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空肠系膜原发性上皮样血管肉瘤引起腹腔出血:病例报告及文献复习
Authors Yang P , Wu Q, Zhou Y, Li Y
Received 6 December 2023
Accepted for publication 12 March 2024
Published 10 April 2024 Volume 2024:17 Pages 327—338
DOI https://doi.org/10.2147/OTT.S453698
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Arseniy Yuzhalin
Abstract: Gastrointestinal angiosarcoma is an extremely rare malignant tumor of the digestive tract, characterized by a very poor prognosis, with few patients surviving more than 1 year after diagnosis. This case report describes a 71-year-old female patient with a 3-year history of intermittent abdominal pain and significant exacerbation of abdominal pain and bloating 2 weeks prior to treatment. After surgical treatment, the pathological and immunohistochemical diagnosis was primary epithelioid angiosarcoma of the jejunal mesentery. The patient refused postoperative adjuvant chemotherapy and died 4 months after diagnosis due to widespread systemic metastasis. In addition, this article reviews 38 previously reported cases of primary gastrointestinal angiosarcoma, aiming to further understand angiosarcoma and thus guide clinical practitioners in providing more comprehensive treatment approaches.
Keywords: gastrointestinal, angiosarcoma, hematochezia