Epithelial Predominant Wilms Tumor in an Adult Patient: Case Report and Literature Review

被引:1
作者
Chapman, Sofia [1 ,2 ]
Lichtbroun, Benjamin [1 ,2 ]
Patel, Hiren [1 ,2 ]
Doppalapudi, Sai Krishnaraya [1 ,2 ]
Thaker, Hatim [3 ]
Smith, Colton [4 ]
Salazar, Cristo Guardado [5 ]
Moerdler, Scott [2 ,6 ]
Ghodoussipour, Saum [1 ,2 ]
机构
[1] Rutgers Canc Inst New Jersey, Sect Urol Oncol, New Brunswick, NJ 08854 USA
[2] Rutgers Robert Wood Johnson Med Sch, New Brunswick, NJ USA
[3] Boston Childrens Hosp, Dept Urol, Boston, MA USA
[4] Rutgers Robert Wood Johnson Med Sch, Dept Pathol Immunol & Lab Med, New Brunswick, NJ USA
[5] Childrens Hosp Los Angeles, Dept Pathol & Lab Med, Los Angeles, CA USA
[6] Rutgers Canc Inst New Jersey, Sect Pediat Hematol & Oncol, New Brunswick, NJ USA
关键词
congenital anomalies; epithelial predominant; Jeune syndrome; renal tumor; Wilms tumor; ABNORMALITIES;
D O I
10.15586/jkcvhl.v11i3.329
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although rare in adults, Wilms tumor is the most common pediatric renal tumor. Treatment typically involves radical nephrectomy followed by adjuvant chemotherapy or radiation, although outcomes differ between children and adults which may be due to challenges in accurately diagnosing these patients. In this article, we present a case report of an adult patient with Jeune syndrome and multiple urologic abnormalities who underwent radical nephrectomy for a large renal mass and was subsequently diagnosed with an epithelial predominant Wilms tumor. Epithelial predominant Wilms tumor may have distinct origins from other Wilms tumor histological subtypes and may incur better outcomes. Herein, we discuss the literature surrounding this rare entity as well as the anticipated treatment course.
引用
收藏
页码:33 / 39
页数:7
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