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颅联体双胎分离术中的手术细微差别——我们的经验及15年随访

Surgical nuances in the separation of craniopagus twins - Our experience and a follow up of 15 years.

作者信息

Pai K Muralidhar, Naidu R Chandrasekhar, Raja A, Rai Y S, Kumar Niranjan, Kini Anand, Joseph Santhosh, Hegde Vinod, Ballal H S, Rao Ramoorthi, Sharma Saroja V, Valakatte Vinay Kumar

机构信息

Department of Neurosurgery, Kasturba Medical College, Mangalore, India.

Department of Neurosurgery, Krishna Institute of Medical Science, Hyderabad, Telangana, India.

出版信息

Neurol India. 2018 Mar-Apr;66(2):426-433. doi: 10.4103/0028-3886.227289.

Abstract

Craniopagus twins are conjoined twins fused at the cranium. This is the rarest anomaly seen in conjoined twins and craniopagus twins account for 2- 6% of conjoined twins. Conjoined twins are also extremely rare, with the anomaly seen in about 10-20 subjects per billion births. A female preponderance has been noted. Craniopagus twins can be classified into complete or partial, depending on whether or not they have shared dural venous sinuses. They can be further classified into angular or total depending on the alignment of the inter-twin longitudinal axis. Surgical separation of these cases can be an elective procedure or an emergency, mandated by the death of one of the twins. Surgical separation of craniopagus twins is a complex exercise needing detailed evaluation and planning. For the successful management of these twins, a multi-disciplinary approach involving neurosurgeons, plastic surgeons, anesthetists, radiologists, pediatric critical care specialists and ancillary staff is mandatory. We present a case of partially successful elective separation of partial angular craniopagus twins performed in 2002.The surviving twin was managed conservatively for a cerebrospinal fluid leak. The patient subsequently developed a pseudomeningocele, necessitating re-exploration, excision of the gliotic tissue, and repair of the dura and the overlying scalp flap. The patient has a skull defect for which cranioplasty has been deferred. The child is neurologically intact. The post-operative evaluation and the detailed periodic neurological assessment till date (with a follow up of 15 years) have been presented in this study.

摘要

颅联体双胞胎是颅骨相连的联体双胞胎。这是联体双胞胎中最罕见的异常情况,颅联体双胞胎占联体双胞胎的2%至6%。联体双胞胎也极为罕见,每十亿例出生中约有10至20例出现这种异常情况。已注意到女性占多数。颅联体双胞胎可根据是否共享硬脑膜静脉窦分为完全型或部分型。根据双胞胎间纵轴的排列情况,它们可进一步分为角型或全型。这些病例的手术分离可以是择期手术,也可能因其中一个双胞胎死亡而成为紧急手术。颅联体双胞胎的手术分离是一项复杂的操作,需要详细评估和规划。为了成功治疗这些双胞胎,必须采用多学科方法,包括神经外科医生、整形外科医生、麻醉师、放射科医生、儿科重症监护专家和辅助人员。我们介绍一例2002年进行的部分角型颅联体双胞胎择期分离手术部分成功的病例。存活的双胞胎因脑脊液漏接受了保守治疗。患者随后出现了假性脑膜膨出,需要再次手术探查、切除胶质组织,并修复硬脑膜和覆盖的头皮瓣。患者存在颅骨缺损,颅骨成形术已推迟。患儿神经功能完好。本研究展示了术后评估以及直至目前(随访15年)详细的定期神经学评估情况。

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