Academic Journal

The First Reported Case of Allogenic Hematopoietic Stem Cell Transplantation for CML Blast Phase (Monocytic Lineage) in the Tyrosine Kinase Inhibitor Era

التفاصيل البيبلوغرافية
العنوان: The First Reported Case of Allogenic Hematopoietic Stem Cell Transplantation for CML Blast Phase (Monocytic Lineage) in the Tyrosine Kinase Inhibitor Era
المؤلفون: Shinya Yamada, Kotaro Arita, Yukio Kondo, Shuichi Mizuta, Hirokazu Okumura
المصدر: Case Reports in Oncology, Vol 15, Iss 2, Pp 535-540 (2022)
بيانات النشر: Karger Publishers, 2022.
سنة النشر: 2022
المجموعة: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
مصطلحات موضوعية: chronic myeloid leukemia, chronic myeloid leukemia blast phase (monocytic lineage), tyrosine kinase inhibitor, hematopoietic stem cell transplantation, hyper-acute graft-versus-host disease, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: Chronic myeloid leukemia (CML) blast phase (monocytic lineage) is extremely rare. A 39-year-old Japanese man was diagnosed with CML blast phase (monocytic lineage). T315I mutation was positive, ponatinib was initially started, and then, allogenic hematopoietic stem cell transplantation (allo-HSCT) was performed. Seven days after allo-HSCT, hyper-acute graft-versus-host disease developed, and medial temporal lobe encephalitis emerged 24 days after allo-HSCT. He was alive for over 1 year after allo-HSCT. This is the first case report of HSCT for CML blast phase (monocytic lineage) in tyrosine kinase inhibitor era. Further cases should be documented for effective treatment regimen and analysis of clinical features.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1662-6575
00052477
Relation: https://www.karger.com/Article/FullText/524770; https://doaj.org/toc/1662-6575
DOI: 10.1159/000524770
URL الوصول: https://doaj.org/article/2947f1c32a934d968b70899d48e5f40f
رقم الانضمام: edsdoj.2947f1c32a934d968b70899d48e5f40f
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:16626575
00052477
DOI:10.1159/000524770