Gurz Selcuk, Temel Necmiye, Tanrivermis Sayit Asli, Sullu Yurdanur
Department of Thoracic Surgery, Ondokuz Mayis University Faculty of Medicine, Samsun, TUR.
Department of Radiology, Ondokuz Mayis University Faculty of Medicine, Samsun, TUR.
Cureus. 2022 Oct 9;14(10):e30113. doi: 10.7759/cureus.30113. eCollection 2022 Oct.
Scapulothoracic bursitis, a rare lesion of the thoracic wall, usually presents as a cystic mass growing at the scapulothoracic interface. Histopathologically, it is characterized by the presence of synovial cells lining the interior of the thickened fibrotic cystic wall and capillary proliferation. A 48-year-old male patient was admitted to our clinic with a complaint of swelling in the back. The magnetic resonance imaging of the lung and mediastinum showed a 43 mm × 130 mm axial lesion in the left infrascapular area between the external muscles and the serratus anterior muscle, hyperintense on T2 sequence, not suppressed on fat-suppressed sequences, with a peripheral minimally contrasted septated collection area. The patient underwent surgical total excision and was discharged on the second postoperative day with no morbidity. Histopathology of the tissue was reported as soft tissue compatible with an inflamed cyst wall with prominent fibroblastic proliferation. Scapulothoracic bursitis lesions can be treated with non-invasive or minimally invasive methods. However, when it becomes a giant lesion occupying space on the thoracic wall and has hemorrhagic content, surgical excision is the treatment of choice.
肩胛胸壁滑囊炎是一种罕见的胸壁病变,通常表现为在肩胛胸壁界面处生长的囊性肿块。组织病理学上,其特征是增厚的纤维化囊壁内有滑膜细胞内衬以及毛细血管增生。一名48岁男性患者因背部肿胀主诉入院。肺部和纵隔的磁共振成像显示,在左侧肩胛下区域,位于外肌和前锯肌之间有一个43毫米×130毫米的轴向病变,在T2序列上呈高信号,在脂肪抑制序列上未被抑制,周边有一个对比度极低的分隔状积液区。患者接受了手术全切,术后第二天出院,无并发症。组织的组织病理学报告为软组织,与伴有显著成纤维细胞增生的炎症性囊壁相符。肩胛胸壁滑囊炎病变可用非侵入性或微创方法治疗。然而,当它成为占据胸壁空间的巨大病变且有出血内容物时,手术切除是首选治疗方法。