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Multicystic Renal Dysplasia with Ipsilateral Ectopic Ureteral Orifice and Seminal Vesicle Cyst: A case report
Korean Journal of Pathology ; : 310-313, 2000.
Article in Korean | WPRIM | ID: wpr-164484
ABSTRACT
Renal dysplasia results from aberrant metanephric histogenesis caused fundamentally by a defect in inducer tissue or responding tissue. Dysplastic kidneys vary tremendously in gross and microscopic appearance but are characterized by abnormal organization and a mixed population of primitive structures, such as fetal or immature cartilage, dysplastic ducts, immature tubules, and undifferentiated mesenchyme. We report a case of unilateral multicystic renal dysplasia associated with an ipsilateral ectopic ureteral orifice entering a seminal vesicle cyst in a 33-year-old man. He was admitted due to primary infertility which had developed three years ago. The his semen analysis revealed oligospermia. No evidence of a family history of renal dysplasia was reported. Microscopic examination showed that the entire kidney was composed of cysts lined by flattened cells, dysplastic ducts and immature tubules surrounded by collars of spindle cells, primitive mesenchyme, and a few aberrantly formed glomeruli.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Oligospermia / Seminal Vesicles / Ureter / Cartilage / Multicystic Dysplastic Kidney / Semen Analysis / Infertility / Kidney / Mesoderm Limits: Adult / Humans / Male Language: Korean Journal: Korean Journal of Pathology Year: 2000 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Oligospermia / Seminal Vesicles / Ureter / Cartilage / Multicystic Dysplastic Kidney / Semen Analysis / Infertility / Kidney / Mesoderm Limits: Adult / Humans / Male Language: Korean Journal: Korean Journal of Pathology Year: 2000 Type: Article