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儿童期多发性皮肤颗粒细胞瘤与神经纤维瘤病。病例报告及文献复习。

Multiple cutaneous granular cell tumors and neurofibromatosis in childhood. A case report and review of the literature.

作者信息

Martin R W, Neldner K H, Boyd A S, Coates P W

机构信息

Department of Dermatology, School of Medicine, Texas Tech University Health Sciences Center, Lubbock 79430.

出版信息

Arch Dermatol. 1990 Aug;126(8):1051-6.

PMID:2166484
Abstract

Multiple cutaneous granular cell tumors have been previously reported in only 26 children or adolescents. An association of these tumors with neurofibromatosis has never been reported previously. We describe a 12-year-old black girl with multiple cutaneous granular cell tumors and neurofibromatosis. Although the histogenesis of these tumors is not completely clear, the findings of ultrastructural and immunohistochemical evaluation of our patient's tumors and the associated neurofibromatosis support a neural crest origin for granular cell tumors.

摘要

此前仅有26例儿童或青少年多发性皮肤颗粒细胞瘤的报道。这些肿瘤与神经纤维瘤病的关联此前从未有过报道。我们描述了一名12岁的黑人女孩,她患有多发性皮肤颗粒细胞瘤和神经纤维瘤病。尽管这些肿瘤的组织发生尚未完全明确,但对我们患者的肿瘤及相关神经纤维瘤病进行超微结构和免疫组化评估的结果支持颗粒细胞瘤起源于神经嵴。

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