Retroperitoneal lymphatic malformation and transverse testicular ectopia: A unique clinical presentation

被引:2
|
作者
Morris, Michael W., Jr. [1 ]
Cauthen, William [1 ]
Bofill, James A. [2 ]
Blewett, Christopher J. [3 ]
Liechty, Kenneth W. [4 ]
机构
[1] Univ Mississippi, Sch Med, Dept Surg, Jackson, MS 39216 USA
[2] Univ Mississippi, Sch Med, Div Maternal Fetal Med, Dept Obstet & Gynecol, Jackson, MS 39216 USA
[3] Univ Mississippi, Sch Med, Div Pediat Surg, Dept Surg, Jackson, MS 39216 USA
[4] Nemours Childrens Hosp, Div Pediat Gen & Fetal Surg, Dept Surg, Orlando, FL USA
关键词
Testicular ectopia; Lymphatic malformation; Sclerotherapy; Fetal MRI; Fetal ultrasound; LYMPHANGIOMA; DIAGNOSIS; ENTITY;
D O I
10.1016/j.jpedsurg.2013.01.032
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
This case report presents a fetal patient diagnosed in utero with a retroperitoneal lymphatic malformation by ultrasound and followed through gestation. At birth the child was noted to have a right inguinal hernia with two palpable testicles. Plan for partial resection and hernia repair with postoperative sclerotherapy was made. At the time of hernia repair, transverse testicular ectopia was diagnosed, and subsequent extraperitoneal transposition orchiopexy was performed following partial resection of the lymphatic malformation. Delayed sclerotherapy in combination with partial resection afforded definitive treatment of the residual lymphatic malformation as the patient demonstrates no recurrence over one year later. This is the first reported case to suggest a direct relationship between transverse testicular ectopia and a retroperitoneal lymphatic malformation. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:E17 / E20
页数:4
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