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Diamond Blackfan Anemia: a Tertiary Care Center Experience

Diamond Blackfan Anemia (DBA) is a rare hypoplastic anemia that presents in infancy with macrocytic anemia and reticulocytopenia. It is a ribosomopathy with autosomal dominant inheritance. In our series of 10 patients with DBA, congenital malformations were observed in 50% of the cases. Age at sympt...

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Autores principales: Singh, Avinash Kumar, Radhakrishnan, Nita, Seth, Tulika, Mishra, Pravas, Mahapatra, Manoranjan, Pati, Haraprasad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Università Cattolica del Sacro Cuore 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684352/
https://www.ncbi.nlm.nih.gov/pubmed/23795277
http://dx.doi.org/10.4084/MJHID.2013.039
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author Singh, Avinash Kumar
Radhakrishnan, Nita
Seth, Tulika
Mishra, Pravas
Mahapatra, Manoranjan
Pati, Haraprasad
author_facet Singh, Avinash Kumar
Radhakrishnan, Nita
Seth, Tulika
Mishra, Pravas
Mahapatra, Manoranjan
Pati, Haraprasad
author_sort Singh, Avinash Kumar
collection PubMed
description Diamond Blackfan Anemia (DBA) is a rare hypoplastic anemia that presents in infancy with macrocytic anemia and reticulocytopenia. It is a ribosomopathy with autosomal dominant inheritance. In our series of 10 patients with DBA, congenital malformations were observed in 50% of the cases. Age at symptom onset ranged from 0–12 months. Age at diagnosis ranged from 4 months to 96 months. Male: female ratio was 9:1. Response to prednisolone was observed in 4 out of the 10 patients (either during initial treatment or during re-challenge). Response to cyclosporine was found to be poor. Bone marrow transplantation was successful in attaining remission in one patient. Malignancies were not reported in any patient possibly due to a short follow up period.
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spelling pubmed-36843522013-06-21 Diamond Blackfan Anemia: a Tertiary Care Center Experience Singh, Avinash Kumar Radhakrishnan, Nita Seth, Tulika Mishra, Pravas Mahapatra, Manoranjan Pati, Haraprasad Mediterr J Hematol Infect Dis Original Article Diamond Blackfan Anemia (DBA) is a rare hypoplastic anemia that presents in infancy with macrocytic anemia and reticulocytopenia. It is a ribosomopathy with autosomal dominant inheritance. In our series of 10 patients with DBA, congenital malformations were observed in 50% of the cases. Age at symptom onset ranged from 0–12 months. Age at diagnosis ranged from 4 months to 96 months. Male: female ratio was 9:1. Response to prednisolone was observed in 4 out of the 10 patients (either during initial treatment or during re-challenge). Response to cyclosporine was found to be poor. Bone marrow transplantation was successful in attaining remission in one patient. Malignancies were not reported in any patient possibly due to a short follow up period. Università Cattolica del Sacro Cuore 2013-06-03 /pmc/articles/PMC3684352/ /pubmed/23795277 http://dx.doi.org/10.4084/MJHID.2013.039 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Singh, Avinash Kumar
Radhakrishnan, Nita
Seth, Tulika
Mishra, Pravas
Mahapatra, Manoranjan
Pati, Haraprasad
Diamond Blackfan Anemia: a Tertiary Care Center Experience
title Diamond Blackfan Anemia: a Tertiary Care Center Experience
title_full Diamond Blackfan Anemia: a Tertiary Care Center Experience
title_fullStr Diamond Blackfan Anemia: a Tertiary Care Center Experience
title_full_unstemmed Diamond Blackfan Anemia: a Tertiary Care Center Experience
title_short Diamond Blackfan Anemia: a Tertiary Care Center Experience
title_sort diamond blackfan anemia: a tertiary care center experience
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684352/
https://www.ncbi.nlm.nih.gov/pubmed/23795277
http://dx.doi.org/10.4084/MJHID.2013.039
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