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Introduction And Importance: Laparoscopic gonadectomy for nonpalpable glands in the inguinal canal, particularly in patients with Complete Androgen Insensitivity Syndrome (CAIS), presents technical challenges and is infrequently reported. While laparoscopic surgery in young women is minimally invasive and offers cosmetic advantages, it may require an additional inguinal incision depending on gonad location.
Case Presentation: A 16-year-old phenotypic female with a chief complaint of primary amenorrhea was diagnosed with 46, XY karyotype and CAIS. She was referred for a gonadectomy. MRI revealed the absence of a uterus, with the right gonad located in the abdominal cavity and the left gonad in the inguinal canal. After discussing the potential need for a secondary incision, a laparoscopic gonadectomy was performed with urological collaboration. During surgery, the gonads were located deep within the inguinal canal and were not palpable. Histopathological examination of the left testis was inconclusive. Four months later, a palpable mass was discovered in the left inguinal region, leading to removal of left testicular tissue via a secondary inguinal incision.
Clinical Discussion: This report highlights the importance of thorough preoperative imaging, collaborative surgical efforts between gynecologists and urologists, and the potential need for secondary surgical intervention when residual gonadal tissue is suspected.
Conclusions: Gonadectomy in patients with CAIS, who typically present to gynecologists due to their female gender identity, requires careful consideration of the potential need for secondary inguinal incisions, particularly in cases involving nonpalpable inguinal gonads.
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http://dx.doi.org/10.1016/j.ijscr.2024.110538 | DOI Listing |
Can Vet J
September 2025
Department of Clinical Studies, Ontario Veterinary College, University of Guelph, 50 Stone Road East, Guelph, Ontario N1G 2W1.
Minimally invasive laparoscopic surgical techniques are desirable in horses and other equids. A new approach called "modified single incision laparoscopic surgery (SILS) for equine cryptorchidectomy" is described, along with the postoperative outcomes of 10 equids. A SILS Port device (Covidien) was placed a 30- to 40-millimeter incision in combination with 1 or 2 15-millimeter para-inguinal incisions to exteriorize the intra-abdominal testicles.
View Article and Find Full Text PDFBMC Urol
August 2025
Department of Pediatrics, Tikur Anbesa Hospital, Addis Ababa, Ethiopia.
Background: Polyorchidism with cryptorchidism is an extremely rare congenital anomaly, particularly in children. Diagnosis and management are significantly more complex in low-middle-income countries (LMICs) due to resource limitations, including absent laparoscopy, increasing risks of torsion, malignancy, and infertility.
Case Presentation: An 8-year-old male from an LMIC presented with a non-palpable left testis.
J Pediatr Adolesc Gynecol
August 2025
Pediatric and Adolescent Gynecology, Department of Surgery, Nationwide Children's Hospital, 700 Children's Drive, Columbus, Ohio 43205-6228.
Background: Up to 10-12% of individuals with Turner Syndrome (TS) have Y chromosome material (e.g. 45,X/46,XY), which can lead to virilization.
View Article and Find Full Text PDFBMC Pregnancy Childbirth
August 2025
Department of Reproductive Medicine, The First People's Hospital of Yunnan Province, Kunming, 650000, Yunnan, China.
Background: For patients with recurrent serous borderline ovarian tumors (BOT) who have undergone unilateral salpingo-oophorectomy, there is a risk of reduced or even lost ovarian reserve after the second surgery; therefore, fertility preservation (FP) prior to re-operation in patients of childbearing age is challenging, and has attracted increasing attention. Here, we discuss the multidisciplinary whole-process management of a patient with recurrent serous BOT, from embryo cryopreservation (EC) before re-fertility-sparing surgery (re-FSS) to successful delivery.
Case Presentation: We describe the treatment of a 28-year-old married, nulliparous female with recurrent serous BOT who requested FP.
Introduction: Congenital lipoid adrenal hyperplasia (CLAH) is a type of congenital adrenal hyperplasia characterized by reduced steroid production. Patients with this endocrine disorder as well as chromosome 46,XY have testes and female external genitalia. Because these individuals are usually raised as female, the testes are removed.
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