大趾远端指骨软骨粘液样纤维瘤1例并文献复习。

IF 1.4 Q3 EMERGENCY MEDICINE
International Journal of Burns and Trauma Pub Date : 2024-12-15 eCollection Date: 2024-01-01 DOI:10.62347/MHUS7790
Latif Zafar Jilani, Mohammad Istiyak, Nikhil Kumar Sharma
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引用次数: 0

摘要

足部软骨粘液样纤维瘤是一种罕见的疾病。我们报告一例CMF在一个7岁的女孩,影响远端指骨的大脚趾。x线片显示溶解性病变累及整个远端指骨,内侧和外侧皮质均被破坏,而关节面保持完整。经组织病理学检查确诊。患者接受了广泛的刮除,然后植骨。随访6个月后,未见复发迹象。本病例报告旨在介绍并强调小儿患者脚趾远端指骨CMF的罕见发生,引起人们对其非典型位置和表现年龄的关注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chondromyxoid fibroma of distal phalanx of great toe: a rare case report with literature review.

Chondromyxoid fibroma (CMF) in the foot is a rare condition. We report a case of CMF in a 7-year-old girl, affecting the distal phalanx of the great toe. Radiographs revealed a lytic lesion involving the entire distal phalanx, with destruction of both the medial and lateral cortices, while the articular surfaces remained intact. The diagnosis was confirmed through histopathological examination. The patient underwent extensive curettage followed by bone grafting. After a six-month follow-up, no signs of recurrence were observed. This case report aims to present and underscore the uncommon occurrence of CMF in the distal phalanx of the toe in a paediatric patient, drawing attention to its atypical location and age of presentation.

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