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先天性皮肤组织细胞增多症X的自然消退:1例报告并讨论疾病分类学及发病机制

Spontaneous regression of congenital cutaneous histiocytosis X: report of a case with discussion of nosology and pathogenesis.

作者信息

Dehner L P, Bamford J T, McDonald E C

出版信息

Pediatr Pathol. 1983 Jan-Mar;1(1):99-106. doi: 10.3109/15513818309048288.

Abstract

Spontaneous regression of histiocytosis X is a rare biologic event as judged by the extensive recorded experience in the literature. We present a case of congenital cutaneous histiocytosis X that resolved without specific therapy in the first week of life. Histologic and ultrastructural studies confirmed the interpretation. This child is an example of so-called pure cutaneous histiocytosis, which, like the other unisystem forms of the disorders, has an excellent prognosis.

摘要

根据文献中广泛记录的经验判断,组织细胞增多症X的自发消退是一种罕见的生物学现象。我们报告一例先天性皮肤组织细胞增多症X,该患儿在出生后第一周未经特殊治疗即自行消退。组织学和超微结构研究证实了这一判断。该患儿是所谓单纯皮肤组织细胞增多症的一个例子,与该疾病的其他单系统形式一样,预后良好。

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