Department of Pathology, Mianyang 404 Hospital, Mianyang, Sichuan Province, China.
Department of Pathology, Santai County People's Hospital, Mianyang, Sichuan Province, China.
Medicine (Baltimore). 2024 Oct 4;103(40):e39719. doi: 10.1097/MD.0000000000039719.
Angiosarcoma is an aggressive neoplasm derived from endothelial cells that may develop anywhere within the body. Here, we report a case of primary gastric epithelioid angiosarcoma initially misdiagnosed as poorly differentiated adenocarcinoma from the preoperative biopsy.
The patient was a 60-year-old male admitted to the hospital due to abdominal discomfort. The gastroscopy examination suggested advanced gastric cardia carcinoma. Subsequent biopsy pathology examination confirmed the diagnosis of poorly differentiated adenocarcinoma. Therefore, the patient underwent radical resection for proximal gastric cancer. Histopathology showed that the tumor cells were epithelioid with rich, eosinophilic cytoplasm. Immunohistochemical examination indicated that the tumor cells were CD34, CD31, and ERG.
Based on clinical, morphological, and immunophenotypic evidence, primary gastric epithelioid angiosarcoma diagnosis was confirmed.
The postoperative Tumor Node Metastasis staging was considered T4aN1Mx. The patient did not receive chemotherapy.
The patient died 3 months after the operation.
Primary gastric epithelioid angiosarcoma is a rare gastric tumor. Given the epithelioid cell features displayed by tumor cells and the high expression of epithelial markers in tumor cells (83%), preoperative diagnosis is difficult and should be differentiated from adenocarcinoma or gastrointestinal stromal tumor.
血管肉瘤是一种来源于内皮细胞的侵袭性肿瘤,可能发生在身体的任何部位。在此,我们报告了一例原发性胃上皮样血管肉瘤的病例,该病例最初在术前活检中被误诊为低分化腺癌。
患者为 60 岁男性,因腹部不适就诊。胃镜检查提示胃贲门癌晚期。随后的活检病理检查证实为低分化腺癌。因此,患者接受了近端胃癌根治性切除术。组织病理学显示肿瘤细胞呈上皮样,细胞质丰富,嗜酸性。免疫组织化学检查显示肿瘤细胞 CD34、CD31 和 ERG 阳性。
根据临床、形态学和免疫表型证据,确诊为原发性胃上皮样血管肉瘤。
术后肿瘤淋巴结转移分期为 T4aN1Mx。患者未接受化疗。
患者术后 3 个月死亡。
原发性胃上皮样血管肉瘤是一种罕见的胃肿瘤。鉴于肿瘤细胞表现出的上皮样细胞特征以及肿瘤细胞中上皮标志物的高表达(83%),术前诊断较为困难,应与腺癌或胃肠道间质瘤相鉴别。