Results 31 to 40 of about 3,098 (225)

Extensive Plexiform Neurofibroma Presenting as Clitoromegaly in Neurofibromatosis Type 1

open access: yesJournal of Behçet Uz Children's Hospital, 2021
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]

open access: yesBMJ Case Reports, 2018
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

Extensive Pelvic Plexiform Neurofibroma Presenting As Clitoromegaly in a 3-Year-Old Female: Presentation and Management with MEK Inhibitor

open access: greenJournal of Pediatric Genetics, 2020
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]

open access: hybridWorld Journal of Advanced Research and Reviews, 2021
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]

open access: bronzeUltrasound in Obstetrics & Gynecology, 2000
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
openalex   +3 more sources

Congenital adrenal hyperplasia with clitoromegaly: a case report

open access: bronzeInternational Surgery Journal
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
openalex   +2 more sources

Clitoromegaly as first presentation of a neurocutaneous syndrome in a 3‐year‐old girl [PDF]

open access: goldClinical Case Reports, 2015
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]

open access: yesJournal 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
doaj   +3 more sources

Painful clitoromegaly caused by rare epithelioid hemangioma

open access: hybridGynecologic Oncology Case Reports, 2012
► 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

open access: yesUrology 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
doaj   +4 more sources

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