OHVIRA syndrome: report of a case in Bolivia

• Rivero Castedo, Leonel ^[1] ; Auza-Santivañez, Jhossmar Cristians ^[2] ; Jimenez-Fernandez, Roberto Carlos ^[3] ; Carrera González, Elier ^[4] ; Rossio López Castillo, Alba ^[5] ; Soneira Pérez, Jorge ^[6]
  1. [1] Universidad Privada Franz Tamayo

     Universidad Privada Franz Tamayo

     Bolivia

     
  2. [2] Ministerio de Salud y Deportes. Instituto Académico Científico Quispe-Cornejo. La Paz, Bolivia
  3. [3] Universidad Católica Boliviana “San Pablo”. Santa Cruz, Bolívia
  4. [4] Hospital Clínico-Quirúrgico Miguel Enríquez. Unidad de cuidados Intensivo. La Habana, Cuba
  5. [5] Hospital de San Lorenzo. Tarija, Bolivia
  6. [6] Hospital Universitario Clínico Quirúrgico “Dr. Miguel Enríquez”. La Habana, Cuba

  Mostrar afiliaciones +
• Localización: Interamerican Journal of Health Sciences (IJHS), ISSN-e 2953-3724, Nº. 4, 2024
• Idioma: inglés
• Enlaces
  • Texto completo
• Resumen

  • Introduction: the OHVIRA Syndrome was described by Herlyn Werner Wunderlich and in 1976 Wunderlichdescribed a grouping of right renal aplasia with bicornuate uterus and simple vagina in the presence of an isolated hematocervix, as a characteristic triad uterus didelphys, intercepted hemivagina and ipsilateral renal anomaly, it is generally performed The diagnosis occurs in puberty at the beginning of menarche, with manifest symptoms of progressive dysmenorrhea and non-specific abdominal pain in the hypochondrium; urinary retention, urinary infection or a pelvic mass usually appear.Clinical case: the case of a 13 - year - old patient is presented, who comes to the clinic with abdominal pain andtransvaginal bleeding. Imaging studies are performed and due to the characteristics of said studies, the presence of OHVIRA Syndrome is suspected.Discussion: once the imaging studies were performed and the diagnosis confirmed, a surgical procedure wasperformed under general anesthesia. Through exploratory laparotomy, a bicornuate uterus was visualized, theright uterus larger than the left, and adherence to the abdominal wall, so an open intervention was decided.Conclusions: OHVIRA syndrome coexists with a rare malformation and is often misdiagnosed as other morecommon etiologies of dysmenorrhea in adolescents, as a consequence it delays a correct and early diagnosis,increasing the risk of kidney damage and its complications. In our clinical case, a timely diagnosis was made andsurgical treatment was subsequently planned with a favorable outcome