Özşen Mine, Tolunay Şahsine, Kocaeli Hasan, Parlak Müfit
Department of Medical Pathology, Uludag University Faculty of Medicine, Bursa, Turkey.
Department of Neurosurgery, Uludag University Faculty of Medicine, Bursa, Turkey.
Indian J Pathol Microbiol. 2023 Jul-Sep;66(3):655-658. doi: 10.4103/ijpm.ijpm_373_21.
Crystal storing histiocytosis is a disorder characterized by local or diffuse infiltration of histiocytes containing crystalline inclusions. This entity has been reported in several organs, however the involvement of the central nervous system (CNS) is extremely rare and to date only 7 cases of crystal storing histiocytosis (CSH) of CNS have been reported in the English literature. More than 90% patients with CSH had an underlying lymphoproliferative or plasma cell disorders, especially multiple myeloma, lymphoplasmacytic lymphoma or monoclonal gammopathy. Radiologically and intraoperatively, CSH may mimic an infectious process or neoplasm, hence its histopathological confirmation is important to facilitate appropriate treatment. In this report, we describe an additional case of crystal storing histiocytosis in a 48 year old female who presented with a mass lesion in the right temporal lobe of the cerebrum.
晶体贮积性组织细胞增多症是一种以含有结晶包涵体的组织细胞局部或弥漫性浸润为特征的疾病。该病症已在多个器官中被报道,然而中枢神经系统(CNS)受累极为罕见,迄今为止,英文文献中仅报道了7例中枢神经系统晶体贮积性组织细胞增多症(CSH)。超过90%的CSH患者存在潜在的淋巴增殖性或浆细胞疾病,尤其是多发性骨髓瘤、淋巴浆细胞淋巴瘤或单克隆丙种球蛋白病。在放射学和手术中,CSH可能类似感染性病变或肿瘤,因此其组织病理学确诊对于促进恰当治疗很重要。在本报告中,我们描述了另外一例晶体贮积性组织细胞增多症病例,患者为一名48岁女性,其大脑右颞叶出现肿块病变。