The patient had multiple anomalies, such as parameatal cyst, urethral duplication, mid-penile hypospadias, and penile chordee.
Parameatal urethral cysts are very rare benign lesions seen in boys, but they can also occur in infants, girls, and adults.
Although cases of urethral duplication and penile hypospadias with chordee cases have been reported, we did not find a parameatal cyst in our patient.
We report for the first time a different variation of urethral duplication accompanied by mid-penile hypospadias, penile chordee, and parameatal cyst; moreover, we believe that the etiology of the these anomalies is the abnormal Mullerian duct termination.
Key words: Arteriovenous malformations; glans penis; parameatal cyst; penis anomalies.
Parameatal uretral kist on tanisi konulan hastaya, histopatolojik tani ve tedavi amach cerrahi eksizyon uygulandi.
Literaturde rapor edilen olgular icinde, parameatal kist, glomus tumoru, bulasici cilt hastaliklari, dermatozlar cogunluktadir.
Parameatal epidermoid ve pilosebase kistlerin cocuklarda glans penisi etkileyen 3 tipi tanimlanmistir.
A parameatal urethral cyst, which is a very rare congenital anomaly, was first reported in two male cases in 1956 by Thompson and Lantin.
Oldukca nadir gorulen konjenital bir anomali olan parameatal uretral kist ilk kez Thompson ve Lantin tarafindan 1956 yilinda iki erkek olguda rapor edilmistir.
Parameatal uretral kist oldukca nadir gorulen benign bir pato1ojidir.
Several terms, including mucus cyst of the penis, genitoperineal cyst of the medium raphe, parameatal
cyst, hydrocystoma and apocrine cystadenoma of the penile shaft, should be considered synonymous.