Chronic granulomatous disease of childhood presenting as gastric outlet obstruction

A case of chronic granulomatous disease of childhood was first diagnosed when a 20-month-old infant developed gastric outlet obstruction. Because of the unusual clinical presentation and negative gastric mucosal biopsies, the diagnosis was delayed. A subsequent full thickness biopsy of the stomach w...

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Veröffentlicht in:The American journal of surgical pathology 1982-10, Vol.6 (7), p.673-676
Hauptverfasser: Varma, V A, Sessions, J T, Kahn, L B, Lipper, S
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container_title The American journal of surgical pathology
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creator Varma, V A
Sessions, J T
Kahn, L B
Lipper, S
description A case of chronic granulomatous disease of childhood was first diagnosed when a 20-month-old infant developed gastric outlet obstruction. Because of the unusual clinical presentation and negative gastric mucosal biopsies, the diagnosis was delayed. A subsequent full thickness biopsy of the stomach wall which led to a correct diagnosis showed a granulomatous infiltrate in the muscularis propria. Characteristic yellow pigment-laden macrophages were seen in the gastric mucosa and pyloric lymph node. Early recognition of this chronic disorder is important not only for proper management but genetic counseling as well.
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subjects Granulomatous Disease, Chronic - complications
Granulomatous Disease, Chronic - diagnosis
Granulomatous Disease, Chronic - pathology
Humans
Infant
Lymph Nodes - pathology
Male
Pyloric Stenosis - etiology
Stomach - pathology
Stomach Diseases - complications
Stomach Diseases - pathology
title Chronic granulomatous disease of childhood presenting as gastric outlet obstruction
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