A 24-year-old male was found to have recurrent epididymitis secondary to ectopic ureteral insertion to the seminal vesicle. His ipsilateral kidney was atrophic and ectopic in the pelvis, suggesting a complex failure of embryological development. He was successfully treated with robot-assisted laparoscopic nephroureterectomy.
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http://dx.doi.org/10.1089/cren.2015.29006.bos | DOI Listing |
J Surg Case Rep
January 2025
Department of Urology, Sapporo Medical University School of Medicine, South 1, West 16, Chuo-ku, Sapporo060-8543, Hokkaido, Japan.
A thoracic kidney is a scarce type of ectopic kidney. We report the case of a 76-year-old man who developed cancer of the ureter, ipsilateral to the thoracic kidney. He presented with abdominal pain in the right upper quadrant.
View Article and Find Full Text PDFCureus
November 2024
Urology, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.
Congenital anomalies are not regularly seen in day-to-day practice. Crossed fused renal anomalies are even rarer. A 50-year-old female patient presented with right-sided pain in the abdomen with intermittent episodes of burning micturition.
View Article and Find Full Text PDFMedicina (Kaunas)
November 2024
Division of Pediatric Surgery, Federico II University Hospital, 80131 Naples, Italy.
Rev Med Inst Mex Seguro Soc
September 2024
Instituto Mexicano del Seguro Social, Hospital de Gineco Obstetricia No. 4 "Luis Castelazo Ayala", División de Obstetricia. Ciudad de México, México.
Background: Abdominal ectopic pregnancy is a rare complication with high maternal and perinatal morbimortality. The objective was to present the multidisciplinary management of an advanced abdominal ectopic pregnancy associated with COVID-19, and a review of the literature.
Clinical Case: 33-year-old multiparous patient with an abdominal ectopic pregnancy of 34 weeks, diagnosed by ultrasound at 27 weeks.
Cureus
October 2024
Pediatric Surgery, Government Medical College, Kozhikode, Kozhikode, IND.
Female hypospadias is an extremely rare condition characterised by urethral meatus placed within the introitus on the anterior vaginal wall, along with foreshortening of the urethra. It is an often missed anomaly that usually co-exists with other genitourinary conditions like ectopic ureter, renal anomalies, septate vagina and bicornuate uterus. A case series of five girls who had hypospadias is being described.
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