Alomari Ahmad I, Spencer Samantha A, Arnold Ryan W, Chaudry Gulraiz, Kasser James R, Burrows Patricia E, Govender Pradeep, Padua Horacio M, Dillon Brian, Upton Joseph, Taghinia Amir H, Fishman Steven J, Mulliken John B, Fevurly Rebecca D, Greene Arin K, Landrigan-Ossar Mary, Paltiel Harriet J, Trenor Cameron C, Kozakewich Harry P
*Divisions of Vascular and Interventional Radiology †Vascular Anomalies Center Departments of ‡Orthopedic Surgery ∥Plastic and Oral Surgery ¶Surgery #Anesthesiology **Radiology ‡‡Pathology ††Division of Hematology/Oncology, Children's Hospital Boston, Harvard Medical School, Boston, MA §Department of Diagnostic and Interventional Imaging, Memorial Hermann and Memorial Hermann Children's Hospital, Houston, TX.
J Pediatr Orthop. 2014 Jan;34(1):109-17. doi: 10.1097/BPO.0b013e3182a1f0b8.
The diagnosis and management of vascular anomalies of the extremities can be challenging as these disorders are uncommon and may clinically overlap. The aim of this paper is to describe the clinical, radiologic, and histopathologic features of fibro-adipose vascular anomaly (FAVA), a previously unrecognized disorder of the limb.
The clinical, imaging, operative, and histopathologic data from patients with a unique intramuscular lesion of the extremities comprising dense fibrofatty tissue and slow-flow vascular malformations were retrospectively reviewed.
Sixteen patients diagnosed with FAVA of the extremity (3 male and 13 female individuals) met the clinical, radiologic, and histopathologic inclusion criteria. The age at presentation ranged from the time of birth to 28 years. The locations of the lesions were: calf (n=10), forearm/wrist (n=3), and thigh (n=3). Fourteen patients presented with severe pain. Seven of the patients with calf lesions had limited ankle dorsiflexion. On imaging, the complex intramuscular lesions replaced muscle fibers with fibrofatty overgrowth and phlebectasia (dilation of the veins). The extrafascial component comprised fatty overgrowth, phlebectasia, and an occasional lymphatic malformation. The histopathologic features comprised dense fibrous tissue, fat, and lymphoplasmacytic aggregates within atrophied skeletal muscle. Adipose tissue also infiltrated skeletal muscle at the periphery of the lesion. There were large, irregular, and sometimes excessively muscularized venous channels and smaller, clustered channels. Other findings include organizing thrombi, a lymphatic component, and dense fibrous tissue-encircled nerves.
The constellation of clinical, radiologic, and histopathologic features constitutes a distinct entity comprising fibrofatty infiltration of muscle, unusual phlebectasia with pain, and contracture of the affected extremity. The clinical and radiologic findings permit the diagnosis of FAVA with major therapeutic implications.
Level III.
四肢血管异常的诊断和管理具有挑战性,因为这些疾病并不常见且在临床上可能存在重叠。本文旨在描述纤维脂肪性血管异常(FAVA)的临床、放射学和组织病理学特征,这是一种此前未被认识的肢体疾病。
回顾性分析了患有独特的四肢肌内病变(包括致密纤维脂肪组织和慢血流血管畸形)患者的临床、影像学、手术及组织病理学数据。
16例被诊断为肢体FAVA的患者(3例男性和13例女性)符合临床、放射学和组织病理学纳入标准。发病年龄从出生到28岁不等。病变部位为:小腿(n = 10)、前臂/腕部(n = 3)和大腿(n = 3)。14例患者出现严重疼痛。7例小腿病变患者存在踝关节背屈受限。影像学检查显示,复杂的肌内病变以纤维脂肪过度生长和静脉扩张(静脉扩张)替代了肌纤维。筋膜外成分包括脂肪过度生长、静脉扩张和偶尔出现的淋巴管畸形。组织病理学特征包括萎缩骨骼肌内的致密纤维组织、脂肪和淋巴浆细胞聚集。脂肪组织也在病变周边浸润骨骼肌。存在大的、不规则的,有时过度肌化的静脉通道以及较小的、成簇的通道。其他发现包括机化血栓、淋巴管成分以及被致密纤维组织环绕的神经。
临床、放射学和组织病理学特征构成了一个独特的实体,包括肌肉的纤维脂肪浸润、伴有疼痛的异常静脉扩张以及受累肢体的挛缩。临床和放射学表现有助于诊断FAVA,并具有重要的治疗意义。
三级。