{"title":"肝小血管肿瘤1例,先前未报道G蛋白α亚家族热点突变","authors":"Minako Yamamura , Yasunori Sato , Kenta Takahashi , Hiep Nguyen Canh , Zihan Li , Kazuyoshi Hosomichi , Atsushi Tajima , Takuro Terada , Yasuni Nakanuma , Kenichi Harada","doi":"10.1016/j.hpr.2022.300660","DOIUrl":null,"url":null,"abstract":"<div><p>Hepatic small vessel neoplasm (HSVN) is a very rare and recently described entity. Moreover, it is a vascular neoplasm of the liver composed of small vessels with infiltrative borders that mimic hepatic angiosarcoma. Based on its lack of atypical morphological features and high proliferative activity, HSVN is thought to be a benign or low-grade neoplasm; however, there is a lack of follow-up information. Here, we present a 51 year-old man with an incidental segment VIII lesion of the liver that displayed plethoric features, which was suspected to be a neoplasm. The patient underwent a segment anterior sectionectomy. The resected liver tumor demonstrated a 2.0 cm by 1.2 cm tan red and partially ill-defined mass, and microscopical examination confirmed HSVN, although the previously identified mutations in HSVN, <em>GNAQ</em>, <em>GNA11</em>, <em>GNA14</em>, and <em>PIK3CA</em> were not detected by genetic testing. The patient’s postoperative recovery was uncomplicated, and abdominal computed tomography at 6 months and 12 months post-surgery revealed no evidence of recurrence. HSVN is a recently described vascular tumor liver with uncertain malignant potential. More research is warranted to establish guidelines for an accurate diagnosis and to elucidate the clinical course of these tumors.</p></div>","PeriodicalId":100612,"journal":{"name":"Human Pathology Reports","volume":"29 ","pages":"Article 300660"},"PeriodicalIF":0.0000,"publicationDate":"2022-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772736X2200072X/pdfft?md5=019d3bc64c67fbffd8afb106318477b6&pid=1-s2.0-S2772736X2200072X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"A case of hepatic small vessel neoplasm without previously reported hotspot mutation of alpha subfamily of G proteins\",\"authors\":\"Minako Yamamura , Yasunori Sato , Kenta Takahashi , Hiep Nguyen Canh , Zihan Li , Kazuyoshi Hosomichi , Atsushi Tajima , Takuro Terada , Yasuni Nakanuma , Kenichi Harada\",\"doi\":\"10.1016/j.hpr.2022.300660\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Hepatic small vessel neoplasm (HSVN) is a very rare and recently described entity. Moreover, it is a vascular neoplasm of the liver composed of small vessels with infiltrative borders that mimic hepatic angiosarcoma. Based on its lack of atypical morphological features and high proliferative activity, HSVN is thought to be a benign or low-grade neoplasm; however, there is a lack of follow-up information. Here, we present a 51 year-old man with an incidental segment VIII lesion of the liver that displayed plethoric features, which was suspected to be a neoplasm. The patient underwent a segment anterior sectionectomy. The resected liver tumor demonstrated a 2.0 cm by 1.2 cm tan red and partially ill-defined mass, and microscopical examination confirmed HSVN, although the previously identified mutations in HSVN, <em>GNAQ</em>, <em>GNA11</em>, <em>GNA14</em>, and <em>PIK3CA</em> were not detected by genetic testing. The patient’s postoperative recovery was uncomplicated, and abdominal computed tomography at 6 months and 12 months post-surgery revealed no evidence of recurrence. HSVN is a recently described vascular tumor liver with uncertain malignant potential. More research is warranted to establish guidelines for an accurate diagnosis and to elucidate the clinical course of these tumors.</p></div>\",\"PeriodicalId\":100612,\"journal\":{\"name\":\"Human Pathology Reports\",\"volume\":\"29 \",\"pages\":\"Article 300660\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2772736X2200072X/pdfft?md5=019d3bc64c67fbffd8afb106318477b6&pid=1-s2.0-S2772736X2200072X-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Human Pathology Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2772736X2200072X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Pathology Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772736X2200072X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
肝小血管肿瘤(HSVN)是一种非常罕见的肿瘤。此外,它是一种肝脏血管肿瘤,由具有浸润性边界的小血管组成,类似于肝血管肉瘤。基于其缺乏非典型形态特征和高增殖活性,HSVN被认为是一种良性或低级别肿瘤;然而,缺乏后续信息。在这里,我们报告一位51岁的男性肝脏偶发的VIII节段病变,表现出过多的特征,怀疑是肿瘤。患者接受了前节段切除术。切除的肝肿瘤显示为2.0 cm × 1.2 cm的棕红色肿块,部分不明确,显微镜检查证实为HSVN,尽管先前鉴定的HSVN、GNAQ、GNA11、GNA14和PIK3CA突变未通过基因检测检测到。患者术后恢复简单,术后6个月和12个月腹部计算机断层扫描显示无复发迹象。HSVN是最近发现的一种肝脏血管肿瘤,其恶性潜能不确定。需要更多的研究来建立准确诊断的指导方针,并阐明这些肿瘤的临床病程。
A case of hepatic small vessel neoplasm without previously reported hotspot mutation of alpha subfamily of G proteins
Hepatic small vessel neoplasm (HSVN) is a very rare and recently described entity. Moreover, it is a vascular neoplasm of the liver composed of small vessels with infiltrative borders that mimic hepatic angiosarcoma. Based on its lack of atypical morphological features and high proliferative activity, HSVN is thought to be a benign or low-grade neoplasm; however, there is a lack of follow-up information. Here, we present a 51 year-old man with an incidental segment VIII lesion of the liver that displayed plethoric features, which was suspected to be a neoplasm. The patient underwent a segment anterior sectionectomy. The resected liver tumor demonstrated a 2.0 cm by 1.2 cm tan red and partially ill-defined mass, and microscopical examination confirmed HSVN, although the previously identified mutations in HSVN, GNAQ, GNA11, GNA14, and PIK3CA were not detected by genetic testing. The patient’s postoperative recovery was uncomplicated, and abdominal computed tomography at 6 months and 12 months post-surgery revealed no evidence of recurrence. HSVN is a recently described vascular tumor liver with uncertain malignant potential. More research is warranted to establish guidelines for an accurate diagnosis and to elucidate the clinical course of these tumors.