RESUMEN
Presentation of two cases of unilateral congenital renal hypoplasia with vesicourethral reflux in two male siblings, no twins, both diagnosed at the age of 24. With no urological history, they present with a dysuria-pollakiuria syndrome which does not even allow to have a clinical suspicion of the final diagnosis. Clinical features of both cases are discussed, and the hyperplasia-reflux association, as well as the possibility of the condition having a hereditary and familial nature, are confirmed by clinical observation as well as radiological and histological data. A literature review is undertaken but published references are very scarce.
Asunto(s)
Riñón/anomalías , Reflujo Vesicoureteral/genética , Adulto , Humanos , Riñón/diagnóstico por imagen , Masculino , Nefrectomía , Radiografía , Uréter/cirugía , Reflujo Vesicoureteral/diagnóstico , Reflujo Vesicoureteral/cirugíaRESUMEN
Exposition of a new case of primary bilateral ureteral endometriosis, a very infrequent condition where early diagnosis before treatment is difficult since no other endometrial foci are found at either the uterus or ovary level or any sites. This condition has an enormous clinical significance because in a very short interval and in a silent manner can cause complete and irreversible damage to the upper urinary tract. The article explains the clinical characteristics of the disease, and discusses the diagnostic procedures available which are generally insufficient. The importance of the histological study is emphasized, and the surgical technique and its complications are described. Also, a literature review is included.