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Secondary cutaneous Epstein-Barr virus-associated diffuse large B-cell lymphoma in a patient with angioimmunoblastic T-cell lymphoma: a case report and review of literature

机译:继发性皮肤爱泼斯坦-巴尔病毒相关的弥漫性大B细胞淋巴瘤在血管免疫母细胞性T细胞淋巴瘤患者中的报道及文献复习

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摘要

Only a few cases of extranodal Epstein-Barr virus (EBV)-associated B-cell lymphomas arising from patients with angioimmunoblastic T-cell lymphoma (AITL) have been described. We report a case of AITL of which secondary cutaneous EBV-associated diffuse large B-cell lymphoma (DLBCL) developed after the initial diagnosis of AITL. A 65-year-old Chinese male patient was diagnosed as AITL based on typical histological and immunohistochemical characteristics in biopsy of the enlarged right inguinal lymph nodes. The patient initially received 6 cycles of chemotherapy with CHOP regimen (cyclophosphamide, vincristine, adriamycin, prednisone), but his symptoms did not disappear. Nineteen months after initial diagnosis of AITL, the patient was hospitalized again because of multiple plaques and nodules on the skin. The skin biopsy was performed, but this time the tumor was composed of large, polymorphous population of lymphocytes with CD20 and CD79a positive on immunohistochemical staining. The tumor cells were strong positive for EBER by in situ hybridization. The findings of skin biopsy were compatible with EBV-associated DLBCL. CHOP-R chemotherapy (cyclophosphamide, doxorubicin, vincristine, prednisone and rituximab) was then administered, resulting in partial response of the disease with pancytopenia and suppression of cellular immunity. To our knowledge, this is the first case of cutaneous EBV-associated DLBCL originated from AITL in Chinese pepole. We suggest the patients with AITL should perform lymph node and skin biopsies regularly in the course of the disease to detect the progression of secondary lymphomas.
机译:仅描述了几例由血管免疫母细胞性T细胞淋巴瘤(AITL)患者引起的结外爱泼斯坦-巴尔病毒(EBV)相关的B细胞淋巴瘤。我们报告的一例AITL的初步诊断后,发展为继发性皮肤EBV相关的弥漫性大B细胞淋巴瘤(DLBCL)。根据典型的右腹股沟淋巴结活检的组织学和免疫组织化学特征,将一名65岁的中国男性患者诊断为AITL。患者最初接受了CHOP方案(环磷酰胺,长春新碱,阿霉素,泼尼松)的6个化疗周期,但症状并未消失。最初诊断为AITL后的19个月,该患者因皮肤上有多个斑块和结节再次入院。进行了皮肤活检,但是这次肿瘤是由大量多态性淋巴细胞组成,在免疫组织化学染色中,CD20和CD79a阳性。通过原位杂交,肿瘤细胞对EBER呈强阳性。皮肤活检的结果与EBV相关的DLBCL相容。然后进行CHOP-R化疗(环磷酰胺,阿霉素,长春新碱,泼尼松和利妥昔单抗),导致该疾病对全血细胞减少症的部分反应,并抑制细胞免疫。据我们所知,这是第一例源自中国人AITL的皮肤EBV相关的DLBCL病例。我们建议AITL患者应在疾病过程中定期进行淋巴结和皮肤活检,以检测继发性淋巴瘤的进展。

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