Herlyn–Werner–Wunderlich syndrome and its complications: A report of two cases and literature review

Abstract

Herlyn–Werner–Wunderlich syndrome (HWWS) is a rare congenital malformation characterized by uterus didelphys, unilateral blind hemivagina, and ipsilateral renal agenesis. The obstructed vagina affects menstrual flow, leading to related clinical symptoms after menarche. However, the age of onset, initial symptoms, and clinical complications differ among patients owing to the different types of vaginal septum. Herein, we report 2 cases. The first case is of a 20-year-old woman who presented with fever; she was diagnosed with vaginitis and pelvic inflammation due to the vaginal septum with ostiole. The second case is of a 12-year-old girl who complained of abdominal pain; she was diagnosed as having pelvic inflammation, omentitis, and suppurative appendicitis due to the atretic vaginal septum.

Herlyn-Werner-Wunderlich Syndrome: About an Uncommon Case Report

“…A proper diagnosis and prompt treatment can prevent the possible complications associated with this syndrome; pyocolpos, endometriosis and infertility [3]. We hereby present an uncommon case of a 13-year-old female patient referred to our department for an episode of acute urine retention associated with a pelvic pain after the onset of puberty in whom the diagnosis of HWW syndrome was made on pelvic MRI.…”