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表现为内生软骨瘤病和脊柱韧带骨化的软骨发育不全:一例报告

Achondroplasia manifesting as enchondromatosis and ossification of the spinal ligaments: a case report.

作者信息

Al Kaissi Ali, Ganger Rudolf, Klaushofer Klaus, Rumpler Monika, Grill Franz

机构信息

Ludwig Boltzmann Institute of Osteology, Hanusch Hospital of WGKK and AUVA Trauma Centre Meidling, 4th Medical Department, Hanusch Hospital, Vienna, Austria.

出版信息

J Med Case Rep. 2008 Aug 11;2:263. doi: 10.1186/1752-1947-2-263.

Abstract

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.

摘要

引言

一名患有软骨发育不全的女孩表现为轻度膝关节疼痛并伴有背部僵硬。骨骼检查显示类似内生软骨瘤的干骺端发育异常和脊柱韧带骨化。脊柱磁共振成像进一步明确了病理情况。

病例报告

一名7岁女孩表现出软骨发育不全的典型表型特征。影像学记录显示干骺端内生软骨瘤病与脊柱骨性强直并存。磁共振成像显示脊柱前后韧带广泛骨化。磁共振成像显示的其他特征包括与椎体前缘终板不规则相关的椎体周边钙化。

结论

内生软骨瘤具有代谢活性,可能在患者一生中持续生长和演变;因此,数年的渐进性钙化并不罕见。脊柱韧带骨化有特定的好发部位,常与老年性强直性椎体骨质增生合并出现。然而,在患有综合征性畸形复合体的儿童中也发现了脊柱韧带骨化。这是一种多因素疾病,复杂的遗传和环境因素相互作用,可能导致脊髓和神经根长期受压,继而发展为脊髓神经根病。我们的患者表现为软骨发育不全、类似内生软骨瘤的干骺端发育异常和脊柱韧带钙化的组合。我们认为沿脊柱韧带的异位骨形成是通过异常的骨化软骨机制发生的。我们推测脊柱韧带骨化和干骺端内生软骨瘤样改变相互关联,在这个特定病例中代表软骨细胞终末分化受损。标准的X线检查仅显示脊柱骨性强直。使用扫描技术已明确了椎体的病理情况。与椎体周边钙化和前缘终板不规则相关的广泛脊柱韧带骨化值得注意。我们报告了一名患有软骨发育不全的女孩可能存在的一种新的脊柱和脊柱外畸形复合体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ac0/2518559/ecbebac6fbdf/1752-1947-2-263-1.jpg

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