Journal List > Korean J Obstet Gynecol > v.54(5) > 1088282

Jeon, You, Kwon, Yoon, Kang, Kim, Chae, Kim, and Kang: A case of the uterus didelphys with unilateral obstructed hemivagina and ipsilateral renal agenesis

Abstract

Uterus didelphys with unilateral obstructed hemivagina, and ipsilateral renal agenesis is a rare congenital anomaly due to Müllerian duct malformation. The most common clinical manifestation is dysmenorrhea, pelvic pain, vaginal or pelvic mass after menarche. Early diagnosis is important, to preserve fertility, to prevent adhesion due to retrograde menstruation, hematometra, hematosalpinx and endometriosis which lead to distorted pelvic anatomy. These anomalies could be diagnosed with ultrasonography and magnetic resonance imaging. Resection or incision of vaginal septum is adequate treatments to relieve symptoms and reserve fertility. We report a case of uterus didelphys with unilateral obstructed hemivagina and ipsilateral renal agenesis with a brief review of the literature.

Figures and Tables

Fig. 1
Transvaginal ultrasonography shows a large paravaginal cystic mass, 4.5×3.5 cm with turbid content.
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Fig. 2
(A) MRI shows uterus didelphys. (B) MRI shows paravaginal cystic mass. (C) MRI shows absence of Lt kidney.
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Fig. 3
Laparoscopic finding shows uterus didelphys and normal finding of both ovaries and salpinges.
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Fig. 4
Diagram of resection of vaginal septum providing drainage of the retained pus.
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Fig. 5
After opertation, the paravaginal mass was disappeared in MRI.
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