Chen J Y, Lin R I, Chao H C, Kong M S, Hsueh C, Lou C C
Department of Pediatrics, Chang Gung Children's Hospital, Taoyuan, Taiwan, R.O.C.
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1998 May-Jun;39(3):203-5.
Neonatal intussusception is an uncommon disease. We report a case of neonatal ileoileocolic intussusception led by an ileal polyp in a female neonate. The patient presented with irritable crying, bilious vomiting and frank bloody stool on the 26th day of life. On physical examination, a mobile abdominal mass was palpated. Abdominal sonography demonstrated a long segment intussusception; associated with a low echogenic mass. At laparotomy, ileoileocolic intussusception led by an ileal polyp was found. Pathology confirmed the diagnosis of polyp. Because intestinal obstruction is the primary manifestation, neonatal intussusception is initially indistinguishable from obstructions due to other reasons like intestinal atresia, congenital bands, necrotizing enterocolitis or midgut volvulus. Our experience showed that although uncommon, intussusception should be considered in the differential diagnosis of intestinal obstruction during the newborn period.
新生儿肠套叠是一种罕见疾病。我们报告一例女性新生儿由回肠息肉导致的回肠-回肠-结肠型肠套叠病例。该患者在出生第26天出现易激惹哭闹、胆汁性呕吐及鲜血便。体格检查时可触及一个可活动的腹部肿块。腹部超声显示长段肠套叠,伴有一个低回声肿块。剖腹探查时发现由回肠息肉导致的回肠-回肠-结肠型肠套叠。病理证实息肉诊断。由于肠梗阻是主要表现,新生儿肠套叠最初难以与因其他原因如肠闭锁、先天性束带、坏死性小肠结肠炎或中肠扭转导致的梗阻相鉴别。我们的经验表明,尽管罕见,但在新生儿期肠梗阻的鉴别诊断中应考虑肠套叠。