Wang Yi, Wu Yeming, Wang Lifeng, Yuan Xiaojun, Jiang Mawei, Li Yuhua
Department of Pediatric Surgery, Xinhua Hospital Affiliated to Medicine School of Shanghai Jiaotong University, Shanghai, China (mainland).
Department of Pathology, Xinhua Hospital Affiliated to Medicine School of Shanghai Jiaotong University, Shanghai, China (mainland).
Med Sci Monit. 2017 Jan 2;23:17-23. doi: 10.12659/msm.900400.
BACKGROUND Sacrococcygeal teratoma (SCT) is a relatively uncommon tumor. Recurrence with poor survival and anorectal dysfunction are the 2 leading problems for patients. Here, we would review the clinic features of patients with SCTs in our hospital to identify risk factors of recurrent SCTs and to analyze anorectal functional sequelae. MATERIAL AND METHODS A retrospective review of all patients with SCTs in our center between 2007 and 2013 was performed. We analyzed the recorded data on each patient and performed follow-up through phone calls. RESULTS Our study included 105 inpatients (78 girls and 27 boys); 104 cases underwent surgical resection, and 62.5% cases had a mature histopathology. The proportion of malignant teratomas rose with increasing age. Fifteen children developed recurrent SCTs with a median of 11.5 months, and most of them had an elevation of AFP levels. Four recurrent children experienced a second tumor relapse. We observed a statistically significant difference in survival rate through Kaplan-Meier method between relapsed (66.7%) and non-relapsed (94.4%) patients. In univariate analysis, incomplete primary resection and malignant histology were proven to increase recurrence risks. Nearly half of patients had at least 1 of the parameters reflecting abnormal bowel function (e.g., involuntary bowel movements, fecal incontinence, and constipation). For those recurrent SCTs patients, difficulty defecating was a major problem. CONCLUSIONS Tumor recurrence affected the prognosis of children with SCT. In our research, incomplete resection and malignant histology were considered risk factors. Constipation was the main problem in anorectal functional sequelae for children who had recurrence.
背景 骶尾部畸胎瘤(SCT)是一种相对罕见的肿瘤。复发、生存预后差及肛门直肠功能障碍是患者面临的两大主要问题。在此,我们回顾我院骶尾部畸胎瘤患者的临床特征,以确定复发性骶尾部畸胎瘤的危险因素,并分析肛门直肠功能后遗症。
材料与方法 对2007年至2013年期间我院所有骶尾部畸胎瘤患者进行回顾性研究。我们分析了每位患者的记录数据,并通过电话进行随访。
结果 我们的研究纳入了105例住院患者(78例女孩和27例男孩);104例患者接受了手术切除,62.5%的病例组织病理学为成熟型。恶性畸胎瘤的比例随年龄增长而上升。15例儿童出现骶尾部畸胎瘤复发,中位复发时间为11.5个月,其中大多数患者甲胎蛋白(AFP)水平升高。4例复发患儿出现第二次肿瘤复发。通过Kaplan-Meier法,我们观察到复发患者(66.7%)和未复发患者(94.4%)的生存率存在统计学显著差异。单因素分析显示,初次切除不完全和恶性组织学被证实会增加复发风险。近一半的患者至少有1项反映肠道功能异常的指标(如不自主排便、大便失禁和便秘)。对于那些复发性骶尾部畸胎瘤患者,排便困难是一个主要问题。
结论 肿瘤复发影响骶尾部畸胎瘤患儿的预后。在我们的研究中,切除不完全和恶性组织学被认为是危险因素。便秘是复发患儿肛门直肠功能后遗症的主要问题。