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Paraspinal extramedullary hematopoiesis in hereditary spherocytosis with a concurrent follicular lymphoma: case report and review of the literature

机译:伴有滤泡性淋巴瘤的遗传性球囊炎的椎旁髓外造血:病例报告和文献复习

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摘要

We report an unusual case of a 70-year-old male with history of hereditary spherocytosis (HS) and secondary paraspinal extramedullary hematopoiesis with a concurrent follicular lymphoma. The lesion presented as a thoracic paraspinal mass of 9 cm, extending longitudinally between T6 and T9 vertebral bodies. Incisional biopsy revealed that this mass included mature hematopoietic tissue compatible with extramedullary hematopoiesis (EMH). The tissue also presented an extensive and diffuse infiltration by an atypical lymphoid population composed predominantly by small cells. The immunohistochemical study revealed that the atypical lymphoid population had a germinal center phenotype, consistent with the diffuse variant of follicular lymphoma (FL). The simultaneous presence of both EMH and FL in the same lesion made the interpretation and the final diagnosis of this case difficult. The presence of EMH in this clinical context may eclipse the diagnosis of the underlying lymphoproliferative neoplasm. The close association between the tumor cells and extramedullary hematopoietic tissue in the absence of lymphadenopathies or other tissue involvement suggests a relationship of this tumor with the recently described primary FL of the bone marrow.
机译:我们报告了一个不寻常的病例,该患者为70岁的男性,具有遗传性球细胞增多症(HS)和继发性脊髓旁髓外造血,并发滤泡性淋巴瘤。病变表现为9 cm的胸椎旁质量,在T6和T9椎体之间纵向延伸。切口活检显示该肿物包括与髓外造血(EMH)相容的成熟造血组织。该组织还表现出由主要由小细胞组成的非典型淋巴样群体的广泛和弥漫性浸润。免疫组织化学研究表明,非典型淋巴样人群具有生发中心表型,与滤泡性淋巴瘤(FL)的弥散变异相一致。在同一病变中同时存在EMH和FL使得对该病例的解释和最终诊断变得困难。在这种临床情况下,EMH的存在可能掩盖了潜在的淋巴增生性肿瘤的诊断。在不存在淋巴腺病或其他组织受累的情况下,肿瘤细胞与髓外造血组织之间的紧密联系表明该肿瘤与最近描述的骨髓原发性FL有关。

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