Department of Musculoskeletal Radiology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
Department of Musculoskeletal Radiology, Royal Orthopaedic Hospital, Birmingham, UK.
Clin Imaging. 2021 Jan;69:374-379. doi: 10.1016/j.clinimag.2020.10.019. Epub 2020 Oct 13.
Mobile wad of Henry (MOH) is a preferred surgical term used to describe the lateral compartment muscles of the forearm consisting of brachioradialis, extensor carpi radialis longus and brevis. The lesions in this compartment are uncommon. In this paper, we describe the largest series of the MOH lesions including their demographics, imaging appearances and importance of surgical anatomy whilst managing MOH lesions via radiological or surgical interventions.
A retrospective search of oncology database for lesions in MOH at our tertiary orthopaedic oncology institute was performed for the last 12 years (2007-2019) after obtaining institutional review board approval. We further analyse data to obtain further clarity of various neoplasms occurring at this particular anatomical site.
We identified 28 patients with MOH lesions with an age range of 8 to 84 years and a male predominance. Imaging-wise, majority of lesions were benign following characteristics of lipomatous tumours, lipomas being the commonest. Other relatively uncommon benign lesions were nodular fasciitis, myositis ossificans and brachioradialis muscle injury; whereas aggressive MOH soft tissue neoplasms included synovial sarcoma and fibrohistiocytoma.
Although majority of MOH lesions are benign, one needs to be aware of spectrum containing uncommon benign and aggressive MOH lesions. When posed with dilemma, the MOH lesions require multidisciplinary approach with close collaboration of the radiologist, the surgeon and the pathologist to decide further management.
Mobile wad of Henry (MOH) 是一个专业的外科术语,用于描述前臂的外侧间隔肌群,包括肱桡肌、桡侧腕长伸肌和短伸肌。该间隔的病变并不常见。本文描述了最大的 MOH 病变系列,包括其人口统计学、影像学表现以及在通过放射或手术干预管理 MOH 病变时的手术解剖学的重要性。
在获得机构审查委员会批准后,我们对我们的三级骨科肿瘤研究所过去 12 年来(2007-2019 年) MOH 中的肿瘤进行了回顾性搜索。我们进一步分析数据,以更清楚地了解发生在这个特定解剖部位的各种肿瘤。
我们共确定了 28 例 MOH 病变患者,年龄 8 至 84 岁,男性居多。影像学上,大多数病变具有脂肪瘤肿瘤的特征,为良性病变。其他相对少见的良性病变包括结节性筋膜炎、骨化性肌炎和肱桡肌损伤;而侵袭性 MOH 软组织肿瘤包括滑膜肉瘤和纤维组织细胞瘤。
尽管大多数 MOH 病变为良性,但人们需要了解包含不常见的良性和侵袭性 MOH 病变的病变谱。当面临困境时,MOH 病变需要多学科方法,由放射科医生、外科医生和病理科医生密切合作,以决定进一步的治疗方案。