Nigam Neha, Rajani Shikha Singh, Rastogi Archana, Patil Anupama, Agrawal Nikhil, Sureka Binit, Arora Asit, Bihari Chhagan
Department of Pathology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Department of Pathology, Institute of Liver and Biliary Sciences, New Delhi, India.
J Lab Physicians. 2019 Oct-Dec;11(4):361-368. doi: 10.4103/JLP.JLP_63_19.
Inflammatory pseudotumor (IPT) of the liver is a rare, tumor-like lesion that is considered to be biologically benign but often mimics malignancy.
The aim of the study was construe clinicopathological features, imaging findings, differential diagnosis, management, and follow-up of IPT involving the liver.
It is a retrospective study.
Cases included were of IPT, diagnosed on histopathology, at our center from June 2009 to December 2016. Details studied were clinical presentation, imaging studies, laboratory investigations, pathological features, treatment, and follow-up of the cases and compared with reports in the literature.
A total of cases of IPT included were 17. The age of the patients ranged from 21 to 62 years. Common presenting features were intermittent fever, upper abdominal pain, and weight loss. Radiological diagnosis varied from neoplastic (13) to infectious etiologies (4), with hepatocellular carcinoma being the most common differential (7/17). Laboratory investigations revealed leukocytosis, hyperbilirubinemia, raised transaminases, and raised serum alkaline phosphatase. Core biopsy of a tumor conceded increased fibrosis along with mixed inflammatory cell infiltrates. Eleven cases were managed conservatively and showed regression or complete recovery. Six patients underwent surgical resection. None of these had any recurrence in median follow-up of 22 months.
IPT of the liver can masquerade as a fatality, either primary or metastatic. It will be well managed with conservative modalities and can avoid redundant hepatectomy, reserved for complicated cases. For this intent, accurate preoperative diagnosis is the requisite, and needle biopsy with or without fine-needle aspiration cytology plays as a significant rescuer in this field.
肝脏炎性假瘤(IPT)是一种罕见的肿瘤样病变,被认为是生物学上的良性病变,但常酷似恶性肿瘤。
本研究旨在分析累及肝脏的IPT的临床病理特征、影像学表现、鉴别诊断、治疗及随访情况。
这是一项回顾性研究。
纳入2009年6月至2016年12月在本中心经组织病理学诊断为IPT的病例。研究的详细内容包括病例的临床表现、影像学检查、实验室检查、病理特征、治疗及随访情况,并与文献报道进行比较。
共纳入17例IPT病例。患者年龄在21至62岁之间。常见的临床表现为间歇性发热、上腹部疼痛和体重减轻。影像学诊断从肿瘤性(13例)到感染性病因(4例)不等,肝细胞癌是最常见的鉴别诊断(7/17)。实验室检查显示白细胞增多、高胆红素血症、转氨酶升高和血清碱性磷酸酶升高。肿瘤的核心活检显示纤维化增加以及混合性炎性细胞浸润。11例采用保守治疗,病情缓解或完全恢复。6例患者接受了手术切除。在中位随访22个月期间,这些患者均无复发。
肝脏IPT可伪装成原发性或转移性致命疾病。采用保守治疗方法可有效管理该病,避免对复杂病例进行不必要的肝切除术。为此,准确的术前诊断是必要的,针吸活检联合或不联合细针穿刺细胞学检查在该领域起着重要的辅助作用。