Thomet C, Belgrado J P, Vankerckove S, Grijseels S, Heijmans S, De Smet S, Vandermeeren L
Lymphology. 2016 Sep;49(3):133-39.
The chondroepitrochlearis muscle is a rare anomaly of the pectoralis major crossing over the neurovascular bundle in the axilla. Often associated with other supernumerary muscles like the arch of Langer, it has been reported in the past as a cause of restriction of arm abduction, cosmetic defects and compression of the ulnary nerve. This case report describes the first known vascular complication due to a chondroepitrochlearis muscle, causing intermittent compression of the axillary vein and thrombosis, associated with pain, upper limb lymphedema, and impaired movements. The diagnosis was suspected from the medical history and confirmed by palpation and dynamic ultrasonography. Surgery was performed to divide the muscle slip with the help of lymphofluoroscopy to prevent damage to the lymphatic structures. Pain and impairment of movement disappeared within a few days after surgery and lymphedema decreased significantly.
肱软骨肌是一种罕见的胸大肌异常,其在腋窝处跨过神经血管束。它常与其他多余肌肉如朗格弓相关联,过去曾有报道称其可导致手臂外展受限、美容缺陷及尺神经受压。本病例报告描述了首例因肱软骨肌导致的血管并发症,引起腋静脉间歇性受压和血栓形成,并伴有疼痛、上肢淋巴水肿及活动障碍。根据病史怀疑诊断,通过触诊和动态超声检查得以确诊。在淋巴荧光镜检查的帮助下进行手术切断肌束,以防止损伤淋巴结构。术后数天内疼痛和活动障碍消失,淋巴水肿明显减轻。