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An Infant with Splenohepatomegaly: A Rare Cause
Osteopetrosis is a rare congenital disorder of bone resorption, caused by failure of osteoclasts to reabsorb immature bone. Malignant infantile osteopetrosis presents in early life with generalized osteosclerosis and decreased bone marrow spaces, resulting in anemia, splenohepatomegaly due to extram...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168642/ https://www.ncbi.nlm.nih.gov/pubmed/25250197 http://dx.doi.org/10.4103/2156-7514.139738 |
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author | Kalyanasundaram, Kathiravan Jegadeesan, Podhini Mohan, Sibi Chakravarthy Ponnurangam, Vinoth N |
author_facet | Kalyanasundaram, Kathiravan Jegadeesan, Podhini Mohan, Sibi Chakravarthy Ponnurangam, Vinoth N |
author_sort | Kalyanasundaram, Kathiravan |
collection | PubMed |
description | Osteopetrosis is a rare congenital disorder of bone resorption, caused by failure of osteoclasts to reabsorb immature bone. Malignant infantile osteopetrosis presents in early life with generalized osteosclerosis and decreased bone marrow spaces, resulting in anemia, splenohepatomegaly due to extramedullary hematopoiesis, cranial nerve compression, and growth failure. It is a fatal condition with death occurring within the first year of life. Bone marrow transplant remains the only curative treatment. We present a report of an infant with splenohepatomegaly, who was diagnosed with malignant infantile osteopetrosis. |
format | Online Article Text |
id | pubmed-4168642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41686422014-09-23 An Infant with Splenohepatomegaly: A Rare Cause Kalyanasundaram, Kathiravan Jegadeesan, Podhini Mohan, Sibi Chakravarthy Ponnurangam, Vinoth N J Clin Imaging Sci Case Report Osteopetrosis is a rare congenital disorder of bone resorption, caused by failure of osteoclasts to reabsorb immature bone. Malignant infantile osteopetrosis presents in early life with generalized osteosclerosis and decreased bone marrow spaces, resulting in anemia, splenohepatomegaly due to extramedullary hematopoiesis, cranial nerve compression, and growth failure. It is a fatal condition with death occurring within the first year of life. Bone marrow transplant remains the only curative treatment. We present a report of an infant with splenohepatomegaly, who was diagnosed with malignant infantile osteopetrosis. Medknow Publications & Media Pvt Ltd 2014-08-30 /pmc/articles/PMC4168642/ /pubmed/25250197 http://dx.doi.org/10.4103/2156-7514.139738 Text en Copyright: © 2014 Kalyanasundaram K. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Case Report Kalyanasundaram, Kathiravan Jegadeesan, Podhini Mohan, Sibi Chakravarthy Ponnurangam, Vinoth N An Infant with Splenohepatomegaly: A Rare Cause |
title | An Infant with Splenohepatomegaly: A Rare Cause |
title_full | An Infant with Splenohepatomegaly: A Rare Cause |
title_fullStr | An Infant with Splenohepatomegaly: A Rare Cause |
title_full_unstemmed | An Infant with Splenohepatomegaly: A Rare Cause |
title_short | An Infant with Splenohepatomegaly: A Rare Cause |
title_sort | infant with splenohepatomegaly: a rare cause |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168642/ https://www.ncbi.nlm.nih.gov/pubmed/25250197 http://dx.doi.org/10.4103/2156-7514.139738 |
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