A rare cause of clitoromegaly: Epidermoid cyst
Archivio Italiano di Urologia e Andrologia, 2019 Clitoromegaly due to non-hormonal causes is rare. In this case, we aimed to present an epidermal cyst that caused clitoromegaly after traditional female circumcision. A 22-year-old African female was referred to our clinic with enlarged clitoris. There is a mobile, soft, nonfluctuant mass with a size of 6 cm originating from the clitoral region at ...
Selman, Karaci +2 more
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Incidental detection of a virilizing Sertoli-Leydig cell tumor during cesarean section: A case report [PDF]
Case Reports in Women's HealthSertoli-Leydig cell tumors are a rare type of sex cord-stromal tumors that are mostly hormonally active (androgenic or estrogenic). Owing to the rarity of this disease, its impact on pregnancy is not fully understood.
Roza Mahyoob +2 more
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Neurofibromatosis Presenting as Painless Clitoromegaly
Urology Journal, 2009 Received June 2008 Accepted September 2008 INTRODUCTION Neurofibromatosis is an autosomal dominant progressive disorder with an incidence of approximately 1 in 3000 live births.(1) Its recognized features include hyperpigmented skin lesions (cafe-au-lait spots), neurofibromas, iris hamartomas, macrocephaly, central nervous system tumors, defects of the
Nicholas G Cost +4 more
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Feminizing Genitoplasty in Congenital Clitoromegaly: A Case Report. [PDF]
CureusCongenital clitoromegaly, also known as macroclitoris, is a rare congenital disorder. It is a cause of poor self-esteem, anxiety, and gender self-perception. It negatively affects social, romantic, and emotional domains. We present a case of female pseudohermaphroditism with congenital clitoromegaly in a 23-year-old woman who attained late menarche at ...
Gattani P +4 more
europepmc +3 more sources
Infected epidermal cyst of the clitoris in an infant [PDF]
Journal of Pediatric Surgery Case Reports, 2021 Clitoral enlargement in the pediatric population is a rare condition, usually related to problems of sexual differentiation, but malignant and benign clitoral lesions have also been described. We report the case of a newborn infant, investigated at birth
M. Doan +3 more
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Apparent Clitoromegaly in a Newborn: A Case of Congenital Adrenal Hyperplasia. [PDF]
CureusSvanadze M +4 more
europepmc +3 more sources
Operative Treatment of Idiopathic Isolated Clitoromegaly – A Clinical Case
Acta Medica BulgaricaIdiopathic clitoromegaly is a relatively rare disease. A case of isolated idiopathic clitoromegaly is presented. It concerns a 31-year-old woman, in whom the clitoris has showed a tendency for progressive enlargement in the last 3-4 years.
Stoyanov S., Ivanova K., Koleva I.
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Microscope-assisted Reduction Clitoroplasty Used to Treat Two Patients with Clitoromegaly
Journal of Nippon Medical School, 2010 We report 2 cases of clitoromegaly, 1 in a patient with true hermaphroditism, and the other in a patient with adrenogenital syndrome. Both were treated surgically with reduction clitoroplasty. There are 3 different clitoroplasty procedures: clitorectomy, clitoral recession, and reduction clitoroplasty.
Masahiro, Murakami +7 more
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Computed Tomography Angiography-Assisted Ovarian Vein Sampling for Diagnosing an Androgen-Producing Leydig Cell Tumor: A Case Report. [PDF]
Case Rep EndocrinolBackground Ovarian Leydig cell tumors, rare androgen‐producing neoplasms, may present with rapidly progressive virilization. Preoperative localization is frequently challenging, particularly when bilateral ovarian abnormalities coexist or radiologic findings are equivocal.
Tomotsune K +11 more
europepmc +2 more sources
MON-252 A (Geni)Tale of Two Diagnosis: Congenital Clitoromegaly with Concurrent Congenital Adrenal Hyperplasia and Mosaic Turner Syndrome [PDF]
J Endocr SocAbigail T. Tisler +2 more
europepmc +3 more sources