Results 201 to 210 of about 2,537 (222)

Clitoromegaly and Megalourethra in Idiopathic Female Intersex

Journal of Urology, 1981
Idiopathic female intersex can present with a varying phenotypic expression but generally includes clitoromegaly in association with either urogenital and/or cloacal anomalies. Additionally, absence of corporeal bodies may exist, resulting in either a markedly enlarged empty phallus or a megalourethra if developmental anomalies of the urogenital sinus ...
R P, Huben, P C, Devine, G A, Harkins, J F, Stecker   +3 more
openaire   +2 more sources

Treatment of clitoromegaly of culturally diverse patients

Journal of Pediatric Urology, 2009
Clitoroplasty is a procedure usually performed in young children, but its long-term psychosexual importance is controversial. We present two adult women from different cultural backgrounds who desired surgery for clitoromegaly.A similar clitoroplasty procedure with preservation of the neurovascular bundle was performed on both patients.
Hasan S, Merali, Patricio C, Gargollo, David A, Diamond   +2 more
openaire   +2 more sources

Pseudo‐clitoromegaly associated with congenital prepubic sinus

International Journal of Urology, 2006
Abstract  We operated on a 12‐year‐old girl who had clitoromegaly and a sinus on the midline prepubic area congenitally. The prepubic sinus appeared to point to the clitoris on the preoperative magnetic resonance image, but the relation between the sinus and clitoromegaly was unclear.
Masa, Hayase, Yoshiyuki, Kojima, Yutaro, Hayashi, Tetsuji, Maruyama, Shoichi, Sasaki, Kenjiro, Kohri   +5 more
openaire   +2 more sources

Idiopathic Female Intersex with Clitoromegaly and Urethral Duplication

Journal of Urology, 1979
Idiopathic female intersex presents in the neonate with characteristic anomalies of the external genitalia, complete and separate phallic and vaginal urethras and vesical outlet obstruction. Management of this disorder should initially focus upon adequate urinary drainage and proper sex assignment in the neonate.
J A, Belis, E E, Hrabovsky
openaire   +2 more sources

Symptomatic Clitoromegaly: Case Report of a Clitoral Hemangioma

Journal of Pediatric and Adolescent Gynecology, 2018
Clitoromegaly is often a sign of an underlying disorder of sexual development. Isolated clitoromegaly might occur as a result of benign or malignant neoplasm.A 10-year-old girl presented with clitoral swelling and discomfort and was noted to have a 5 × 2 × 2 cm, tender, cystic mass in the left periclitoral area.
Chandler A, Kasuske, Keith A, Hansen
openaire   +2 more sources

Giant Epidermoid Inclusion Cyst of the Clitoris Mimicking Clitoromegaly

Journal of Lower Genital Tract Disease, 2013
We describe a rare case of clitoromegaly due to a large clitoral cyst that occurred spontaneously without any declared previous female genital mutilation. The cyst was excised successfully with good cosmetic results.
Eftekhar Hassan, Al-Ojaimi, Maryam Mohd, Abdulla   +1 more
openaire   +2 more sources

Hemangioma of the Clitoris Presenting as Clitoromegaly: A Case Report

Journal of Pediatric and Adolescent Gynecology, 2009
A 20-year-old woman with massive clitoral enlargement is presented to discuss the differential diagnosis and the treatment of this condition.
Bruni, Vincenzina, Pontello, Valentina, Dei, Metella, Alessandrini, Marco, Li Marzi, Vincenzo, Nicita, Giulio   +5 more
openaire   +4 more sources

Isolated Transient Neonatal Clitoromegaly with Hyperandrogenism of Unknown Etiology

Journal of Pediatric and Adolescent Gynecology, 2009
Neonatal clitoromegaly is usually attributed to androgen stimulation secondary to congenital adrenal hyperplasia or in utero androgen exposure. We present a unique case of transient, isolated neonatal clitoromegaly, associated with increased androgen levels of unidentifiable cause, which spontaneously resolved when the androgen levels normalized.
T, Dumont, A Y, Black, A, Ahmet, N A, Fleming   +3 more
openaire   +2 more sources

Congenital Adrenal Hyperplasia Presenting with Posterior Labial Fusion Without Clitoromegaly

Pediatrics, 1980
In females with congenital adrenal hyperplasia, 21-hydroxylase deficiency without salt loss is usually recognized in the neonate because of ambiguous genitalia (ie, clitoromegaly with or without labial fusion), or at a later age because of progressive virilization and/or accelerated linear growth.
W N, Marshall, E S, Lightner
openaire   +2 more sources

A 26-Month-Old With Clitoromegaly

Clinical Pediatrics, 2023
Yi Yan Heng, Erica A. Eugster
openaire   +2 more sources