Primary pulmonary presentation extranodal NK/T-cell lymphoma, small cell variant, illustrating the value of flow EBER in situ hybridisation assay.

IF 1 4区 医学 Q4 HEMATOLOGY
Soham Kale, Zbigniew Rudzki, Bernard Maybury, Kaviya Selvapandian, Gerald Langman, Claire Shannon-Lowe
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引用次数: 0

Abstract

A 57-year-old male from Guinea presented with 6 months of progressive shortness of breath, productive cough, and occasional night sweats. A lung biopsy revealed an angiocentric pulmonary infiltrate of small bland lymphocytes and lymphoepithelial lesions mimicking a MALT lymphoma. The infiltrate expressed CD3, CD56, and Epstein-Barr virus-encoded RNA with little Ki-67 staining. Blood EBV copies were 519 IU/mL. FDG-PET scan showed no uptake outside the thorax. A diagnosis of small-cell variant pulmonary NK/T-cell lymphoma was made. Following asparaginase/cisplatin-based treatment, the patient developed recurrent cough, and nasal biopsy suggested lymphoma relapse. Following transplant conditioning, the patient developed symptoms of fever and cough, with rising blood EBV load. Lymphoma progression was suspected. A flow RNA assay demonstrated a small population of EBER + CD8 + T-cells in blood. NK/T-cell lymphoma usually present with sino-nasal symptoms. The small-cell variant is rare. The diagnosis is challenging when the clinical presentation and cytological features are atypical. POT1 variants have not been reported in ENKTL to our knowledge, but germline variants have been associated with lymphomas. A multicolour EBER hybridisation flow assay can help identify the cellular origin of EBV reactivation.

原发性肺表现为结外NK/ t细胞淋巴瘤,小细胞变异,说明流式EBER原位杂交试验的价值。
来自几内亚的一名57岁男性,表现为6个月进行性呼吸短促、咳嗽和偶尔盗汗。肺活检显示以血管为中心的肺浸润性小淋巴细胞和淋巴上皮病变,类似于MALT淋巴瘤。浸润表达CD3、CD56和Epstein-Barr病毒编码RNA, Ki-67染色较少。血EBV拷贝数为519 IU/mL。FDG-PET扫描未见胸外摄取。诊断为小细胞变异性肺NK/ t细胞淋巴瘤。在以天冬酰胺酶/顺铂为基础的治疗后,患者出现复发性咳嗽,鼻腔活检提示淋巴瘤复发。移植后,患者出现发热和咳嗽症状,血液中eb病毒载量升高。怀疑淋巴瘤进展。流式RNA分析显示血液中有少量的EBER + CD8 + t细胞。NK/ t细胞淋巴瘤通常表现为鼻鼻症状。小细胞变异是罕见的。当临床表现和细胞学特征不典型时,诊断是具有挑战性的。据我们所知,在ENKTL中尚未报道POT1变异,但种系变异与淋巴瘤有关。多色EBER杂交流动试验可以帮助确定EBV再激活的细胞起源。
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来源期刊
Journal of Hematopathology
Journal of Hematopathology HEMATOLOGYPATHOLOGY-PATHOLOGY
CiteScore
0.80
自引率
0.00%
发文量
45
期刊介绍: The Journal of Hematopathology aims at providing pathologists with a special interest in hematopathology with all the information needed to perform modern pathology in evaluating lymphoid tissues and bone marrow. To this end the journal publishes reviews, editorials, comments, original papers, guidelines and protocols, papers on ancillary techniques, and occasional case reports in the fields of the pathology, molecular biology, and clinical features of diseases of the hematopoietic system. The journal is the unique reference point for all pathologists with an interest in hematopathology. Molecular biologists involved in the expanding field of molecular diagnostics and research on lymphomas and leukemia benefit from the journal, too. Furthermore, the journal is of major interest for hematologists dealing with patients suffering from lymphomas, leukemias, and other diseases. The journal is unique in its true international character. Especially in the field of hematopathology it is clear that there are huge geographical variations in incidence of diseases. This is not only locally relevant, but due to globalization, relevant for all those involved in the management of patients.
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