Haque Saadiya A, Xiang Ying, Ozdemirli Metin, Shad Aziza, Kallakury Bhaskar
Department of Pathology;
Pediatr Rep. 2010 Jun 18;2(1):e11. doi: 10.4081/pr.2010.e11.
Hepatosplenic T-cell lymphoma (HSTL) is rare, being derived from cytotoxic T-cells, and manifests as an extranodal systemic lymphoma. We present an unusual case of a seventeen-year-old female, with no significant prior medical history, presenting with a hepatosplenic T-cell lymphoma. The diagnosis was confirmed by histological examination, immunohistochemisty, and flow cytometry. A staging work-up demonstrated bone marrow involvement by HSTL with concomitant intranuclear parvoviral inclusions.
肝脾T细胞淋巴瘤(HSTL)较为罕见,起源于细胞毒性T细胞,表现为结外系统性淋巴瘤。我们报告了一例不寻常的病例,一名17岁女性,既往无重大病史,被诊断为肝脾T细胞淋巴瘤。诊断通过组织学检查、免疫组织化学和流式细胞术得以证实。分期检查显示该肝脾T细胞淋巴瘤累及骨髓,并伴有核内细小病毒包涵体。