包涵体纤维瘤病
Inclusion body fibromatosis.
作者信息
Zardawi I M, Earley M J
出版信息
J Pathol. 1982 Jun;137(2):99-107. doi: 10.1002/path.1711370203.
PMID:6283048
Abstract
The clinical and pathological features of two further cases of the condition previously described as Recurring Digital Fibrous Tumour of Childhood are presented. The ultrastructural appearance of the characteristic cell inclusions bears some resemblance to Mallory's hyaline and suggest increased functional activities in the fibroblasts carrying these unusual dense bodies. Retention of abnormal metabolic products in fibroblasts is the most likely explanation. The term Inclusion Body Fibromatosis is proposed for this entity.
摘要
本文报告了另外两例曾被描述为儿童复发性指纤维瘤病的病例的临床和病理特征。特征性细胞内含物的超微结构外观与马洛里透明变性有一些相似之处，提示携带这些异常致密小体的成纤维细胞功能活动增强。成纤维细胞中异常代谢产物的潴留是最可能的解释。为此实体提出“包涵体纤维瘤病”这一术语。
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