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Osteopetrosis: a rare case of portal hypertension

Osteopetrosis is a rare genetic bone disorder characterized by a defect in osteoclasts recruitment and function. Its manifestations are numerous and they mainly include skeletal and dental deformities, cranial nerve entrapment and infections. Over time, osteoclastic expansion invades bone marrow lea...

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Autores principales: Khsiba, Amal, Nasr, Sahar, Hamzaoui, Lamine, Mahmoudi, Moufida, Mohamed, Asma Ben, Yaakoubi, Manel, Medhioub, Mouna, Azouz, Mohamed Moussadek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9704036/
https://www.ncbi.nlm.nih.gov/pubmed/36457539
http://dx.doi.org/10.2144/fsoa-2022-0028
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author Khsiba, Amal
Nasr, Sahar
Hamzaoui, Lamine
Mahmoudi, Moufida
Mohamed, Asma Ben
Yaakoubi, Manel
Medhioub, Mouna
Azouz, Mohamed Moussadek
author_facet Khsiba, Amal
Nasr, Sahar
Hamzaoui, Lamine
Mahmoudi, Moufida
Mohamed, Asma Ben
Yaakoubi, Manel
Medhioub, Mouna
Azouz, Mohamed Moussadek
author_sort Khsiba, Amal
collection PubMed
description Osteopetrosis is a rare genetic bone disorder characterized by a defect in osteoclasts recruitment and function. Its manifestations are numerous and they mainly include skeletal and dental deformities, cranial nerve entrapment and infections. Over time, osteoclastic expansion invades bone marrow leaving little space for hematopoietic cells. As a result, extramedullary hematopoiesis takes place in the reticular system mainly in the spleen and liver. In these patients, portal hypertension can occur as a result of extramedullary hematopoiesis associated splenomegaly. We are reporting in this article a rare case of spontaneous bacterial peritonitis associated with portal hypertension in a patient with osteopetrosis.
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spelling pubmed-97040362022-11-30 Osteopetrosis: a rare case of portal hypertension Khsiba, Amal Nasr, Sahar Hamzaoui, Lamine Mahmoudi, Moufida Mohamed, Asma Ben Yaakoubi, Manel Medhioub, Mouna Azouz, Mohamed Moussadek Future Sci OA Case Report Osteopetrosis is a rare genetic bone disorder characterized by a defect in osteoclasts recruitment and function. Its manifestations are numerous and they mainly include skeletal and dental deformities, cranial nerve entrapment and infections. Over time, osteoclastic expansion invades bone marrow leaving little space for hematopoietic cells. As a result, extramedullary hematopoiesis takes place in the reticular system mainly in the spleen and liver. In these patients, portal hypertension can occur as a result of extramedullary hematopoiesis associated splenomegaly. We are reporting in this article a rare case of spontaneous bacterial peritonitis associated with portal hypertension in a patient with osteopetrosis. Future Science Ltd 2022-11-15 /pmc/articles/PMC9704036/ /pubmed/36457539 http://dx.doi.org/10.2144/fsoa-2022-0028 Text en © 2022 Sahar Nasr https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Case Report
Khsiba, Amal
Nasr, Sahar
Hamzaoui, Lamine
Mahmoudi, Moufida
Mohamed, Asma Ben
Yaakoubi, Manel
Medhioub, Mouna
Azouz, Mohamed Moussadek
Osteopetrosis: a rare case of portal hypertension
title Osteopetrosis: a rare case of portal hypertension
title_full Osteopetrosis: a rare case of portal hypertension
title_fullStr Osteopetrosis: a rare case of portal hypertension
title_full_unstemmed Osteopetrosis: a rare case of portal hypertension
title_short Osteopetrosis: a rare case of portal hypertension
title_sort osteopetrosis: a rare case of portal hypertension
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9704036/
https://www.ncbi.nlm.nih.gov/pubmed/36457539
http://dx.doi.org/10.2144/fsoa-2022-0028
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