Results 121 to 130 of about 193,360 (208)

Effect of autoimmune diseases on aplastic anemia: a bidirectional two-sample Mendelian randomization study

Hematology
Objectives: Numerous observational research avenues have identified a possible correlation between aplastic anemia and autoimmune diseases, rooted in analogous dysfunctional immune responses.
Qiuni Chen, Chuanyang Lu, Chunling Wang, Liang Yu   +3 more
doaj   +1 more source

Disseminated Histoplasmosis in a Patient with Aplastic Anemia

, 2014
Histoplasmosis is a systemic mycosis which has a worldwide distribution.Though common in immunocompromised patients, disseminated histoplasmosis has rarely been reported in patients with aplastic anemia.
Prashant Durgapal, Immaculata Xess, Ruma Ray, Tulika Seth, Pravas Mishra, Manoranjan Mahapatra, Sanjeev Kumar Sharma, Sunil Gupta, Sanjay Sharma, Anjan Mukherjee   +9 more
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Outcome of pregnancy and disease course among women with aplastic anemia treated with immunosuppression

, 2002
peer-reviewedBackground: 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 ...
MCCANN, SHAUN, McCann S, Symeonidis A, Passweg J, Nachbaur D, Frickhofen N, Marin P, Tichelli A, Bacigalupo A, Socié G, Barge R, Schrezenmeier H, Hows J, Marsh J   +13 more
core   +1 more source

Development and Validation of a Nomogram Based on Red Blood Cell and Reticulocyte Parameters for Differentiating Thalassemia Trait From Iron Deficiency Anemia

Journal of Clinical Laboratory Analysis, Volume 40, Issue 19, October 2026.
Thalassemia trait (TT) and iron deficiency anemia (IDA) are the primary causes of microcytic hypochromic anemia with overlapping hematological features, making their differential diagnosis challenging, so this study developed and validated a nomogram integrating red blood cell (RBC) count, mean corpuscular volume (MCV), reticulocyte percentage (RET ...
Yong Chen, Yazhen Mao, Jie Liu, Yice Lin, Dandan Chen   +4 more
wiley   +1 more source

Original Articles Relapse of aplastic anemia in children after immunosuppressive therapy: a report from the Japan Childhood Aplastic Anemia Study Group

, 2011
Background Although the therapeutic outcome of acquired aplastic anemia has improved markedly with the introduction of immunosuppressive therapy using antithymocyte globulin and cyclosporine, a significant proportion of patients subsequently relapse and ...

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Reversible Eltrombopag‐Associated Bone Marrow Fibrosis With Hematologic Recovery After Drug Withdrawal in ASXL1‐Mutated Hypoplastic Myelodysplastic Syndrome: A Case Report

eJHaem, Volume 7, Issue 5, October 2026.
ABSTRACT Hypoplastic myelodysplastic syndrome (MDS) often overlaps clinically with aplastic anemia and frequently involves clonal hematopoiesis. Thrombopoietin receptor agonists (TPO‐RAs), including eltrombopag, are increasingly used to treat cytopenias in hypoplastic marrow failure syndromes; however, their long‐term effects on clonal dynamics and ...
Kyoko Yoshihara, Ikuo Matsuda, Yasuhito Nannya, Mami Samori, Naru Tomigaki, Saki Takahashi, Chisato Ohe, Satoshi Yoshihara   +7 more
wiley   +1 more source

Atypical Presentation of UBE2T‐Related Fanconi Anemia With Immune‐Mediated Thrombocytopenia and Hematopoietic Somatic Mosaicism: A Case Report

eJHaem, Volume 7, Issue 5, October 2026.
ABSTRACT Fanconi anemia (FA) is a genetically heterogeneous disorder of chromosome instability leading to bone marrow failure (BMF) and other manifestations. We report a case of FA in which two atypical features initially obscured the diagnosis: the presence of T cell‐mediated thrombocytopenia, and somatic mosaicism leading to normal chromosome ...
Bridget T. Kiely, Alison A. Bertuch
wiley   +1 more source

Spontaneous remission of aplastic anemia: a retrospective analysis

Haematologica, 2001
BACKGROUND AND OBJECTIVES: Although acquired aplastic anemia is usually a chronic disorder, a small proportion of patients with aplastic anemia was reported to recover spontaneously without specific therapy such as allogeneic bone marrow transplantation ...
JH Lee, JH Lee, YR Shin, JS Lee, WK Kim, HS Chi, CJ Park, KH Lee   +7 more
doaj  

Expanded Umbilical Cord Blood Transplantation in Cerebral X‐Linked Adrenoleukodystrophy: A Case Report

eJHaem, Volume 7, Issue 5, October 2026.
ABSTRACT Umbilical cord blood transplantation is a viable source of stem cells due to accessibility and low incidence of chronic graft‐versus‐host disease despite human‐leukocyte‐antigen mismatching. Disadvantages of low stem cell dose in larger recipients include delayed immune reconstitution, graft rejection, and mortality.
Rachel E. Granberg, Thomas Pfeiffer, Sanil Sansar, Rafael Galindo, Shalini Shenoy   +4 more
wiley   +1 more source

Aplastic Anaemia in a Chronic Lymphocytic Leukaemia Patient Treated With Acalabrutinib, a Bruton Tyrosine Kinase Inhibitor—Case Report

eJHaem, Volume 7, Issue 5, October 2026.
ABSTRACT Introduction Although Immune cytopenias such as immune thrombocytopenia (ITP), autoimmune haemolytic anaemia (AIHA) and pure red blood cell aplasia (PRCA) are well documented associations with chronic lymphocytic leukaemia (CLL), aplastic anaemia (AA) is seemingly rare. Case This report describes a case of AA in a CLL patient post commencement
Zachray Wei, Tamara Marconi, Lucy Tuck, Stephen Ting   +3 more
wiley   +1 more source