(系统性肥大细胞增多症)。

Q4 Medicine

Medicina cutanea ibero-latino-americana Pub Date : 1990-01-01

J Redondo Mateo, M Vaquero Perez, L Guinea Esquerdo

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引用次数: 0

摘要

我们记录了一位70岁男性的系统性肥大细胞增多症病例，其临床表现以腹部症状(疼痛和腹泻)和晕厥发作开始，发现肝脾肿大，皮肤，骨骼和骨髓受累。丘疹红斑病变出现在以前的结肠镜切除术的疤痕组织。抓挠这些病变部位会产生瘙痒。组织学上发现乳腺细胞浸润，符合系统性肥大细胞增多症的诊断，并伴有Köebner的现象。我们回顾了系统性肥大细胞增多症最显著的特征。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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[Systemic mastocytosis].

We record a case of systemic mastocytosis in a 70 year old male whose clinical picture started with abdominal symptomatology (pain and diarrhea) and syncopal episodes, who was found to have hepatosplenomegaly and skin, bone and bone-marrow involvement. Papulo-erythematous lesions appeared over the scar tissue of a previous colyscectomy. Scratching of these lesions produced urtication. Histologically an infiltration of mastocytes was found, being compatible with the diagnosis of systemic mastocytosis with Köebner's phenomenon. We review the most remarkable characteristics of systemic mastocytosis.

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来源期刊

Medicina cutanea ibero-latino-americana Medicine-Dermatology

自引率

0.00%

发文量

期刊介绍： La Revista Medicina Cutánea Ibero-Latino-Americana se adhiere a los “Requisitos de uniformidad para manuscritos presentados para publicación en revista biomédicas” elaborados por el Comité Internacional de Editores de Revista Médicas