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| Percutaneous liver biopsy: retrospective study of primary and secondary hepatic lymphoma in twenty-one patients |
| Yan-Feng Bai, Ji-Min Liu, Xiu-Ming Zhang, Chao-Zhe Jiang, Xiao Xu and Shu-Sen Zheng |
Hangzhou, China
Author Affiliations: Department of Pathology (Bai YF, Liu JM, Zhang XM and Jiang CZ); Division of Hepatobiliary Pancreatic Surgery (Xu X and Zheng SS), the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China; and Department of Pathology and Molecular Medicine, Faculty of Health Sciences, McMaster University, Hamilton L8S 4K1, Canada (Liu JM)
Corresponding Author: Shu-Sen Zheng, MD, PhD, FACS, Division of Hepatobiliary Pancreatic Surgery, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China (Tel: +86-571- 87236570; Fax: +86-571-87236628; Email: shusenzheng@zju.edu.cn) |
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Abstract BACKGROUND: Hepatic lymphoma (HL) is categorized as primary and secondary hepatic lymphoma (PHL and SHL). This disorder can present as hepatic mass or mass-like lesion. Chemotherapy often is the first line treatment for patients with HL. Thus, an accurate pre-management histological diagnosis is essential to potentially improve clinical outcomes. The present study was to explore the prevalence of HL in ultrasound guided liver biopsies for hepatic mass or mass-like lesions, to investigate HL associated clinicopathological features, to raise the awareness of early recognition and proper diagnosis of this entity, and to assess specimen adequacy in needle core biopsy.
METHODS: Twenty-one cases of HL were enrolled. Clinical and pathological characteristics were evaluated, quality of biopsies was assessed and pertinent literature was reviewed.
RESULTS: HL was diagnosed in 0.94% of 2242 liver biopsy cases with ambiguous clinical presentation, laboratory tests and image studies. There were two cases of PHL (0.09%), and nineteen cases of SHL (0.85%). Histopathologically, diffuse large B-cell lymphoma was the most common type, followed by B-cell lymphoma not otherwise specified, T-cell lymphoma, Hodgkin’s lymphoma, and B-cell chronic lymphocytic leukemia/small lymphocytic lymphoma. Additionally, three lymphocytic infiltration patterns were documented microscopically. The nodular infiltration was the most common type.
CONCLUSIONS: HL is a rare entity and histopathology along with ancillary tests remains the only way to make the diagnosis. Clinicians’ awareness of this entity and early liver biopsy are essential in patient management.
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2017, Vol. 16 
