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肝血管平滑肌脂肪瘤伴巨大血管瘤。

Hepatic angiomyolipoma with a giant hemangioma.

作者信息

Tani Aya, Yoshida Hiroshi, Mamada Yasuhiro, Taniai Nobuhiko, Mineta Sho, Yoshioka Masato, Kawano Yoichi, Ueda Junji, Naito Zenya, Uchida Eiji

机构信息

Surgery for Organ Function and Biological Regulation, Graduate School of Medicine, Nippon Medical School.

出版信息

J Nippon Med Sch. 2011;78(5):317-21. doi: 10.1272/jnms.78.317.

Abstract

Hepatic angiomyolipoma is a rare hepatic mesenchymal tumor. We report a case of hepatic angiomyolipoma that was successfully resected along with a giant hemangioma. A 53-year-old Japanese woman was admitted to our hospital for further evaluation of a liver tumor in segment 4. The tumor was detected on positron emission tomography during a health check-up. Abdominal ultrasonography revealed a well-defined mass of mixed echogenicity, 1.5 cm in diameter, in segment 4, and a giant hemangioma of mixed echogenicity, 7 cm in diameter, in segment 7. On enhanced computed tomography, the tumor in segment 4 showed hyperattenuation in the early phase and hypoattenuation in the delayed phase. On magnetic resonance imaging, the tumor in segment 4 showed hypointensity on T1-weighted images, hyperintensity on T2-weighted images, and hyperintensity on diffusion-weighted images. On angiography, the tumor in segment 4 appeared as a circumscribed hypervascular mass in the early phase and a slightly hypovascular mass in the delayed phase. The imaging findings suggested a primary hepatocellular carcinoma. The patient consented to resection of the tumor in segment 4 along with the giant hemangioma in segment 7. These tumors were resected with tumor-free surgical margins by partial resection of segments 4 and 7 of the liver. The cut surface of the resected specimen of segment 4 showed a yellowish tumor consisting of mature adipose tissue. The histopathological diagnoses of the resected specimens were angiomyolipoma in segment 4 and cavernous hemangioma in segment 7. The tumor in segment 4 consisted of mature lipocytes with angiomatous and small lymphocytic components, but no mitotic figures. The tumor showed immunoreactivity to smooth muscle antigen and homatropine methylbromide 45 and no immunoreactivity to AE/E3. The postoperative course was uneventful, and the patient remains well 1 year after the operation.

摘要

肝血管平滑肌脂肪瘤是一种罕见的肝脏间叶性肿瘤。我们报告一例肝血管平滑肌脂肪瘤,该肿瘤与巨大血管瘤一起成功切除。一名53岁的日本女性因进一步评估肝脏第4段肿瘤而入住我院。该肿瘤在健康体检的正电子发射断层扫描中被发现。腹部超声检查显示,第4段有一个边界清晰、直径1.5厘米的混合回声肿块,第7段有一个直径7厘米的混合回声巨大血管瘤。增强计算机断层扫描显示,第4段肿瘤在早期呈高密度,延迟期呈低密度。磁共振成像显示,第4段肿瘤在T1加权图像上呈低信号,T2加权图像上呈高信号,扩散加权图像上呈高信号。血管造影显示,第4段肿瘤在早期表现为边界清晰的高血运肿块,延迟期表现为略低血运肿块。影像学表现提示为原发性肝细胞癌。患者同意切除第4段肿瘤及第7段巨大血管瘤。通过部分切除肝脏第4段和第7段,以无瘤手术切缘切除了这些肿瘤。第4段切除标本的切面显示为一个由成熟脂肪组织组成的黄色肿瘤。切除标本的组织病理学诊断为第4段血管平滑肌脂肪瘤和第7段海绵状血管瘤。第4段肿瘤由成熟的脂肪细胞以及血管性和小淋巴细胞成分组成,但未见有丝分裂象。该肿瘤对平滑肌抗原和甲基溴化后马托品呈免疫反应,对AE/E3无免疫反应。术后过程顺利,患者术后1年情况良好。

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