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手部单一射线或单一神经分布的小儿多发性软骨瘤病的罕见表现:一项多中心病例系列研究。

Rare Presentation of Pediatric Multiple Enchondromatosis Limited to Single Ray or Single Nerve Distribution in the Hand: A Multicenter Case Series.

机构信息

Department of Orthopaedic Surgery and Sports Medicine, University of Kentucky.

Shriners Hospitals for Children Medical Center, Lexington.

出版信息

J Pediatr Orthop. 2022 Aug 1;42(7):e788-e792. doi: 10.1097/BPO.0000000000002189. Epub 2022 May 17.

Abstract

BACKGROUND

Multiple enchondromas in the pediatric hand is a relatively rare occurrence and the literature regarding its incidence and treatment is sparse. Within this rare subset of patients, we identified a unique cohort in which lesions are confined to multiple bones in a single ray or adjacent rays within a single nerve distribution. We review the clinical and pathologic characteristics and describe the indications for and outcomes of treatment in this unique subset of patients as well as offer conjectures about its occurrence.

METHODS

Institutional review board (IRB)-approved retrospective multicenter study between 2010 and 2018 identified subjects with isolated multiple enchondromas and minimum 2-year follow-up. Data analyzed included demographics, lesion quantification and localization, symptoms and/or fracture(s), treatment of lesion(s), complications, recurrence, and presence of malignant transformation.

RESULTS

Ten patients were evaluated with average age at presentation of 9 years (range: 4 to 16) and mean clinical follow-up of 6 years (range: 2.8 to 8.6). Five subjects had multiple ray involvement in a single nerve distribution and 5 had single ray involvement with an average of 4 lesions noted per subject (range: 2 to 8). All children in the study had histopathologic-proven enchondromas and underwent operative curettage±bone grafting. Indications for surgical intervention included persistent pain, multiple prior pathologic fractures, impending fracture and deformity. During the study period three subjects experienced pathologic fracture treated successfully with immobilization. Recurrence was noted in 40% at an average of 105 weeks postoperatively (range: 24 to 260) and appears higher than that reported in the literature. No case of malignant transformation was observed during the study period.

CONCLUSIONS

A rare subset of pediatric patients with multiple enchondromas of the hand is described with lesions limited to a single ray or single nerve distribution. Further awareness of this unique subset of patients may increase our understanding of the disease and improve patient outcomes.

LEVEL OF EVIDENCE

Level IV-therapeutic (case series).

摘要

背景

儿童手部多发性内生软骨瘤较为罕见,其发病率和治疗方法的相关文献也较为稀少。在这一罕见病例中,我们发现了一个独特的亚组,其病变局限于单一神经支配的单一射线或相邻射线的多个骨骼中。我们回顾了这些患者的临床和病理特征,并描述了这一独特亚组患者的治疗适应证和治疗结果,同时对其发病机制进行了推测。

方法

通过机构审查委员会(IRB)批准的回顾性多中心研究,纳入 2010 年至 2018 年间患有孤立性多发性内生软骨瘤且随访时间至少 2 年的患者。分析的数据包括患者的人口统计学资料、病变的定量和定位、症状和/或骨折、病变的治疗、并发症、复发以及恶性转化的存在。

结果

共评估了 10 名患者,平均就诊年龄为 9 岁(范围:4 至 16 岁),平均临床随访时间为 6 年(范围:2.8 至 8.6 年)。5 名患者存在单一神经支配下的多射线受累,5 名患者存在单一射线受累,平均每个患者有 4 个病变(范围:2 至 8 个)。所有研究中的患儿均经组织病理学证实为内生软骨瘤,并接受了手术刮除术+植骨术。手术干预的适应证包括持续疼痛、多次病理性骨折、即将发生的骨折和畸形。在研究期间,有 3 名患者发生了病理性骨折,通过固定治疗获得了成功。40%的患者在术后平均 105 周(范围:24 至 260 周)时出现复发,这一复发率似乎高于文献报道。在研究期间未观察到恶性转化病例。

结论

描述了手部多发性内生软骨瘤的一个罕见亚组,其病变局限于单一射线或单一神经支配。进一步了解这一独特的患者亚组可能会提高我们对该疾病的认识,并改善患者的治疗效果。

证据等级

IV 级-治疗性(病例系列研究)。

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