一例无症状免疫受损患者的原发性中枢神经系统霍奇金淋巴瘤与淋巴增殖障碍的比较——一例病例报告和文献复习

Godbe Kn, Guilliams El, Benko Mj, Grider Dj, Stump Ms
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摘要

原发性中枢神经系统(CNS)霍奇金淋巴瘤极为罕见。一名82岁的女性在绊倒并撞到头部后出现在急诊室,导致头部撕裂,没有其他明显的伤害。头部CT显示一高密度区,与顶枕出血或肿块相符。她被转移到三级保健机构,在那里头部MRI显示一个涉及转移性疾病的顶枕肿块。没有发现转移性疾病的主要来源或证据。肿瘤被切除,并确定为典型的霍奇金淋巴瘤,混合细胞型。患者无并发症,出院回家。建议患者未来的治疗包括PET扫描和放疗。在与美国国立卫生研究院淋巴瘤专家协商后,根据患者的类风湿关节炎史,患者的诊断改为非典型淋巴增生性疾病,伴有Reed-Sternberg/Hodgkin样细胞,并接受免疫抑制剂治疗。文献回顾显示,几例原发性中枢神经系统霍奇金淋巴瘤病例与本研究中的患者极为相似。该病例被诊断为非典型淋巴细胞增生性疾病,这使人们怀疑以前报道的中枢神经系统原发性霍奇金病是否被误诊为该患者的病理染色,并且免疫抑制剂史非常相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Central Nervous System Hodgkin Lymphoma versus Lymphoproliferative Disorder in an Asymptomatic Immunocompromised Patient - A Case Report and Review of the Current Literature
Primary central nervous system (CNS) Hodgkin’s lymphoma is extremely rare. An 82 year old female presented to the Emergency Department after she tripped and hit her head, resulting in a head laceration with no other apparent injuries. Head CT revealed a hyperdense area consistent with either a parieto-occipital hemorrhage or mass. She was transferred to a tertiary care institution, where head MRI revealed a parieto-occipital mass concerning for metastatic disease. No primary source or evidence of metastatic disease were found. The tumor was resected and identified to be a classical Hodgkin’s lymphoma, mixed cellularity type. The patient had no complications and was discharged home. Recommendations for patient’s future treatment included a PET scan and radiotherapy. After a consultation with a lymphoma expert at the NIH, the patient’s diagnosis was changed to an atypical lymphoproliferative disorder with Reed-Sternberg/Hodgkin like cells based on the patient’s history of rheumatoid arthritis treated with an immunosuppressant. A review of the literature revealed several primary CNS Hodgkin’s lymphoma cases that were extremely similar to the patient in this study. This case’s diagnosis as an atypical lymphoproliferative disorder casts doubt on if previously reported cases of CNS primary Hodgkin’s disease were misclassified as the pathological staining of this patient and the immunosuppressant history are extremely similar.
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