Rongstad Mallory, Moyer Jarod, Mifflin Rachel, Condit Kevin, Rongstad Kurt
Drexel University College of Medicine, United States.
University of Wisconsin Hospitals and Clinics, United States.
Int J Surg Case Rep. 2025 Apr;129:111164. doi: 10.1016/j.ijscr.2025.111164. Epub 2025 Mar 17.
Synovial chondromatosis is a rare, benign metaplasia of the synovium characterized by the formation of cartilaginous nodules. This condition can lead to joint stiffness, pain, and damage. It is most common in the knee but has been described in various joints, including the hand. Due to its low prevalence and nonspecific symptoms, delayed diagnosis may lead to complications such as local invasion, pain, osteoarthritis, and, rarely, malignant transformation. Surgical intervention is often indicated after conservative management fails.
This report describes the complex case of synovial chondromatosis of the second metacarpophalangeal (MCP) joint in an 18-year-old female. Multiple surgical interventions culminated in amputation of her second ray for definitive management.
This case underscores the complexities of diagnosing and managing synovial chondromatosis, particularly in rare locations like the hand. Despite radiographic and pathological evidence, a definitive diagnosis was delayed, contributing to prolonged morbidity. The aggressive and recurring nature of this case highlights the need to consider synovial chondromatosis in refractory hand and finger joint pain, regardless of patient age or gender. Questions remain about whether earlier aggressive intervention could reduce recurrence or if earlier amputation could improve outcomes.
This case highlights the challenges of diagnosing and managing recurrent synovial chondromatosis in the hand. Early recognition and aggressive intervention may prevent prolonged morbidity and functional impairment. Further research is needed to determine whether earlier amputation could improve outcomes in refractory cases.
滑膜软骨瘤病是一种罕见的滑膜良性化生,其特征是形成软骨结节。这种情况可导致关节僵硬、疼痛和损伤。它最常见于膝关节,但也见于包括手部在内的各种关节。由于其发病率低且症状不具特异性,延迟诊断可能导致局部侵袭、疼痛、骨关节炎等并发症,很少会发生恶变。保守治疗失败后通常需要手术干预。
本报告描述了一名18岁女性第二掌指关节滑膜软骨瘤病的复杂病例。多次手术干预最终导致其第二掌骨截肢以进行确定性治疗。
该病例强调了滑膜软骨瘤病诊断和治疗的复杂性,尤其是在手部等罕见部位。尽管有影像学和病理学证据,但确诊仍被延迟,导致发病时间延长。该病例的侵袭性和复发性性质凸显了在难治性手部和手指关节疼痛中考虑滑膜软骨瘤病的必要性,无论患者年龄或性别如何。关于早期积极干预是否可以减少复发或早期截肢是否可以改善预后仍存在疑问。
该病例凸显了手部复发性滑膜软骨瘤病诊断和治疗的挑战。早期识别和积极干预可能预防发病时间延长和功能损害。需要进一步研究以确定早期截肢是否可以改善难治性病例的预后。