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原发性肝淋巴瘤——一例病例报告及文献综述

Primary lymphoma of the liver - a case-report and a review of the literature.

作者信息

Franchi R, Abbiati C, Signaroldi A, Quadrelli G, Maggioni M, Sbalzarini G

机构信息

OSPED CIV CASALPUSTERLENGO,SERV RADIOL,I-20071 CASALPUSTERLENGO,ITALY. UNIV MILAN,CATTEDRA ANAT & ISTOL PATOL 2,MILAN,ITALY.

出版信息

Oncol Rep. 1995 Nov;2(6):1017-9. doi: 10.3892/or.2.6.1017.

DOI:10.3892/or.2.6.1017
PMID:21597845
Abstract

A case of primary lymphoma of the liver in a 72-year-old man is reported. The patient showed a three to four month history of abdominal ache, low grade fever, and weight loss. The presence of a large mass occupying the V and VT hepatic segments was demonstrated; no other organs were involved and no evidence of lymphoadenopathy was found. Laboratory tests showed a remarkable increase in ESR, LDH and alkaline phosphatase while CEA and alpha-1 fetoprotein were within the normal values. Two ultrasound-guided needle biopsies on the hepatic lesion did not produce any significant tissue for diagnosis. Therefore the V and VI hepatic segments were excised; a hard, greyish mass with the largest diameter of 6.5 cm, was found at laparatomy. Histology of the surgical specimen showed the presence of a malignant non-Hodgking's B-cell lymphoma, centroblastic-centrocytic, diffuse type (working formulation: G) of intermediate grade of malignancy. Staging was completed with lymphography, and bone marrow biopsy; both proved normal. After the operation adjuvant chemotherapy was commenced (COP for six cycles). Follow-up has so far shown no signs of recurrence after 24 months. In conclusion, the diagnosis of primary lymphoma of the liver is very difficult and is often reached only after histologic evaluation of the surgical specimen. Moreover, this disease has a much more favourable prognosis than the hepatocellular carcinoma and other primary or secondary liver cancers; therefore accurate investigations are important to reach the correct diagnosis.

摘要

报告了一例72岁男性原发性肝淋巴瘤病例。患者有三到四个月的腹痛、低热和体重减轻病史。影像学检查显示肝脏V段和VII段有一个大肿块;未累及其他器官,也未发现淋巴结肿大。实验室检查显示血沉、乳酸脱氢酶和碱性磷酸酶显著升高,而癌胚抗原和甲胎蛋白在正常范围内。对肝脏病变进行两次超声引导下穿刺活检均未获取到有诊断意义的组织。因此,切除了肝脏V段和VI段;剖腹手术时发现一个坚硬的灰色肿块,最大直径为6.5厘米。手术标本组织学检查显示为恶性非霍奇金B细胞淋巴瘤,中心母细胞-中心细胞型,弥漫型(工作分类:G),恶性程度为中度。通过淋巴管造影和骨髓活检完成分期检查;结果均正常。术后开始辅助化疗(COP方案,共六个周期)。随访至今,24个月后未发现复发迹象。总之,原发性肝淋巴瘤的诊断非常困难,通常只有在对手术标本进行组织学评估后才能确诊。此外,这种疾病的预后比肝细胞癌和其他原发性或继发性肝癌要好得多;因此,准确的检查对于做出正确诊断很重要。

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