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Archives of Gynecology and Obstetrics

, Volume 286, Issue 3, pp 785–791 | Cite as

Diagnostic challenges of hemihematocolpos and dysmenorrhea in adolescents: obstructed hemivagina, didelphys or bicornuate uterus and renal aplasia is a rare female genital malformation

  • Irini Tzialidou-Palermo
  • Constantin S. von KaisenbergEmail author
  • Guillermo-José Garcia-Rocha
  • Hans-Walter Schloesser
  • Ina Baehr
  • Cordula Schippert
Reproductive Medicine

Abstract

Objectives

To develop a clear diagnostic and therapeutic strategy for adolescents presenting with abdominal pain and vaginal tumor caused by congenital female genital anomalies, such as blind hemivagina and uterine anomalies, as the lack of the correct diagnosis of the underlying anatomical genitourinary malformation frequently leads to destructive surgical procedures.

Methods

Retrospective study, study group: patients with double/bicornuate uterus, blind hemivagina and hematocolpos (n = 13), controls: patients with uterine malformation and complete vertical vaginal septum (n = 11), analysis for: menarche, age at onset of symptoms, type of malformation, symptoms leading to admission and diagnostic/surgical techniques applied.

Results

Median age at diagnosis study group 19.85 (SD ± 6.23, range 13–23 years) versus controls 26.09 years (SD ± 7.44, 16–36 years); predominance of imperforated hemivagina: 69.2 % right-sided versus 30.8 % left-sided septum; renal agenesis ipsilateral to imperforate hemivagina 100 % study group versus 9.1 % controls; 84.6 % previous surgical interventions in the study group, such as partial removal of the septum and re-obliteration, unilateral salpingo-ovarectomy and vaginal drainage of pyometra. We used a single transvaginal surgical procedure, including removal of the obstructed vaginal septum and marsupialization of the blind hemivagina.

Conclusions

A diagnostic and therapeutic algorithm for young women presenting with progressive dysmenorrhea and abdominal pain and/or vaginal tumor reduces destructive interventions.

Keywords

Hemivagina Hemihematocolpos Dysmenorrhea Renal aplasia Mullerian anomalies Female genital tract malformations 

Notes

Acknowledgments

We acknowledge the oral contributions of Rizwan Rehimi, from the group of Professor Dr. rer. nat. Beate Brand-Saberi, Ruhr-University Bochum, Department of Anatomy and Molecular Embryology, Building MA, 5/158, 44780 Bochum, Germany.

Conflict of interest

The authors declare that they have no conflict of interest. They have full control of all primary data and agree to allow the Journal to review their data if requested.

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Copyright information

© Springer-Verlag 2012

Authors and Affiliations

  • Irini Tzialidou-Palermo
    • 1
  • Constantin S. von Kaisenberg
    • 1
    Email author
  • Guillermo-José Garcia-Rocha
    • 1
  • Hans-Walter Schloesser
    • 1
  • Ina Baehr
    • 2
  • Cordula Schippert
    • 1
  1. 1.Department of Obstetrics, Gynecology and Reproductive MedicineHannover Medical SchoolHannoverGermany
  2. 2.Department of Anatomy and Cell BiologyMartin-Luther-University Halle-WittenbergHalle (Saale)Germany

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