颅内受累的婴儿肌纤维瘤病罕见病例

IF 1.4 Q3 PEDIATRICS
Global Pediatric Health Pub Date : 2024-08-15 eCollection Date: 2024-01-01 DOI:10.1177/2333794X241266564
Fatima Zahrae El Mansoury, Zakia El Yousfi, Ayman El Farouki, Siham El Haddad, Nazik Allali, Latifa Chat
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引用次数: 0

摘要

婴幼儿肌纤维瘤病是一种发生在婴幼儿时期的增生性疾病,其特征是由各种间质成分组成的结节性或弥漫性病变。颅内受累的报道并不多见。在此,我们介绍了一例罕见的颅内实质受累的 3 岁女孩的病例,她的组织学模式在现有的婴儿肌纤维瘤病患者文献中已有记载。随后的核磁共振成像随访显示没有复发迹象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Case of Infantile Myofibromatosis With Intra Cranial Involvement.

Infantile myofibromatosis is a proliferative disorder occurring during infancy and early childhood, marked by the development of nodular or diffuse lesions consisting of various mesenchymal elements. Intracranial involvement is infrequently reported. Here, we present the case of a 3-year-old girl exhibiting a rare manifestation of IM with intracranial parenchymal involvement, displaying a histological pattern documented in existing literature on patients with infantile myofibromatosis. Subsequent MRI follow-up revealed no signs of recurrence.

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来源期刊
Global Pediatric Health
Global Pediatric Health Nursing-Pediatrics
CiteScore
2.20
自引率
0.00%
发文量
105
审稿时长
12 weeks
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