Aberrant CD3 positive plasmablastic lymphoma of small bowel in a HIV negative, EBV negative patient: A case report.

IF 0.5 Indian journal of pathology & microbiology Pub Date : 2025-07-01 Epub Date: 2025-02-07 DOI:10.4103/ijpm.ijpm_228_24
Umama Idrees, Mayurakshi Das, Anuradha Sekaran, Duvvur N Reddy
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Abstract

Abstract: Plasmablastic lymphoma (PBL) is an aggressive lymphoma with the proliferation of plasmablastic cells with a plasma cell immunophenotype and immunonegativity for B-cell markers. Here we present a case of jejunal PBL in an 82-year-old human immunodeficiency virus (HIV) negative and Epstein-Barr (EBV) negative male who presented with subacute intestinal obstruction and histopathological examination showed a large cell lymphoma with plasmablastic differentiation diffusely infiltrating full thickness of the jejunal wall. Neoplastic cells were immunopositive for CD138, MUM-1, EMA, and CD56, along with aberrant expression of pan T-cell marker CD3. No restrictions for kappa and lambda light chains were noted. Ki67 index was >90%. Tumor cells were immunonegative for CD20, CD5, CD7, CD30, and PAX 5. Suspicion of this rare and high-grade lymphoma in immunocompetent patients and at extra-nodal locations along with awareness of diagnostic pitfalls in its immunoprofile will aid in accurate diagnosis and prognostication.

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1例HIV阴性、EBV阴性患者发生小肠异常CD3阳性浆母细胞淋巴瘤。
摘要:浆母细胞淋巴瘤(PBL)是一种侵袭性淋巴瘤,伴有浆细胞免疫表型和b细胞标记物免疫阴性的浆母细胞增殖。我们报告一例82岁男性空肠PBL,表现为亚急性肠梗阻,组织病理学检查显示大细胞淋巴瘤伴质母细胞分化,弥漫性浸润全层空肠壁。肿瘤细胞CD138、MUM-1、EMA和CD56免疫阳性,泛t细胞标志物CD3异常表达。kappa和lambda轻链没有限制。Ki67指数为bb0.90 %。肿瘤细胞对CD20、CD5、CD7、CD30和pax5均呈免疫阴性。在免疫功能正常的患者和淋巴结外部位怀疑这种罕见的高级别淋巴瘤,并意识到其免疫谱的诊断缺陷,将有助于准确的诊断和预后。
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