Primary Central Nervous System Histiocytic Sarcoma Arising After Precursor B-Cell Acute Lymphoblastic Leukemia

Alan F Brown, H. Fan, J. Floyd, J. Henry, Russell A Higgins
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引用次数: 11

Abstract

Abstract Histiocytic sarcomas (HSs) are rare malignant neoplasms derived from histiocytes that may be associated with other hematolymphoid neoplasms. Histiocytic sarcomas rarely occur in the CNS and have not previously been reported in conjunction with prior B-cell lymphoblastic leukemia. We report the case of a 23-year-old man who presented with primary CNS HS 7 years after achieving remission for precursor B-cell acute lymphoblastic leukemia (B-ALL). Molecular studies revealed clonal immunoglobulin heavy-chain (IGH) gene rearrangement within the HS, suggesting linkage to his previous B-ALL. Previously reported post-ALL HSs show a strong predilection for young males (male-to-female ratio, 20:1), whereas cases of primary CNS HS without previous ALL affected older adults with balanced sex predilection. The patient's survival at 60 months exceeds expectations when compared with that of other reported cases of de novo primary CNS HS (n = 18) and post-ALL HS at all sites (n = 19). In addition, we discuss the potential relationship between B-ALL and HS posed by other authors.
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前体b细胞急性淋巴母细胞白血病后发生的原发性中枢神经系统组织细胞肉瘤
组织细胞肉瘤(HSs)是一种罕见的起源于组织细胞的恶性肿瘤,可能与其他血淋巴肿瘤有关。组织细胞肉瘤很少发生在中枢神经系统,以前没有报道与既往b细胞淋巴母细胞白血病合并。我们报告一例23岁的男性在前体b细胞急性淋巴母细胞白血病(B-ALL)缓解7年后出现原发性中枢神经系统综合征。分子研究显示,HS内克隆性免疫球蛋白重链(IGH)基因重排,提示与先前的B-ALL有关。先前报道的ALL后HS表现出强烈的年轻男性偏好(男女比例为20:1),而没有ALL前的原发性中枢神经系统HS病例影响的是性别偏好平衡的老年人。与其他报道的原发性中枢神经系统HS (n = 18)和all后所有部位HS (n = 19)的新生病例相比,患者的60个月生存率超过预期。此外,我们还讨论了其他作者提出的B-ALL与HS之间的潜在关系。
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