Multilobed Osteochondroma of the Posterior Humeral Midshaft: A Rare Morphological Variant.

IF 0.4 Q4 ORTHOPEDICS
Case Reports in Orthopedics Pub Date : 2026-07-18 eCollection Date: 2026-01-01 DOI:10.1155/cro/7763381
Feras Abuqweider, Abdul Haq Mahmoud Shahin, Anas R A Bayyoud Qasrawi, Ranya Abu Khalaf, Abdallah Badarna, Hanin Shatrit, Momen Sulyman, Mostafa Ibraheem, Qais Alnjoom
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Abstract

Osteochondroma, or osseocartilaginous exostosis, is the most common benign bone tumor, accounting for approximately 30%-35% of benign bone lesions and predominantly arising from the metaphyseal regions of long bones in young males. Mid-diaphyseal origin and multilobed morphology are exceptionally uncommon and may present diagnostic and surgical challenges. We report a rare case of a solitary, multilobed osteochondroma arising from the posterior humeral midshaft in an 18-year-old male. The patient presented with a 1-year history of a gradually enlarging, painless mass over the lateral aspect of the left upper arm, without functional limitation or neurovascular symptoms. Physical examination revealed a firm, immobile, nontender mass with intact distal neurovascular status. Magnetic resonance imaging demonstrated a pedunculated osseous lesion measuring 6.5 × 3.3 × 2.3 cm, exhibiting continuity with the humeral medullary cavity and a distinctive three-lobed configuration, including a bilobed stalk. The cartilage cap thickness measured approximately 4 mm, with no surrounding soft tissue abnormalities. Surgical excision was performed via a posterior longitudinal approach, with careful identification and preservation of the radial nerve. Intraoperatively, three distinct pedunculated bony stalks arising from the posterior humeral midshaft were excised en bloc. Histopathological analysis confirmed a benign osteochondroma, showing mature trabecular bone capped by hyaline cartilage without atypia or malignant features. To the best of our knowledge, no previous report has specifically described this combination of posterior humeral mid-diaphyseal location and multilobed morphology. This case expands the anatomical and morphological spectrum of osteochondroma and highlights the critical role of advanced imaging in preoperative planning, particularly for lesions in proximity to major neurovascular structures. Recognition of such atypical presentations is essential to ensure accurate diagnosis, safe surgical management, and avoidance of iatrogenic complications.

肱骨后中轴多叶性骨软骨瘤:一种罕见的形态学变异。
骨软骨瘤或骨软骨外生性增生是最常见的良性骨肿瘤,约占良性骨病变的30%-35%,主要发生于年轻男性长骨干骺端。干骺端中部起源和多叶形态异常罕见,可能给诊断和手术带来挑战。我们报告一个罕见的病例孤立,多叶骨软骨瘤产生于肱骨后中轴在一个18岁的男性。患者有1年的左上臂外侧无痛性肿块逐渐增大的病史,无功能限制或神经血管症状。体格检查显示一个坚固、不能动、无压痛的肿块,远端神经血管状态完好。磁共振成像显示有带梗骨性病变,尺寸为6.5 × 3.3 × 2.3 cm,显示出与肱骨腔的连续性和独特的三叶结构,包括双叶茎。软骨帽厚度约为4mm,周围无软组织异常。手术切除通过后纵入路进行,仔细识别和保存桡神经。术中,从肱骨后中轴产生的三个明显带梗的骨柄被整体切除。组织病理学分析证实为良性骨软骨瘤,显示成熟的骨小梁被透明软骨覆盖,无异型或恶性特征。据我们所知,以前没有报道专门描述过这种肱骨后骨干中段位置和多叶形态的组合。本病例扩展了骨软骨瘤的解剖和形态学谱,并强调了术前计划中先进成像的关键作用,特别是靠近主要神经血管结构的病变。识别此类非典型表现对于确保准确诊断、安全手术处理和避免医源性并发症至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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