Results 1 to 10 of about 13,550 (223)

Pure Red Cell Aplasia That Developed 13 Years After Thymoma Treatment: A Case Report and Literature Review [PDF]

Thoracic Cancer
A 47‐year‐old woman was diagnosed with invasive thymoma 13 years ago. She had undergone repeated surgeries, as well as chemotherapy and radiation therapy. Chemotherapy was discontinued after the patient developed normocytic anemia, which was unresponsive
Kento Kono, Kazuhisa Nakashima, Yukari Tsubata, Tsutomu Takahashi, Keita Kawakado, Takashi Yanagawa, Makoto Nagasaki, Tamio Okimoto, Takeshi Isobe   +8 more
doaj   +3 more sources

Clonal hematopoiesis in adult pure red cell aplasia

Scientific Reports, 2021
Idiopathic pure red cell aplasia (PRCA) and secondary PRCA associated with thymoma and large granular lymphocyte leukemia are generally considered to be immune-mediated.
Naohito Fujishima, Junki Kohmaru, Souichi Koyota, Keiji Kuba, Tomoo Saga, Ayumi Omokawa, Yuki Moritoki, Shigeharu Ueki, Fumihiro Ishida, Shinji Nakao, Akira Matsuda, Akiko Ohta, Kaoru Tohyama, Hiroshi Yamasaki, Kensuke Usuki, Yasuhiro Nakashima, Shinya Sato, Yasushi Miyazaki, Yasuhito Nannya, Seishi Ogawa, Kenichi Sawada, Kinuko Mitani, Makoto Hirokawa   +22 more
doaj   +2 more sources

Pure red cell aplasia and seronegative myasthenia gravis in association with thymoma

Journal of Community Hospital Internal Medicine Perspectives, 2020
Pure red cell aplasia is an uncommon paraneoplastic syndrome of thymoma. Myasthenia gravis is the most common paraneoplastic syndrome associated with thymoma. We present a case of a 79-year-old Pacific Islander female who presented with profound fatigue,
Sun Yong Lee, Amandeep Gill, Syung Min Jung   +2 more
doaj   +2 more sources

Daratumumab for treatment-refractory acquired idiopathic pure red cell aplasia

Haematologica, 2022
Not available.
Naseema Gangat, Jonathan Bleeker, Douglas Lynch, Horatiu Olteanu, Louis Letendre, Ayalew Tefferi   +5 more
doaj   +2 more sources

Pure red cell aplasia secondary to erythropoietin therapy [PDF]

Clinical Medicine
We report a case series of two patients with chronic kidney disease (CKD) who developed erythropoietin-induced pure red cell aplasia following a change in erythropoietin preparation.
Gwenno Mair Edwards, Abdulfattah A Alejmi   +1 more
doaj   +2 more sources

Rational management approach to pure red cell aplasia

Haematologica, 2018
Pure red cell aplasia is an orphan disease, and as such lacks rationally established standard therapies. Most cases are idiopathic; a subset is antibody-mediated.
Suresh Kumar Balasubramanian, Meena Sadaps, Swapna Thota, Mai Aly, Bartlomiej P. Przychodzen, Cassandra M. Hirsch, Valeria Visconte, Tomas Radivoyevitch, Jaroslaw P. Maciejewski   +8 more
doaj   +2 more sources

Pembrolizumab-induced Pure Red Cell Aplasia Successfully Treated with Intravenous Immunoglobulin

Internal medicine, 2020
We herein report a 64-year-old man who was treated with pembrolizumab for relapsed Hodgkin lymphoma. After the third administration of pembrolizumab, he showed acute anemia with a positive direct anti-globulin test.
Atsushi Isoda, Yuri Miyazawa, Kenichi Tahara, Masahiro Mihara, Akio Saito, Morio Matsumoto, Morio Sawamura   +6 more
openalex   +3 more sources

A riboflavin transporter deficiency presenting as pure red cell aplasia: a pediatric case report [PDF]

Frontiers in Pediatrics
IntroductionRiboflavin transporter deficiency (RTD) is a rare genetic disorder that affects riboflavin transport, leading to impaired red blood cell production and resulting in pure red cell aplasia.
Jingying Cheng, Jiafeng Yao, Shasha Zhao, Lingling Fu, Liqiang Zhang, Jin Jiang   +5 more
doaj   +2 more sources

Pure Red Cell Aplasia (PRCA) and Cerebellar Hypoplasia as Atypical Features of Polyglandular Autoimmune Syndrome Type I (APS-1): Two Sisters With the Same AIRE Mutation but Different Phenotypes

Frontiers in Pediatrics, 2019
The polyglandular autoimmune syndrome type I is a rare hereditary autosomal recessive disease. We describe a child with the classic triad of the disease and her sister with pure red cell aplasia and cerebellar hypoplasia.
Matteo Chinello, Margherita Mauro, Gaetano Cantalupo, Rita Balter, Massimiliano De Bortoli, Virginia Vitale, Ada Zaccaron, Elisa Bonetti, Rossella Gaudino, Elena Fiorini, Simone Cesaro   +10 more
doaj   +2 more sources

Effective treatment of refractory monoclonal gammopathy‐associated pure red cell aplasia with isatuximab, pomalidomide and dexamethasone [PDF]

eJHaem
Monoclonal gammopathy‐associated pure red cell aplasia (MG‐PRCA) is characterized by the absence or pronounced hypoplasia of erythroid precursors in the bone marrow, causing reticulocytopenia and a normocytic, normochromic anaemia in a patient with a ...
Christian Sebastian Michel, Eva Marie Fehr, Hildegard Nolte, Joachim Beck, Andreas Kreft, Katharina Theresa Rauschkolb‐Olk, Bjoern Jacobi, Matthias Theobald, Markus Munder   +8 more
doaj   +2 more sources