General Surgery, Fiona Stanley Hospital, Murdoch, Western Australia, Australia
Anatomical Pathology, Australian Clinical Labs, Clayton, Victoria, Australia.
BMJ Case Rep. 2023 Nov 15;16(11):e254963. doi: 10.1136/bcr-2023-254963.
Hepatic reactive lymphoid hyperplasia is an uncommon benign condition, often found incidentally as a solitary liver lesion. The chronic inflammatory reaction associated with autoimmune conditions and malignancies has been postulated as a possible aetiology. The diagnosis is challenging as it often mimics various malignancies radiologically and histologically, hence the diagnosis being made only after surgical resection. Lymphadenopathy is common with primary biliary cholangitis, though rarely reported with reactive lymphoid hyperplasia. We report a case of hepatic reactive lymphoid hyperplasia associated with portacaval lymphadenopathy in a patient with primary biliary cholangitis, diagnosed after surgical resection. We propose lesional biopsy be considered in patients with primary biliary cholangitis found to have a solitary lesion with supporting low-risk clinical and radiological features.
肝反应性淋巴组织增生是一种不常见的良性病变,常作为孤立性肝病变偶然发现。与自身免疫性疾病和恶性肿瘤相关的慢性炎症反应被认为是一种可能的病因。由于其在影像学和组织学上常模仿各种恶性肿瘤,因此诊断具有挑战性,只有在手术切除后才能做出诊断。原发性胆汁性胆管炎常伴有淋巴结病,尽管很少有反应性淋巴组织增生的报道。我们报告了一例原发性胆汁性胆管炎患者伴门腔淋巴结病的肝反应性淋巴组织增生,该病例在手术切除后诊断。我们建议对发现具有支持低风险临床和影像学特征的孤立性病变的原发性胆汁性胆管炎患者考虑进行病变活检。