Journal of Pediatric Surgery
Volume 44, Issue 9 , Pages e1-e3, September 2009

Laparoscopic management of persistent mullerian duct syndrome

  • Sandesh V. Parelkar

      Affiliations

    • Department of Pediatric Surgery, King Edward Memorial Hospital, Parel, Mumbai, India 400002
  • ,
  • Rahul Kumar Gupta

      Affiliations

    • Department of Pediatric Surgery, King Edward Memorial Hospital, Parel, Mumbai, India 400002
    • Corresponding Author InformationCorresponding author. Tel.: +91 9833112941.
  • ,
  • Sanjay Oak

      Affiliations

    • King Edward Memorial Hospital, Parel, Mumbai, India 400002
  • ,
  • Beejal Sanghvi

      Affiliations

    • Department of Pediatric Surgery, King Edward Memorial Hospital, Parel, Mumbai, India 400002
  • ,
  • Deepak Kaltari

      Affiliations

    • Department of Pediatric Surgery, King Edward Memorial Hospital, Parel, Mumbai, India 400002
  • ,
  • Raj Shekhar Patil

      Affiliations

    • Department of Pediatric Surgery, King Edward Memorial Hospital, Parel, Mumbai, India 400002
  • ,
  • Advait Prakash

      Affiliations

    • Department of Pediatric Surgery, King Edward Memorial Hospital, Parel, Mumbai, India 400002
  • ,
  • Pradeep Shimoga

      Affiliations

    • Department of Pediatric Surgery, King Edward Memorial Hospital, Parel, Mumbai, India 400002

Received 25 March 2009; received in revised form 13 May 2009; accepted 18 May 2009.

Abstract 

Persistent mullerian duct syndrome (PMDS), characterized by the presence of mullerian structures in a virilized male, frequently presents as undescended testis, either intraabdominal or within a hernial sac. We describe a 10-month-old infant with PMDS successfully managed by the laparoscopic approach. At the age of 1.5 months, the patient presented with a left inguinal hernia and bilateral nonpalpable gonads in another center and underwent left inguinal exploration. The uterus and a gonadlike structure along with the hernia sac were found in the inguinal canal. Left inguinal herniotomy was performed after reduction of the uterus and gonadlike structure. No gonadal biopsy was obtained. The patient was further investigated in the same center. His karyotype was 46,XY. Magnetic resonance imaging of the abdomen and pelvis revealed a uterinelike structure posterior to the urinary bladder, but neither testis nor ovaries were visualized. At 10 months of age, he was referred to our department for further management. A laparoscopic single-stage orchiopexy was performed. Both testes were identified and brought to the scrotum by splitting the uterus in the midline and then bringing the testes with the vas and attached uterine tissue into the scrotum. The aim of placement of well-vascularized testes in the scrotum was achieved as confirmed on follow-up color Doppler ultrasound study 6 months postoperatively, which showed normal vascularity. Laparoscopic surgical techniques for this condition are also discussed.

Key words: Laparoscopic orchiopexy, Persistent mullerian duct syndrome

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PII: S0022-3468(09)00451-5

doi:10.1016/j.jpedsurg.2009.05.033

Journal of Pediatric Surgery
Volume 44, Issue 9 , Pages e1-e3, September 2009