Concomitant Classic Hodgkin Lymphoma of Lymph Node and cMYC-Positive Burkitt Leukemia/Lymphoma of the Bone Marrow Presented Concurrently at the Time of Presentation: A Rare Combination of Discordant Lymphomas.

IF 3 Q2 Medicine
Clinical Medicine Insights-Blood Disorders Pub Date : 2016-08-03 eCollection Date: 2016-01-01 DOI:10.4137/CMBD.S39908
Dina S Soliman, Shehab Fareed, Einas Alkuwari, Halima El-Omri, Ahmad Al-Sabbagh, Amna Gameel, Mohamed Yassin
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引用次数: 3

Abstract

Discordant lymphoma is rare condition in which different types of malignant lymphomas occurring in different anatomic sites. The two diseases may present clinically as concurrent or sequential disease (10). Herein we are reporting a Pakistani female in her 60s, a carrier of hepatitis B virus with multiple comorbidities presented with cervical lymphadenopathy, diagnosed as Hodgkin's lymphoma, mixed cellularity. During the staging workup, the patient was discovered to have extensive bone marrow (BM) involvement by Burkitt leukaemia/lymphoma (BL). Cytogenetic analysis revealed positivity for t(8;14)(q24;q32) confirmed by Fluorescence In Situ Hybridization (FISH) for IGH/MYC. Epstein-Barr virus (EBV) was demonstrated heavily in our case, with (EBV) DNA of 24,295,560 copies/ml by PCR at time of presentation, in addition, the neoplastic cells in both diagnostic tissues (cervical lymph node and BM) demonstrated positivity for EBV. A diagnosis of concomitant EBV related discordant lymphoma (classical Hodgkin lymphoma (cHL) and Burkitt lymphoma (BL) in leukemic phase was made. Among all reported cases, this case is highly exceptional because it is the first case of discordant/composite lymphoma, with this combination and concomitant presentation. Since we are dealing with a case with an exceptionally rare combination, we found it significant to elaborate more on its clinical features, contributing factors including EBV role, response to treatment, complications, and prognosis.

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合并淋巴结经典霍奇金淋巴瘤和cmyc阳性伯基特白血病/骨髓淋巴瘤:罕见的不协调淋巴瘤组合。
不协调性淋巴瘤是一种罕见的情况,不同类型的恶性淋巴瘤发生在不同的解剖部位。这两种疾病在临床上可表现为并发或顺序性疾病(10)。在此,我们报告一名60多岁的巴基斯坦女性,乙型肝炎病毒携带者,多发性合并症表现为宫颈淋巴结病,诊断为霍奇金淋巴瘤,混合细胞性。在分期检查中,患者被发现有广泛的骨髓(BM)累及伯基特白血病/淋巴瘤(BL)。细胞遗传学分析显示,荧光原位杂交(FISH)证实t(8;14)(q24;q32)为IGH/MYC阳性。Epstein-Barr病毒(EBV)在我们的病例中被大量证实,(EBV) DNA在提出时通过PCR检测为24,295,560拷贝/ml,此外,两个诊断组织(颈部淋巴结和BM)的肿瘤细胞均显示EBV阳性。在白血病期诊断合并EBV相关的不协调性淋巴瘤(经典霍奇金淋巴瘤(cHL)和伯基特淋巴瘤(BL)。在所有报告的病例中,这个病例是非常特殊的,因为它是第一个不协调/复合淋巴瘤的病例,这种组合和伴随的表现。由于我们正在处理一个异常罕见的合并病例,我们发现有必要详细阐述其临床特征,影响因素包括EBV的作用,对治疗的反应,并发症和预后。
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来源期刊
CiteScore
3.70
自引率
0.00%
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审稿时长
8 weeks
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