Rare but Potentially Fatal Presentations of Diffuse Large B-cell Lymphoma: Leukemic Phase or Hemophagocytic Syndrome in Bone Marrow.

IF 1.9 Q3 PATHOLOGY Clinical Pathology Pub Date : 2022-01-09 eCollection Date: 2022-01-01 DOI:10.1177/2632010X211070774
Wan Awatif Wan Mohd Zohdi, Ahmad Zulhimi Ismail, Nurasyikin Yusof, Azlin Ithnin, Salwati Shuib, Noraidah Masir, Sivakumar Palaniappan, Nor Rafeah Tumian
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Abstract

Diffuse large B-cell lymphoma (DLBCL) is a type of non-Hodgkin Lymphoma commonly presenting as a solid tumor either by nodal or extra-nodal manifestations. Here we describe two atypical presentations of lymphoma, finally resulting in the diagnosis of DLBCL. Case 1: A 53-year-old man with a previous history of nasopharyngeal carcinoma presented with a two-week history of B-symptoms and hyperleukocytosis. Peripheral blood film showed 78% abnormal mononuclear cells. Immunohistochemical stain showing Ki-67 of 90%, negative c-myc, BCL2 and BCL6, and negative c-MYC with fluorescence in-situ hybridization studies on the trephine biopsy, concluded the diagnosis of CD5+ DLBCL of ABC subtype. He received intravenous cyclophosphamide and oral prednisolone for cytoreduction, followed by 6 cycles of chemo-immunotherapy. However, he succumbed due to severe sepsis after the completion of therapy. Case 2: A 56-year-old lady who was initially investigated for pyrexia of unknown origin was noted to have hemophagocytosis upon bone marrow aspirate examination. The bone marrow trephine biopsy revealed some atypical clusters of B-cells positive for CD20 which was inconclusive. PET-CT scan noted an enlarged hypermetabolic spleen without lymphadenopathy. Splenic biopsy with immunohistochemical studies revealed DLBCL of ABC subtype. The diagnosis was consistent with primary splenic DLBCL. She became unwell post splenic biopsy and was admitted to the intensive care unit where she passed away 2 weeks later from Candida and Sternotrophomonas septicemia. These cases highlight the atypical presentations of a common subtype of NHL in our center. Arriving at the definitive diagnosis can be difficult especially when patients are acutely ill, hampering the necessary invasive procedures for diagnosis. The outcomes of both cases are briefly discussed hoping to spread awareness among clinicians on the rare and acutely critical presentations of DLBCL.

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弥漫性大b细胞淋巴瘤罕见但可能致命的表现:骨髓白血病期或噬血细胞综合征。
弥漫性大b细胞淋巴瘤(DLBCL)是一种非霍奇金淋巴瘤,通常表现为实体瘤,有淋巴结或结外表现。这里我们描述了两个非典型的淋巴瘤表现,最终导致DLBCL的诊断。病例1:53岁男性,既往鼻咽癌病史,有两周b症状和白细胞增多史。外周血膜显示78%的单核细胞异常。免疫组化染色显示Ki-67为90%,c-myc、BCL2、BCL6阴性,环甲活检c-myc荧光原位杂交阴性,诊断为ABC亚型CD5+ DLBCL。静脉注射环磷酰胺和口服强的松龙减少细胞,随后化疗免疫治疗6个周期。然而,在治疗完成后,他因严重的败血症而死亡。病例2:一位56岁的女士,她最初因不明原因的发热而接受调查,在骨髓抽吸检查时发现有噬血细胞症。骨髓穿刺活检显示一些不典型的CD20阳性b细胞簇,这是不确定的。PET-CT扫描显示脾脏高代谢肿大,无淋巴结病变。脾活检和免疫组化研究显示为ABC亚型DLBCL。诊断符合原发性脾大细胞淋巴瘤。她在脾活检后感到不适,并被送进重症监护室,2周后因念珠菌和胸养单胞菌败血症去世。这些病例突出了我们中心NHL常见亚型的非典型表现。达到明确的诊断可能是困难的,特别是当病人是急性疾病,阻碍了必要的侵入性诊断程序。本文简要讨论了这两个病例的结果,希望能在临床医生中传播对罕见和急性关键的DLBCL表现的认识。
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来源期刊
Clinical Pathology
Clinical Pathology PATHOLOGY-
CiteScore
2.20
自引率
7.70%
发文量
66
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