Multicystic Nephroma-Report of Two Rare Cases in a Span Of Seven Years

Angioimmunoblastic Lymphadenopathand Report of Two Rare Cases

Angioimmunoblastic Lymphadenopathy (AIL) is an uncommon disorder which begins  with constitutional symptoms. The majority of the patients .has generalized l?7111ph­ adenopathy, , hepatosplenomegaly and about 40% show cutaneous manifestations such as maculopapular eruption, purpura, urticaria or erythroderma. Histhopatho­Iogy of lymphnodes has a characteristic picture. The etiology of AIL is unk...

Congental Glucose- Galactose Malabsorption a Rare Cause of Diarrhea in Infancy Period: Report of Two Cases

A report of two cases of pyknodysostosis in two children

pyknodysostosis is a rare bone disease characterzed with short stature,wide fontaneles,small chin,hyperdensity of bones,erosion of tufts of the disatl phalanges,and narrowing of the mandibular angle. pyknodysostosis is inheritted as an autosomal recessive disease and may be seen in both sexes at any age.the patients have normal life span.short stature and bone fractures are their major problems...

a cross-comparative dtudy between two textbook series in terms of the presentation of politeness

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Multicystic nephroma in an elderly man. Case report.

Multicystic nephroma is a relatively rare tumor of the kidney presenting unclear histological origin. Abdominal mass is a common onset sign in children while abdominal flank pain or abdominal discomfort, hematuria and recurrent urinary tract infections usually affect adults. Preoperative diagnosis is impossible especially in the adult variant of the tumor where clear cells carcinoma with cystic...