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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...

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Autores principales: Kalyanasundaram, Kathiravan, Jegadeesan, Podhini, Mohan, Sibi Chakravarthy, Ponnurangam, Vinoth N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
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.
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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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