Results 51 to 60 of about 1,235 (149)

SARS-CoV-2 infection in an infant with non-respiratory manifestations: a case report

Egyptian Pediatric Association Gazette, 2021
Background Coronavirus disease (COVID-19) presents in children usually with less severe manifestations than in adults. Although fever and cough were reported as the most common symptoms, children can have non-specific symptoms. We describe an infant with
Muhammad Adel, Ahmed Magdy
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Immune‐Mediated Multilineage Cytopenias in Thymoma: A Retrospective Case Series

Thoracic Cancer, Volume 17, Issue 2, January 2026.
Thymoma‐associated immune dysregulation can drive multilineage cytopenias through T‐cell–mediated mechanisms. Patients show heterogeneous marrow involvement, frequent relapse, and variable lineage‐specific responses to immunosuppressive therapy, with sirolimus demonstrating activity in T‐cell‐driven phenotypes. ABSTRACT Background Thymoma is associated
Naibo Hu, Yansong Wei, Weinan Lin, Xifeng Dong, Huaquan Wang   +4 more
wiley   +1 more source

Pure Red Cell Aplasia with Del(20q) Sensitive for Immunosuppressive Treatment

Case Reports in Hematology, 2020
Pure red cell aplasia (PRCA) is a rare syndrome that only affects the erythroid lineage. It is defined by a normocytic, normochromic anemia with a marked reticulocytopenia and severe reduction or absence of erythroid precursors in the bone marrow ...
Anh Khoi Vo, Hilde Kollsete Gjelberg, Randi Hovland, Marte Karen Lindstad Brattås, Øystein Bruserud, Håkon Reikvam   +5 more
doaj   +1 more source

Pyridoxine Refractory Sideroblastic Anemia: Diagnosis and Misdiagnosis

Clinical Pediatric Hematology-Oncology, 2022
We report the case of a 7-year-old girl who was originally diagnosed at the age of 6 months with transfusion-dependent red cell aplasia based on a combination of severe anemia, reticulocytopenia and bone marrow findings. Since early infancy due to severe
Muhammad Matloob Alam, Abdulrhman Alathaibi, Ruwayd Adel Attar, Muhammad Kashif, Hamdan Saeed Al-Ghamdi, Sultan Abdulaziz Alharthi, Abdulmohsen Bokhary, Muteb Althomali   +7 more
doaj   +1 more source

Rapid Recovery from Chronic PRCA by MSC Infusion in Patient after Major ABO-Mismatched alloSCT

Case Reports in Medicine, 2012
Pure red cell aplasia (PRCA) is a rare complication in recipients of allogenic stem cell from ABO incompatible donors. It is characterized by reticulocytopenia and by an absence of red cell cell precursors in the bone marrow.
Vera Sergeevicheva, Irina Kruchkova, Elena Chernykh, Ekaterina Shevela, Alexander Kulagin, Andrey Gilevich, Igor Lisukov, David Sergeevichev, Vladimir Kozlov   +8 more
doaj   +1 more source

Pure Red Cell Aplasia Associated With Thymic Tumors, a Nationwide Retrospective Study

American Journal of Hematology, Volume 100, Issue 12, Page 2230-2237, December 2025.
ABSTRACT Pure red cell aplasia (PRCA) is the most frequent autoimmune cytopenia associated with thymic tumors (TTs). In a nationwide retrospective study, we included 41 patients (22 women, median age 62 years). At PRCA diagnosis, the mean hemoglobin level was 6.6 ± 2.1 g/dL, and the reticulocyte count was 6 ± 5 × 109/L. PRCA was diagnosed before TT (8%,
Mylène Hemmer, Sylvain Moinard, Olivier Lambotte, Marion Malphettes, Louis Terriou, Bertrand Lioger, Guillaume Le Guenno, Jean‐François Viallard, Marc Michel, Hervé Lobbes   +9 more
wiley   +1 more source

Parvovirus B19-triggered acute hemolytic anemia and thrombocytopenia in a child with Evans syndrome

Mediterranean Journal of Hematology and Infectious Diseases, 2018
Background: Human parvovirus B19 (HPV-B19) is the etiologic agent of erythema infectiosum, of transient aplastic crises in individuals with underlying chronic hemolytic disorders, and of chronic pure red cell aplasia in immunocompromised individuals ...
ELPIS MANTADAKIS
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Congenital Dyserythropoietic Anemia Type III Associated With a Novel KIF23 Variant (c.2132A>G; p.Gln711Arg): A Case Report

Clinical Case Reports, Volume 13, Issue 9, September 2025.
ABSTRACT Congenital dyserythropoietic anemia type III (CDA III) is an extremely rare inherited disorder characterized by ineffective erythropoiesis, multinucleated erythroblasts in the bone marrow, and variable clinical gravity. We report the case of a 6‐year‐old boy, presenting with abdominal distension, failure to thrive, dark urine, intermittent ...
Ahmad Hamammdi, Kareem Sultan Tamimi, Adam Qabaha, Omar Bsharat, Kareem Ibraheem, Ahmad Batran   +5 more
wiley   +1 more source

Intersecting Anemias: PARP Inhibitor‐Induced Toxicity and Autoimmune Hemolysis—A Case Report

eJHaem, Volume 6, Issue 4, August 2025.
ABSTRACT We present a case of a 71‐year‐old woman with a history of high‐grade serous ovarian adenocarcinoma, treated with neoadjuvant chemotherapy, surgery, and adjuvant chemotherapy. A maintenance treatment combining bevacizumab and olaparib was introduced consecutively. Bevacizumab was stopped 7 months later due to neurological complications.
Julien Dereme, Konstantinos Asonitis, Francesco Grandoni, Aikaterini Liapi, Apostolos Sarivalasis, Gerasimos Tsilimidos   +5 more
wiley   +1 more source

RIFAMPICIN INDUCED PURE RED CELL APLASIA

Zdravniški Vestnik, 2008
BACKGROUND Pure red cell aplasia (PRCA) is a rare condition of severe anemia characterized by anabsence of erythroid precursor in the bone marrow, severe reticulocytopenia and normalplatelet and leukocyte count.
Marija Čeh
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