Suppr超能文献

先天性婴儿指纤维瘤病:一例病例报告及文献复习

Congenital infantile digital fibromatosis: a case report and review of the literature.

作者信息

Adegoke Omolade O, Ajao Akinlabi E, Ano-Edward Gbemi H

机构信息

University of Ibadan College of Medicine, Pathology; University College Hospital Ibadan, Pathology.

Bowen University, Department of Surgery; University College Hospital Ibadan, Department of Surgery.

出版信息

Afr Health Sci. 2020 Dec;20(4):1865-1869. doi: 10.4314/ahs.v20i4.42.

Abstract

Infantile digital fibromatosis (IDF), also called inclusion body fibromatosis is an uncommon benign tumour occurring in the digits of young children. In about a third of cases, it is congenital and the diagnosis is based on the presence of peculiar intracytoplasmic inclusions on histology. Recurrence rate post-surgery is high. However, spontaneous regression has been reported. We present a case of a 5-month-old infant who had excision of a right second toe mass, which has been present from birth. Histological examination revealed this to be infantile digital fibromatosis. To the best of our knowledge, no report of this has been made in Nigeria. It is important that this diagnosis be entertained in young children with masses on the digits as this will influence the management instituted.

摘要

婴儿指部纤维瘤病(IDF),也称为包涵体纤维瘤病,是一种发生于幼儿手指的罕见良性肿瘤。约三分之一的病例为先天性,诊断基于组织学上特殊的胞质内包涵体的存在。手术后复发率较高。然而,也有自发消退的报道。我们报告一例5个月大婴儿,其出生时即存在的右第二趾肿物被切除。组织学检查显示为婴儿指部纤维瘤病。据我们所知,尼日利亚尚无此类报告。对于手指有肿物的幼儿考虑这一诊断很重要,因为这将影响所采取的治疗措施。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验