A rare case of synovial chondromatosis of the inferior TMJ compartment. Diagnosis and treatment aspect.

D. Sozzi, G. Bocchialini, G. Novelli, M. Valente, F. Moltrasio, A. Bozzetti
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引用次数: 14

Abstract

AIM Synovial Chondromatosis (SC) is a rare, benign non neoplastic arthopathy characterized by the metaplastic development of cartilaginous nodules within the synovial membrane. In only 3% of all cases does it affect the temporomandibular joint (TMJ) and cases that arise from the lower compartment are rarely found in literature. The aim of this paper is to report a new case of SC of the inferior TMJ compartment with the description of the clinical, therapeutic and histopathological findings. CASE REPORT This article presents a 68-year-old woman with preauricular swelling on the right side, pain, crepitus and limited joint motion. This patient was evaluated by preoperative clinical manifestation, CT scan and MR images. Both showed multiple, calcified loose bodies in the inferior compartment. Based on these images as well as the patient's signs and symptoms, a surgical intervention was performed. A good functional recovery with no signs of recurrence at 36 months of follow up was obtained. CONCLUSION Among cases of synovial chondromatosis in literature, only twelve originating in the lower compartment have been reported, this one included. In all the cases treated for SC in the lower compartment, both in literature and in our case report, surgical treatment led to healing.
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颞下颌关节下腔滑膜软骨瘤病1例。诊疗方面。
滑膜软骨瘤病(SC)是一种罕见的良性非肿瘤性关节炎,其特征是滑膜内软骨结节的化生发展。在所有病例中,只有3%的病例会影响颞下颌关节(TMJ),文献中很少发现起源于下腔室的病例。本文报告一例新的颞下颌关节下腔室SC,并对其临床、治疗和组织病理学结果进行了描述。病例报告:这篇文章介绍了一位68岁的女性,右侧耳前肿胀,疼痛,毛骨悚然,关节活动受限。通过术前临床表现、CT扫描及MR影像对患者进行评价。下腔室均可见多发钙化松散体。根据这些图像以及患者的体征和症状,进行手术干预。随访36个月,功能恢复良好,无复发迹象。结论在文献报道的滑膜软骨瘤病病例中,只有12例起源于下腔室,包括这一例。在所有治疗下腔室SC的病例中,无论是在文献中还是在我们的病例报告中,手术治疗都导致了愈合。
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