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Clitorornegaly in type 2 neurofibrornatosis: A case report and review of the literature

  • H. Ytiksel1,*,
  • A. R. Odabasi1
  • S. Kafkas1
  • E. Onur2
  • M. Turgut3

1Assist. Prof, Departments of Obstetrics and Gynecolog, Turkey

2Prof, Departments of Obstetrics and Gynecology, Turkey

3Assist. Prof, Department of Neurosurgery, Adnan Menderes University, Faculty of Medicine, Aydm, Turkey

DOI: 10.12892/ejgo200305447 Vol.24,Issue 5,September 2003 pp.447-451

Published: 10 September 2003

*Corresponding Author(s): H. Ytiksel E-mail:

Abstract

Objective: Genitourinary neurofibromatosis (NF) is a rare disorder and clitoral involvement has been reported infrequently. In the English literature there are only 26 reported cases with clitoral involvement in NF.

Case: A 28-year-old female with clitoral enlargement, previously diagnosed with NF 2, was successfully treated by removal of the clitoral mass that increased in size during the previous two years. Clitoroplasty was performed while preserving the glans of clitoris. Histopathologic examination revealed plexiform neurofibroma.

Conclusion: To the best of our knowledge the patient is the 27th reported clitoromegaly case with NF, but the first case reported with NF 2 or central NF in the English literature.

Keywords

Clitoromegaly; Clitoroplasty; Hypertrophy of clitoris; Neurofibromatosis 2

Cite and Share

H. Ytiksel,A. R. Odabasi,S. Kafkas,E. Onur,M. Turgut. Clitorornegaly in type 2 neurofibrornatosis: A case report and review of the literature. European Journal of Gynaecological Oncology. 2003. 24(5);447-451.

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