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十二指肠平滑肌肉瘤及其多次复发:三年随访后的良好手术结果。

Duodenal leiomyosarcoma and its multiple recurrences: good surgical result after three years of follow-up.

作者信息

Pedrazzoli S, Sperti C, Militello C, Chiappetta A, Pomerri F, Petrin P

出版信息

Ital J Surg Sci. 1984;14(4):321-6.

PMID:6533116
Abstract

Duodenal leiomyosarcoma is a rare tumor and its current prognosis is poor. A case of duodenal leiomyosarcoma is described which recurred five years after the first intestinal resection, and was treated successfully with pancreaticoduodenectomy (PCD), extensive small bowel resection, and transverse, descending and sigmoid colon removal. The patient is still alive three years after this operation. Preservation of the stomach and the first duodenal portion after PCD most likely reduced the malabsorption, which is expected following such radical intestinal resection. This experience suggests an aggressive surgical approach to duodenal leiomyosarcomas, even when metastases are present.

摘要

十二指肠平滑肌肉瘤是一种罕见肿瘤,目前其预后较差。本文描述了一例十二指肠平滑肌肉瘤患者,该患者在首次肠道切除术后5年复发,随后成功接受了胰十二指肠切除术(PCD)、广泛小肠切除术以及横结肠、降结肠和乙状结肠切除术。该患者术后3年仍然存活。PCD术后保留胃和十二指肠第一部极有可能减少了这种根治性肠道切除术后预期会出现的吸收不良。这一经验表明,即使存在转移,对十二指肠平滑肌肉瘤也应采取积极的手术方法。

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