Results 21 to 30 of about 1,685 (160)

Preterm ovarian hyperstimulation syndrome mimicking clitoromegaly

Pediatrics and Neonatology, 2023
Zeynep Alize Ay, Saygin Abali, Ayse Korkmaz, Serdar Beken   +3 more
doaj   +3 more sources

Clitoromegaly: beyond testosterone [PDF]

BMJ 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. On examination, there was clitoral enlargement (3×1 cm), a plexiform neuroma involving right labia majora (figure 1)
Darshana Sudip Thakur, Chaitanya G Yerawar, Meghana Phiske, Nikhil M Bhagwat   +3 more
openaire   +2 more sources

Clitoromegaly caused by ovarian stimulation in a preterm newborn: ovarian hyperstimulation syndrome of preterm babies

The Turkish Journal of Pediatrics, 2020
Background. Preterm ovarian hyperstimulation syndrome (POHS) is an uncommon disorder characterized by prematurity, hypogastric and upper leg swelling, high serum estradiol and gonadotropin levels, and ovarian cysts.
Elvan Bayramoğlu, Şenay Savaş Erdeve, Betül Emine Derinkuyu, İstemi Han Çelik, Semra Çetinkaya, Zehra Aycan   +5 more
doaj   +1 more source

Extensive Plexiform Neurofibroma Presenting as Clitoromegaly in Neurofibromatosis Type 1

Journal 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, Gülçin Arslan, Beyhan Özkaya, Sinan Genç, Behzat Özkan   +4 more
doaj   +1 more source

Virilizing Adrenocortical Carcinoma Oncocytic Variant in a Child with Heterosexual Precocious Puberty and a Literature Review

Journal of Pediatric Research, 2022
Androgen-secreting adrenal tumors are aggressive cancers in childhood; however, they are rare in clinical practice. Children with adrenal carcinoma usually present with peripheral precocious puberty, premature pubarche, signs of virilization and ...
Seyran Bulut, Gönül Çatlı, Berna Eroğlu Filibeli, Hayrullah Manyas, İlkay Ayrancı, Rabia Meral, Deniz Kızmazoğlu, Bumin Nuri Dündar   +7 more
doaj   +1 more source

Idiopathic Non-hormonal Clitoromegaly in a Young Female: A Case Report [PDF]

Journal of Clinical and Diagnostic Research
Clitoromegaly may be either congenital or acquired and is primarily caused by elevated androgen levels during foetal development, childhood, or puberty. We describe an unusual case of clitoromegaly in a young female who presented with genital pruritus,
Naganitya Vangala, Adarshlata Singh, Bhushan Madke, Sree Ramya Talasila, Soham Meghe   +4 more
doaj   +1 more source

Reduction Clitoroplasty with Preservation of the Dorsal Neurovascular Pedicle in a 6-Year-Old Female: A Case Report [PDF]

Archives of Aesthetic Plastic Surgery, 2016
A 6-year-old female presented to our hospital with clitoromegaly. On physical examination, she demonstrated evidence of precocious pubic hair and clitoromegaly. The relaxed clitoris measured 3.7 cm in length.
Hyochun Park, Wonwoo Kim, Hoonnam Kim, Hyeonjung Yeo   +3 more
doaj   +1 more source

An unusual case of type a posterior cloaca associated with 46xx disorder of sexual differentiation with y duplication of urethra

Journal of Indian Association of Pediatric Surgeons, 2022
We report an infant reared as a girl who presented with ambiguous genitalia and urine coming per rectum. On examination, she had minimal clitoromegaly with labial fusion and Y urethral duplication.
Rahul K Gupta, Pooja Tiwari, Sandesh V Parelkar, Beejal V Sanghvi, Kedar P Mudkhedkar, Satej S Mhaskar, Rujuta S Shah   +6 more
doaj   +1 more source

Clitoral Epidermoid Cyst Presenting as Pseudoclitoromegaly of Pregnancy

American Journal of Perinatology Reports, 2013
Objective Acquired clitoromegaly is rare and may result from hormonal and nonhormonal causes, and evaluation of the pregnant patient with clitoromegaly invokes a specific set of differential diagnoses.
Jing W. Hughes, Marsha K. Guess, Adam Hittelman, Sallis Yip, John Astle, Lubna Pal, Silvio E. Inzucchi, Antonette T. Dulay   +7 more
doaj   +1 more source

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, Fabian S Sanchez, Arthur G Weinberg, Korgun Koral, Linda A Baker   +4 more
doaj   +3 more sources