Chalasani Sreelatha, Hennick Mark R, Hocking William G, Shaw Gene R, Lawler Benjamin
Department of Internal/Hospital Medicine, Marshfield Clinic, Marshfield, Wisconsin 54449, USA.
Clin Med Res. 2013 Feb;11(1):31-5. doi: 10.3121/cmr.2012.1092. Epub 2012 Sep 20.
Histiocytic sarcoma (HS) is a very rare hematopoietic neoplasm that has been reported in association with other hematological malignancies. Presentation of HS in the central nervous system is even less common. Diagnosis of HS requires the presence of histiocytic markers and the systematic exclusion of markers of other cell lineages. Primary HS central nervous system tumors are aggressive and generally have poor outcomes. There are no standard treatment guidelines due to lack of clinical trials and a limited number of case reports. Here we present a unique case with two primary histiocytic lesions in the brain, refractory to systemic and radiation therapies, that developed after being treated for T-cell acute lymphoblastic leukemia 16 years prior.
组织细胞肉瘤(HS)是一种非常罕见的造血系统肿瘤,已有报道其与其他血液系统恶性肿瘤相关。HS在中枢神经系统中的表现更为罕见。HS的诊断需要存在组织细胞标志物,并系统排除其他细胞谱系的标志物。原发性HS中枢神经系统肿瘤具有侵袭性,总体预后较差。由于缺乏临床试验和有限的病例报告,尚无标准治疗指南。在此,我们报告一例独特病例,该患者在16年前接受T细胞急性淋巴细胞白血病治疗后,脑部出现两个原发性组织细胞病变,对全身治疗和放疗均无效。