Results 31 to 40 of about 3,098 (225)
Extensive Plexiform Neurofibroma Presenting as Clitoromegaly in Neurofibromatosis Type 1
Neurofibromatosis type 1 (NF1) is an autosomal-dominant disorder with multisystem involvement. Genitourinary involvement of neurofibromatosis type 1 is rare condition and involvement of plexiform neurofibroma can cause painful clitoromegaly. A 9-year-old
Özlem Nalbantoğlu+4 more
doaj +2 more sources
Clitoromegaly: beyond testosterone [PDF]
A 9-year-old girl was presented for evaluation of clitoromegaly (figure 1). There was no evidence of adrenarche, thelarche or accelerated growth. The parents denied a history suggestive of adrenal crisis or progressive hyperpigmentation.
D. S. Thakur+3 more
semanticscholar +3 more sources
Plexiform neurofibroma (PN) involvement of the external genitalia in patients with neurofibromatosis type I (NF1) is a rare cause of nonhormonal clitoromegaly. We present a 3-year-old female with known NF1 who presented with clitoromegaly.
Richelle C. Waldner+3 more
openalex +3 more sources
Idiopathic clitoromegaly: Reduction clitoroplasty at Al-Rahma Hospital Zanzibar Tanzania: A case report and review of the literature [PDF]
We present a case of 5 years old female with of idiopathic clitoromegaly managed by reduction clitoroplasty, preserving the dorsal neurovascular bundle and extensive network of nerves around the corpora to the glans Clitoromegaly is an embarrassing ...
Mohammed Mbarouk+4 more
openalex +2 more sources
P52Ultrasonographic diagnosis of an approach to a case with intrauterine clitoromegaly [PDF]
IntroductionAdrenal androgens are one of the important determinants of sexual differentiation in fetal period. Increased circulating levels of adrenal androgens as seen in congenital adrenal hyperplasia, interact with genital skin androgen receptors and induce clitoral enlargement, fusion of labial folds and cause migration of the urethral‐vaginal ...
B. Tekin, Hikmet Hassa, Tanser Şenses
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Congenital adrenal hyperplasia with clitoromegaly: a case report
Congenital adrenal hyperplasia (CAH) is a rare but significant medical disorder that affects the adrenal glands, causing excessive production of androgens, a group of hormones responsible for the characteristics associated with male sexual development ...
Kevin Piether, Nunik Agustriani
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Clitoromegaly as first presentation of a neurocutaneous syndrome in a 3‐year‐old girl [PDF]
Key Clinical MessageA rare cause of clitoral hypertrophy in a child is neurofibromatosis type 1 (NF1). Although evaluation, including karyotype and hormonal studies, is necessary to exclude ambiguous genitalia, the diagnosis of neurofibromatosis as a possible cause of clitoromegaly may help avoid lengthy and sometimes invasive interventions.
Zacharoula Karabouta+2 more
openalex +4 more sources
Infected epidermal cyst of the clitoris in an infant [PDF]
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
doaj +3 more sources
Painful clitoromegaly caused by rare epithelioid hemangioma
► Painful clitoromegaly may be caused by an infiltrating epithelioid hemangioma tumor. ► Epithelioid hemangiomas are usually benign. ► Rare forms are the aggressive epithelioid hemangioendotheliomas or epithelioid angiosarcomas. ► Endocrine and infectious causes of clitoromegaly must be ruled out.
Heidi J. Gray+2 more
openalex +4 more sources
Neurofibromatosis Presenting as Painless Clitoromegaly
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
doaj +4 more sources