Takiyama Akihiro, Nishihara Hiroshi, Tateishi Ukihide, Kimura Taichi, Wang Lei, Marukawa Katsuji, Itoh Tomoo, Hashino Satoshi, Nagashima Kazuo, Tanaka Shinya
Laboratory of Molecular and Cellular Pathology, Hokkaido University School of Medicine, Kita-Ku, Sapporo, Japan.
Neuropathology. 2008 Dec;28(6):640-4. doi: 10.1111/j.1440-1789.2008.00903.x. Epub 2008 Apr 1.
Lymphomatoid granulomatosis (LYG) in the CNS is an uncommon lymphoproliferative disease with characteristic angiocentric lymphoreticular proliferative and granulomatous lesions exhibiting low-grade malignant potential. Here we report a rare case of CNS-LYG, which disseminated to the lymph node and bone marrow. A 50-year-old man was diagnosed with CNS-LYG based on brain biopsy showing perivascular infiltration of CD3-positive small T-lymphocytes without overt nuclear atypism. Eight months after the initial neurological symptoms, inguinal lymph node swelling was found and histopathologically diagnosed as peripheral T-cell lymphoma. TCRgamma-gene rearrangement study using both paraffin-embedded specimens of brain and inguinal lymph node demonstrated an identical clonal band. Considering the clinical course, we concluded lymph node involvement of CNS-LYG, suggesting the malignant potential of CNS-LYG.
中枢神经系统的淋巴瘤样肉芽肿病(LYG)是一种罕见的淋巴增殖性疾病,具有特征性的血管中心性淋巴网状细胞增殖和肉芽肿性病变,显示出低度恶性潜能。在此,我们报告一例罕见的中枢神经系统LYG病例,该病例已扩散至淋巴结和骨髓。一名50岁男性基于脑活检显示CD3阳性小T淋巴细胞血管周围浸润且无明显核异型性而被诊断为中枢神经系统LYG。在出现初始神经症状8个月后,发现腹股沟淋巴结肿大,经组织病理学诊断为外周T细胞淋巴瘤。使用脑和腹股沟淋巴结的石蜡包埋标本进行的TCRγ基因重排研究显示出相同的克隆条带。考虑到临床病程,我们得出结论,该病例为中枢神经系统LYG累及淋巴结,提示中枢神经系统LYG具有恶性潜能。