Granular cell tumor of the esophagus.
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Biomedical subjects
Publications and source records attributed to K Chawla.
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To date, only two cases of renal angiomyolipoma with associated lymph node involvement have been described. The authors report a third instance of this unusual entity.
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Familial achalasia most often has been recorded in siblings, and only rarely (twice previously) in a parent and offspring. This report concerns a third case of achalasia in a parent and offspring (mother and son). Clinical and radiographic features of the esophageal achalasia are presented. The possibility that genetic factors may play a role in the etiology of this disorder is discussed.
Five cases of pancreatic pseudocyst are presented with unusual manifestations. Clinical features of each entity are discussed to enable one to diagnose the rare manifestations and complications of pancreatic pseudocyst. Reasonable understanding of such cases enables accurate diagnostic work-up for confirmation and early surgical intervention.
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Renal ischemia and infarction present with one basic characteristic: an area of low attenuation on a CT scan. We present three cases of renal ischemia and infarction with various underlying causes.
Solitary innominate artery aneurysms are very rare in the pediatric age group. They may be seen in association with multiple aneurysms or occasionally in patients with connective tissue disease. Magnetic resonance appears to be a very useful noninvasive technique capable of demonstrating flowing blood and vascular lumen without injection of contrast media.
An asymptomatic case of a Bochdalek hernia with progressive herniation of the right ureter is presented. The diagnosis was made by computed tomography (CT).
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An extremely rare case of branchiogenic cyst of the larynx in young adult male is reported. Relevant literature is reviewed.