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表现为孤立性骨软骨瘤的颞骨纤维结构不良:一例报告

Fibrous Dysplasia of Temporal Bone Presented as a Solitary Osteochondroma: A Case Report.

作者信息

Tambe Deepak A, Patel Saumil K, Sayed Saif Rahamathulla, Mahajan Swapnil R

机构信息

Department of Orthopaedics, Dr. Balasaheb Vikhe Patil Rural Medical College, Pravara Medical Trust, Pravara Institute of Medical Sciences, Ahmednagar, Maharashtra, India.

Department of Orthopaedics, Sharanam Hospital, Dholka, Gujarat, India.

出版信息

J Orthop Case Rep. 2022 Jun;12(6):53-57. doi: 10.13107/jocr.2022.v12.i06.2862.

Abstract

INTRODUCTION

Fibrous dysplasia is a benign disorder of unknown etiology. It represents a disturbance of normal bone development - a defect in osteoblastic differentiation and maturation that originates in the mesenchymal precursor of the bone. It is characterized by slow progressive replacement of bone by abnormal isomorphic fibrous tissue. Temporal bone involvement is extremely rare. We report an unusual case of fibrous dysplasia presented like a solitary osteochondroma.

CASE REPORT

A 14-year-old girl presented with the complaints of slow-growing swelling on the left temporal region in scalp near left eye for 2 years. The swelling was small to begin with, which increased gradually over a period of 2 years. There were no other presenting symptoms. Hearing was normal. Parents of the patient were concerned with cosmesis only. She had undergone 3D CT scan of skull where it showed bony outgrowth with features suggestive of exostosis. This bony outgrowth had cortex in continuity to cortex of temporal bone and medullary canal same as that of the temporal bone and ground-glass appearance. Repeat CT scan showed bony outgrowth with cortical continuity and had pedicle. It was suggestive of pedunculated osteochondroma. There was no evidence of malignant transformation as swelling showed calcified osteoid-like mass throughout. Hence, the clinical and radiological diagnosis of the left temporal bone solitary osteochondroma was made. However, histopathology showed irregularly shaped bony trabeculae in fibrous stroma of variable cellularity without accompanying osteoblast rimming. Thus, diagnosis was fibrous dysplasia of bone. Histopathological slide was reviewed by two independent pathologists with same conclusion.

CONCLUSION

Our case was unique in that the lesion presented clinically and radiologically as solitary osteochondroma. However, in hindsight, lack of cartilage cap on CT scan should have prompted us to look for another diagnosis. To the best of our knowledge, this was unique varied presentation of fibrous dysplasia of temporal bone.

摘要

引言

骨纤维异常增殖症是一种病因不明的良性疾病。它代表了正常骨发育的紊乱——一种起源于骨间充质前体的成骨细胞分化和成熟缺陷。其特征是异常的同形纤维组织缓慢渐进性地替代骨组织。颞骨受累极为罕见。我们报告一例表现类似孤立性骨软骨瘤的不寻常骨纤维异常增殖症病例。

病例报告

一名14岁女孩因左眼附近头皮左侧颞部缓慢生长的肿胀就诊,病程2年。肿胀起初较小,在2年期间逐渐增大。无其他伴随症状。听力正常。患者父母仅关注外观问题。她接受了头颅三维CT扫描,显示有骨赘形成,具有外生性骨疣的特征。这个骨赘的皮质与颞骨皮质连续,髓腔与颞骨相同,呈磨玻璃样外观。重复CT扫描显示骨赘有皮质连续性且有蒂。提示为带蒂骨软骨瘤。由于整个肿胀显示为钙化的类骨样肿块,无恶性转化证据。因此,做出了左侧颞骨孤立性骨软骨瘤的临床和放射学诊断。然而,组织病理学显示在细胞成分各异的纤维基质中有不规则形状的骨小梁,无成骨细胞环绕。因此,诊断为骨纤维异常增殖症。组织病理学切片由两位独立病理学家复查,得出相同结论。

结论

我们的病例独特之处在于该病变在临床和放射学上表现为孤立性骨软骨瘤。然而,事后看来,CT扫描上缺乏软骨帽本应促使我们寻找其他诊断。据我们所知,这是颞骨骨纤维异常增殖症独特的多样表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c7/10092386/b0e6c1d1673b/JOCR-12-53-g001.jpg

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