O'Driscoll Christopher J L, Spinner Robert J
Department of Neurologic Surgery, Mayo Clinic, Rochester, Minnesota.
J Neurosurg Case Lessons. 2024 Nov 18;8(21). doi: 10.3171/CASE24596.
Snapping triceps is a dynamic condition in which a portion of the medial head of the triceps dislocates over the medial epicondyle during flexion or extension. Pushed by the triceps, the ulnar nerve typically also dislocates over the medial epicondyle, causing neuropathy. Posttraumatic cubitus varus deformities resulting from pediatric supracondylar fractures have been associated with snapping triceps. This is the first case of snapping triceps associated with cubitus varus due to distal humeral malunion, which occurred in an adult.
A 23-year-old man sustained a left distal humeral fracture from arm wrestling, which was treated nonoperatively, healing in a varus malunion. Within several months, he developed ulnar neuropathy and snapping at the medial elbow, which was diagnosed as a dislocating ulnar nerve and was treated with ulnar nerve transposition. He presented 8 years later with continued ulnar neuritis symptoms and snapping and was found to have snapping medial triceps. He chose nonoperative treatment.
Snapping triceps, presenting as snapping at the elbow with ulnar nerve symptoms, can be incorrectly diagnosed as isolated ulnar nerve dislocation. Unrecognized snapping triceps leads to persistent symptoms after ulnar nerve transposition. The patient in this case demonstrated that an altered triceps line of pull can cause snapping triceps regardless of how the cubitus varus originated. https://thejns.org/doi/10.3171/CASE24596.
肱三头肌弹响是一种动态病症,在屈肘或伸肘过程中,肱三头肌内侧头的一部分会在内上髁上方脱位。在肱三头肌的推动下,尺神经通常也会在内上髁上方脱位,导致神经病变。小儿髁上骨折导致的创伤后肘内翻畸形与肱三头肌弹响有关。这是首例因肱骨远端畸形愈合导致肘内翻并伴有肱三头肌弹响的病例,发生在一名成年人身上。
一名23岁男性因掰手腕导致左肱骨远端骨折,未接受手术治疗,愈合后出现内翻畸形愈合。几个月内,他出现了尺神经病变以及内侧肘部弹响,被诊断为尺神经脱位,并接受了尺神经移位术治疗。8年后,他因持续的尺神经炎症状和弹响前来就诊,被发现存在肱三头肌内侧弹响。他选择了非手术治疗。
表现为肘部弹响并伴有尺神经症状的肱三头肌弹响,可能会被错误地诊断为单纯的尺神经脱位。未被识别的肱三头肌弹响会导致尺神经移位术后症状持续存在。该病例中的患者表明,无论肘内翻如何形成,肱三头肌拉力线的改变都可能导致肱三头肌弹响。https://thejns.org/doi/10.3171/CASE24596