Hereditary Multiple Exostoses in the Hands and Fingers: Early Presentation and Early Surgical Treatment in Family Members. Case Reports

Author:

Ohkuma Rika1,McCarthy Edward F.2,Deune E. Gene13

Affiliation:

1. Department of Plastic Surgery, Johns Hopkins School of Medicine, Johns Hopkins Outpatient Center, 601 N. Caroline Street, Suite 8161, Baltimore, MD 21287, USA

2. Department of Pathology, Johns Hopkins Hospital, Johns Hopkins Weinberg Building, 401 N. Broadway, Suite 2261, Baltimore, MD 21231, USA

3. Department of Orthopaedic Surgery, Johns Hopkins School of Medicine, Johns Hopkins Outpatient Center, 601 N. Caroline Street, Suite 5243, Baltimore, MD 21287, USA

Abstract

Hereditary multiple exostosis (HME) is a benign condition with multiple bony tumors with cartilage caps (osteochondromas), mainly presenting in the long and flat bones. Usually the presentation for HME is between 2 and 10 years of age and most are seen by 4 years of age (Khan et al. 2009). In this paper, we report a family with three members (father, son, and a daughter) who had very early presentations of HME in the fingers within the first 2 years of age. The son presented with bony nodules at 7 months of age, and he required surgery at 13 months of age for a severe functional deformity of his left ring finger. He also had an unusual histological presentation on his osteochondroma that consists of only subperiosteal cartilage without ossification.

Publisher

SAGE Publications

Subject

Orthopedics and Sports Medicine,Surgery

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Natural History and Characteristics of Hand Exostoses in Multiple Hereditary Exostoses;The Journal of Hand Surgery;2021-09

2. Tumors of the Nail Apparatus and Adjacent Tissues;Baran & Dawber's Diseases of the Nails and their Management;2018-12-07

3. Trigger finger in a hereditary multiple exostoses disease: A unique case report;European Journal of Plastic Surgery;2018-11-27

4. A giant multi-lobed osteochondroma of the phalanx in an adult: A case report;International Journal of Surgery Case Reports;2017

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