Zobrazeno 1 - 10
of 405
pro vyhledávání: '"Reticulocytopenia"'
Autor:
Mona M Alfaraj, Hussain H Al Saeed
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 1, Pp 1-6 (2020)
Pure red cell aplasia (PRCA) is a type of normocytic or sometimes macrocytic anemia characterized by reticulocytopenia. The cause of hypo erythropoiesis is varied. It could be of a congenital or an acquired type. A congenital PRCA is different than a
Externí odkaz:
https://doaj.org/article/de457e5351d84e8eb4f9eb55bba7f010
Publikováno v:
Turkish Journal of Hematology, Vol 39, Iss 3, Pp 211-212 (2022)
Externí odkaz:
https://doaj.org/article/9519dcf061a047fdbbfeaa1eef0c0383
Publikováno v:
Терапевтический архив, Vol 91, Iss 7, Pp 121-126 (2019)
Eight patients were observed with a rare combination of thymoma and pure red cell aplasia of bone marrow (PRCA), of which seven women were between 44 to 68 years old. The diagnosis of PRCA was established before the detection of thymoma in 1 patient,
Externí odkaz:
https://doaj.org/article/3d60d155f225429b98a644a93944846a
Publikováno v:
European Journal of Case Reports in Internal Medicine (2020)
Autoimmune haemolytic anaemia (AIHA) is an uncommon condition characterized by increased destruction of erythrocytes associated with reticulocytosis in the great majority of cases. We present the case of a 68-year-old woman with jaundice and malaise.
Externí odkaz:
https://doaj.org/article/834b27737a134bfdbfbace62707ee7a2
Publikováno v:
J Zhejiang Univ Sci B
Pure red cell aplasia (PRCA) is a well-recognized complication of ABO major mismatched allogeneic hematopoietic stem cell transplantation (allo-HSCT), with a reported incidence of 10%-20% (Zhidong et al., 2012; Busca et al., 2018). It is clinically c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d200df9f5a080a7e320c7532b3d76b60
https://doi.org/10.1631/jzus.b2000532
https://doi.org/10.1631/jzus.b2000532
Publikováno v:
Transfusion. 61:1908-1915
BACKGROUND The anti-M antibody can lead to hemolytic disease of the fetus and newborn (HDFN) and adverse fetal outcomes, especially in the Asian population. However, fetal erythropoiesis resulting from M alloimmunization needs further investigation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6255536515ddc9511bd064ce354b634
https://doi.org/10.1111/trf.16350
https://doi.org/10.1111/trf.16350
Autor:
Jianyong Li, Yao He, Lang Cheng, Jian-Fu Zhang, Ming Hong, Ruinan Lu, Guangsheng He, Xiaoqing Liu, Run Zhang
Publikováno v:
International Journal of Hematology. 114:124-128
Acquired pure red cell aplasia is a rare condition characterized by normocytic normochromic anemia with severe reticulocytopenia. In refractory acquired pure red cell aplasia, the low response rate of immunosuppressive therapy also constitutes a chal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afea9910852e195078a9a4eb5b29c092
https://doi.org/10.1007/s12185-021-03100-2
https://doi.org/10.1007/s12185-021-03100-2
Autor:
Sheila S. McThenia, Vilmarie Rodriguez, Lezlie H. Andersen, Craig D. Tauscher, Jennifer L. Oliveira, Eapen K. Jacob, Emily Patterson
Publikováno v:
Transfusion. 61:974-978
Background Hemolytic disease of the fetus and newborn (HDFN) attributable to anti-M is rare, although case reports implicate anti-M in varying severities of HDFN, including fetal hydrops and intrauterine death. Case description We describe the case o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb369bb5593a0198ea8c9b9ac14478d4
https://doi.org/10.1111/trf.16252
https://doi.org/10.1111/trf.16252
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Publikováno v:
Journal of Veterinary Internal Medicine
Background Breed predispositions, survival, and prognostic factors have not been evaluated in dogs with nonregenerative immune-mediated anemia (nrIMA). Hypothesis/objectives To describe clinicopathologic variables, evaluate their associations with su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e5b3efdca4158587abb9eab3191286f
https://doi.org/10.1111/jvim.15986
https://doi.org/10.1111/jvim.15986