A Unique Case of Hereditary Multiple Osteochondromas in the Feet

Clara J. Devota, Kelly R. Kamnikar, Carolyn V. Isaac, Joseph T. Hefner
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Abstract

This report describes the differential diagnosis of osseous growths in the first metatarsals of an adult male previously unreported in the literature. Examination of the remains via macroscopic analysis and conventional radiography identified unusual bilateral growths arising from the lateral aspects of the first metatarsals with growth directed towards the tarsometatarsal joint. Two exostoses in the ribs were also observed. Using the available evidence, hereditary multiple osteochondromas (HMO) was determined the likely causative disorder for the pedal growths based on the presence of cartilage caps on the ends of the growths, a lack of articular morphology, and the presence of a rib exostosis consistent with HMO. The potential bilateral expression of HMO in the first metatarsals in this case challenges the dominating diagnostic criteria that HMO growths are directed away from the growth plate and only occur in the metaphysis, expanding the spectrum of HMO’s manifestation in the human skeleton. Medical records for the decedent provided no indication of a disorder associated with the development of osteochondromas, nor any indication that medical treatment was undertaken to manage the growths.
一个独特的遗传性多发性足部骨软骨瘤病例
本报告描述了一名成年男性第一跖骨骨生长的鉴别诊断,此前未见文献报道。通过宏观分析和常规x线摄影检查发现,第一跖骨外侧出现异常的双侧生长,生长方向为跗跖关节。在肋骨也观察到两处外生骨瘤。根据现有的证据,遗传性多发性骨软骨瘤(HMO)被确定为可能导致脚部生长的疾病,原因是生长末端存在软骨帽,缺乏关节形态,并且存在与HMO一致的肋骨外生。在本病例中,HMO在第一跖骨的潜在双侧表达挑战了HMO生长远离生长板且仅发生在干骺端的主要诊断标准,扩大了HMO在人类骨骼中的表现范围。死者的医疗记录没有显示出患有与骨软骨瘤有关的疾病,也没有任何迹象表明为控制骨软骨瘤的生长而进行了治疗。
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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