Primary Colonic Epithelioid Angiosarcoma with Hepatic Metastasis: A Case Report.

Taehan Yongsang Uihakhoe chi Pub Date : 2022-03-01 Epub Date: 2021-10-18 DOI:10.3348/jksr.2021.0064
Jiyun Lim, Seong Sook Hong, Jiyoung Hwang, Hyun-Joo Kim, So-Young Jin
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Abstract

Colonic angiosarcoma is an extremely rare and aggressive malignant tumor with poor prognosis. We report a case of colonic epithelioid angiosarcoma with colonic obstruction and rapidly progressive hepatic metastasis in a 44-year-old female. Abdominal CT revealed a heterogeneously enhancing irregular mass in the ascending colon, causing proximal bowel distension. The patient underwent surgery, and histopathological examination revealed a poorly differentiated carcinoma. A follow-up liver dynamic MRI after 4 months revealed newly developed diffusely scattered numerous small nodules in both hepatic lobes with peripheral and nodular marked arterial hyperenhancement, raising the suspicion of hepatic angiosarcoma. A pathologic second opinion was obtained, and additional immunohistochemistry revealed colonic epithelioid angiosarcoma. The patient showed progressive hepatic metastasis on follow-up abdominal CT after 6 months and died 8 months after initial diagnosis. We describe an educational case of colonic angiosarcoma, a rare malignant tumor, with rapidly progressive hepatic metastasis that showed radiologic findings suggestive of angiosarcoma and enabled a re-diagnosis for proper treatment and prognosis prediction.

Abstract Image

原发性结肠上皮样血管肉瘤伴肝转移1例。
摘要结肠血管肉瘤是一种极为罕见且侵袭性的恶性肿瘤,预后差。我们报告一例44岁女性的结肠上皮样血管肉瘤合并结肠梗阻及快速进展性肝转移。腹部CT显示升结肠一不规则肿块,引起近端肠膨胀。患者接受手术,组织病理学检查显示为低分化癌。随访4个月后肝脏动态MRI示双叶新发弥漫性散在性大量小结节,周围及结节性动脉明显增高,怀疑肝血管肉瘤。病理第二意见,和额外的免疫组织化学显示结肠上皮样血管肉瘤。6个月后随访腹部CT显示进展性肝转移,初步诊断后8个月死亡。我们报告一例具有教育意义的结肠血管肉瘤病例,这是一种罕见的恶性肿瘤,具有快速进展的肝转移,其放射学表现提示血管肉瘤,并使其重新诊断,以进行适当的治疗和预后预测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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