Stringer M D, Brereton R J, Drake D P, Kiely E M, Agrawal M, Mouriquand P D, Tam P K
Department of Paediatric Surgery, Hospital for Sick Children, London, England.
J Pediatr Surg. 1994 Apr;29(4):501-3. doi: 10.1016/0022-3468(94)90077-9.
Seven full-term infants with aganglionosis extending into the small bowel presented with clinical, radiological, and operative features of meconium ileus. Misdiagnosis resulted in inappropriate treatment. The correct diagnosis was eventually established by rectal suction biopsy, mostly after either recurrent intestinal obstruction or stomal dysfunction, and after cystic fibrosis had been excluded. For two patients, the results of rectal suction biopsies were initially misleading. Two infants died. Extensive intestinal aganglionosis should be considered a rare possibility in all infants with meconium ileus. In such cases, histological examination of the appendix may avoid this potential pitfall.
7名患有延伸至小肠的神经节缺失症的足月儿表现出胎粪性肠梗阻的临床、放射学及手术特征。误诊导致了不恰当的治疗。最终通过直肠吸引活检确诊,多数是在反复肠梗阻或造口功能障碍后,且排除囊性纤维化之后。有2例患者,直肠吸引活检结果最初产生了误导。2名婴儿死亡。对于所有患有胎粪性肠梗阻的婴儿,应考虑存在广泛肠道神经节缺失症这种罕见可能性。在此类病例中,阑尾的组织学检查可能会避免这一潜在陷阱。