Nejat Farideh, Habibi Zohreh, Goudarzi Mehrdad, Azad Mahdi Souraki, Moradi Ehsan, Heidari Vahid, Kadivar Maliheh, Soltani Zahra Ebrahim, Kouchakzadeh Leila
Departments of 1 Neurosurgery.
Anesthesiology.
J Neurosurg Pediatr. 2017 Oct;20(4):307-313. doi: 10.3171/2017.1.PEDS16306. Epub 2017 Jul 14.
Craniopagus is a very rare congenital anomaly that tends to affect females more often than males. It is classified as partial or total. Most affected twins are either stillborn or die during the perinatal period. Those who survive birth should undergo detailed radiological evaluations soon after their condition becomes stable so that the precise anatomy of the conjoined part can be defined and surgery can be planned in detail by a multidisciplinary team. Recommendations for decreasing the risk of unsuccessful surgery include performing surgery on an elective basis after extensive preoperative radiological evaluations as well as when the twins are at an acceptable age and weight for a complex surgical separation, generally as staged procedures. In addition, the operation should be performed by a well-equipped expert multidisciplinary team. When one of the conjoined twins dies, however, surgical separation cannot be postponed because the shared circulatory system predisposes the alive child to life-threatening complications, including coagulopathy. The authors report on the successful separation of craniopagus twins performed on an emergency basis at 32 weeks of gestational age because of the sudden death of one of them. At the time of separation surgery, the twins each weighed 1250 g. To the best of the authors' knowledge, this is the youngest age and lowest weight yet reported for successful surgical separation. The surviving twin developed a pseudomeningocele, which required a second operation and placement of a cystoperitoneal shunt 4 months after the operation. Additional surgery is planned to repair a cranial defect that resulted from the pseudomeningocele, but his general physical and mental condition was otherwise good at latest follow-up (12 months after separation surgery).
颅联体是一种非常罕见的先天性异常,女性比男性更易受影响。它分为部分性或整体性。大多数受影响的双胞胎要么死产,要么在围产期死亡。那些存活下来的婴儿在病情稳定后应尽快接受详细的影像学评估,以便确定联体部位的精确解剖结构,并由多学科团队详细规划手术。降低手术失败风险的建议包括在进行广泛的术前影像学评估后择期进行手术,以及当双胞胎达到可接受的年龄和体重以进行复杂的手术分离时,通常采用分期手术。此外,手术应由设备精良的专家多学科团队进行。然而,当其中一个联体双胞胎死亡时,手术分离不能推迟,因为共享的循环系统会使存活的婴儿易发生危及生命的并发症,包括凝血病。作者报告了因其中一个双胞胎突然死亡而在孕32周时紧急进行的颅联体双胞胎成功分离手术。分离手术时,每个双胞胎体重1250克。据作者所知,这是成功进行手术分离所报告的最年轻年龄和最低体重。存活的双胞胎出现了假性脑脊膜膨出,这需要在手术后4个月进行二次手术并放置囊腹膜分流管。计划进行额外的手术来修复由假性脑脊膜膨出导致的颅骨缺损,但在最新随访(分离手术后12个月)时,他的总体身体和精神状况良好。