Mishalany H, Mahnovski V, Woolley M
Surgery. 1982 Jan;91(1):38-41.
Congenital asplenia has been traditionally described in association with cardiopulmonary anomalies (Ivemark syndrome). A case of congenital asplenia with duplication of the hindgut and genitourinary tract, myelomeningocele, situs inversus abdominis, and imperforate anus generated interest in review of the gastrointestinal anomalies of 36 patients who died of the disease in Childrens Hospital of Los Angeles. A significant number were found to have situs inversus, malrotation of the bowel, esophageal varices, duplication and hypoplasia of the stomach, Hirschsprung's disease, imperforate anus, and duplication of the hindgut. These patients present with symptoms referable to their gastrointestinal anomalies and may not draw attention to the concomitant cardiopulmonary anomalies or to the absence of the spleen. It becomes important, therefore, to establish the presence of the spleen in infants suffering from various anomalies of the gastrointestinal tract because of the overwhelming septicemia that is known to complicate the clinical management of these patients.
先天性无脾症传统上被描述为与心肺异常相关(艾弗马克综合征)。一例患有后肠和泌尿生殖道重复畸形、脊髓脊膜膨出、腹内脏器反位和肛门闭锁的先天性无脾症病例,引发了对洛杉矶儿童医院36例死于该病患者的胃肠道异常情况进行回顾研究的兴趣。发现相当一部分患者存在腹内脏器反位、肠旋转不良、食管静脉曲张、胃重复畸形和发育不全、先天性巨结肠、肛门闭锁以及后肠重复畸形。这些患者会出现与胃肠道异常相关的症状,可能不会引起对伴随的心肺异常或无脾情况的关注。因此,对于患有各种胃肠道异常的婴儿,确定脾脏的存在很重要,因为已知严重败血症会使这些患者的临床治疗复杂化。