Cured case of relapsed acute myeloid leukemia with giant central nervous system chloroma

Y. Bashir, Nusrat Bashir, Shabeer Ahmed, S. Geelani, Asif Ahmed, J. Rasool
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Abstract

Myeloid leukemias are a heterogenous group of disease characterized by infiltration of blood, bone marrow and other tissues by neoplastic cells of hematopoietic origin. Rarely, patients may present with symptoms from a mass lesion located in soft tissues. The mass lesion represents a tumor of leukemic cells and is called granulocytic sarcoma or chloroma. This is more commonly seen in monocytic subtype with abnormalities of chromosome 11. In general, they are felt to augur a poorer prognosis, with a poorer response to treatment and worse survival. There have been few case reports of orbital and central nervous system (CNS) chloroma in pediatric age group who have done better than only a medullary disease. Here, we present a case of acute myelogenous leukemia M2 who had two relapses one medullary and one extramedullary (CNS relapse with giant CNS chloroma). Patient was reinduced with same drugs and was advised to go for allogenic stem cell transplantation, which he could not. Subsequently presented with features of raised  Intracranial tension (ICT) and was diagnosed to have extramedullary relapse in the form of giant CNS chloroma. He was treated with surgical debulking of the tumor, fludarabine, AraC, idarubicin, and G-CSF chemotherapy protocol (FLAG-IDA) chemo, and local intraspinal triple therapy 5 years back and stands cured at present.
复发性急性髓性白血病合并巨大中枢神经系统氯瘤1例
髓性白血病是一种异质性的疾病,其特征是造血来源的肿瘤细胞浸润血液、骨髓和其他组织。很少,患者可能会出现软组织肿块病变的症状。肿块病变代表白血病细胞肿瘤,称为粒细胞肉瘤或氯瘤。这在11号染色体异常的单核细胞亚型中更为常见。一般来说,他们被认为预示着预后较差,对治疗的反应较差,生存率较差。在儿童年龄组中,眼眶和中枢神经系统(CNS)氯瘤的治疗效果优于单纯髓系疾病的病例报道很少。这里,我们报告一个急性髓性白血病M2的病例,他有两次复发,一次髓系和一次髓外(中枢神经系统复发伴巨大中枢神经系统氯瘤)。患者再次使用相同的药物进行诱导,并被建议进行同种异体干细胞移植,但他不能。随后表现为颅内压升高(ICT),并被诊断为髓外复发,表现为巨大中枢神经系统氯瘤。患者于5年前接受手术切除肿瘤、氟达拉滨、AraC、依达柔比星、G-CSF化疗方案(FLAG-IDA)化疗和局部椎管内三联治疗,目前痊愈。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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