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空肠小肠重复畸形

[Jejunal small intestine duplication].

作者信息

Peiper M, Zornig C

机构信息

Abteilung für Allgemeinchirurgie, Universitäts-Krankenhaus Eppendorf, Hamburg.

出版信息

Langenbecks Arch Chir. 1994;379(6):358-60.

PMID:7845162
Abstract

Duplications of the alimentary tract are rare. Most of them are diagnosed during infancy or childhood, when they become symptomatic and a palpable mass is found. Major complications are bleeding, perforation, ileus and pancreatitis. In the majority of cases the gastro-intestinal duplication is localized in the small bowel. Correct preoperative diagnosis by means of imaging techniques is rare. Because there is no malignancy surgery is only necessary in symptomatic cases.

摘要

消化道重复畸形很罕见。它们大多在婴儿期或儿童期被诊断出来,此时会出现症状并可摸到肿块。主要并发症有出血、穿孔、肠梗阻和胰腺炎。在大多数情况下,胃肠道重复畸形位于小肠。通过影像学技术进行术前正确诊断很罕见。由于不存在恶性病变,仅在出现症状的病例中才需要手术。

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