Abstract
Hydrohaematometrocolpos may occur secondary to isolated imperforate hymen, genital tract duplications, and complex urogenital sinus or cloacal abnormalities. The presenting symptoms and relation to menarche provide clues to the diagnosis. Examination of the abdomen, introitus, and vagina may confirm the diagnosis and assist in clarification of the anatomy. In genital duplications ultrasonography further delineates the pelvic anatomy and demonstrates unilateral renal agenesis. We have reviewed our 10-year experience and present an approach for the diagnosis and investigation of these patients.
Similar content being viewed by others
References
Lewis BV, Brant HA (1966) Gynaecological complications associated with Mullerian duct abnormalities. Obstet Gynaecol 28: 315–322
Tarry WF, Ducket JW, Stephens FD (1986) The Mayer-Rokitansky syndrome: pathogenesis, classification and management. J Urol 135: 648–652
Tran ATB, Arensman RM, Faltermann W (1987) Diagnosis and management of hydrohaematometrocolpos syndrome. Am J Dis Child 141: 632–634
Author information
Authors and Affiliations
Additional information
Offprint requests to: P. M. Davidson
Rights and permissions
About this article
Cite this article
Sawyer, S.M., Davidson, P.M., Beasley, S.W. et al. Management of hydrohaematometrocolpos syndromes. Pediatr Surg Int 4, 347–350 (1989). https://doi.org/10.1007/BF00183404
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00183404