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诊断肾发育不全、加特纳管囊肿与同侧苗勒管梗阻并存的情况。

Diagnosing the combination of renal dysgenesis, Gartner's duct cyst and ipsilateral müllerian duct obstruction.

作者信息

Sheih C P, Li Y W, Liao Y J, Huang T S, Kao S P, Chen W J

机构信息

Department of Pediatrics, Taipei Municipal Women and Children's Hospital, Taiwan.

出版信息

J Urol. 1998 Jan;159(1):217-21. doi: 10.1016/s0022-5347(01)64071-0.

DOI:10.1016/s0022-5347(01)64071-0
PMID:9400484
Abstract

PURPOSE

We describe the differential points in the diagnosis of the combination of renal dysgenesis, Gartner's duct cyst and ipsilateral müllerian duct obstruction. Various imaging studies and urological procedures were performed. We report our experience in detecting these anomalies in 10 girls and review the literature.

MATERIALS AND METHODS

Ten girls, 7 to 13 years old, with this combination of anomalies were identified in the last 10 years. Imaging studies as well as urological procedures were selectively performed, especially at puberty following menarche. Patients received long-term followup with ultrasound.

RESULTS

Cystic dilation of Gartner's duct protruded into the bladder and presented as a ureterocele in 5 patients and posterior to the bladder in 5. Surgical removal of a partial portion of a Gartner's duct cyst was performed in 5 patients for alleviation of urinary symptoms. Unilateral müllerian duct obstruction was demonstrated in all 10 patients. Excision of the vaginal septum was performed in 6 patients for relief of genital obstruction.

CONCLUSIONS

When cystic dilatation of the pelvis, especially a ureterocele-like cyst without ureteral dilatation, is found in girls with ipsilateral renal dysgenesis, the possibility of a Gartner's duct cyst should be considered. For early detection and treatment of unilateral obstruction of duplicated müllerian ducts pelvic sonography should be performed at puberty, especially just after menarche, in girls with renal dysgenesis and ipsilateral Gartner's duct cyst.

摘要

目的

我们描述肾发育不全、加特纳管囊肿和同侧苗勒管梗阻合并症诊断中的鉴别要点。进行了各种影像学检查和泌尿外科手术。我们报告在10名女孩中检测到这些异常的经验并复习文献。

材料与方法

在过去10年中,确定了10名年龄在7至13岁之间患有这种异常合并症的女孩。选择性地进行了影像学检查以及泌尿外科手术,特别是在初潮后的青春期。患者接受了超声长期随访。

结果

加特纳管的囊性扩张突入膀胱,在5例患者中表现为输尿管囊肿,在5例患者中位于膀胱后方。5例患者进行了加特纳管囊肿部分切除术以缓解尿路症状。所有10例患者均证实存在单侧苗勒管梗阻。6例患者进行了阴道纵隔切除术以缓解生殖道梗阻。

结论

当在患有同侧肾发育不全的女孩中发现盆腔囊性扩张,尤其是无输尿管扩张的输尿管囊肿样囊肿时,应考虑加特纳管囊肿的可能性。对于患有肾发育不全和同侧加特纳管囊肿的女孩,应在青春期,尤其是初潮后不久进行盆腔超声检查,以早期发现和治疗重复苗勒管的单侧梗阻。

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