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Question Category:Diagnostic dilemma |
Baby, 10 year old,febrile low grade, marasmic,anemic, distended abdomin, no visceromegaly, chronic constipation, gut sounds audible.
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Question Category:Diagnostic dilemma |
An 8 yr old girl,weight 30Kgs, apparently in a healthy condition, developed low grade fever for 3 days associated with nausea and 3-4 episodes of vomiting. She was adviced ofloxacin and domperidone by a local pediatrician. Fever did not respond well to these medications and a repeat advice was sought and was asked to continue the same. On day 3, she started complaining of 'Burning sensation' in feet and would'nt allow anyone to touch them and would feel comfortable with application of cold. Her extremities were cold & for this unusual complaint, was taken to a hospital where she was admitted for observations and some IV fluids were administered. Two hours following infusions, she developed agitated behaviour and on examination her blood pressure was found to be progressively falling and hence was shifted to ICU. ECG done showed Ventricular tachycardia and despite adequate intervention succumbed to her illness. All her investigations were within normal limits including electrolytes. No history of diarrhea, oligouria, any congenital anamolies, birth injuruies or cardiac complaints , previous hospitalization.
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Question Category:Diagnostic dilemma |
how to differentiate scarlet fever from atypical measles[measles in immunised childeren
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Question Category:Diagnostic dilemma |
child present with dismorphology long phitlum and hypotonia and mental retardation what the syndrome have these feature????
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Question Category:Diagnostic dilemma |
14 year old girl gall stone splenomegaly Hb 7 gm%, Reticulocyte 3.2%, TLC 3,400/cmm, platelet normal, hypochromia (low mch), microcytosis (low mcv), anisocytosis, poikilocytosis, ovalocytosis, RDW abnormally high, LDH abnormally high. ESR 45 mm 1st hour. What may be the probable diagnosis?
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Question Category:Diagnostic dilemma |
A 6 years female child (referred from orthopedics department for ruling out any metabolic disease)presented with progressive left genu valgum since last one year and proportionate short stature.There is past history of jaundice 8 months back for 6 days, mild grade undocumented pyrexia off & on (almost once every month) relieved by one day of antipyretics.There is no history of trauma or joint swelling or pain ever in the affected knee and elsewhere, no history of chronic diarrhoea/constipation. On examination she had severe pallor,abdominal distention, firm splenomegaly, coarse facies (? hemolytic),one cutaneous birth mark (? cafe au lait spot).Left genu valgum,compensatory scoliosis,Limblengths are equal,. Blood Investigations revealed pancytopenia, RF positive. PBF-RBCS are normocytic hypochromic,WBCs- no atypical cells. Ophthalmoscopy- no iridocyclitis.USG abdomen- firm 5cm splenoegaly, liver normal,no ascites. Bone marrow- erythroid hyperplasia with dyserythropoiesis. X ray left kneejoint shows growth arrest lines atlower end of femur and upper end of tibia,no joint destruction,no signs of scurvy or rickets, normal density. Xray spine shows scoliosis. Vertebral bodies are normal-no collapse or beaking. Xray wrist has 3 carpals and the epiphysis for the lower ends of radius and ulna are also visible. Can this hypersplenism & bony deformity be explained by a single diagnosis. what is the differential diagnosis and the further line of management.
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Question Category:Diagnostic dilemma |
4 month baby admitted with excessive crying which resolved in 2 hours .as a part of investigation xray wasdone which showed cardiomegaly(ct ratio 80%).The Treating physician considered possibilaty of dilated cardiomyopathy just because of cardiomyopathy after 2 hours of admission patient was asumptomatic. o/e no murmur no other significant finding .Then 2D ECHO was done which was absolutely normal. Still the physician insisted that it is dilated cardiomyopathy and started on carvedilol and digoxin. Is it rational?
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Question Category:Diagnostic dilemma |
A 6 years old child presented to us with complaints of reccurrent pyoderma localized to face for 4 years; otitis media for 3 years; crusting from nose for 2 years. On examination child has hepatosplenomegaly and generalised lymphadenopathy.All other systemic examination found to be normal. Investigation revealed nomal CBC; XRay and bone marrow. Blood culture was sterile. What is the diagnotic possibilities?
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Question Category:Diagnostic dilemma |
a 11 month female infant presented with swelling of left hand & lower end of left forearm.All investigations including color doppler were normal.after 2 months of onset of this problem,there is slight hypertrophy of left arm.what can be the diagnosis & definitive investigation?
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Question Category:Diagnostic dilemma |
Dear sir 2young couple, closely relative to each have a big problem .They have 6 children 3 alive & 3 died due to unknown cause. Those who died usually the problem started at the age 4-6month as chest infection which is resistant to treatment.Those who died are male & female. The 1st died at 4m, 2nd died at 6m, 3rd died at 2year after a protracted course of illness started as LRT infection & lymphadenopathy . The age of the alive children are 8y (female) , 3y(female), 18m(male).The 1st & 3rd are totally normal.The 2nd child is 3y(female) run the same illness LRT infection , lymphadenopathy, FTT progress to chronic lung disease + clubbing of fingure+ chronic exuding ,fascial widespreading skin infection . Those who died & this pt. are fully vaccinated ,while those survived are not vaccinated . On exam. Chronically ill child under weight dyspenic with + clubbing of fingure Vital sign are normal apart from tachypenia Generalized lymphadenopathy, Resp. system: bilatrel rhonchi & crepition Cvs. System: normal Soft abdomen, mild hepatosplenomegaly Investigation: Cbc normal GOT+GPT normal Blood urea & creatinin normal Immunoglobuline assay normal ESR 50 Sweat test normal Toxoplasmosis titer: -ve Blood , urine, stool culture are –ve Tt reaction –ve ACE normal Sputum for Tb bacilli –ve Gastric aspirate for Tb bacilli –ve Bone scan normal Abdominal sonar normal Cxr & CAT scan chest infection & hilar lymphadenopathy +lung fibrosis. Lymph node & lung biopsy :Follcular hyperplastic lymphadenitis with evidence of progressive transformation of germinal centers & occasional mini clusters of epitheloid & giant cells without true granuloma formation or caseation necrosis. This is most consistent with: a. progressive transformation of germinal centers. b. Toxoplasmosis & other specific(none-Tb) infection. The skin lesion as seen by an expert dermatologist to be mostly as Tb of skin. What is your opinion about this case? Waiting your advice.
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Question Category:Diagnostic dilemma |
The last time i asked pediatric on call a question on leukodystrophy it was answered very generally. It lacked the personal touch and my query was'nt satisfied. I again have a patient whom we think to be a certain leukodystrophy?? MRI postponed due to delay in arranging funds by the family. The sequence of findings is as follows- Male child 14 yrs of age. Presenting with difficulty in walking speech and abnormal behaviour since last 4 yrs with increased tone in all the four limbs. His mother confirms an increased skin pigmentation along with the problems started. Our first doubt was ALD. But family also has an elder FEMALE sibling who had simmilar problems starting around the same age with increased pigmentation and is presently 18 yrs old. CECT in this boy is suggestive of hypodensities in both cerebral hemispheres and basal ganglia (CECT done outside). Now can you please suggest some disorder which encompasses both the siblings? Please help me at the earliest.
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