Huang Chao, Guo Wenlai, Qu Wenrui, Zhu Zhe, Li Rui
Hand and Foot Surgery, The Second Hospital of Jilin University, No 218, Lane Ziqiang, Nanguan District, Changchun City, Jilin, P.R. China.
Medicine (Baltimore). 2019 May;98(19):e15587. doi: 10.1097/MD.0000000000015587.
Chondroid lipoma (CL) is a rare benign tumor. No relevant epidemiological reports have been published on CL, and there is a lack of uniform diagnostic and treatment criteria for the tumor.
Here, we report a case of CL with a mass on the left buttock for 2 weeks, and further illuminate its diagnosis and treatment.
The diagnosis of CL was rendered according to the pathological indices.
The tumor was resected completely under spinal anesthesia.
The patient was followed-up for 6 months and showed no tumor recurrence or metastasis and there was resolution of the patient's lower-limb numbness and pain.
The case study presented here provides evidence that CL could be effectively diagnosed by using ultrasound, puncture or biopsy, and/or magnetic resonance imaging. Furthermore, the patient recovered without any complications after completely resecting the tumor.
软骨样脂肪瘤(CL)是一种罕见的良性肿瘤。目前尚未发表关于CL的相关流行病学报告,且该肿瘤缺乏统一的诊断和治疗标准。
在此,我们报告一例左臀部肿物2周的CL病例,并进一步阐明其诊断和治疗方法。
根据病理指标诊断为CL。
在脊髓麻醉下将肿瘤完整切除。
对患者进行了6个月的随访,未见肿瘤复发或转移,患者下肢麻木和疼痛症状消失。
本病例研究表明,CL可通过超声、穿刺活检和/或磁共振成像有效诊断。此外,肿瘤完整切除后患者恢复良好,无任何并发症。