Case Series
Article 1013
Authors:
Roopa M<sup>*</sup>
Abstract:
Background: High intra- and inter-observer variability in the follicular assessment using 2D ultrasound (US) is still a concern. To solve this issue, a software solution, which automatically
provides follicles’ count and their diameters using 2D US images obtained by a manual sweep of an ovary. The primary objective of this study was to compare result of the automated solution with manual 2D US-based assessment.
Case Series
Article 1014
Authors:
Roopa M<sup>*</sup>
Abstract:
Background: Stage III and IV uterine prolapse are associated with urinary incontinence. Type of urinary continence, symptoms and relation to urodynamic studies has been variably described.
Methods: Design of the study. It was prospective interventional study. Setting study was conducted in tertiary care teaching hospital in south India. Participants: 51 patients with grade III and grade IV prolapse.
Intervention: Urinary symptoms evaluation and urodynamic study was done before and after pessary.
Case Report
Article 1015
Authors:
Aswathy P, Priya PV, Sankar S
Abstract:
Background: Accessory and cavitated uterine mass (ACUM) is a rare clinical entity. Reported cases of ACUM have no communication with main uterine cavity. Here we report a case of mullerian anomaly resembling ACUM but having communication with main uterine cavity. Case Presentation: 47 year old lady presented with lower abdominal distension and pain. Radiological evaluation: large pelvic cyst suggestive of pyometra or a peritoneal cyst. Laparotomy finding: a fully developed normal uterus and a large cystic mass near the left broad ligament suggestive of a degenerating broad ligament leiomyoma. The mass was removed along with uterus. Histopathological finding: uterus showed normal morphology and the broad ligament mass showed a circumscribed cystic lesion with morphology similar to uterus with a narrow communication between two. Diagnosis: Accessory and Cavitated uterine mass- communicating type. Conclusion: ACUM is a rare Mullerian anomaly often misdiagnosed as degenerating leiomyoma or adenomyoma and so may be under reported.
