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肝脏炎性假瘤(IPT)及肝脏IPT样病变的临床病理特征与转归

Clinicopathologic features and outcomes of hepatic inflammatory pseudotumour (IPT) and hepatic IPT-like lesions.

作者信息

Nguyen Eric D, Wen Kwun Wah, Kakar Sanjay, Balitzer Dana J

机构信息

Department of Pathology, University of California, San Francisco, San Francisco, CA, USA.

Cellnetix Pathology & Laboratories, Seattle, WA, USA.

出版信息

Histopathology. 2025 Mar;86(4):525-535. doi: 10.1111/his.15357. Epub 2024 Oct 31.

Abstract

AIMS

Hepatic inflammatory pseudotumours (IPTs) are nonneoplastic hepatic masses characterized by variably fibroblastic stroma and inflammatory infiltrate, hypothesized to arise as part of a response to infection or prior surgery. The aim of this study was to evaluate the clinicopathologic features and outcomes of biopsy-proven hepatic IPT as well as other cases with IPT-like histologic features.

METHODS AND RESULTS

A database search at our institution identified cases with a pathologic diagnosis of hepatic IPT (n = 80) between 2000 and 2023. Histologic features (stromal quality, inflammatory cell components, granulomas, and necrosis) were evaluated. Past medical and surgical history, microbiologic studies, and outcomes were reviewed retrospectively. Patients frequently had a past medical history of malignancy (34%), biliary disease (15%), or prior intraabdominal surgery (24%), and often presented with multifocal hepatic lesions (36%). Variable inflammatory backgrounds were present, including histiocytic (36%), lymphoplasmacytic (34%), or neutrophilic (24%). Specific organisms were identified in 15% of cases, most commonly Klebsiella and Staphylococcus species. Most patients with available clinical follow-up demonstrated radiologic resolution and/or had repeat negative biopsy; a minority of patients (8%) were subsequently diagnosed with neoplastic hepatic lesions. No significant association was seen between histologic features and the subsequent clinical or pathologic diagnosis of hepatic neoplastic lesions.

CONCLUSIONS

Hepatic IPT is a heterogeneous entity that can present in a variety of clinical scenarios and show a wide morphologic spectrum. These lesions often regress spontaneously or with antibiotics. A subset of cases with hepatic IPT-like histologic features were subsequently diagnosed with malignancy, emphasizing the need for continued follow-up and repeat biopsy depending on clinical and radiologic features.

摘要

目的

肝炎性假瘤(IPT)是一种非肿瘤性肝肿块,其特征为不同程度的纤维母细胞性间质和炎症浸润,推测其发生是对感染或既往手术的一种反应。本研究的目的是评估经活检证实的肝IPT以及其他具有IPT样组织学特征的病例的临床病理特征和预后。

方法与结果

对我们机构的数据库进行检索,确定了2000年至2023年间病理诊断为肝IPT的病例(n = 80)。评估了组织学特征(间质质量、炎症细胞成分、肉芽肿和坏死)。回顾性分析既往病史和手术史、微生物学研究及预后。患者常有恶性肿瘤病史(34%)、胆道疾病(15%)或既往腹部手术史(24%),且常表现为多灶性肝病变(36%)。存在多种炎症背景,包括组织细胞性(36%)、淋巴浆细胞性(34%)或中性粒细胞性(24%)。15%的病例中鉴定出特定病原体,最常见的是克雷伯菌属和葡萄球菌属。大多数有临床随访资料的患者显示影像学消退和/或再次活检阴性;少数患者(8%)随后被诊断为肝脏肿瘤性病变。组织学特征与随后肝脏肿瘤性病变的临床或病理诊断之间未发现显著关联。

结论

肝IPT是一种异质性实体,可出现在多种临床情况下,形态学谱广泛。这些病变通常可自发消退或经抗生素治疗后消退。一部分具有IPT样组织学特征的病例随后被诊断为恶性肿瘤,强调根据临床和影像学特征持续随访和再次活检的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31e8/11791728/1f36ca835a04/HIS-86-525-g001.jpg

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