后纵隔原发性软骨瘤伴霍纳综合征：一例报告。
Primary chondroma of posterior mediastinum with Horner's syndrome: a case report.
机构信息
Department of Lung Cancer Surgery, Tianjin Key Laboratory of Lung Cancer Metastasis and Tumor Microenvironment, Tianjin Lung Cancer Institute, Tianjin Medical University General Hospital, Anshan Road No.154, Heping District, Tianjin, 300052, China.
出版信息
World J Surg Oncol. 2018 Oct 17;16(1):209. doi: 10.1186/s12957-018-1511-6.
BACKGROUND
Chondroma is a slowly growing, benign cartilaginous tumor which predominantly occurs in long bones of the hands and feet. Primary mediastinal chondroma is rare, especially with Horner's syndrome.
CASE PRESENTATION
We reported the case of a 31-year-old woman with a posterior mediastinum mass associated with Horner's syndrome. After complete dissection of the mass, a pathological diagnosis of the primary mediastinal chondroma was rendered. The patient has shown no local recurrence or distal disease in a 3.5-year follow-up period.
CONCLUSIONS
The preoperative diagnosis of chondroma should combine various examinations for comprehensive evaluation. Complete surgical resection should be the first choice of the treatment due to the risk of malignancy.
背景
软骨瘤是一种缓慢生长的良性软骨肿瘤，主要发生在手和脚的长骨中。原发性纵隔软骨瘤很少见，特别是伴有霍纳综合征。
病例介绍
我们报告了一例 31 岁女性患者，其存在后纵隔肿块合并霍纳综合征。在完全切除肿块后，做出了原发性纵隔软骨瘤的病理诊断。在 3.5 年的随访中，患者未出现局部复发或远处疾病。
结论
软骨瘤的术前诊断应结合各种检查进行综合评估。由于存在恶性风险，完整的手术切除应是首选治疗方法。
Zotero 插件