Harwal Rahul, Joseph Rosemary Livin Jose, Raju Prabhakaran, Chidambaranathan Sugumar, Bharathi Vidya Jayanthi J, Obla Lakshmanamoorthy Naganath Babu
Institute of Surgical Gastroenterology, Madras Medical College and Rajiv Gandhi Government General Hospital, Chennai, India.
ACG Case Rep J. 2023 Jan 20;10(1):e00962. doi: 10.14309/crj.0000000000000962. eCollection 2023 Jan.
Perivascular epithelioid cell tumors (PEComas) are rare mesenchymal neoplasms, and liver PEComas are extremely rare. They are usually discovered incidentally, and diagnostic pitfalls are frequent owing to similar imaging characteristics to other liver neoplasms. We present a patient whose evaluation was consistent with a right-sided hepatocellular carcinoma for which right hepatectomy was performed. Based on the final histopathological examination and immunohistochemistry, a diagnosis of PEComa was made. Immunohistochemistry plays a crucial role in arriving at the diagnosis, and resection represents the standard of care. A long-term follow-up is recommended because the natural history of PEComas is unpredictable.
血管周上皮样细胞肿瘤(PEComas)是罕见的间叶性肿瘤,而肝脏PEComas极其罕见。它们通常是偶然发现的,由于其影像学特征与其他肝脏肿瘤相似,诊断陷阱屡见不鲜。我们报告一例患者,其评估结果与右侧肝细胞癌相符,遂行右半肝切除术。基于最终的组织病理学检查和免疫组化结果,诊断为PEComa。免疫组化在诊断过程中起着关键作用,手术切除是标准的治疗方法。由于PEComas的自然病程不可预测,建议进行长期随访。