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Missing Cells: Pathophysiology, Diagnosis, and Management of (Pan)Cytopenia in Childhood

Peripheral blood cytopenia in children can be due to a variety of acquired or inherited diseases. Genetic disorders affecting a single hematopoietic lineage are frequently characterized by typical bone marrow findings, such as lack of progenitors or maturation arrest in congenital neutropenia or a l...

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Autores principales: Erlacher, Miriam, Strahm, Brigitte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500095/
https://www.ncbi.nlm.nih.gov/pubmed/26217651
http://dx.doi.org/10.3389/fped.2015.00064
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author Erlacher, Miriam
Strahm, Brigitte
author_facet Erlacher, Miriam
Strahm, Brigitte
author_sort Erlacher, Miriam
collection PubMed
description Peripheral blood cytopenia in children can be due to a variety of acquired or inherited diseases. Genetic disorders affecting a single hematopoietic lineage are frequently characterized by typical bone marrow findings, such as lack of progenitors or maturation arrest in congenital neutropenia or a lack of megakaryocytes in congenital amegakaryocytic thrombocytopenia, whereas antibody-mediated diseases such as autoimmune neutropenia are associated with a rather unremarkable bone marrow morphology. By contrast, pancytopenia is frequently associated with a hypocellular bone marrow, and the differential diagnosis includes acquired aplastic anemia, myelodysplastic syndrome, inherited bone marrow failure syndromes such as Fanconi anemia and dyskeratosis congenita, and a variety of immunological disorders including hemophagocytic lymphohistiocytosis. Thorough bone marrow analysis is of special importance for the diagnostic work-up of most patients. Cellularity, cellular composition, and dysplastic signs are the cornerstones of the differential diagnosis. Pancytopenia in the presence of a normo- or hypercellular marrow with dysplastic changes may indicate myelodysplastic syndrome. More challenging for the hematologist is the evaluation of the hypocellular bone marrow. Although aplastic anemia and hypocellular refractory cytopenia of childhood (RCC) can reliably be differentiated on a morphological level, the overlapping pathophysiology remains a significant challenge for the choice of the therapeutic strategy. Furthermore, inherited bone marrow failure syndromes are usually associated with the morphological picture of RCC, and the recognition of these entities is essential as they often present a multisystem disease requiring different diagnostic and therapeutic approaches. This paper gives an overview over the different disease entities presenting with (pan)cytopenia, their pathophysiology, characteristic bone marrow findings, and therapeutic approaches.
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spelling pubmed-45000952015-07-27 Missing Cells: Pathophysiology, Diagnosis, and Management of (Pan)Cytopenia in Childhood Erlacher, Miriam Strahm, Brigitte Front Pediatr Pediatrics Peripheral blood cytopenia in children can be due to a variety of acquired or inherited diseases. Genetic disorders affecting a single hematopoietic lineage are frequently characterized by typical bone marrow findings, such as lack of progenitors or maturation arrest in congenital neutropenia or a lack of megakaryocytes in congenital amegakaryocytic thrombocytopenia, whereas antibody-mediated diseases such as autoimmune neutropenia are associated with a rather unremarkable bone marrow morphology. By contrast, pancytopenia is frequently associated with a hypocellular bone marrow, and the differential diagnosis includes acquired aplastic anemia, myelodysplastic syndrome, inherited bone marrow failure syndromes such as Fanconi anemia and dyskeratosis congenita, and a variety of immunological disorders including hemophagocytic lymphohistiocytosis. Thorough bone marrow analysis is of special importance for the diagnostic work-up of most patients. Cellularity, cellular composition, and dysplastic signs are the cornerstones of the differential diagnosis. Pancytopenia in the presence of a normo- or hypercellular marrow with dysplastic changes may indicate myelodysplastic syndrome. More challenging for the hematologist is the evaluation of the hypocellular bone marrow. Although aplastic anemia and hypocellular refractory cytopenia of childhood (RCC) can reliably be differentiated on a morphological level, the overlapping pathophysiology remains a significant challenge for the choice of the therapeutic strategy. Furthermore, inherited bone marrow failure syndromes are usually associated with the morphological picture of RCC, and the recognition of these entities is essential as they often present a multisystem disease requiring different diagnostic and therapeutic approaches. This paper gives an overview over the different disease entities presenting with (pan)cytopenia, their pathophysiology, characteristic bone marrow findings, and therapeutic approaches. Frontiers Media S.A. 2015-07-13 /pmc/articles/PMC4500095/ /pubmed/26217651 http://dx.doi.org/10.3389/fped.2015.00064 Text en Copyright © 2015 Erlacher and Strahm. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Erlacher, Miriam
Strahm, Brigitte
Missing Cells: Pathophysiology, Diagnosis, and Management of (Pan)Cytopenia in Childhood
title Missing Cells: Pathophysiology, Diagnosis, and Management of (Pan)Cytopenia in Childhood
title_full Missing Cells: Pathophysiology, Diagnosis, and Management of (Pan)Cytopenia in Childhood
title_fullStr Missing Cells: Pathophysiology, Diagnosis, and Management of (Pan)Cytopenia in Childhood
title_full_unstemmed Missing Cells: Pathophysiology, Diagnosis, and Management of (Pan)Cytopenia in Childhood
title_short Missing Cells: Pathophysiology, Diagnosis, and Management of (Pan)Cytopenia in Childhood
title_sort missing cells: pathophysiology, diagnosis, and management of (pan)cytopenia in childhood
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500095/
https://www.ncbi.nlm.nih.gov/pubmed/26217651
http://dx.doi.org/10.3389/fped.2015.00064
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