Osseous bilateral pseudotumour of the thumb in severe haemophilia A – A case report

P. Mandal, Rishu Vidhrati, Debasis Gantait
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Abstract

Abstract Pseudotumour is a rare complication of haemophilia, categorised as osseous or non-osseous (soft tissue) lesions based on anatomic location. The bones most frequently involved are the larger ones; pseudotumours of small bones are rare. Here we present a rare case of pseudotumours of both thumbs in a 10-year-old male with severe haemophilia A, successfully treated with factor replacement therapy. This case highlights the possibility of treating such cases conservatively, but also the need for education to enable early intervention to prevent potential complications that could be life-threatening.
严重血友病A伴双侧拇指骨性假瘤1例
假性肿瘤是血友病的一种罕见并发症,根据解剖位置分为骨性或非骨性(软组织)病变。最常见的是那些较大的骨头;小骨的假肿瘤是罕见的。在这里,我们提出一个罕见的病例假肿瘤的两个拇指在一个10岁的男性严重血友病a,成功地治疗了因子替代疗法。该病例强调了保守治疗此类病例的可能性,但也需要进行教育,使早期干预能够预防可能危及生命的潜在并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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