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1.
J Pediatr Adolesc Gynecol ; 36(6): 541-544, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37451429

ABSTRACT

OBJECTIVES: The objectives of the study were to compare the demographic characteristics, presenting complaints, timeliness of diagnosis, and treatments given to all patients diagnosed with obstructive hemivagina ipsilateral renal agenesis (OHVIRA) between the adolescent group (age 10-19) and the adult group (age 20 and above) and to propose a feasible screening test consisting of routine bedside ultrasound to detect renal anomalies in addition to pelvic ultrasound during the assessment of females with gynecologic complications in resource-limited settings. METHOD AND ANALYSIS: We conducted a retrospective cohort analysis of all patients with OHVIRA at our institution, Sabah Women and Children's Hospital, Malaysia, between the 2013 and 2022. Data were collected by reviewing patients' medical notes. RESULTS: There were a total of 18 patients diagnosed with OHVIRA from 2013 to 2022, aged 10-41 years old. Nine patients (50%) presented during adolescence. Most (88.9%) came with symptoms such as abdominal pain, urinary symptoms, abnormal uterine bleeding, foul-smelling vaginal discharge, and primary infertility, whereas only 2 patients (11.1%) were asymptomatic and diagnosed incidentally. Acute abdomen was more common in the adolescent group (P = .015). No significant difference was found on the side of the renal anomaly. CONCLUSION: Presenting symptoms vary and are often mimicked other gynecologic or surgical conditions, making the diagnosis difficult and delayed. Some patients were incidentally diagnosed while being managed for other problems, and it was not uncommon to have unnecessary surgery before the correct diagnosis was made. We suggest that all female patients with abdominal and pelvic complaints should be screened for renal anomaly during pelvic scan to improve diagnostic rates.


Subject(s)
Abnormalities, Multiple , Vagina , Child , Adult , Adolescent , Female , Humans , Young Adult , Malaysia , Retrospective Studies , Vagina/abnormalities , Abnormalities, Multiple/surgery , Kidney/diagnostic imaging , Kidney/abnormalities , Syndrome , Uterus/abnormalities
2.
J Pediatr Adolesc Gynecol ; 32(1): 74-77, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30248506

ABSTRACT

BACKGROUND: Ovotesticular disorders of sex development is a condition defined as the presence of ovarian tissue containing ovarian follicles and testicular tissue containing seminiferous tubules in the same individual. CASE: We report on a 19-year-old who is phenotypically male, with a 46,XX/46,XY mosaicism karyotype, who presented later in life with cyclical abdominal pain that resembled menstrual cramps and unilateral undescended testes. SUMMARY AND CONCLUSION: He underwent laparoscopic hysterectomy and right salpingo-oophorectomy, resulting in cessation of his symptoms and improved sperm count.


Subject(s)
Hysterectomy/methods , Laparoscopy/methods , Ovotesticular Disorders of Sex Development/surgery , Salpingo-oophorectomy/methods , Adult , Female , Hormone Replacement Therapy/methods , Humans , Male , Mosaicism , Ovary/surgery , Ovotesticular Disorders of Sex Development/diagnosis , Ovotesticular Disorders of Sex Development/drug therapy , Sperm Count , Spermatogonia , Testosterone/therapeutic use , Treatment Outcome , Young Adult
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