نتایج جستجو برای: severe acquired aplastic anemia

تعداد نتایج: 541227  

Journal: :International journal of clinical and experimental pathology 2014
Aya Furuya Mitsuaki Ishida Keiko Hodohara Miyuki Yoshii Hiroko Okuno Akiko Horinouchi Ryota Nakanishi Ayumi Harada Muneo Iwai Keiko Yoshida Akiko Kagotani Takashi Yoshida Hidetoshi Okabe

It is well established that Down's syndrome exhibits a predisposition to development of leukemia, however, association between aplastic anemia and Down's syndrome is exceptional. Herein, we describe a case of aplastic anemia occurring in Down's syndrome following post-transplant lymphoproliferative disorder (PTLD) after bone marrow transplantation (BMT). A 27-year-old Japanese male with Down's ...

Journal: :Hematology. American Society of Hematology. Education Program 2005
Blanche P Alter

Aplastic anemia may be inherited or acquired. The distinction between these lies not in the age of the patient, but in the clinical and laboratory diagnoses. Adult hematologists must consider adult presentations of the inherited disorders, in order to avoid incorrect management of their patients. Physicians for adult patients must also realize that children with inherited disorders now survive ...

Journal: :Haematologica 2012
Andrea Bacigalupo Gérard Socié Hubert Schrezenmeier Andre Tichelli Anna Locasciulli Monika Fuehrer Antonio M Risitano Carlo Dufour Jakob R Passweg Rosi Oneto Mahmoud Aljurf Catherine Flynn Valerie Mialou Rose Marie Hamladji Judith C W Marsh

BACKGROUND Bone marrow has been shown to be superior to peripheral blood, as a stem cell source, in young patients (<20 years of age) with acquired aplastic anemia undergoing a matched sibling transplant. The aim of this study was to test whether this currently also holds true for older patients with acquired aplastic anemia. DESIGN AND METHODS We analyzed 1886 patients with acquired aplastic...

Journal: :Blood 1983
N K Ramsay T H Kim P McGlave A Goldman M E Nesbit W Krivit W G Woods J H Kersey

A preparative regimen, consisting of total lymphoid irradiation and cyclophosphamide, was utilized in 40 patients with severe aplastic anemia undergoing allogeneic marrow transplantation. This regimen was successful in decreasing rejection in these previously transfused patients, as only one patient rejected the marrow graft. Twenty-nine of the 40 transplanted patients are surviving from 1.5 to...

Journal: :Blood 1975
B M Camitta J M Rappeport R Parkman D G Nathan

Despite androgens and intensive supportive care, satisfactory survival in severe aplastic anemia remains at 20% or less. Histocompatible bone marrow transplantation can restore normal hematopoiesis in approximately 40% of similarly severe individuals. Delay of transplantation for 3 wk after diagnosis allows time for proper evaluation and for many spontaneous recoveries. Further delay increases ...

Journal: :JAMA 2015
Shahinaz M Gadalla Tao Wang Michael Haagenson Stephen R Spellman Stephanie J Lee Kirsten M Williams Jason Y Wong Immaculata De Vivo Sharon A Savage

IMPORTANCE Telomeres protect chromosome ends and are markers of cellular aging and replicative capacity. OBJECTIVE To evaluate the association between recipient and donor pretransplant leukocyte telomere length with outcomes after unrelated donor allogeneic hematopoietic cell transplantation (HCT) for patients with severe aplastic anemia. DESIGN, PARTICIPANTS, AND SETTING The study included...

Journal: :Journal of Nippon Medical School = Nippon Ika Daigaku zasshi 2007
Kenji Tajika Taro Mizuki Kazutaka Nakayama Hiroki Yamaguchi Kazuo Dan

Immunosuppressive therapy and stem cell transplantation from an HLA-identical donor are the major effective treatments for severe aplastic anemia. However, treatments still need to be developed for patients who do not have a HLA-identical donor and have not shown a clinical response to immunosuppressive therapy. We herein report on 2 patients in whom this problem could be overcome by transplant...

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