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巨指(趾)症的病理学

Pathology of macrodactyly.

作者信息

Desai P, Steiner G C

机构信息

Department of Pathology, Hospital for Joint Diseases Orthopaedic Institute, New York, NY 10003.

出版信息

Bull Hosp Jt Dis Orthop Inst. 1990 Fall;50(2):116-25.

PMID:2175658
Abstract

Macrodactyly is an unusual congenital anomaly in which there is hamartomatous proliferation of the soft tissue of the affected digit. It is usually present at birth or recognized during adolescence. Eleven cases are presented. All showed abnormal accumulation of adipose tissue in the affected digits. In five cases, prominent endoneural and perineural fibrosis was noted. Two cases also demonstrated focal neural and vascular proliferation. This is an unusual finding in macrodactyly and may be a part of the abnormal hamartomatous proliferation that is observed in this condition. None of the patients had clinical evidence of neurofibromatosis. One patient had the Proteus syndrome.

摘要

巨指症是一种罕见的先天性异常,受累手指的软组织存在错构瘤样增生。通常在出生时即存在或在青春期被发现。本文报告了11例病例。所有病例均显示受累手指脂肪组织异常堆积。5例可见明显的神经内膜和神经束膜纤维化。2例还表现为局灶性神经和血管增生。这在巨指症中是不寻常的发现,可能是这种疾病中观察到的异常错构瘤样增生的一部分。所有患者均无神经纤维瘤病的临床证据。1例患者患有变形综合征。

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