Aydin F, Bartholomew P M, Vinson D G
Department of Pathology, Tulane University School of Medicine, New Orleans, LA, USA.
Arch Pathol Lab Med. 1998 Apr;122(4):361-5.
To present, to our knowledge, the first case of primary central nervous system T-cell lymphoma in the setting of acquired immunodeficiency syndrome. Design.Clinical, radiological, laboratory, and pathological data from a young patient at advanced stage of acquired immunodeficiency syndrome were studied.
A 38-year-old white man with stage CIII human immunodeficiency virus infection presented with headaches. Cerebrospinal fluid culture was positive for mycobacterium. He had facial herpes simplex virus and disseminated cytomegalovirus infections. Magnetic resonance imaging of the brain showed multiple areas of patchy or ring-shaped contrast enhancement in the periventricular zone of the right frontoparietal region. Stereotactic brain biopsy showed perivascular CD3 (pan T-cell marker)-positive lymphocytic infiltrates with partial necrosis extending into the neuropil. Not a single cell was labeled with L26, a B-cell marker. Negative and positive controls were appropriate. Special stains for cytomegalovirus, herpes simplex virus, Epstein-Barr virus, acid-fast bacilli, and fungi were negative. Gene rearrangement studies showed rearranged Tgamma and Tbeta bands. Polymerase chain reaction with a primer specific for Epstein-Barr virus genome-encoding nuclear antigen 1 region was positive. Human T-cell leukemia/lymphoma virus I work-up was negative. The patient was treated for mycobacteria. Four months later, he presented with a paravertebral neck mass. Needle biopsy showed a T-cell lymphoma with morphology similar to that in the brain.
To our knowledge, this case represents the first example of T-cell lymphoma of the brain in a patient with advanced stage of acquired immunodeficiency syndrome. Epstein-Barr virus may play a role in T-cell lymphomagenesis. The other unique finding is the complete absence of B cells in a central nervous system lesion. The underlying mechanism eradicating the B cells is unknown.
据我们所知,报告首例获得性免疫缺陷综合征背景下的原发性中枢神经系统T细胞淋巴瘤病例。设计:对一名处于获得性免疫缺陷综合征晚期的年轻患者的临床、放射学、实验室和病理数据进行研究。
一名38岁的白人男性,患有CIII期人类免疫缺陷病毒感染,出现头痛症状。脑脊液培养显示结核分枝杆菌阳性。他患有面部单纯疱疹病毒感染和播散性巨细胞病毒感染。脑部磁共振成像显示右额顶叶区域脑室周围有多个斑片状或环形强化区域。立体定向脑活检显示血管周围CD3(全T细胞标志物)阳性淋巴细胞浸润,部分坏死延伸至神经毡。没有一个细胞被B细胞标志物L26标记。阴性和阳性对照均合适。巨细胞病毒、单纯疱疹病毒、EB病毒、抗酸杆菌和真菌的特殊染色均为阴性。基因重排研究显示Tγ和Tβ带重排。针对EB病毒基因组编码核抗原1区域的引物进行的聚合酶链反应呈阳性。人类T细胞白血病/淋巴瘤病毒I检测为阴性。该患者接受了抗分枝杆菌治疗。四个月后,他出现了椎旁颈部肿块。针吸活检显示为T细胞淋巴瘤,其形态与脑部相似。
据我们所知,该病例代表了获得性免疫缺陷综合征晚期患者脑部T细胞淋巴瘤的首例。EB病毒可能在T细胞淋巴瘤的发生中起作用。另一个独特的发现是中枢神经系统病变中完全没有B细胞。清除B细胞的潜在机制尚不清楚。