CENTRAL NERVOUS SYSTEM RELAPSE OF MULTIPLE MYELOMA

M. Qubtia, M. Nasir, Memoona Mian, A. Hameed
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Abstract

Multiple myeloma (MM) is a plasma cell disorder primarily involving bone marrow. Extramedullary involvement is less common, with central nervous system (CNS) myelomatosis being a rare entity and such presentation carries extremely dismal prognosis. We present case of a 40 years old male with MM who was initially treated with 6 cycles of Cyclophosphamide, Thalidomide and Dexamethasone resulting in complete response. 2 years later he presented with CNS myelomatosis and scrotal involvement and was initially treated with Bortezomib and dexamethasone, cranial irradiation and intrathecal Methorexate, Cytarabine, Hydrocortisone (TRIO IT), along with radical orchiectomy and testicular radiation during the course of treatment. However, after initial response his disease showed clinical and radiological progression after 4 months of therapy. He was switched to high dose Methotrexate (HD-MTX) with TRIOITand later Lenalidamide and dexamethasone (Len/dex) was added to the above regimen. He continued to show good clinical response but his cytology remained persistently positive, therefore, HD-MTX was discontinued in the later course of treatment. Subsequently he was started on best supportive care only, when his neurological status deteriorated further. He survived almost 9 months after a diagnosis of CNS myelomatosis. Patients with multiple myeloma, presenting with neurological symptoms should always be investigated for the possibility of CNS MM. CNS relapse is a fatal disease with poor prognosis. Recommended treatment must include a systemic anti-MM regimen that crosses the BBB (ideally Immunomodulatory drugs (IMiDs) IMiDs-dexamethasone based therapy), CNS irradiation and intrathecal chemotherapy.Key words: Multiple myeloma, central nervous system myelomatosis, therapy
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中枢神经系统多发性骨髓瘤复发
多发性骨髓瘤(MM)是一种主要累及骨髓的浆细胞疾病。髓外受累不常见,中枢神经系统(CNS)骨髓瘤病是一种罕见的实体,这种表现预后非常差。我们报告了一例40岁男性MM患者,他最初接受了6个周期的环磷酰胺、沙利度胺和地塞米松治疗,完全缓解。2年后,他出现中枢神经系统骨髓瘤病和阴囊受累,最初接受硼替佐米和地塞米松、颅照射和鞘内甲氨喋呤、阿糖胞苷、氢化可的松(TRIO IT)治疗,同时在治疗过程中进行根治性睾丸切除术和睾丸放射治疗。然而,在最初的反应后,他的疾病在治疗4个月后表现出临床和放射学进展。患者改用高剂量甲氨蝶呤(HD-MTX)联合trioitd治疗,后在上述方案中加入来那胺和地塞米松(Len/dex)。他继续表现出良好的临床反应,但他的细胞学仍然持续呈阳性,因此,在治疗的后期停止了HD-MTX。随后,当他的神经系统状况进一步恶化时,他开始接受最好的支持治疗。在被诊断为中枢神经系统骨髓瘤病后,他活了近9个月。出现神经系统症状的多发性骨髓瘤患者应经常检查中枢神经系统MM的可能性,中枢神经系统复发是一种预后不良的致命疾病。推荐的治疗方案必须包括通过血脑屏障的全身抗mm方案(理想情况下是免疫调节药物(IMiDs), IMiDs-地塞米松为基础的治疗),中枢神经系统照射和鞘内化疗。关键词:多发性骨髓瘤,中枢神经系统骨髓瘤,治疗
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