Hilar and Extrahepatic Inflammatory Pseudotumour: A Case Report and Systematic Literature Review.

IF 1.3 Q3 MEDICINE, GENERAL & INTERNAL Cureus Pub Date : 2025-02-26 eCollection Date: 2025-02-01 DOI:10.7759/cureus.79727
Nicole Hawkins, David Sun, Panuwat Pornkul, Kaeun Bae, Matan Ben David
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Abstract

Inflammatory pseudotumor (IPT) is a benign inflammatory lesion that is exceptionally rare in the biliary tree. Its clinical and radiological presentation mimics neoplastic disease, so diagnosis often relies on histology. Surgical resection is the mainstay of treatment. A case of histologically confirmed IPT in a 52-year-old female, successfully managed with surgical resection, is presented. A systematic literature review was conducted following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines to identify case reports and case series of IPT involving the extrahepatic bile ducts and liver hilum. Searches of PubMed and Embase (from January 1960 to December 2024) yielded 23 original articles that met inclusion criteria. Data on clinical presentation, management, and outcomes were analyzed. A total of 33 cases of hilar and extrahepatic IPT have been reported in the literature. Obstructive jaundice was the most common presentation (79% n=26/32) accompanied by biochemical elevation of liver function tests (91% n=21/23) and bilirubin (77% n=17/22). Surgical resection was the most common treatment (82% n=27/33) with excellent outcomes and only one case of recurrence. However, the follow-up period was relatively short (median of one year). Of five cases initially treated with steroids, three were successfully managed with steroids alone. The other two cases proceeded to surgical resection due to disease progression. Serum immunoglobulin-G4 was high in successfully managed cases and not reported in failed cases. Hilar and extrahepatic IPT is a rare pathology with a similar presentation to neoplastic disease, which can make diagnosis and management challenging. Surgical resection is the mainstay of management, however, in select cases, preoperative biopsy may help avoid unnecessary surgical intervention. Further studies with extended follow-up are needed to optimize diagnostic and therapeutic strategies.

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肝门及肝外炎性假瘤1例报告及系统文献复习。
炎性假瘤(IPT)是一种良性炎性病变,在胆道树异常罕见。它的临床和放射学表现与肿瘤疾病相似,因此诊断往往依赖于组织学。手术切除是治疗的主要方法。一例组织学证实IPT在一个52岁的女性,成功地管理与手术切除,提出。根据系统评价和荟萃分析(PRISMA)指南的首选报告项目进行系统文献综述,以确定涉及肝外胆管和肝门的IPT病例报告和病例系列。PubMed和Embase检索(从1960年1月到2024年12月)得到23篇符合纳入标准的原创文章。我们分析了临床表现、管理和结果的数据。文献报道肝门及肝外IPT共33例。梗阻性黄疸是最常见的表现(79% n=26/32),并伴有肝功能生化升高(91% n=21/23)和胆红素升高(77% n=17/22)。手术切除是最常见的治疗方法(82% n=27/33),预后良好,只有1例复发。然而,随访期相对较短(中位为1年)。在最初使用类固醇治疗的5例病例中,有3例仅使用类固醇治疗成功。另外2例因病情进展而行手术切除。血清免疫球蛋白g4在治疗成功的病例中较高,而在治疗失败的病例中未见报道。肝门和肝外IPT是一种罕见的病理,其表现与肿瘤疾病相似,可使诊断和治疗具有挑战性。手术切除是主要的治疗方法,然而,在某些情况下,术前活检可能有助于避免不必要的手术干预。需要进一步的研究和长期随访来优化诊断和治疗策略。
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