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一名患有胎粪性腹膜炎的早产儿空肠先天性纤维肉瘤

Congenital fibrosarcoma of the jejunum in a premature infant with meconium peritonitis.

作者信息

Shima Y, Ikegami E, Takechi N, Migita M, Hayashi Z, Araki T, Tanaka Y, Sugiyama M, Hashizume K

机构信息

Department of Premature and Neonatal Medicine, Japanese Red Cross Katsushika Maternity Hospital, Tokyo, Japan.

出版信息

Eur J Pediatr Surg. 2003 Apr;13(2):134-6. doi: 10.1055/s-2003-39560.

Abstract

We report an unusual case of perforation of a congenital fibrosarcoma of the jejunum in utero and secondary meconium peritonitis. Prenatal ultrasound showed polyhydramnios and fetal ascites from 25 gestational weeks in the absence of other fetal congenital anomalies. A 2200 g baby girl was born at 34 weeks gestation, presenting with severe generalized edema and respiratory distress immediately after birth. Plain radiography revealed progressive abdominal distension and pneumoperitoneum. The baby subsequently underwent surgery at the age of one day. A perforation of the upper jejunum, which had resulted in meconium peritonitis, was discovered intraoperatively and the perforated section of the intestine was resected and anastomosed successfully. The postoperative course was uneventful. Pathological examination confirmed that the perforation was caused by rupture of a congenital fibrosarcoma originating from the jejunum. Rupture of a malignant tumor is an extremely rare cause of peritonitis in the fetus and neonate.

摘要

我们报告了一例罕见的先天性空肠纤维肉瘤宫内穿孔并继发胎粪性腹膜炎的病例。产前超声显示,自孕25周起出现羊水过多和胎儿腹水,且无其他胎儿先天性异常。一名体重2200克的女婴在孕34周时出生,出生后立即出现严重全身性水肿和呼吸窘迫。腹部平片显示腹胀进行性加重和气腹。该婴儿随后在出生一天后接受了手术。术中发现上段空肠穿孔导致胎粪性腹膜炎,切除了穿孔的肠段并成功吻合。术后过程顺利。病理检查证实穿孔是由起源于空肠的先天性纤维肉瘤破裂所致。恶性肿瘤破裂是胎儿和新生儿腹膜炎极为罕见的原因。

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