IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Klein Dantis, Ramandeep Singh, Paramdeep Singh
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引用次数: 0

摘要

背景:遗传性多发性骨软骨瘤(HMO)是一种良性肿瘤,主要影响膝关节周围的骨骼、肱骨近端、手腕、骨盆以及较小程度的肋骨。虽然肋源性骨软骨瘤并不常见且通常无症状,但它们可导致继发于肿瘤相关压力的胸膜、心包和膈损伤。我们提出一个独特的病例血管相关的巨大骨软骨瘤肋骨是遗传性的,起源于右第二,第三和第四肋骨压迫症状在一个年幼的孩子。该患儿接受了广泛的局部切除和聚丙烯网片重建,并成功管理,无复发。案例展示:患者为9岁男性,右胸充盈和疼痛2个月,伴有第1代和第2代亲属的相似病史,均为遗传性,ct扫描显示右侧第2至第4根肋骨前部出现无根肋骨骨软骨瘤,伴大软骨帽。骨性生长4.5 × 2.5 cm,在右上肺叶凹陷。其软骨帽位于腋窝动脉后上方2.5 × 4.8 cm处,三维体积重建图像显示腋窝和锁骨下动脉与病变邻近。活检结果不确定,没有恶性细胞,因此他接受了广泛的局部肿瘤切除和聚丙烯网重建。随访1个月、3个月、6个月和9个月均无异常,胸曲度正常,无复发迹象。结论:本病例说明了在成长中的儿童中应用先进的成像技术进行儿科胸壁重建的手术挑战和成功的结果,强调了个性化创新方法在治疗罕见骨骼异常中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Paediatric vascular-related hereditary giant rib osteochondroma: report of a successful chest wall reconstruction.

Background: Hereditary multiple osteochondromas (HMO) are benign neoplasms that predominantly affect the bones around the knee joint, proximal humerus, wrist, pelvis, and to a lesser extent, the rib. Although rib-origin osteochondromas are uncommon and often asymptomatic, they can lead to pleural, pericardial, and diaphragmatic injuries secondary to tumour related pressure. We are presenting a unique case of a vascular-related giant osteochondroma rib that is hereditary, originating from the right second, third, and fourth ribs causing compression symptoms in a young child. The child underwent wide local excision and reconstruction using polypropylene mesh that was managed successfully with no recurrence.

Case presentation: A 9-year-old male experiencing fullness and pain in the right chest for two months with a parallel medical history of swellings in first- and second-generation relatives that is hereditary in origin underwent contrast-enhanced computed tomography revealing a sessile rib osteochondroma arising from the anterior aspects of the right second to fourth ribs with an associated large cartilaginous cap. The bony growth measured 4.5 × 2.5 cm indenting the right upper lobe while, its cartilaginous cap measured 2.5 × 4.8 cm posterior-superiorly seen encasing the axillary artery and 3D volumetric reconstructive image revealed the proximity of the axillary and subclavian artery with the lesion. A biopsy was inconclusive with no malignant cells, so he underwent wide local excision of the tumour and reconstruction with polypropylene mesh. Follow-ups at one, three, six, and nine months were uneventful with normal thoracic curvature and no sign of recurrence.

Conclusion: This case illustrates the surgical challenges addressed and the successful outcome of a paediatric chest wall reconstruction in a growing child, utilizing advanced imaging techniques, to underscore the importance of an individualized, innovative approach in managing rare skeletal anomalies.

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来源期刊
Journal of Cardiothoracic Surgery
Journal of Cardiothoracic Surgery 医学-心血管系统
CiteScore
2.50
自引率
6.20%
发文量
286
审稿时长
4-8 weeks
期刊介绍: Journal of Cardiothoracic Surgery is an open access journal that encompasses all aspects of research in the field of Cardiology, and Cardiothoracic and Vascular Surgery. The journal publishes original scientific research documenting clinical and experimental advances in cardiac, vascular and thoracic surgery, and related fields. Topics of interest include surgical techniques, survival rates, surgical complications and their outcomes; along with basic sciences, pediatric conditions, transplantations and clinical trials. Journal of Cardiothoracic Surgery is of interest to cardiothoracic and vascular surgeons, cardiothoracic anaesthesiologists, cardiologists, chest physicians, and allied health professionals.
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