Lee Sunhyang, Ko Su Yeon, Park Woon-Ju
Department of Radiology, Daejin Medical Center Bundang Jesaeng General Hospital, Seongnam, Korea.
Department of Radiology, Jeju National Universitiy College of Medicine, Jeju, Korea.
Radiol Case Rep. 2021 Nov 10;17(1):152-155. doi: 10.1016/j.radcr.2021.10.001. eCollection 2022 Jan.
Lymphatic malformations (LMs) are rare, with more than 90% occurring during childhood. Most LMs are located in the head, neck and axilla. LMs in chest wall are extremely rare, particularly in adults. This report describes a 45-year-old man with a large macrocystic LM in the right anterior chest wall. Computed tomography showed a ∼15 cm sized, well-defined, homogeneous and hypoattenuated mass without enhancement in the right anterior chest wall. On ultrasonography (US), the mass was circumscribed and anechoic, with internal septations and posterior acoustic enhancement. Following surgical excision, the mass was diagnosed as a macrocystic LM.
淋巴管畸形(LMs)较为罕见,90%以上发生于儿童期。大多数淋巴管畸形位于头、颈和腋窝。胸壁淋巴管畸形极为罕见,尤其是在成人中。本报告描述了一名45岁男性,其右前胸壁有一个巨大的大囊型淋巴管畸形。计算机断层扫描显示右前胸壁有一个大小约15厘米、边界清晰、均匀且低密度的肿块,无强化。超声检查显示该肿块边界清晰、无回声,内部有分隔且后方有回声增强。手术切除后,该肿块被诊断为大囊型淋巴管畸形。