Results 1 to 10 of about 1,434 (146)

Post–COVID-19 pure red cell aplasia: A case report and literature review [PDF]

SAGE Open Medical Case Reports
Pure red cell aplasia is a rare hematologic disorder characterized by severe normocytic anemia, reticulocytopenia, and absence of erythroid precursors.
Alanoud Al Shmarri, Duha Marwan Naji, Elmustafa Abdalla, Abdulrahman F. Al-Mashdali, Mohammed Ahmed, V-Ayah Elhadi, Deena Mudawi, Mohammad Abdulgayoom, Imran Ahmad, Samah Kohla, Sarah Elkourashy, Shehab F. Mohamed   +11 more
doaj   +3 more sources

Vitamin B12 Deficiency‐Associated Pseudo‐Thrombotic Microangiopathy in a Patient on Longstanding Oral B12 Supplementation [PDF]

Clinical Case Reports
Vitamin B12 deficiency is a common cause of normocytic or megaloblastic anemia. In 2.5% of cases, it can manifest as pseudo‐thrombotic microangiopathy (pseudo‐TMA), which mimics thrombotic thrombocytopenic purpura (TTP), an emergent hemolytic ...
Hanna K. Bertucci, Benjamin M. Moy, Regina Stein   +2 more
doaj   +3 more sources

Neonatal Diamond‐Blackfan anemia with persistent neutropenia caused by an RPS15A variant [PDF]

Pediatr Investig
Pediatric Investigation, EarlyView.
Hong Zheng, Kaimei Wang, Jian Wang, Jianpei Fang, Dunhua Zhou, Kunyin Qiu   +5 more
wiley   +2 more sources

H Syndrome Associated With Pure Red Cell Aplasia, Rosai–Dorfman Disease, and Sensorineural Hearing Loss: Phenotypic Variability in Three Children With the Same SLC29A3 Mutation [PDF]

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT H syndrome is a rare autosomal recessive disorder caused by mutations in the SLC29A3 gene. We report three pediatric patients with a homozygous c.1309G>A (p.Gly437Arg) mutation presenting with distinct phenotypic variations. These cases expand the clinical spectrum and emphasize the importance of early genetic diagnosis and family counseling.
Mohammad Najajrah, Hadeel I. Bouzia, Nermin K. Darawi, Fatima S. Hajjaj, Nour H. Moosa, Noor M. Awad   +5 more
wiley   +2 more sources

Splenic Sequestration and Suspected Transient Aplastic Crisis in Sickle-Cell SC/Hemoglobin-G Disease in an Adult: A Case Report [PDF]

Clinical Medicine Insights: Case Reports
Acute Splenic Sequestration Crisis (ASSC) and Transient Aplastic Crisis (TAC) are severe, but distinct, hematologic complications of sickle cell disease (SCD). ASSC typically presents with acute splenomegaly and anemia due to red blood cell (RBC) pooling,
Evani Patel MD, Simon Gunter MD, Lee Hartner MD   +2 more
doaj   +2 more sources

A 2-month-old boy with hemolytic anemia and reticulocytopenia following intravenous immunoglobulin therapy for Kawasaki disease: a case report and literature review. [PDF]

Korean Journal of Pediatrics, 2016
Herein, we report a rare case of hemolytic anemia with reticulocytopenia following intravenous immunoglobulin therapy in a young infant treated for Kawasaki disease.
Soo Hyun Kim, Dong Hyun Cha, Youn Ho Shin   +2 more
exaly   +2 more sources

Repeated Response to Daratumumab in Refractory MGUS‐Associated Pure Red Cell Aplasia Persisting After Allogeneic Transplantation: A Case Report [PDF]

eJHaem, Volume 7, Issue 5, October 2026.
ABSTRACT Pure red cell aplasia (PRCA) is usually managed as a disorder driven predominantly by cellular immune mechanisms, but plasma cell‐directed therapy may be relevant in selected cases associated with monoclonal gammopathy. We report a case of refractory PRCA associated with IgG‐kappa monoclonal gammopathy of undetermined significance (MGUS). A 64‐
Kyoko Yoshihara, Toshimitsu Matsui, Ikuo Matsuda, Mami Samori, Yoshiyuki Fujita, Saki Takahashi, Fuyuki Yamagata, Nobuto Utsunomiya, Chisato Ohe, Satoshi Yoshihara   +9 more
wiley   +2 more sources

Pure Red Cell Aplasia as an Isolated Paraneoplastic Manifestation of Thymoma: A Case Report and Literature Review [PDF]

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Thymomas are epithelial tumors of the anterior mediastinum and are frequently associated with paraneoplastic autoimmune disorders. Pure red cell aplasia (PRCA) is a rare but clinically significant complication, caused by immune‐mediated suppression of erythropoiesis.
Heba Amer, Modar Alajlani, Mhd Rashad Jamle, Hareth Almanfe, Mohammad Shbat, Mohammad Abd Alrahman Saif, Anas Abdulrazzak, Ahmed Nabhan, Bassam Darwish   +8 more
wiley   +2 more sources

Refractory autoimmune hemolytic anemia with poor erythropoietic compensation in combined immunodeficiency: A case series [PDF]

Pediatr Allergy Immunol
Pediatric Allergy and Immunology, Volume 37, Issue 8, August 2026.
Letizia Baldini, Mattia Moratti, Alessandro Ruggi, Francesco Licciardi, Fraia Melchionda, Maura Fois, Maria Elena Cantarini, Elena Facchini, Veronica Barat, Giovanni Del Borrello, Bruno Fattizzo, Elena Sabattini, Clara Bertuzzi, Riccardo Masetti, Francesca Conti   +14 more
wiley   +2 more sources

Case Report: From complete remission to severe anemia: pure red cell aplasia emerged after VRd regimen in multiple myeloma [PDF]

Frontiers in Oncology
Pure red cell aplasia (PRCA) is a rare disorder characterized by severe reticulocytopenia and absence of erythroid precursors. Its association with multiple myeloma (MM) therapy is uncommon.
Xiaoqing Zhang, Ting Hu, Hongmei Dai, Hua Yuan   +3 more
doaj   +2 more sources