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Achondroplasia manifesting as enchondromatosis and ossification of the spinal ligaments: a case report
INTRODUCTION: A girl presented with achondroplasia manifested as mild knee pain associated with stiffness of her back. A skeletal survey showed enchondroma-like metaphyseal dysplasia and ossification of the spinal ligaments. Magnetic resonance imaging of the spine further clarified the pathological...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518559/ https://www.ncbi.nlm.nih.gov/pubmed/18694487 http://dx.doi.org/10.1186/1752-1947-2-263 |
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author | Al Kaissi, Ali Ganger, Rudolf Klaushofer, Klaus Rumpler, Monika Grill, Franz |
author_facet | Al Kaissi, Ali Ganger, Rudolf Klaushofer, Klaus Rumpler, Monika Grill, Franz |
author_sort | Al Kaissi, Ali |
collection | PubMed |
description | INTRODUCTION: A girl presented with achondroplasia manifested as mild knee pain associated with stiffness of her back. A skeletal survey showed enchondroma-like metaphyseal dysplasia and ossification of the spinal ligaments. Magnetic resonance imaging of the spine further clarified the pathological composites. CASE PRESENTATION: A 7-year-old girl presented with the classical phenotypic features of achondroplasia. Radiographic documentation showed the co-existence of metaphyseal enchondromatosis and development of spinal bony ankylosis. Magnetic resonance imaging showed extensive ossification of the anterior and posterior spinal ligaments. Additional features revealed by magnetic resonance imaging included calcification of the peripheral vertebral bodies associated with anterior end-plate irregularities. CONCLUSION: Enchondromas are metabolically active and may continue to grow and evolve throughout the patient's lifetime; thus, progressive calcification over a period of years is not unusual. Ossification of the spinal ligaments has a specific site of predilection and often occurs in combination with senile ankylosing vertebral hyperostosis. Nevertheless, ossification of the spinal ligaments has been encountered in children with syndromic malformation complex. It is a multifactorial disease in which complex genetic and environmental factors interact, potentially leading to chronic pressure on the spinal cord and nerve roots with subsequent development of myeloradiculopathy. Our patient presented with a combination of achondroplasia, enchondroma-like metaphyseal dysplasia and calcification of the spinal ligaments. We suggest that the development of heterotopic bone formation along the spinal ligaments had occurred through an abnormal ossified enchondral mechanism. We postulate that ossification of the spinal ligaments and metaphyseal enchondromatous changes are related to each other and represent impaired terminal differentiation of chondrocytes in this particular case. Standard radiographic examination showed spinal bony ankylosis only. The pathological composites of the vertebrae have been clarified using scanning technology. Extensive spinal ligament ossification associated with calcification of the peripheral vertebral bodies and anterior end-plate irregularities were notable. We report what may be a novel spinal and extraspinal malformation complex in a girl with achondroplasia. |
format | Text |
id | pubmed-2518559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25185592008-08-21 Achondroplasia manifesting as enchondromatosis and ossification of the spinal ligaments: a case report Al Kaissi, Ali Ganger, Rudolf Klaushofer, Klaus Rumpler, Monika Grill, Franz J Med Case Reports Case Report INTRODUCTION: A girl presented with achondroplasia manifested as mild knee pain associated with stiffness of her back. A skeletal survey showed enchondroma-like metaphyseal dysplasia and ossification of the spinal ligaments. Magnetic resonance imaging of the spine further clarified the pathological composites. CASE PRESENTATION: A 7-year-old girl presented with the classical phenotypic features of achondroplasia. Radiographic documentation showed the co-existence of metaphyseal enchondromatosis and development of spinal bony ankylosis. Magnetic resonance imaging showed extensive ossification of the anterior and posterior spinal ligaments. Additional features revealed by magnetic resonance imaging included calcification of the peripheral vertebral bodies associated with anterior end-plate irregularities. CONCLUSION: Enchondromas are metabolically active and may continue to grow and evolve throughout the patient's lifetime; thus, progressive calcification over a period of years is not unusual. Ossification of the spinal ligaments has a specific site of predilection and often occurs in combination with senile ankylosing vertebral hyperostosis. Nevertheless, ossification of the spinal ligaments has been encountered in children with syndromic malformation complex. It is a multifactorial disease in which complex genetic and environmental factors interact, potentially leading to chronic pressure on the spinal cord and nerve roots with subsequent development of myeloradiculopathy. Our patient presented with a combination of achondroplasia, enchondroma-like metaphyseal dysplasia and calcification of the spinal ligaments. We suggest that the development of heterotopic bone formation along the spinal ligaments had occurred through an abnormal ossified enchondral mechanism. We postulate that ossification of the spinal ligaments and metaphyseal enchondromatous changes are related to each other and represent impaired terminal differentiation of chondrocytes in this particular case. Standard radiographic examination showed spinal bony ankylosis only. The pathological composites of the vertebrae have been clarified using scanning technology. Extensive spinal ligament ossification associated with calcification of the peripheral vertebral bodies and anterior end-plate irregularities were notable. We report what may be a novel spinal and extraspinal malformation complex in a girl with achondroplasia. BioMed Central 2008-08-11 /pmc/articles/PMC2518559/ /pubmed/18694487 http://dx.doi.org/10.1186/1752-1947-2-263 Text en Copyright © 2008 Al Kaissi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 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 | Case Report Al Kaissi, Ali Ganger, Rudolf Klaushofer, Klaus Rumpler, Monika Grill, Franz Achondroplasia manifesting as enchondromatosis and ossification of the spinal ligaments: a case report |
title | Achondroplasia manifesting as enchondromatosis and ossification of the spinal ligaments: a case report |
title_full | Achondroplasia manifesting as enchondromatosis and ossification of the spinal ligaments: a case report |
title_fullStr | Achondroplasia manifesting as enchondromatosis and ossification of the spinal ligaments: a case report |
title_full_unstemmed | Achondroplasia manifesting as enchondromatosis and ossification of the spinal ligaments: a case report |
title_short | Achondroplasia manifesting as enchondromatosis and ossification of the spinal ligaments: a case report |
title_sort | achondroplasia manifesting as enchondromatosis and ossification of the spinal ligaments: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518559/ https://www.ncbi.nlm.nih.gov/pubmed/18694487 http://dx.doi.org/10.1186/1752-1947-2-263 |
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