نتایج جستجو برای: severe acquired aplastic anemia

تعداد نتایج: 541227  

2013
Beatriz Stela Pitombeira Alessandra Paz Annelise Pezzi Bruna Amorin Vanessa Valim Alvaro Laureano Andrea Wieck Lisandra Rigoni Érica Ottoni Gustavo Fisher Liane Daudt Lucia Silla

Background. Allogeneic hematopoietic stem cell transplantation (HSCT) is still associated with a high transplant-related mortality rate. In 2009, the EBMT risk score was validated as a simple tool to predict the outcome after allogeneic HSCT for acquired hematological disorders. Objectives. The aim of this study was to validate the applicability of the EBMT risk score for allogeneic HSCT on Sou...

Journal: :Blood 2002
Seiji Kojima Takaharu Matsuyama Shunichi Kato Hisato Kigasawa Ryoji Kobayashi Atsushi Kikuta Hisashi Sakamaki Koichiro Ikuta Masahiro Tsuchida Yasutaka Hoshi Yasuo Morishima Yoshihisa Kodera

We retrospectively analyzed results for 154 patients with acquired severe aplastic anemia who received bone marrow transplants between 1993 and 2000 from unrelated donors identified through the Japan Marrow Donor Program. Patients were aged between 1 and 46 years (median, 17 years). Seventy-nine donor-patient pairs matched at HLA-A, -B, and -DRB1 loci, as shown by DNA typing. Among the 75 misma...

Journal: :Annals of internal medicine 2002
André Tichelli Gérard Socié Judith Marsh Renée Barge Norbert Frickhofen Shaun McCann Andrea Bacigalupo Jill Hows Pedro Marin David Nachbaur Argiris Symeonidis Jakob Passweg Hubert Schrezenmeier

BACKGROUND Aplastic anemia may develop during pregnancy and sometimes improves spontaneously after delivery. The effects of pregnancy on aplastic anemia after immunosuppressive treatment and of aplastic anemia on the outcome of pregnancy have not been described. OBJECTIVE To determine the outcome of pregnancy and the disease course among women with aplastic anemia who received immunosuppressi...

Journal: :Blood 1985
G D Goss M A Wittwer W R Bezwoda J Herman A Rabson L Seymour D P Derman B Mendelow

Bone marrow transplantation for severe idiopathic aplastic anemia was undertaken in a patient, using his monozygotic twin brother as the donor. In spite of the use of syngeneic bone marrow, failure of engraftment occurred on two occasions. In vitro studies demonstrated that natural killer (NK) cells from the recipient markedly inhibited the growth of donor bone marrow granulocyte progenitor cel...

Journal: :Internal medicine 1994
H Inoue K Shinohara J Nomiyama E Oeda

We report a case of severe and fatal aplastic anemia during an episode of infectious mononucleosis caused by Epstein-Barr (EB) virus infection. The 13-year-old female patient had shown normal hematological findings and had previously undergone repeated chemotherapy and autologous bone marrow transplantation for refractory non-Hodgkin malignant lymphoma (NHL). She was probably in an immuno-suppr...

Journal: :Blood 1985
F R Appelbaum M A Cheever A Fefer R Storb E D Thomas

Two patients with aplastic anemia were treated with high-dose cyclophosphamide and marrow transplantation from their normal, genetically identical twin. Both patients rapidly recovered normal marrow function, but marrow failure recurred 13 and 18 months later. Because donor and host pairs were identical twins, these cases of graft failure could not have resulted from the usual cause of graft fa...

Journal: :Current oncology 2010
J Oh G J Kutas P Davey M Morrison J R Perry

Temozolomide (TMZ) is an oral alkylating agent used during concurrent and adjuvant chemotherapy for newly diagnosed glioblastoma multiforme. Temozolomide is generally well tolerated and improves survival; however, severe adverse events have occasionally been reported. Here, we report the case of a patient who developed aplastic anemia with related complications in the setting of concurrent TMZ ...

1989
Chong Won Park Chi Hwa Han Choon Coo Kim Dong Jip Kim Hak Ki Kim

Journal: :JAMA 2003
Stephen Rosenfeld Dean Follmann Olga Nunez Neal S Young

CONTEXT In most patients, aplastic anemia results from T-cell-mediated immune destruction of bone marrow. Aplastic anemia can be effectively treated by stem cell transplantation or immunosuppression. OBJECTIVE To assess long-term outcomes after immunosuppressive therapy. DESIGN, SETTING, AND PATIENTS Cohort of 122 patients (31 were < or =18 years and 91 were >18 years) with severe aplastic ...

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