| Literature DB >> 26692686 |
L I Smith-Harrison1, Mehul S Patel1, Ryan P Smith1, Noah S Schenkman1.
Abstract
Persistent Müllerian duct syndrome is a rare genetic disorder characterized by a male with retained Müllerian structures. Remnant excision must be considered due to the possibility of malignant degeneration. We review a case of delayed diagnosis in a 25-year-old man presenting with hematuria. Preoperative counseling must emphasize the risk of malignancy versus the risks to fertility. The da Vinci robot offers a novel, safe approach for excision of the relevant Müllerian structures. Dissection should be limited to structures superior to the cavernosal neurovascular bundles to preserve the continence and erectile function. A semen analysis is recommended preoperatively to determine effects on fertility.Entities:
Keywords: Laparoscopic surgery; Persistent Mullerian duct syndrome; robotic surgery
Year: 2015 PMID: 26692686 PMCID: PMC4660717 DOI: 10.4103/0974-7796.164859
Source DB: PubMed Journal: Urol Ann ISSN: 0974-7796
Figure 1Magnetic resonance urogram revealed a right unicornuate uterus. A tubular structure (white arrow) originating from the endocervical canal travels medially along the superior aspect of the right seminal vesicle to the midline where it inserts into the prostatic urethra
Figure 2Fluoroscopy confirming communication between the Müllerian remnant and the verumontanum orifice
Figure 3Intra-operative photograph showing the Mullerian remnant (arrow) as adhesions are taken down. Three working arms and helper suction are appreciated as well
Figure 4Continued dissection of the remnant structure with bilateral seminal vesicles demonstrated