From the *Department of Clinical Physiology, Nuclear Medicine & PET, Rigshospitalet, Copenhagen University Hospital, Copenhagen; †Department of Orthopedic Surgery, Odense University Hospital, University of Southern Denmark, Odense; ‡Musculoskeletal Tumor Section, Department of Orthopedic Surgery, Rigshospitalet, University of Copenhagen, Copenhagen; and §Department of Nuclear Medicine, Odense University Hospital, University of Southern Denmark, Odense, Denmark.
Clin Nucl Med. 2017 Dec;42(12):e519-e522. doi: 10.1097/RLU.0000000000001856.
Angiosarcomas are highly malignant and rare tumors of vascular or lymphatic endothelial cell origin with a poor prognosis. Lymphangiosarcoma associated with chronic lymphedema is known as Stewart-Treves syndrome. Stewart-Treves syndrome is primarily described in patients with lymphedema of an upper extremity occurring after breast cancer surgery including radical axillary lymph node dissection and subsequent radiotherapy. It is rarely described in the presence of idiopathic chronic lymphedema of the lower extremities. We present a case of lymphangiosarcoma visualized on F-FDG PET/CT, where Stewart-Treves syndrome is secondary to probably a combination of idiopathic chronic lymphedema of the lower extremities and systemic immunosuppressive treatment.
血管肉瘤是一种起源于血管或淋巴管内皮细胞的高度恶性和罕见肿瘤,预后不良。与慢性淋巴水肿相关的淋巴管肉瘤被称为Stewart-Treves 综合征。Stewart-Treves 综合征主要发生在乳腺癌手术后上肢淋巴水肿的患者中,包括腋窝淋巴结清扫术和随后的放疗。在下肢特发性慢性淋巴水肿的情况下很少描述。我们报告了一例 F-FDG PET/CT 上显示的淋巴管肉瘤病例,Stewart-Treves 综合征可能是下肢特发性慢性淋巴水肿和全身免疫抑制治疗的综合作用所致。