How I treat acquired aplastic anemia

A Bacigalupo - Blood, The Journal of the American Society of …, 2017 - ashpublications.org
Acquired severe aplastic anemia (SAA) is a rare hematologic disease associated with
significant morbidity and mortality. Immune destruction of hemopoietic stem cells plays an …

Advances in understanding the pathogenesis of acquired aplastic anaemia

L Luzzatto, AM Risitano - British Journal of Haematology, 2018 - Wiley Online Library
This review examines the evidence that bone marrow failure (BMF) in aplastic anaemia (AA)
is due to loss of haematopoietic stem cells (HSC s), which, in turn, is caused by deranged …

[HTML][HTML] Impact of CD34 cell dose and conditioning regimen on outcomes after haploidentical donor hematopoietic stem cell transplantation with post-transplantation …

LJ Arcuri, SK Nabhan, R Cunha, S Nichele… - Biology of Blood and …, 2020 - Elsevier
Severe aplastic anemia (SAA) is a life-threatening disease that can be cured with allogeneic
cell transplantation (HCT). Haploidentical donor transplantation with post-transplantation …

Aplastic anemia: first-line treatment by immunosuppression and sibling marrow transplantation

JR Passweg, JCW Marsh - Hematology 2010, the American …, 2010 - ashpublications.org
Newly diagnosed aplastic anemia is a serious condition, with more than 75%(higher in
young patients) becoming long-term survivors if diagnosed and treated appropriately. First …

Clinical management of aplastic anemia

AE DeZern, RA Brodsky - Expert review of hematology, 2011 - Taylor & Francis
Acquired aplastic anemia is a potentially fatal bone marrow failure disorder that is
characterized by pancytopenia and a hypocellular bone marrow. Hematopoietic stem-cell …

Late effects among pediatric patients followed for nearly 4 decades after transplantation for severe aplastic anemia

JE Sanders, AE Woolfrey, PA Carpenter… - Blood, The Journal …, 2011 - ashpublications.org
Aplastic anemia (AA), a potentially fatal disease, may be cured with marrow transplantation.
Survival in pediatric patients has been excellent early after transplantation, but only limited …

Аллогенная трансплантация гемопоэтических стволовых клеток у детей: настоящее, проблемы, перспективы

БВ Афанасьев, ЛС Зубаровская… - … детской гематологии и …, 2015 - cyberleninka.ru
Трансплантация гемопоэтических стволовых клеток (ТГСК) является ведущим методом
лечения злокачественных заболеваний системы крови и наследственных …

Autologous hematopoietic recovery after allogeneic hematopoietic stem cell transplantation: A case-based review

X Shi, X Liu, Y Tang, Y Tan, W Han, S Gao - Transplant Immunology, 2023 - Elsevier
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is widely applied for the
treatment of hematologic malignancies, but autologous hematopoietic recovery (AR) after …

Graft failure after allogeneic hematopoietic stem cell transplantation in pediatric patients with acute leukemia: autologous reconstitution or second transplant?

T Rostami, MR Rostami, AH Mirhosseini… - Stem Cell Research & …, 2024 - Springer
Background Graft failure (GF) is a rare but serious complication after allogeneic
hematopoietic stem cell transplantation (HSCT). Prevention of graft failure remains the most …

[HTML][HTML] Relapse of aplastic anemia with majority donor chimerism (donor-type aplasia) occurring late after bone marrow transplantation

A Shaw, JR Passweg, J De La Fuente, R Bajwa… - Biology of Blood and …, 2020 - Elsevier
There have been sporadic reports of the development of delayed disease recurrence after
bone marrow transplantation for severe aplastic anemia despite sustained majority or full …