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骶尾部畸胎瘤的泌尿和肛肠并发症:产前和产后的预测因素。

Urologic and anorectal complications of sacrococcygeal teratomas: prenatal and postnatal predictors.

机构信息

The Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia, Philadelphia PA.

Division of Urology, Children's Hospital of Philadelphia, Philadelphia PA.

出版信息

J Pediatr Surg. 2014 Jan;49(1):139-42; discussion 142-3. doi: 10.1016/j.jpedsurg.2013.09.042. Epub 2013 Oct 8.

Abstract

PURPOSE

Anorectal and urologic sequelae are observed in long-term survivors of sacrococcygeal teratoma (SCT). In this study we evaluate the incidence and predictors of anorectal and urologic complications in SCT.

METHODS

A retrospective review was performed for all SCT patients who underwent resection at a single institution between 2000 and 2012. Enrollment criteria included a minimum of 12months follow-up. Categorical variables were analyzed by Fisher's exact test and continuous variables by Mann Whitney test (p<0.05).

RESULTS

Forty-five patients were studied. Anorectal complications occurred in 29%, including severe chronic constipation (n=13) and fecal incontinence (n=4). Urologic complications occurred in 33%, including neurogenic bladder (n=12), vesicoureteral reflux (n=5), and urinary incontinence (n=7). Prenatal imaging by fetal MRI demonstrated mass effect with obstruction of the bowel (n=4) or bladder and collecting system (n=7) in a subset of patients with postnatal complications (anorectal 4/4, PPV 100%; urologic 6/7, PPV 86%). Postnatal complications were associated with obstructive findings on prenatal imaging, prenatal therapeutic interventions, Altman classification, perineal reconstruction, and tumor recurrence. No anorectal or urologic complications occurred in patients with Altman type I tumors.

CONCLUSIONS

Urologic and anorectal complications are common in patients with SCT. Higher Altman classification and prenatal imaging suggestive of intestinal or urologic obstruction should prompt focused prenatal counseling and postnatal screening for anorectal and urologic dysfunction.

摘要

目的

骶尾部畸胎瘤(SCT)的长期幸存者会出现肛肠和泌尿科后遗症。本研究旨在评估 SCT 患者肛肠和泌尿科并发症的发生率和预测因素。

方法

对 2000 年至 2012 年期间在一家机构接受手术切除的所有 SCT 患者进行回顾性分析。纳入标准为至少随访 12 个月。采用 Fisher 精确检验分析分类变量,采用 Mann-Whitney 检验分析连续变量(p<0.05)。

结果

共纳入 45 例患者。29%的患者发生肛肠并发症,包括严重慢性便秘(n=13)和粪便失禁(n=4)。33%的患者发生泌尿科并发症,包括神经性膀胱(n=12)、输尿管反流(n=5)和尿失禁(n=7)。胎儿 MRI 产前影像学检查显示,在一组有产后并发症的患者中,肿瘤占位效应导致肠道(n=4)或膀胱和集合系统(n=7)梗阻。产前并发症(肛门直肠 4/4,PPV 100%;泌尿科 6/7,PPV 86%)与产前影像学的梗阻表现、产前治疗干预、Altman 分类、会阴重建和肿瘤复发有关。Altman Ⅰ型肿瘤患者无肛肠或泌尿科并发症。

结论

SCT 患者的泌尿科和肛肠并发症很常见。较高的 Altman 分类和提示肠道或泌尿系统梗阻的产前影像学表现应提示进行有针对性的产前咨询和肛肠、泌尿科功能障碍的产后筛查。

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