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2例短指畸形患者手部皮肤钙化症

Cutis Calcinosis of the Hand in 2 Patients With Symbrachydactyly.

作者信息

Bougioukli Sofia, El-Farra Mohamed H, Mahabir Roshan, Wright Joan, Miric Nina Lightdale

机构信息

Department of Orthopaedic Surgery, Keck School of Medicine, University of Southern California, Los Angeles, CA.

University of California Riverside School of Medicine, Riverside, CA.

出版信息

J Hand Surg Glob Online. 2022 Dec 8;5(2):242-245. doi: 10.1016/j.jhsg.2022.11.005. eCollection 2023 Mar.

Abstract

Cutis calcinosis of the hand in the setting of symbrachydactyly is presented in 2 unique patients. Both lesions were treated based on the standard of care protocols with resection of the calcified mass and hand reconstruction, as appropriate. The patients healed uneventfully without recurrence of the calcification at a the 1-year follow-up. The association between symbrachydactyly and calcinosis cutis is discussed along with a hypothesis on the pathophysiologic mechanism that could potentially explain this unusual occurrence and why it might be more common than previously identified.

摘要

本文介绍了2例患有并指畸形伴手部皮肤钙化症的独特患者。根据护理标准方案,对两处病变均进行了钙化肿块切除及必要的手部重建治疗。在1年的随访中,患者愈合良好,钙化未复发。本文讨论了并指畸形与皮肤钙化症之间的关联,并提出了一种病理生理机制假说,该假说可能解释了这种不寻常的现象以及为何它可能比之前所认为的更为常见。

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