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原发性脾血管肉瘤破裂至结肠。表现为肛门出血。

Ruptured primary splenic angiosarcoma into the colon. Presentation as anal bleeding.

作者信息

Jiménez-Heffernan J A, Hardisson D, Prieto-Nieto M I, Burgos E

机构信息

Department of Pathology, University Hospital La Paz, Madrid, Spain.

出版信息

Acta Gastroenterol Belg. 1999 Apr-Jun;62(2):248-51.

Abstract

A 71-year-old woman presented with a six month history of constipation and abdominal discomfort, with anal bleeding during the last days. Ultrasonography and CT-scan of the abdomen showed a large heterogeneous mass that was located in the splenic region, but the nature and origin of the tumour could not be clearly established preoperatively. The clinical diagnosis was of abdominal tumour with colonic and splenic involvement, and a left hemicolectomy and splenectomy were performed. Pathologic examination revealed a primary angiosarcoma of the spleen with penetration and fistulization of the tumour into the large bowel. The patient received adjuvant radiation therapy, but she died of extensive metastastic disease from her primary angiosarcoma of the spleen nine months after surgery. In summary, splenic angiosarcoma is very difficult to diagnose preoperatively. This highly aggressive neoplasm has an overall poor prognosis, specially if it is associated with rupture and haemoperitoneum. As this case highlights, unusual forms of rupture may lead to atypical clinical presentations, increasing even more the difficulty in the diagnosis.

摘要

一名71岁女性,有6个月便秘及腹部不适病史,近几日出现肛门出血。腹部超声及CT扫描显示脾区有一巨大不均匀肿块,但术前无法明确肿瘤的性质及起源。临床诊断为累及结肠和脾脏的腹部肿瘤,遂行左半结肠切除术及脾切除术。病理检查显示为脾脏原发性血管肉瘤,肿瘤侵犯并瘘入大肠。患者接受了辅助放疗,但术后9个月死于脾脏原发性血管肉瘤广泛转移。总之,脾脏血管肉瘤术前很难诊断。这种侵袭性很强的肿瘤总体预后较差,尤其是伴有破裂和腹腔积血时。正如本病例所示,不寻常的破裂形式可能导致非典型临床表现,进一步增加诊断难度。

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