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原发性硬化性胆管炎患者的原发性肝黏膜相关B细胞淋巴瘤——一例最终需要肝移植的病例

Primary Hepatic Mucosa-Associated B-Cell Lymphoma in a Patient with Primary Sclerosing Cholangitis-A Case Ultimately Requiring Liver Transplantation.

作者信息

Novak Jerica, Đokić Mihajlo, Petrič Miha, Vozlič Diana, Živanović Milanka, Ranković Branislava, Trotovšek Blaž

机构信息

Department of Abdominal Surgery, University Medical Center Ljubljana, Zaloska 7, 1000 Ljubljana, Slovenia.

Medical Faculty Ljubljana, University of Ljubljana, Vrazov trg 2, 1000 Ljubljana, Slovenia.

出版信息

Diagnostics (Basel). 2025 Aug 19;15(16):2082. doi: 10.3390/diagnostics15162082.

Abstract

Primary hepatic extranodal marginal zone lymphoma of mucosa-associated type (MALT) is an extremely rare liver neoplasm. The lesions are often misdiagnosed for the most common primary hepatic malignancy, such as hepatocellular carcinoma and cholangiocarcinoma. As the diagnosis is most often made after the resection, there are still no clear guidelines for the optimal treatment of these patients. A 30-year-old male patient with known primary sclerosing cholangitis (PSC) was treated at the Department of Abdominal Surgery Ljubljana due to a mass in the right liver, believed to be an intrahepatic cholangiocarcinoma. Due to the extent of the disease, extended right hepatectomy with the resection of the hepatocholedochus, lymphadenectomy, and hepaticojejunal anastomosis were performed. After the surgery, the patient developed a small-for-size syndrome and therefore necessitated a liver transplantation (LT) that was afterwards successfully performed. This case highlights the diagnostic challenges of differentiating primary hepatic MALT lymphoma from cholangiocarcinoma on imaging, especially in patients with underlying liver disease. Preoperative confirmation of the malignant disease could potentially change treatment course in our patient. Therefore, a serious surgical complication with development of small-for-size syndrome after major hepatectomy could potentially be prevented. Regarding the underlying liver disease, the patient could probably be a candidate for LT with the bridging chemotherapy. Primary hepatic MALT lymphoma is an extremely rare liver lesion but remains a valid option in a differential diagnosis of liver lesions in patients with chronic viral infection or autoimmune disease, especially in settings of cirrhosis. Moreover, a high level of suspicion must be raised in young patients with solitary liver mass and autoimmune liver disease. Surgical resection is the best way to achieve elimination of the disease.

摘要

原发性肝黏膜相关型结外边缘区淋巴瘤(MALT)是一种极其罕见的肝脏肿瘤。这些病变常被误诊为最常见的原发性肝脏恶性肿瘤,如肝细胞癌和胆管癌。由于大多数情况下在切除术后才做出诊断,对于这些患者的最佳治疗仍没有明确的指南。一名30岁已知患有原发性硬化性胆管炎(PSC)的男性患者因右肝肿物在卢布尔雅那腹部外科接受治疗,该肿物被认为是肝内胆管癌。由于疾病范围,进行了扩大的右肝切除术,包括肝门胆管切除、淋巴结清扫和肝空肠吻合术。术后,患者出现了小肝综合征,因此需要进行肝移植(LT),随后成功实施。该病例突出了在影像学上区分原发性肝MALT淋巴瘤与胆管癌的诊断挑战,尤其是在有潜在肝脏疾病的患者中。术前对恶性疾病的确诊可能会改变我们这位患者的治疗过程。因此,有可能预防在大肝切除术后出现小肝综合征这一严重手术并发症。关于潜在的肝脏疾病,该患者可能是接受桥接化疗的肝移植候选者。原发性肝MALT淋巴瘤是一种极其罕见的肝脏病变,但在慢性病毒感染或自身免疫性疾病患者,尤其是肝硬化患者的肝脏病变鉴别诊断中仍是一个有效的选项。此外,对于患有孤立性肝肿物和自身免疫性肝病的年轻患者必须高度怀疑。手术切除是实现疾病消除的最佳方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fae/12385175/203195b030cf/diagnostics-15-02082-g001.jpg

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