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两名跗骨型轴前多指畸形患者的手术重建技术:两个真性拇趾。

Surgical Reconstruction Technique of Two Patients With Tarsal Type Preaxial Polydactyly: Two True Prehalluces.

作者信息

Ferman Daniel H, Bauler Laura D, Bovid Karen

机构信息

Third-Year Medical Student, Western Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, MI.

Assistant Professor, Department of Biomedical Sciences, Western Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, MI.

出版信息

J Foot Ankle Surg. 2019 Jul;58(4):814-820. doi: 10.1053/j.jfas.2018.12.011.

Abstract

Polydactyly of the foot occurs in 1.7 cases per 1000 live births, comprising 45% of congenital abnormalities of the foot. Most reported cases of polydactyly of the foot are postaxial, and 15% are preaxial; of those, tarsal type preaxial polydactyly (a true prehallux) occurs in only 3% of cases. Because of this rarity, there is minimal literature available to guide management or surgical reconstruction. Two newborns presented with similar tarsal type preaxial polydactylies in the context of multiple congenital anomalies at a single institution. Patient 1 presented at birth with an accessory digit arising medially from the right foot at the medial malleolus. Two weeks later, genetically unrelated, patient 2 presented at birth with an accessory digit arising medially from the right foot at the talus. Both patients underwent resection of the extra digit and reconstruction including transfer of the accessory anterior tibial tendon arising from the preaxial extra digit to the remaining first ray. Two years after surgery, both patients are walking well with preserved dorsiflexion strength. Given the rarity of true prehallux cases, reported surgical treatment and outcomes are lacking. This case demonstrates the management of 2 patients to better guide future patient care. Although nonsurgical treatment with shoewear modification is an option, surgical reconstruction facilitated wearing typical shoes while preserving ambulatory ability. Both patients in this series had an accessory anterior tibial tendon. Surgical transfer of the tendon prevented loss of dorsiflexion strength and foot drop postoperatively.

摘要

足部多指畸形的发生率为每1000例活产中有1.7例,占足部先天性畸形的45%。大多数报道的足部多指畸形病例为轴后型,15%为轴前型;其中,跗骨型轴前多指畸形(真正的拇前趾)仅占病例的3%。由于这种罕见性,可供指导治疗或手术重建的文献极少。在一家机构中,有两名新生儿在患有多种先天性畸形的情况下出现了类似的跗骨型轴前多指畸形。患者1出生时右足内踝内侧有一个副趾。两周后,与患者1无血缘关系的患者2出生时右足距骨内侧有一个副趾。两名患者均接受了多余趾切除及重建手术,包括将来自轴前多余趾的副胫前肌腱转移至剩余的第一跖骨。术后两年,两名患者行走良好,背屈力量保留。鉴于真正的拇前趾病例罕见,缺乏已报道的手术治疗方法及结果。本病例展示了对两名患者的治疗过程,以更好地指导未来的患者护理。虽然通过修改鞋具进行非手术治疗是一种选择,但手术重建有助于患者穿着普通鞋子,同时保留行走能力。本系列中的两名患者均有副胫前肌腱。肌腱的手术转移防止了术后背屈力量丧失和足下垂。

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