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A Rare Case of Partial Unilateral Corpus Cavernosum Agenesis With Concomitant Multiple Genitourinary Anomalies.
Baydilli, Numan; Akinsal, Emre Can; Selvi, Ismail; Golbasi, Abdullah; Imamoglu, Hakan; Ekmekcioglu, Oguz.
Afiliação
  • Baydilli N; Department of Urology, Erciyes University Medical School, Kayseri, Turkey.
  • Akinsal EC; Department of Urology, Erciyes University Medical School, Kayseri, Turkey.
  • Selvi I; Department of Urology, Karabük University Training and Research Hospital, Karabük, Turkey. Electronic address: ismselvi33@hotmail.com.
  • Golbasi A; Department of Urology, Erciyes University Medical School, Kayseri, Turkey.
  • Imamoglu H; Department of Radiology, Erciyes University Medical School, Kayseri, Turkey.
  • Ekmekcioglu O; Department of Urology, Erciyes University Medical School, Kayseri, Turkey.
Urology ; 143: 234-237, 2020 09.
Article em En | MEDLINE | ID: mdl-32439555
ABSTRACT
Congenital penile agenesis is a rare condition with an incidence of 1 in 30 million, while other congenital malformations of the cavernous bodies are much less common. In a few cases in the literature, it has been reported that the reason for consulting a physician with these conditions is the insufficient erection. As a first reported case, we present a 16-year-old male patient with partial unilateral corpus cavernosum agenesis accompanying genitourinary anomalies.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pênis / Anormalidades Múltiplas / Doenças da Bexiga Urinária / Divertículo / Doenças dos Genitais Masculinos Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Adolescent / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pênis / Anormalidades Múltiplas / Doenças da Bexiga Urinária / Divertículo / Doenças dos Genitais Masculinos Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Adolescent / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article