Li Jialin, Qian Ming, Huang Xiaoyi, Zhao Li, Yang Xinghai, Xiao Jianru
Department of Orthopedics Oncology, Changzheng Hospital Department of Pathology, Changhai Hospital Nursing School, Second Military Medical University, Shanghai, China.
Medicine (Baltimore). 2017 Dec;96(49):e8950. doi: 10.1097/MD.0000000000008950.
Epidermoid cysts are slow-growing, benign tumor which account for less than 1% of all intraspinal tumors and epidermoid cyst with Atypical Hyperplasia is very rare. Surgical resection is the standard treatment of the tumor, but recurrence is not uncommon after incomplete resection. Inappropriate treatment can lead to repeated recurrent. Here, we reported a case of repeated recurrent epidermoid cyst with atypical hyperplasia treated with radiotherapy after surgery.
A 40-year-old female presenting with intraspinal epidermoid cyst showed incomplete paraplegia in lower limbs.
Back pain reappeared 19 months later after surgical treatment. The patient suffered marked weakness in both limbs, along with obvious muscle atrophy and sensation deficiency of warmth and pain in left lower limb. MRI demonstrated a cystic mass with solid content and peripheral strengthen in enhanced scan.
Extended excision with intraoperative local chemotherapy and postoperative radiotherapy was performed and a dramatic reversal of symptoms was gained 4 weeks after surgery, with a total dose of 46 Gy. Postoperative pathological examination revealed epidermoid cyst with mild to moderate atypical hyperplasia.
No acute side effects of the treatment were reported. Back pain obviously alleviated within 48 hours after surgery, while weakness and numbness of the lower limbs gradually improved and nearly disappeared in the 3-monthly follow-up visit. Until now, no recurrence is found during the 5-years follow-up.
Our study highlights that incomplete excision has led to repeated recurrent epidermoid cyst, but its complete removal with adjuvant radiotherapy has achieved remission of symptoms. Atypical hyperplasia discovered by pathological examination reminds us the possibility of malignant transformation and ensures the necessity of adequate treatment.
表皮样囊肿是生长缓慢的良性肿瘤,占所有脊柱内肿瘤的比例不到1%,而伴有非典型增生的表皮样囊肿非常罕见。手术切除是该肿瘤的标准治疗方法,但不完全切除后复发并不少见。不恰当的治疗可导致反复复发。在此,我们报告了1例伴有非典型增生的表皮样囊肿反复复发,术后接受放疗的病例。
一名40岁女性因脊柱内表皮样囊肿就诊,表现为下肢不完全性截瘫。
手术治疗19个月后背痛复发。患者双下肢明显无力,伴有明显肌肉萎缩及左下肢温痛觉减退。MRI显示囊性肿块,增强扫描有实性成分及周边强化。
行扩大切除术,术中局部化疗及术后放疗,术后4周症状显著改善,总剂量46 Gy。术后病理检查显示为伴有轻度至中度非典型增生的表皮样囊肿。
未报告治疗的急性副作用。术后48小时内背痛明显缓解,下肢无力及麻木逐渐改善,在3个月的随访中几乎消失。截至目前,5年随访期间未发现复发。
我们的研究强调,不完全切除导致表皮样囊肿反复复发,但完整切除并辅助放疗可实现症状缓解。病理检查发现非典型增生提醒我们存在恶变的可能性,并确保了充分治疗的必要性。