Showing posts with label diagnosis. Show all posts
Showing posts with label diagnosis. Show all posts

Peritonsiler abscess (PTA / Quinsy) 9


COMPLICATIONS
Complications that can arise in the abscess is peritonsiler (Fachruddin, 2002):
1. Spontaneous abscess rupture, causing hemorrhage, or pulmonary aspiration pyernia.
2. Spreading infection and abscess to the area, causing parafaring abscess parafaring.
3. If there is spreading to the region may lead to intracranial sinus thrombus Cavemosus, meningitis and brain abscess.
4. Nephritis, peritonitis, mediastinitis.

PROGNOSIS
Most of the patients treated with antibiotics and adequate drainage in the area will return abscces recover within a few days. A small percentage of complaints indicates a further abscess, and it is necessary tonsilektomi action. In addition, if the patient reported back pain throat complaints that persist after incision and drainage is appropriate, action may be indicated tonsilektomi (Gosselin, 2008).

CONCLUSION
1. Peritonsiler abscess (PTA) is an infection that occurred in the area - the area around tonsila Palatina caused by aerobic and anaerobic bacteria.
2. Pathophysiology of PTA is certainly not known, but one thing is widely agreed that the occurrence of an abscess is associated with inflammation of the tonsils previous events.
3. Management is done in cases of abscess peritonsiler with adequate antibiotics when the stadium infiltrates. Arise when the abscess is incision and should be followed by drainage tonsilektomi action.
4. Complications that can arise due to inadequate handling and complete. As if there is an appropriate treatment, the prognosis would be good then.
Read More - Peritonsiler abscess (PTA / Quinsy) 9

Peritonsiler abscess (PTA / Quinsy) 7


DIAGNOSIS
Information from patients is needed to make the diagnosis peritonsiler abscess. Patients had a history of pain in the esophagus is one that supports peritonsilar abscess. History of acute pharyngitis and tonsillitis accompanied by a lack of comfort in unilateral pharingeal (Steyer, 2007).
The diagnosis is rarely in doubt if the inspector saw a large swelling peritonsilaris, pushing past the midline uvula, with edema of the palate molle and protrusion of tissue from the midline. Palpation if possible to distinguish abscess from cellulitis (Adams, 1997).
In the investigation can be done:
1. Laboratory tests such as complete blood, electrolytes, and blood culture. Which is the "gold standard" for diagnosing abscess peritonsilar is by collecting pus from the abscess using a needle aspiration (Jevuska, 2007).
2. Radiological examination in anteroposterior position only shows "distortion" of the network but not useful for certain locations who abscess (Daley, 2007).
3. On CT scan can be seen on the tonsils hipodens areas that indicate the presence of fluid in the affected tonsils besides that it also can be seen in an asymmetrical enlargement of the tonsils. This examination can help to plan the operation (Daley, 2007).
4. Ultrasound, a technique is simple and noninvasive and can help in distinguishing between cellulitis and the beginning of the abscess. This examination can also determine a more focused selection before surgery and drainage for sure.
Read More - Peritonsiler abscess (PTA / Quinsy) 7

Peritonsiler abscess (PTA / Quinsy) 4


Some microorganisms that can cause acute or chronic tonsillitis can also be a PTA-causing organisms. Aetiology peritonsiler abscess most frequently encountered is a species of aerobic and anaerobic gram-positive are usually found in the culture, usually bacterial beta-hemolytic Streptococcus group A. The next most common is from Staphilokokus groups, pneumococcal, and Haemophilus. And other microorganisms that can be found in the culture including Laktobasillus, groups such as filamentosa shaped Actinomyces sp., Mikrokokus, Neisseria sp., Diphtheria bacteria, Bacteroides sp., And some bacteria other non-sporulation (Gosselin, 2008). Sometimes the infection continues to be tonsila cellulitis difusa of the palate extends tonsila mole. Continuation of this process causes abscesses peritonsilaris. These disorders can occur quickly, with the beginning of tonsillitis, or the end of the course of the disease of acute tonsillitis. This can happen even if given penicillin. Usually unilateral and more frequently in children older and younger adults (Adams, 1997).
Read More - Peritonsiler abscess (PTA / Quinsy) 4

how to choose baby's sex? 1


As a newborn, the first question most asked is: 'baby is a boy or a girl? "Genital appearance to answer what the baby gender. The term 'sex' refers to biological differences between men and women; the term 'gender' refers to the social status that distinguishes men and women. Generally assumed the position of gender in social behavior (Stewart, 1999).
A thousand years ago, has noted that the man had tried and wanted to choose the sex of the child. Efforts are made through traditional ceremonies, mostly superstitious and magical practices, and others mask shallow knowledge.
Likewise feeling anxious to failure because not getting the sex of the child who is expected to be the problem since time immemorial.
Medically, selecting the sex of the baby is very possible. Even with knowing the nature of sperm, a more practical effort can be done individually by the husband-wife (Hasuki, 2006).
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hypertension crisis 5 DIAGNOSIS



Knowing the previous history and clinical findings are very important to distinguish between hypertension and hypertensive emergency urgency. Information about previous history of hypertension should include that have been diagnosed, the duration, degree, and control of blood pressure taken. Also find information about the previous history should take precedence in the discovery of the organ - the target organ affected, the situation during hypertension, and findings - that there are other findings.
Some other things that can be asked related to the occurrence of hypertensive crisis:
 Drugs - drugs
- Antihypertensive therapy previously obtained.
- The use of substances - substances "over - the - counter", as an example of a drug - a drug simpatomimetik.
- The use of drugs - drugs such as cocaine.
 Date of last menstrual
 other health problems (ex: hipertens earlier, thyroid disease, Cushing's syndrome, systemic lupus, and kidney disease).
 assessment of complaints that lead to hypertension crisis clinical findings:
-  chest pain of ischemic heart muscle or myocardium
- Back pain  aortic dissection
- Difficulty in breathing  pulmonary edema or congestive heart failure
- Symptoms - anxiety symptoms  neurologist, vision problems, level of chaos that changes - change (hypertension enselopati)
Physical examination should be given priority on things - things that can explain the crisis of hypertension in the emergency situation.
 Alerts - vital signs
 blood pressure should be measured in standing and sitting position (if possible  assess whether or not the volume depletion
 blood pressure should also be measured on both arms  significant differences leading to the aortic dissection.
Funduskopi examination may include changes that are consistent from chronic hypertension. Acute changes include arterial spasm (focal or diffus), retinal edema, bleeding in the retina (surface and shape as a tongue of fire, or deep and wide), exudate in the retina (hard or like cotton wool), or papiledema.
Examination focused on the cardiovascular whether there is a sign - a sign of heart failure (such as the lungs ronkhi voice, increased jugular venous pressure, askultasi emergence of S3 in the heart, and peripheral edema) or aortic dissection. Results further possibility of compensation can occur from an artery that is usually caused by a decrease in pulse rate, and this may result in ischemic brain, muscles, or digestive tract. Additional sound new murmur or mitral insufficiency penigkatan than may sound as a result of increased left ventricular afterload.
With the heart - the heart, neurological examination can directly explain the sign - a sign that will soon happen / is happening. Symptoms often arise as a result of hypertension among other enselopati, disorientation, decreased level of consciousness, and in some cases focal neurological deficit or seizures comprehensive or specific focal only. Enselopati hypertension is a stand-alone diagnosis, where the existence of other lesions (cont: stroke, subarachnoid hemorrhage, mass lesions) could be set aside. This is possible because of cerebral edema caused by the loss of autoregulation of cerebral blood vessels that appear because of hypertension weight.
The laboratory should be done immediately upon discovery of clinical symptoms and explain the important results for the ongoing situation. Routine blood tests can determine the presence or absence of mikroangiopati hemolytic anemia. Examination of urine can also indicate a hematuri, proteinuri or sediment on the state azotermia or kidney failure. Urine examination to determine the levels metanefrin can also be done to eliminate the possibility of pheokromositoma. Increased levels of serum urea and creatinine, metabolic acidosis, and hypokalemia can be seen on the blood chemistry tests which can indicate a decrease in kidney function. Aldosterone levels and plasma rennin can also be examined to rule out the existence of primary hiperaldosteronism in patients with significant hypokalemia previously not received diuretic drugs at the time of attack .. Hypokalemia which is the description of secondary aldosteronism, is at approximately 50% of patients with hypertensive crisis. In patients with elevated blood pressure due to natriuresis, serum sodium levels are usually lower than the state of primary aldosteronism. This happens because the increase in hydrostatic pressure peritubuler kidney-related increase in arterial pressure. This Natriuresis causes a secondary decrease in sodium reabsorbsi. Laboratory tests that can be done as an alternative to support the diagnosis of hypertensive crisis, among others, toxicology tests, pregnancy testing, and endocrine examinations.
Hipertropi the left ventricle and changes associated with ischemia or infarction can be seen on electrocardiography examination. Photo roentgens thoracic show evidence of heart enlargement, pulmonary edema, or a widened mediastinum, where it all can lead to aortic dissection. In addition, to further strengthen the suspicion of aortic dissection, can be performed chest CT examination, transesofageal ekhokardiografi, or with aortic arteriogram. Ekhokardiografi two dimensions can be used to distinguish pure diastole dysfunction of the heart during systole dysfunction sign - a sign of heart failure appear. All this may help in determining the therapy given and the provision of long-term therapy.
Head CT scan can be performed on patients with symptoms of neurological disorders. Sign - a sign that may arise from this investigation, among others, brain hemorrhage, brain edema, or ischemia in the brain.
In the end, it is important to determine the cause of secondary hypertension (eg hypertension renovaskular) which may cause the crisis. Test with a single dose of captopril may be given, especially in patients who did not receive drug therapy for hypertension before. Aktvitas levels of plasma rennin known in advance and then the patients were given 25 to 50 mg of captopril, 60 minutes and then re-examined rennin levels. The sensitivity value is a good test, but for very low spesifisitasnya. For further examination, such as Doppler ultrasound, MRI renal angiography, angiography with contrast, may be done to better diagnosis.
Using Skrening captopril test for secondary causes of the crisis of hypertension:
METHOD
o Patients receive adequate intake of salt and not getting a diuretic drug.
o Stop all hypertension medications three weeks before the test, if possible.
o The patient is seated at least 30 minutes, take blood samples and determined aktvitas levels of plasma rennin.
o captopril 50 mg diluted in 10 ml of water, the patient should immediately take the solution.
o After 60 minutes, take back the blood sample and measured re-elevated levels of plasma rennin.
INTERPRETATION
Expressed a positive test if:
 There was elevated levels of plasma rennin or more 12 ng/ml/jam.
and
 absolute increase in plasma rennin levels of 10 ng / ml / hour or more.
and
 Increased levels of plasma rennin > 150 % or > 400 % if the lower threshold value of plasma rennin levels were < 3 ng / ml / days.
Read More - hypertension crisis 5 DIAGNOSIS

cancer lungs: 11 Prognosis


A. Small Cell Lung Cancer (SCLC):
 With a change therapy in the past 15 - 20 years the possibility of life on average (median survival time) who had < 3 months increased to 1 year.
 The possibility Disease Limited group average life up to 1-2 years, while 20% of it remained alive in 2 years.
 30 % died because of local complications of the tumor.
 70 % died of carsinomatosis.
 50 % metastasize to the brain (autopsy)

B. Non-Small Cell Lung Cancer (NSCLC):
 Most important in the prognosis of lung cancer is to determine the stage of the disease.
 Compared with other types of NSCLC, karsinomaskuamosa not as bad as others. In patients who performed surgery, the possibility of life after 5 years was 30 % surgey.  Survival after surgery, 70 % on Occult carcinoma; 35 - 40 % in stage 1; 10 - 15% in stage II and less than 10 % at stage III.
 75 % of squamous carcinoma died of complications torakal, 25 % because of the extra torakal, 2 % of them died because of the central nervous system disorders.
 40 % of adenocarcinoma and large cell carcinoma died of complications torakal, 5 for 55 extra torakal.
 15 % of adenocarcinoma and large cell carcinoma metastatic to the brain and 8 - 9 % die from central nervous system disorders.
 The possibility of life on average tumor metastases patients varies from 6 months to 1 year, where it is highly dependent on performance status (Karnofsky scale), extent of disease, the weight loss in the last 6 months.
Read More - cancer lungs: 11 Prognosis

cancer lungs: 10 DIAGNOSTIC PROCEDURES

A. Photo chest roentgens in Posterior-anterior (PA) and lateral
Simple initial examinations that can detect lung cancer. Mayo Clinic Study of the USA, found 61 % of lung tumors were detected in routine examination with normal chest roentgens images, whereas sputum cytologic examination can detect only 19 % . In lung cancer, breast examination roentgens photo also necessary to re-evaluate its doubling time. Reported that most lung cancer has a doubling time of 37 - 465 days. When the doubling time> 18 months, mean tumor benign. The signs of other tumors are benign lesions, concentric spherical, solid and calcification of the firm.

Inspection photos chest roentgens tomography more accurate ways to support the possibility of lung tumors, when the usual way breast images can not confirm the presence of tumors. Investigations another radiologist who sometimes is also necessary bronkografi, fluoroscopy, superior vena cavografi, ventilation / perfusion scanning, ultrasound sonography.

In photos roentgens primary lung cancer can be seen as a solitary round shadow or cause the collapse of a lobe due to bronchial tumor block. Early cancer can be very small and irregular shape, but usually will be fine when growing up. While the picture radiologist for secondary lung tumors does not indicate where the location of the primary tumor.

B. Examination Computed Tomography and Magnetic Resonance Imaging

CT scan at thorax, more sensitive than normal chest image examination, because it can detect abnormalities or nodules with a minimum diameter of 3 mm, although false positives for abnormalities of this magnitude can reach 25 - 60 %. If this facility possible, a CT scan could be a second screening examination after normal chest images. Magnetic Resonance Imaging examination (MRI) is not routinely done, because he is limited to assessing the invading tumor abnormalities in the vertebrae, spinal medulla, the mediastinum, in addition to cost is also quite expensive.

MR examination thorax not superior to CT scan thorax. We are developing a technique that is more accurate imaging of Positron Emission Tomography (PET) can distinguish benign and malignant tumors based on differences in metabolism of biochemical substances case of glucose, oxygen, proteins, nucleic acids. Examples of substances used methionine 11 C and F - 18 fluorodeoxyglucose (FD6).

Tumors less than 1 cm, somewhat difficult to detect because of the small size is less resolusion by PET Scanner. Sensitivity and specificity reported how PET is 83-93% 60-90% sensitive and specific.

Some false positives to be found also a sign of malignant lesions such as inflammation and infection and tuberculosis aspergilosis. Although it is known from several studies PET examination has better accuracy values than CT scans.

C. Inspection of Bone Scanning

This examination is required if the expected signs of metastases to the bone. Tumor incidence of non small cell lung cancer (NSCLC) to bone was reported by 15 %.

D. Sputum cytology examination

Sputum cytology examination is done routinely, especially when patients have complaints such as cough. Cytologic examination does not always give positive results because it depends on:
 Location of tumors of the bronchus
 Type of tumor
 Engineering issued a sputum
 The number of sputum examination. Examination is recommended 3 - 5 days in a row
 When sputum examination (sputum must be fresh)

In lung cancer, which is central to good sputum examination can give positive results up to 67 - 85 % in squamous cell carcinoma. Sputum cytology examination is recommended as a routine examination and screening for early diagnosis of lung cancer, and they are developing early diagnosis using sputum examination staining with immune MAB with antigen antibody 624 H 12 for SCLC (small cell lung cancer) and 703 D4 antibodies to antigens NSCLC (non small cell lung carcinoma). Reports from the National Cancer Institute USA this technique gives results 91 %, 88 % sensitive and specific.

Other cytologic examination for lung cancer diagnostics can be performed on pleural fluid, aspiration of cervical lymph nodes, supraklavikula, rinse and bronchus on bronchoscopy sweep.

E. Histopathology examination

Histopathologic examination is the gold standard for diagnosis of lung cancer to obtain biopsy specimens in a way through:

Bronchoscopy. Modification of fiber-optic bronchoscopy may include:
 Trans bronchial lung biopsy (TBLB) with the demands of fluoroscopy or ultrasound.
 Recently fuorescence examination was developed by using fluorescence bronchoscopy exchanging agent such as Hp D (hemato porphyrin derivate) gave fluorescence concentrates in cancer tissue. The newer technique is to auto fluorescence bronchoscopy. The results of this examination showed 50% more sensitive than white light bronchoscopy for detection of carcinoma in situ and severe dysplasia.
 Ultrasound bronchoscopy, also developed at this time to detect peripheral tumors, endobronkial tumors, lymph node lesions of the mediastinum and hilar regions.
 positive result with bronchoscopy can be reached: 95 % for centrally located tumors and 70-80% for tumors of peripheral location.
 Trans-bronchial-Needle Aspiration (TBNA). Working against lymph nodules in the hilar or mediastinal. The result will be better when guided by CT scan.

How to examination by bronchoscopy is to insert a tube pipe flexible bronchoscope into the airways. In this way doctors can look inside the lungs and lung tissue samples taken for laboratory examination.


Trans Torakal biopsy (TTB)
If the patient has cavities fluid in the lungs, the doctor may take a sample by inserting a thin needle into the chest between the ribs. Fluid is then examined in the laboratory, to see whether or not cancer cells. Raised a number of liquids with a biopsy or torasentesis can also improve breathing.

Biopsy with TTB especially for lesions located peripheral to the size of < 2 cm sensitivity reached 90 - 95 %. Complications pneumothorak can reach 20 - 25 % and haemoptysis up to 20 %. With better preparation, these complications can be minimized. Examination results will be better if there is demand for CT scans, ultrasound, or fluoroscopy. Biopsy of lymph nodes palpable, can be done in Daniel's biopsy of the lymph-nodes scalaneus supraklavikular. Torakoskopi. Biopsy of the tumor in the pleura give better results than by way torakoskopi blind (blind). For tumors located on the surface of the pleural biopsy with the way visceralis Video Assisted Thoracoscopy has a sensitivity and specificity to 100 %, whereas complications occur is very small. Mediatinoskopi. More than 20 % of lung cancers metastasize to the mediastinum, especially Small Cell and Large Cell Ca Ca. to obtain tumor metastases or lymph nodes involved can be done by mediastinoskopi where mediastinoskopi inserted through the supra-sternal incision. This can help assess how far the cancer has spread and whether the operation is wise choice to remove the tumor. Biopsy results positive value 40 %. From other studies on the false negative values obtained mediastinoskopi of 8 - 12 (followed by Thoracotomy).

Thoracotomy for lung cancer diagnostic procedures done when non-invasive and invasive previously failed to find tumor cells.
Read More - cancer lungs: 10 DIAGNOSTIC PROCEDURES

cancer lungs: 9 Early Detection


Complete anamnesis and thorough physical examination is the key to proper diagnosis. In addition to clinical symptoms mentioned above, several factors need to be considered in patients with suspected lung cancer, including: factors of age, smoking habits, a history of cancer in the family, exposure to carcinogenic substances or exposed to the fungus, and infections that can cause solitary pulmonary nodule. Finding lung cancer at an early stage is very difficult because at this stage there are no complaints or symptoms. The size of tumors at early stages is relatively small (<1cm)> 40 years, smoking> 1 pack per day and / or working in polluted environment that allows happens lung cancer (factory paint, plastic, asbestos, etc.) . Research conducted by the NCI on cancer research center 3 for> 20 years of more than 30,000 volunteers male heavy smokers, where half undergo intensive screening with sputum cytologic examination every 4 months and chest roentgens images (PA and lateral) of each year and a half other as the control group. The results of this study showed a positive early-stage tumors in the first group of 45% and 15% in the control group. Patients with lung cancer has a 5-year rate of survival by 35% compared to the control group 13%. In this study, examination of malignant cells by cytologic examination of sputum more easily find squamous cell carcinoma, while the image more chest roentgens found adenocarcinoma and squamous cell carcinoma. Small cell carcinoma rare detected in early stages. Overall the study concluded that there is a positive value (benefits) in the early detection of lung cancer.
Read More - cancer lungs: 9 Early Detection

skin; verruca 5 Veruka and Malignancy


Diagnosis Banding
Verruca plantar must be distinguished from regions where lesions callositis waxy, thick, yellowish and there are no capillaries in the peel. Cron occur in places affected by pressure and are usually smaller and pain with blockage in the middle.
Veruka Plana should be distinguished liken Planus which shows a purplish and diskolorasi Wickham stria. Planus liken lesions usually associated with itching and certain mucosal lesions.
Nevus epidermal similar verruca digitata or verruca filiformis. Molluscum contagiosum lesions are white with papul seen umbilikasi or in the middle of the curve.

Verruca and Malignancy
Verruca benign in individuals imunokompeten almost never become malignant. There are a few reports of lesions that begin as verruca and later became squamous cell carcinoma is invasive. The combination of verruca periungual with genital HPV disease should be special attention.
Verukous many lesions occur in individuals with immunosuppression and in patients who receive organ transplants is about 50% of patients with renal transplants develop into verruca, five years after transplantation. Exposure to sunlight increases the incidence of lesions verruca and act as kokarsinogen. Changes displasi almost certainly happen and very little relationship between the clinical symptoms with the histological picture. The lesions are a particular form of the virus verruca, Keratosis Bowenoid or diesel or keratoakantoma or squamous karsinomata. Some types of HPV have been found in benign squamous lesions and malignant in patients with immunocompromise and a role in the initiation and progression of malignant processes.
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skin; verruca 4 diagnosis


Special forms

Epidermodysplasia verruciformis
Epidermodysplasia verruciformis is inherited disorder in which there are subtle defect-mediated immunity by cells and is an area of HPV infection and persistent. Lesion is very diverse forms, can be flat, resembling verruca lesions, macular hyperpigmentation, red, or atrophy, or plaque-like Pityriasis versicolor. Flat form and which resemble lesions frequently located in verruca extremities and face and a thicker plaque can mimic seboroik Keratosis. Lesions found to contain many types of HPV that cause verruca including Plana, but some types that do not cause disease in normal individuals. There is a risk of developing into squamous cell carcinoma of the skin exposed to the sun (sun-exposed).

Bowenoid papulosis
Also known as intraepitelial neoplasms of the vulva, penis, and anal (NIV, NIP, NIA). Bowenoid papulosis appears as a small papul, usually multiple, sometimes located on the surface of pigmented mucosa and skin in the anogenital region of both sexes. Usually found in young adults but no association of age and there is a strong relationship with HPV type 16 infection.

Focal epithelial hyperplasia
Also known as Heck's disease, is a rare benign lesions, which reduced noise without gender predisposition. Lesions characteristic of multiple noduler firmly bounded on the oral mucosa. The disease is usually found in native Americans and the Inuit in Greenland, is reported rarely found in other countries. HPV types 13 and 32 as an agent cause in patients with genetic predisposition.

Epithelioma carcinoma cuniculatum and verukosa
Epitelioma kunikulatum a squamous cell carcinoma appears as mass with a smooth consistency bulbus software on your feet. Multiple sinus open to the surface and when pressed, the lesions become like a giant plantar verruca, but the difference between rapid growth and local invasion.
Verukosa carcinoma developed in the cavum of oral and genital mucosal lesions, and look like cauliflower.

Diagnosis
Verruca diagnosis is established based on clinical examination but can also be supported by the histological picture of epidermal acanthuses with papillomatosis, hiperkeratosis, and parakeratosis with a protrusion and grooves in the middle of verruca. Dermis capillaries protruding and blood clot blockage. There are a wide keratinocytes with eccentric piknosis cell nucleus surrounded by a halo perinuklear (koilosit is characteristic of papilloma associated with HPV). HPV-infected cells had few granules and a lump of eosinophils keratohialin basofilik granules. Verruca Plana acanthuses only slightly and does not occur hiperkeratosis and parakeratosis or papillomatosis.
Characterization of HPV is very little done, but useful in some cases of genital verruca in children with suspected sexual abuse. Knowledge of the genotype of HPV in benign verruca therapy does not affect the election.
Read More - skin; verruca 4 diagnosis

treat melasma : 8 diagnosis


Melasma Diagnosis
Melasma diagnosed only with clinical examination. To determine the type of melasma, Wood-ray examination is done. While the examination histopatologik only done in some cases.

Melasma Diagnosis Letter
a. Addison Disease
Addison disease is a disease caused insufiensi adrenal, where the increase occurred between kortikotropin and MSH, which is marked by symptoms that are often not typical, such as stiff-stiff, weak, anoreksia, Nausea, stomach aches, Gastroenteritis, diarrhea and emotions that are not stable. Insufiensi adrenal is triggered by infection or destructs autoimmune nonspecific on the adrenal gland. Diseases that often cause infection of Addison disease is tuberculosis. There is destructs cortex adrenal cause feedback inhibition hypothalamus gland and anterior pituitary lost, the consequences kortikotropin sekresi ongoing. Kortikotropin MSH and progenitor of both components is the same hormone. When kortikotropin parsed from prohormon, together with the MSH released. Consequences arising hiperpigmentasi crimson / bronze (Bronze hyperpigmentation) that way.
b. Drug induced photosensitivity is kutaneus disease as a result of the combination of chemical reaction and light, where the actual exposure of one of them does not cause disease. This disease is usually because of drugs or chemicals or systemic topical.
c. Discoid lupus eritematous (LED) is a disease that attacks the system connective and vascular caused autoimmune process and the interaction between genetic factors and immunologic, virus infection and hormonal. LED going on which The speck in the skin eritematosa and atrophy without ulserasi. Deviation localise usually symmetrical in the face, ears or neck.
d. Hiperpigmentasi post-infection occurs after inflammation of the skin. Aberration is very common and tend to settle on the dark skin. The clinical hiperpigmentasi can be found following the pattern and distribution of skin disease.
e. Efelid aberration is a form of skin The speck-The speck of black or brown in areas exposed to sunlight. It was revealed that familial factors are autosomal dominant, and usually occurs in the summer. Localization on the face, neck, shoulder, back and hands.
f. Ookronosis the pigment in the dermis hill that often occur because the stack metabolite hidrokuinon in the dermis.
Read More - treat melasma : 8 diagnosis

juvenil diabetes: 10 handling


Handling

Diabetes mellitus, if not managed properly can lead to the occurrence of various chronic diseases, such as serebrovaskuler disease, coronary heart, blood vessel leg, eye disease, kidney and nerve. If the blood glucose level can always be better, hopefully all the chronic difficult can be prevented, at least resist.
Manage diabetes mellitus in the short term objective is the complaints / symptoms and to maintain healthy and feeling comfortable. For the longer term, more objective, namely to prevent penyulit, both makroangiopati, mikroangiopati and neuropati, with the final goal morbiditas reduce mortality and DM.
To achieve this, various efforts made to improve metabolik aberration that occurred in DM patients, such as deviation of blood glucose, lipid, and various aberration that also affect the achievement of long-term goals, such as blood pressure and body weight.

Main pillars of the management of Diabetes mellitus:
1. Education
Education initials are important both in making families feel safe and able to deal with insulin injections, blood glucose test, test keton urin, hipoglikemia, and other penatalaksaan they should do. This usually requires the presence of both parents for about 3 days (but depending on the speed of learning).

2. Diet / medical nutrition therapy
Medical nutrition therapy is a therapy that is non farmakologis recommended for the diabetisi. Medical nutrition therapy, in principle, this is a pattern of eating that is based on the nutrient status diabetisi and diet modifications based on individual needs.
Goals of nutrition therapy for patients with diabetes mellitus type 1 is:
- Maintaining the blood glucose level near normal with the way insulin therapy on dietary patterns of each individual exercise and physical activity.
- Obtain blood pressure and lipid content is optimal.
- Provide enough calories and maintain ideal body weight, growth and development is normal.
- Reducing risk factors and prevent the occurrence of complications, both acute (hipoglikemia, a disease not related to diabetes), chronic (hypertension, hiperlipidemia, kidney disease, kardiovaskuler disease, complications, and other micro and makrovaskuler).
- Improving health with the selection of the appropriate type of food.
Planning must be adjusted according to the eating habits of each individual. Number of entries calorie foods that come from carbohydrate is more important than the source or type of karbohidratnya.
Standard is recommended that food with the composition:
- Carbohydrate: 60-70%
- Protein: 10-15%
- Fat: 20-25%
Exchange system created in 1950 by the American Dietetic Association, the American Diabetes Association, and the U.S. Public Health Service used as a tool to control your diet, and indicate the type of food that can be consumed by diabetic patients. Category of food that enter into the exchange system is divided into 6 groups: rice / bread, meat, vegetables, fruit, milk and fat. Each portion can be because it contains nutrients that are similar in the amount of calories, carbohydrates, protein and fat.
Now five years of data available to show that glucose control in children who get a diet "sugar limited" freedom to eat food with other appropriate taste, diet versus an exchange of special American Diabetes Association (initially developed to control body weight and are still useful when the body weight is a problem). If you use the exchange diet, calorie Feed 24 hours is calculated as 1000 kkal plus the additional 100 kkal per year until 2500 kkal age. Calories are usually divided into 55% from carbohydrate, 20% of the protein, and 25% from fat. Snack is provided at the time of peak insulin activity, or before exercise to prevent hipoglikemia (usually 3-4 hours in the afternoon and sometimes at 10-11 pm) and dense snack containing protein and fat should be consumed consistently before bedtime to prevent hipoglikemia nokturna.

3. Insulin
Most children with medium or heavy ketonuria is not asidosis and so does not suffer dehydration requiring fluid therapy intravena, beginning diterapi (treatment is usually the way) with regular insulin intramuskular (per hour) or sub kutan (every 2-3 hours) with a dose of 0,1-0,2 units per kg body weight. If ketonuria is reduced, a mixture of regular insulin with insulin starts working long with dose 0,5-1,0 units per kg (total dose) per 24 hours. When there is no ketonuria at the beginning, usually indicates insulin endogen production of larger, initial dose is usually 0,25-0,5 units per kg body weight per 24 hours. Duapertiga of the total dose is usually given in the morning and 1 / 3 in the afternoon, more good 30-60 minutes before eating. Children under the age of 4 years and usually only need ½ to 2 units of regular insulin, children aged 4-12 years old need 1-5 units of regular insulin, and puber children need 5-10 units of regular insulin. The remaining doses of insulin given as a long-term. Doses are usually strictly monitored through the first week on the phone and dititrasi appropriate monitoring of blood glucose at home. At puberty, insulin dose increased in general and can reach up to 1.5 units per kg body weight per 24 hours. (11)
Method infus intravena low dose continuously, where the main dose of 0.1 U / kg regular insulin, followed by a infus constant 0.1 U / kg / hour. This method is effective, simple and easy to understand the physiological, and has received wide as insulin delivery method is selected during ketoasidosis. This measure provides a continuous insulin in plasma is steadily approaching the peak reached in normal individuals during oral glucose tolerance test. Presumably, the same steady level attained at the cellular level and allows the response metabolik steady without fluctuations that have occurred in the insulin injection in snatches. Worries that the insulin can be attached to the glass and the pipe was not based, and effective delivery of insulin can be given without the use of albumin or gelatin is added to the infusat. Moreover, insulin can be given infus drops with gravity without the use of special pumps, pumps, although such help. Set infus to insulin associated with a separate pipe infus used for fluid and electrolyte therapy recommended dose adjustments so that each can be separately .. After the amount of insulin for the first 6-8 hours is calculated, this amount is added to the bottles 250-500 ml 0.9% physiological salt.

Farmakokinetik the insulin used
Type of Insulin ONSET drug peak time duration drug effects
Lispro, aspart, glulisine 5 - 15 minutes 45 - 75 minutes 2 - 4 hours
Regular 30 minutes ± 2 - 4 hours 5 - 8 hours
NPH ± 2 hours 6 - 10 days 18 - 28 hours
Insulin glargine ± 2 hours There is no peak of 20 -> 24 hours
Insulin detemir ± 2 hours There is no peak of 6 - 24 hours
4. Sports / physical training
Patients with diabetes, physiological response, depending on the sport at the time of the plasma insulin level at the time. This response increase the risk of a patient on hypoglycemia especially when doing physical activities, the more weight in terms of intensity, duration and frequency.
Children who follow sports require monitoring of blood glucose level is greater (before, after, and when doing activities that are in long time) and giving the right dose of insulin.
In the child with a dose of insulin that remains, should be given a snack before exercise. Some children even require additional carbohydrate after exercise because the exercise intensity can affect the blood glucose level due to increased release katekolamin, so that often occur during sports hypoglycemia if not traet as above.
In the patients who use insulin pumps, insulin infuse value given should be reduced 30 to 70% for physical activity to prevent hypoglycemia.
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juvenil diabetes: 9 Diagnosis


Diagnosis

Children who have diagnosed diabetes mellitus, for the purpose of simple can be divided into three general categories: (1) people who have a history of diabetes impressive, especially poliuria with polidipsia and failure to increase body weight despite a high appetite, (2) those who are suffering while glukosuria or settle, and (3) those who have clinical manifestations acidosis metabolic with or without stupor or coma. In all cases the diagnosis diabetes mellitus depending on the hiperglikemia associated with glukosuria with or without ketonuria. When symptoms of classic poliuria and polidipsia accompanied with hyperglycemia and glukosuria, glucose tolerance test is not required to support the diagnosis.
The findings glukosuria with or without hyperglycemia level of light entering the hospital during the trauma or infection, or even increased during the emotional connection is usually not indicate the existence of diabetes, in most circumstances this glukosuria less during healing. Because this condition may indicate a limited capacity to sekresi insulin, which appear by increasing stress hormone plasma level, patients should be re-checked for possible tommorrow hyperglycemia or clinical signs of diabetes mellitus. On this condition, glucose tolerance test should be conducted several weeks after recovery from acute illness by using a glucose loading dose adjusted to body weight. Evidence shows that this test may be abnormal in most of HLA-DR3 and HLA-DR4, and they have the antibody cell islands or autoantibodi insulin detected.
Screening procedures such as determination of blood glucose after eating (postpandrial) or oral glucose tolerance test has detected a low number on the child, even on those who are considered at risk even though, such as sibling children diabetic. Because screening procedure is not recommended in children.
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juvenil diabetes: 8 clinical manifestation

Clinical manifestation
Clinical manifestation of diabetes mellitus is associated with the consequences metabolic deficiency insulin. Patients who have insulin deficient can not maintain the fasting plasma glucose level is normal, or glucose tolerance after carbohydrate meals. If hiperglikemy severe kidney and exceed the threshold, then glukosuria arise. Glukosuria this will lead to diuresis osmotic the expenditure increase urine (poliuria) and emerged feeling thirsty (polidipsia). Because glucose lost with urine, the patient experienced a negative calorie balance and body weight decreased. Hunger is the greater (polifagia) will may arise as a result of the loss of calories. Patients complain tired and nod.
Purulent skin infections and vaginitis in girls monilia teens sometimes arise at the time of diabetes diagnosis. This infection is a rare clinical manifestation of diabetes only in children, and a thorough history will always show the poliuria and polidipsia. Ketoasidosis often cause some early (around 25%) diabetic children. Initial manifestation may be relatively minor and consist of vomiting, dehydration and poliuria. In the case of longer and heavier, the Kussmaul breathing, and no smell aseton on brething. Stomach pain or stiffness can have and can resemble appendicitis or pankreatitis. There was a bluntness brain and eventually coma. Laboratory findings, including glukosuria, ketonuria, hiperglikemia, ketonemia, and asidosis metabolik. Leukositosis is prevalent, and amilase can increase serum nonspecific; serum lipase is usually not increased. On those with the stomach aches, pain can not be assumed that the findings of this evidence is the need for emergency surgery before the therapy fluid, electrolyte, insulin has been tried according to correct dehydration and acidosis; manifestation stomach often lost after a few hours in treatment.
After starting the insulin therapy, type I diabetics may experience ketoasidosis if they pass a one-time inject insulin due to stress or infection, accident or serious illn

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juvenil diabetes: 2 etiology


Epidemiology
DM is a disease with great consequences to health and social. Not only because of the high prevalence of complications, but because cronic and a high death rate.
Prevalence of DM in the world continues to increase. In 1995, prevalence 4.0%. In the year 2025 is estimated to be 5.4%. In developing countries increased prevalence is more light. In 1995 it was found 84 million cases of DM and in the year 2025 this figure will increase to 228 million.
The occurrence of diabetes was 7 years before diagnosis, so morbidity and early mortality occurred in cases that are not detected.

Etiology and Pathogenesis
Developments in understanding the etiology and pathogenesis DM revitedthe previous classification. Although all types of DM by the hyperglycemia, but pathogenesis occurrence hyperglycemia very different. 2005 American Diabetes Association (ADA) to make the classification, the diabetes is type 4, among others, type 1 DM, type 2 DM, type DM, and DM in pregnancy. Diagnostic criteria of DM, according to the ADA in 2005 is:
1. When blood sugar 200 mg / dl if the typical complaints,
2. Fasting blood sugar 126 mg / dl.
3. Plasma glucose level 200 mg / dl at 2 hours after glucose load at 75 grams TTGO.
Diabetes mellitus is not a single form, but presumably is a heterogeneous group of aberration is the difference between the pattern and the genetic mechanism and etiology patofisiologi other disturbances that cause glucose tolerance. National Diabetes Data Group has put the classification category and diabetes glucose intolerance based on the knowledge of the present. This classification has been accepted and supported by various diabetes associations around the world by researchers and Pediatrics. Three main forms of diabetes and some forms of carbohydrate intolerance were identified: Type I Diabetes (Diabetes mellitus Juvenil), type II diabetes, and secondary diabetes.
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hiv - aids 7 diagnosis


Diagnosis
Some of the diagnostic steps that can be done on a baby suspected of HIV infection obtain the mother pregnant. (Pusponegoro, 2004)

anamnesis
• Historical mother user of drugs including drug through the blood vessel.
• Historical mother receiving a blood transfusion or components, and without the filter of HIV test
• Historical aberration sexual orientation and behavior in the mother (female bisexual)
• Historical imunologis mother with a bad response.

Physical examination
Neonatus on clinical symptoms can be:
• BBLR or fail to grow.
• Infection channel repeated breath, otitis media, sinusitis, sepsis, monoliasis repetitive, sometimes happens nonspesifik infection with symptoms hepatosplenomegali, limfadenopati, and fever.
• Disturbance of progressive motor

Examination support
• CT-Scan  not have to see kalsifikasi basaltic ganglia and atrofi on korteks serebri.
• HIV antibody inspection  in children> 18 months, declared positive if the IgG anti-HIV (+) with the Blot and ELISA checks. In the infant <18> 95% baby age 3-6 months.
If test HIV, most of the babies born by HIV-positive mothers showed positive results. This means that there is antibody to HIV in the blood. However, the baby receives the mother's antibody, in order to protect the body's immune system so that the form fully. So positive test results in early life does not mean the baby being infected.
If the baby was infected, the body's immune system will form antibody against HIV, and HIV tests will continue to show positive results. If the baby is not infected, antibody from the mother will be lost so that the test results became negative after approximately 6-12 months.
A test other, similar to viral load tests can be used to determine if the baby is infected, usually several weeks after birth. This test, the search for the virus antibody is not, at this time only available in some large cities, and the price is quite expensive. (anonymous, 2007)
Both culture and virus-specific assessment RRP HIV, can be successful in the diagnosis of infection from the list of blood samples fetus. Amniocentesis and has kordosentesis can be done successfully in pregnant women with HIV sero-positive, but the way and time to perform the procedure invasive this problem because the chronology of transmission of HIV is not definitive. There are also concerns about the possibility of transmission to the fetus as a result of the procedure itself, especially kordosentesis. (Parks, 2000)
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Dermatitis 6


Conclusion

1. Dermatitis is inflammation Numularis on the skin lesi in the form of coin or currency somewhat oval, with a firm boundary efflorescence form papulovesikel, usually wet, so easily broken.
2. The cause of dermatitis numularis not clear, is a bacterial infection may etiology basic agent, and the many factors that influence.
3. Histopatologis overview dermatitis numularis; epidermis visible hiperkeratosis, akantosis, edema interselular, and at the end of the dermis occurs blood vessel dilation, and grannulated cells limfosit inflammation and monosit.
4. Generally, dermatitis numularis diagnose based on the description klinisnya.
5. To treat dermatitis numularis, explore possible causes must be first or the factors that influence the occurrence of this dermatitis.
6. Principles of therapy used: antihistamine, corticosteroid, and antibiotics.
7. Disease recurrence is relapse.
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Pankreas 3: Diabetes Diagnostic



DM diagnosis

Terms: 2 times made in the measurement
Fasting glucose level 126 mg / dl is the best index to the value of 2 hour glucose 200 mg / dl = diabetic complications first appear retinopati the diabetic
When in including a high risk category and the results certainly have not done so TTGO DM (oral glucose tolerance test) each year, namely;
1. three days before the test, eating and regular sports
2. fasting 10 - 12 minutes
3. check sugar fasting
4. drink 75 grams of glucose + 250 ml of water and drink within 5 minutes
5. do check GD X 4 ½ hours each
results:
- Well, if the GD 70 - 110 mg / dl
- If value:
<200>dl after 2 hours, including the normal Confirmation TTGO not be done if there are special circumstances such as hyperglycemia DM, acidosis, BB came down fast, etc. DM implementation There are 3 ways:

1. Diet Planning

Namely the search for daily calorie needs in a way:
A. - Use the formula:

BB ideal = [TB cm - 100] - 10%


Reduction of 10% do not apply to the men <160 poor =" <90%" normal =" 90-110%" more =""> 110-120%
Fat => 120%

BB ideal X 30 (men) or 25 (women) = needs basaltic

Daily Needs Needs = Basal + type of work
Light = 10%
Medium = 20%
Weight = 40-100%
Lean patients, pregnant, breastfeeding, grow flowers = 20-30%

B. - Search for integrity without looking at the type of daily activities (dg find RDW% (Relative Body Weight))

BB kg
RDW = ------------------- X 100%
TB -100 cm

Lean = BB X 40-60 kal / day
Normal X 30 = BB
Tallowy X 20 = BB
X = Obest BB 10-15

Example;
Patients 50 kg DM BB, TB 150 cm, how much needs kal / day?

50 kg
RDW = ------------------- X 100% = 100% (normal category)
150 cm -100

So calorie needs per day X 30 = BB
50 X 30 = 1500 kal / day
The proposed menu of food choices;
KH = 60-70%
Protein = 10-15%
Fat = 20-25%

2. Physical Exercise
Exercise method with X CRIPE 3-4 every week
Continuous ongoing = no stop
= Rhythmical contraction and relaxation of regular
Interval = fast and slow lapse of regular cross -
= Progressive training of the light to heavy
Endurance time = survive in a certain time

3. Use of Drugs
a. Group Sulfonilurea
BB is used for normal, often causing hypoglycemia
I work:
- Stimulation of insulin release stored
- Lower threshold sekresi insulin
- Improve insulin sekresi
drug sample;
* Clorpropamid & glibenclamid
- Insufficiency risk of renal and not recommended on the parents
* Tolbutamid & glikuidon
- Both for parents and people with kidney dysfunction and hepar
b. Group Biguanid
used for people with fat and not BB meyebabkan hipoglikemia
I work:
- Improve insulin sensitivity in hepar and perifer
- Decrease in intestinal glucose absorbs
- Reduce the glucose level at the time hiperglikenia
drug sample; metformin

c. Inhibitor α Glukosidase
how it works with preventing α glukosidase down so that the absorption of glucose
example drugs; acarbose

d. Insulin Sensitizing Agent
how to work with insulin to increase sentitifitas
sample drugs; thoazolidinediones


e. Insulin
indication of insulin:
1. DM weight of the BB is going down fast
2. ketoasidosis, acidosis lactate, comma hiperosmolar
3. DM with heavy infection and surgery
4. DM pregnancies that occurred in the uncontrollable
5. not susceptible to the OHO or contraindicate
drug sample;
short work actrapid =
work is being = monotrad, NPH, insulatrad
long work = PZI
mix = mixtrad


Diabetes Complications

a. Comma HYPOGLYCEMIA
coma is due to glucose in the blood is too low.
This is caused by:
1. people with DM in the early stages.
2. DM treatment on:
a. the use of insulin
b. sulfonilurea users (not for biguanid)
c. that the mother of baby DM
3. non-DM patients with history gastrektomi, tumor, Addison disease, liver disease, and others.
There are 2 phases in hipoglikemia
1. aware phase (phase I)
Lack of glucose in the brain activation caused nerve autonomy hypothalamus that result in enzyme release epinephrine giving effect:
- sweat, trembling
- Headache, palpitasi (due to brain glucose down)
2. phase is not aware (phase II)
The least degree of glucose in the blood supply the brain cause metabolic disturbances that result in disrupted function of the brain interference occurs. Characteristics-characteristics:
- The strange behavior
- Sensory of the more obtuse
- Coma

Note:
Somogyi effect: a result of insulin at the time hyperglycemia that are not measurable, so that the hormone increased opposition and improve the regulatory measure glucose in the range hyperglycemia.
Prevention: the provision of glucose is carried out gradually revealed.

Diagnosis hyperglycemia commas:
Enforcement of this diagnosis is based on the Trias WHIPPLE:
1. hypoglycemia with symptoms of the Ssp
2. glucose level <50 dl
3. symptoms disappear with the glucose handling:
1. ABC, rest, then measure GDS
2. if aware of: water solution of sugar
3. if not aware give mucosa cheek with honey / sugar / syrup
4. if you are not aware: infus D40%, 50 ml bolus every 30 minutes to realize, and every day watching GDS
5. if still not aware of the GDS is above normal: manitol 2 mg / kg every 6 hours BB dexametason or 10 mg / kg bolus + BB 2 mg every 6 hours (because of edema suspected cerebri)
6. avoid the high glucose level, because it will aggravate edema. Glucose should level 90-180 mg / dl
7. if the patient has a history with the urea sulfonil of 1-2 mg of glukagon im not will susceptible

b.HYPERGLIKEMIA - The principle of KAD and KHHNK same - Both due to the effect defisiensi insulin:
1. Hiperglikemia
2. Dehydration (due to loss due to diuresis osmotik ion Na, K, P, Mg), ion interference.
3. Hipovolemia, hiperosmolar
4. Lipolisis, asidosis
5. Nitrogen balance is negative because the protein used glukoneogenesis
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