1型神经纤维瘤病患儿中伪装成神经纤维瘤的皮肤血管平滑肌脂肪瘤：一例报告

Cutaneous angiomyolipoma masquerading as a neurofibroma in a child with neurofibromatosis type 1: a case report.

作者信息

Carrau Diana, Kahwash Samir, Pearson Gregory

机构信息

College of Medicine, Ohio State University, Columbus, Ohio.

Department of Anatomic Pathology, Nationwide Children's Hospital, Columbus, Ohio.

出版信息

Pediatr Dermatol. 2015 May-Jun;32(3):423-4. doi: 10.1111/pde.12398. Epub 2015 Jan 30.

DOI:10.1111/pde.12398

PMID:25640861

Abstract

Angiomyolipomas are benign tumors composed of blood vessels, smooth muscle, and adipose tissue that are frequently associated with tuberous sclerosis. Cutaneous angiomyolipomas are rare and typically present in men in the fifth or sixth decade of life. We present a case of a cutaneous angiomyolipoma masquerading as a neurofibroma in a 13-year-old boy with a history of neurofibromatosis type 1.

摘要

血管平滑肌脂肪瘤是由血管、平滑肌和脂肪组织组成的良性肿瘤，常与结节性硬化症相关。皮肤血管平滑肌脂肪瘤罕见，通常见于50或60岁男性。我们报告1例13岁患1型神经纤维瘤病的男孩，其皮肤血管平滑肌脂肪瘤伪装成神经纤维瘤。