Huda Tanweerul, Parwez Mohammad Masoom, Pandya Bharati
Department of General Surgery, AIIMS, Bhopal, Madhya Pradesh, India.
Gastrointest Tumors. 2021 Apr;8(2):58-62. doi: 10.1159/000513963. Epub 2021 Feb 18.
Hepatic EHE (epithelioid hemangioendothelioma) is an uncommon entity of vascular origin and a low-grade malignant tumor. Primary hepatic EHE is rare. These tumors can be multifocal at presentation like in the soft tissues, bones, brain, liver, and small intestine. First described by Weiss and Enzinger in 1982 as a malignant vascular neoplasm with indolent behavior. We report the case of a 23-year-old male, known case of chronic liver disease, who presented with incisional hernia following exploratory laparotomy 8 months back, performed for intestinal obstruction. Contrast-enhanced computed tomography abdomen revealed an incisional hernia with a large defect along with multiple lesions in the liver (suspected metastases) and peritoneal deposits and a few discrete lung nodules. Some areas of interloop collections were also noted. Biopsies were taken from the liver which revealed benign cirrhotic lesion. Relevant to the findings, multiple biopsies were performed and fluid was sent for evaluation. The liver biopsy came out positive for borderline vascular malignancy (epithelioid hemangioendothelioma). This was confirmed with the immunohistochemistry report. Epithelioid hemangioendothelioma occurs mostly in soft tissues of extremity and lungs. The involvement of the liver may be seen as metastasis or rarely as a primary tumor. The incidence of primary malignant hepatic hemangioendothelioma is about 0.1/100,000; the mean age at the time of diagnosis is 41.7 years, and male:female ratio is 2:3. Liver transplantation, hepatectomy, chemoembolization, radiotherapy, and chemotherapeutic agents are reported treatment regimens. Malignant EHE of liver presents as multiple hepatic nodules. Being locally aggressive, it can invade the peritoneum, gut, and lungs. Orthoptic liver transplantation appears to be the only remedy because of the multifocal nature of the disease. Partial hepatectomy is possible for localized tumors.
肝脏上皮样血管内皮瘤(EHE)是一种罕见的血管源性低度恶性肿瘤。原发性肝脏EHE较为罕见。这些肿瘤在发病时可呈多灶性,如同在软组织、骨骼、脑、肝脏和小肠中那样。1982年由韦斯和恩津格首次描述为一种具有惰性生物学行为的恶性血管肿瘤。我们报告一例23岁男性病例,该患者为慢性肝病患者,8个月前因肠梗阻接受剖腹探查术后出现切口疝。腹部增强计算机断层扫描显示有一个大缺损的切口疝,同时肝脏有多个病变(怀疑为转移灶)、腹膜种植以及一些散在的肺结节。还发现了一些肠袢间积液区域。对肝脏进行了活检,结果显示为良性肝硬化病变。鉴于这些发现,进行了多次活检并送检液体进行评估。肝脏活检结果显示为临界性血管恶性肿瘤(上皮样血管内皮瘤)阳性。免疫组化报告证实了这一结果。上皮样血管内皮瘤大多发生于四肢软组织和肺部。肝脏受累可表现为转移,极少情况下为原发性肿瘤。原发性恶性肝脏血管内皮瘤的发病率约为0.1/10万;诊断时的平均年龄为41.7岁,男女比例为2:3。据报道,治疗方案包括肝移植、肝切除术、化疗栓塞、放疗和化疗药物。肝脏恶性EHE表现为多个肝结节。由于其具有局部侵袭性,可侵犯腹膜、肠道和肺部。由于该病具有多灶性,原位肝移植似乎是唯一的治疗方法。对于局限性肿瘤可行部分肝切除术。