Autologous Hematopoietic Cell Transplant as an Effective Treatment Modality for Systemic Sclerosis and Multiple Myeloma.

IF 2.1 Q3 HEMATOLOGY Journal of Blood Medicine Pub Date : 2025-01-06 eCollection Date: 2025-01-01 DOI:10.2147/JBM.S489627
Hamda Memon, Ricardo Parrondo, Julianna Schreurs, Ernesto Ayala, Madiha Iqbal
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Abstract

Systemic sclerosis (SSc) is a multi-system disease characterized by a dysregulated immune system. Autologous hematopoietic cell transplantation (AHCT) is the only treatment that has been shown to confer significant benefit in controlling disease and improving survival for patients with SSc. A diagnosis of multiple myeloma (MM) after the diagnosis of SSc is rare and optimal treatment in such cases remains unclear. We here report a case of a female patient who was diagnosed with MM while she was undergoing evaluation for AHCT due to SSc. A novel conditioning regimen for AHCT, with therapeutic efficacy in SSc and MM was offered to the patient, resulting in long term remission of both diseases.

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自体造血细胞移植作为系统性硬化症和多发性骨髓瘤的有效治疗方式。
系统性硬化症(SSc)是一种以免疫系统失调为特征的多系统疾病。自体造血细胞移植(AHCT)是唯一被证明在控制SSc患者疾病和提高生存率方面具有显著益处的治疗方法。多发性骨髓瘤(MM)在SSc诊断后的诊断是罕见的,在这种情况下的最佳治疗尚不清楚。我们在此报告一例女性患者,她因SSc而接受AHCT评估时被诊断为MM。为患者提供了一种新的AHCT调理方案,对SSc和MM具有治疗效果,导致两种疾病的长期缓解。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
94
审稿时长
16 weeks
期刊介绍: The Journal of Blood Medicine is an international, peer-reviewed, open access, online journal publishing laboratory, experimental and clinical aspects of all topics pertaining to blood based medicine including but not limited to: Transfusion Medicine (blood components, stem cell transplantation, apheresis, gene based therapeutics), Blood collection, Donor issues, Transmittable diseases, and Blood banking logistics, Immunohematology, Artificial and alternative blood based therapeutics, Hematology including disorders/pathology related to leukocytes/immunology, red cells, platelets and hemostasis, Biotechnology/nanotechnology of blood related medicine, Legal aspects of blood medicine, Historical perspectives. Original research, short reports, reviews, case reports and commentaries are invited.
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