Patil Sampat Dumbre, Parekh Hemant, Patil Vaishali Dumbre, Joshi Kartikeya
Orthopaedic Department, Noble Hospital, Hadapsar, Pune- 411013, Maharashtra, India.; Orthopaedic Department, Shri Prayagdham Trust Charitable Hospital, UruliKanchan, Pune- 412202, Maharashtra, India.
Orthopaedic Department, SmtKashibaiNavale Medical College and General Hospital, S. No 49/1, Westerly Bypass Road, Narhe (Ambegaon), Pune - 411 041, Maharashtra. India.
J Orthop Case Rep. 2014 Apr-Jun;4(2):64-8. doi: 10.13107/jocr.2250-0685.171.
Congenital hallux varus of secondary type is associated with polydactyly, syndactyly or other congenital deformities of the foot. Such congenital deformities can be addressed in childhood with soft tissue reconstructive procedures. In adulthood, treatment of these deformities is challenging because of soft tissue contractures and rigid bony deformities. To our knowledge, this is the first case report demonstrating the management of neglected secondary congenital hallux varus in adults.
We present here a case of a 23 years old male patient who presented to us with untreated congenital hallux varus of secondary type. Patient had an extra great toe (polydactyly) with syndactyly. We have treated this patient in two stages. First stage consisted of excision of the extra great toe and gradual correction of medial great toe. In second stage, metatarsophalangeal joint fusion was done. We have follow up of this case for more than 2.5 years.
Severe neglected congenital deformities presenting in adulthood pose unique problems of soft tissue contractures and permanent bony deformities. Congenital neglected hallux varus with polydactyly and syndactyly is a rare deformity. Its correction was challenging as patient presented to us in adulthood. A staged approach of gradual soft tissue distraction and then metatarsophalangeal joint fusion has resulted in satisfactory aesthetic and functional outcome.
继发性先天性拇内翻与多指畸形、并指畸形或足部其他先天性畸形相关。此类先天性畸形在儿童期可通过软组织重建手术进行治疗。在成年期,由于软组织挛缩和僵硬的骨性畸形,治疗这些畸形具有挑战性。据我们所知,这是首例关于成人继发性先天性拇内翻漏诊病例治疗的报告。
我们在此呈现一名23岁男性患者的病例,该患者因未治疗的继发性先天性拇内翻前来就诊。患者有一个额外的大脚趾(多指畸形)并伴有并指畸形。我们分两个阶段对该患者进行了治疗。第一阶段包括切除额外的大脚趾并逐步矫正内侧大脚趾。第二阶段进行了跖趾关节融合术。我们对该病例进行了超过2.5年的随访。
成年期出现的严重先天性畸形漏诊会带来软组织挛缩和永久性骨性畸形等独特问题。伴有多指畸形和并指畸形的先天性拇内翻漏诊是一种罕见的畸形。由于患者成年后前来就诊,其矫正具有挑战性。采用逐步软组织牵张然后进行跖趾关节融合的分期方法,已取得了令人满意的美学和功能效果。