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Caudal regression syndrome and a pelvic kidney: case report
被引:1
|作者:
Hage, Dany
[1
]
Iwanaga, Joe
[1
]
Dumont, Aaron S.
[1
]
Tubbs, R. Shane
[1
,2
,3
,4
,5
]
机构:
[1] Tulane Univ, Sch Med, Dept Neurosurg, Tulane Ctr Clin Neurosci, 1430 Tulane Ave, New Orleans, LA 70112 USA
[2] Tulane Univ, Sch Med, Dept Struct & Cellular Biol, 1430 Tulane Ave, New Orleans, LA 70112 USA
[3] Ochsner Hlth Syst, Dept Neurosurg, New Orleans, LA USA
[4] Ochsner Hlth Syst, Ochsner Neurosci Inst, New Orleans, LA USA
[5] St Georges Univ, Dept Anat Sci, St Georges, Grenada
关键词:
Caudal regression syndrome;
Pelvic kidney;
Magnetic resonance imaging;
Renal malformation;
Spinal agenesis;
FAILURE;
D O I:
10.5115/acb.20.057
中图分类号:
R602 [外科病理学、解剖学];
R32 [人体形态学];
学科分类号:
100101 ;
摘要:
Caudal regression syndrome (CRS) is a rare congenital variation. A high incidence of renal and genitourinary malformations has been observed in patients with CRS, with the most common being neurogenic bladder and renal agenesis. We report a rare case report documenting both CRS and a pelvic kidney found during a diagnostic magnetic resonance imaging. Although renal anatomy variants are found in patients with CRS, a pelvic kidney is normally not part of the constellation of findings in this malformation. As seen in our patient, a pelvic kidney should be considered in patients suspected of having CRS.
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页码:509 / 511
页数:3
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