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多发性胃肠道血管畸形:两例报告。

Multiple Gastrointestinal Haemangiomatosis: A Report of Two Cases.

机构信息

Department of Paediatric Surgery, Sefako Makgatho Health Sciences University, Ga-Rankuwa, South Africa.

出版信息

Afr J Paediatr Surg. 2024 Jan 1;21(1):78-80. doi: 10.4103/ajps.ajps_87_22. Epub 2024 Jan 20.

Abstract

Gastrointestinal (GI) haemangiomatosis is a very rare cause of GI bleeding in children. Due to this fact, making the diagnosis sometimes is delayed. In this case report, two different patients with multiple GI haemangiomatosis are presented. Of note is an 8 year old male with a previous history of a vascular malformation of the face presented with features of bowel obstruction (intussusception) and a history of recurrent blood in stool. At laparotomy, multiple haemangiomatosis were seen on the small bowel, right colon, liver, diaphragm and on the body of the gallbladder. Surgical management with excision of the enteric lesions and stapled anastomosis was done.

摘要

胃肠道(GI)血管瘤病是儿童胃肠道出血的一个非常罕见的原因。由于这个事实,有时会延误诊断。在本病例报告中,介绍了两名患有多发性胃肠道血管瘤病的不同患者。值得注意的是,一名 8 岁男性,有面部血管畸形病史,表现为肠梗阻(肠套叠)特征和反复便血病史。剖腹手术时,在小肠、右结肠、肝脏、膈肌和胆囊体上可见多处血管瘤病。采用切除肠内病变和吻合器吻合的手术治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e1/10903737/2c09da898c7d/AJPS-21-78-g001.jpg

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