Woywodt A, Verhaart S, Kiss A
Department of Surgery, University of the Witwatersrand, Johannesburg, Gauteng Province, Republic of South Africa.
J Pediatr Surg. 1998 Sep;33(9):1423-5. doi: 10.1016/s0022-3468(98)90026-4.
A 4-day-old black male underwent laparotomy for intestinal obstruction. At surgery, multiple jejunal atresias (type IV) of the jejunum were detected. As an incidental finding, atresia of the appendix was also present. The jejunal atresia was repaired, and resection of the tip of the cecal pole and atretic appendix was performed. Gross and histological examination confirmed the presence of a type IV atresia of the jejunum and a cordlike (type II) atresia of the appendix with inflammatory changes in the tip of the appendix. The boy made an uneventful recovery. Examination of all organ systems did not show any associated findings, and the family history was unremarkable. To our best knowledge, this case represents the first case of atresia of the appendix described in the literature.
一名4日龄黑人男性因肠梗阻接受剖腹手术。手术中,发现空肠存在多处空肠闭锁(IV型)。作为偶然发现,阑尾也存在闭锁。对空肠闭锁进行了修复,并切除了盲肠极尖端和闭锁的阑尾。大体和组织学检查证实存在空肠IV型闭锁以及阑尾条索状(II型)闭锁,阑尾尖端有炎症改变。患儿恢复顺利。对所有器官系统的检查未发现任何相关异常,家族史也无明显异常。据我们所知,该病例是文献中描述的首例阑尾闭锁病例。