肝脏 ›› 2022, Vol. 27 ›› Issue (3): 352-354.

• 其他肝病 • 上一篇    下一篇

肝脏血管周上皮样细胞肿瘤临床病理观察

周兵, 康玉斌, 王洁   

  1. 332000 江西 九江市第一人民医院病理科(周兵,王洁);九江学院护理学院(康玉斌)
  • 收稿日期:2021-02-23 出版日期:2022-03-31 发布日期:2022-05-31
  • 通讯作者: 周兵,Email:zhoubinglili@163.com
  • 基金资助:
    江西省卫生厅科技计划资助项目(202120056)

Perivascular epithelioid cell tumor in liver: a clinicopathological analysis

ZHOU Bing1, KANG Yu-bin2, WANG Jie1   

  1. 1. Department of Pathology, Jiujiang Frist Hospital, Jiangxi 332000,China;
    2. Nursing College of Jiujiang University, Jiangxi 332000, China
  • Received:2021-02-23 Online:2022-03-31 Published:2022-05-31
  • Contact: ZHOU Bing,Email:zhoubinglili@163.com

摘要: 目的 探讨肝脏血管周上皮样细胞肿瘤(PEComa)的临床病理特征、诊断与鉴别诊断及预后。方法 回顾性分析3例肝脏原发的PEComa,观察其临床表现、组织病理学及相关免疫组化表型,收集随访资料并复习相关文献。结果 3例患者均为女性,年龄39~60岁之间。2例无明显临床症状,1例因腹部胀痛入院。镜下见肿瘤与肝组织界限尚清,上皮样瘤细胞呈实性片状或巢状生长,胞浆嗜酸或透亮,间质见丰富的血管网,2例可见脂肪空泡。免疫组化主要表达Vim 、HMB45、Melan-A 和SMA。平均随访37个月,未见肿瘤复发或转移。结论 肝脏PEComa罕见,易与其它肝脏肿瘤相混淆,特异性的组织学特征和免疫组织化学标记在诊断及鉴别诊断上具有重要价值。

关键词: 血管周上皮样细胞肿瘤, 肝脏肿瘤, 临床病理学

Abstract: Objective To investigate clinicopathologic characteristics, diagnosis and differential diagnosis and prognosis of perivascular epithelioid cell tumor (PEComa) of liver.Methods The clinical and pathological features of 3 cases with liver PEComa were analyzed by histopathological and immunohistochemical testing. Clinical and follow-up information was obtained. The published relevant literatures were reviewed.Results All 3 patients were females, aged from 39 to 60 years. The most common symptoms were cough with sputum and exertional dyspnea; 2 case was asymptomatic and 1 case with bellyache. Microscopically, the boundary between tumor and normal liver tissue was clear, the epithelioid tumor cells were solid lamellar or nested arrangement, the cytoplasm was eosinophilic or translucent, abundant vascular network and fat vacuoles were found in the stroma. Immunohistochemically, the tumor cells were positive for Vim, HMB45, Melan-A and SMA. The average follow-up was 37 months, no tumor recurrence or metastasis was found.Conclusion PEComa of liver is rare and the clinical symptoms are atypical, definite diagnosis depends on characteristic histological morphology and immunohistochemical findings.

Key words: Perivascular epithelioid cell tumor, Liver neoplasma, Clinicopathologic