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Fortuitous detection of adult malrotated ectopic kidney during acute appendicitis: A unique case report.
Touati, Med Dheker; Khefacha, Fahd; Ben Othmane, Mohamed Raouf; Belhadj, Anis; Saidani, Ahmed; Chebbi, Faouzi.
Afiliación
  • Touati MD; General Surgery Department, Mahmoud El Matri Hospital, R534+F9H, Rue de la Faculté de Médecine, Tunis, Tunisia; Faculty of Medicine of Tunis, University of Tunis El Manar, R534+F9H, Rue de la Faculté de Médecine, Tunis, Tunisia. Electronic address: dhekertouati@gmail.com.
  • Khefacha F; General Surgery Department, Mahmoud El Matri Hospital, R534+F9H, Rue de la Faculté de Médecine, Tunis, Tunisia; Faculty of Medicine of Tunis, University of Tunis El Manar, R534+F9H, Rue de la Faculté de Médecine, Tunis, Tunisia.
  • Ben Othmane MR; General Surgery Department, Mahmoud El Matri Hospital, R534+F9H, Rue de la Faculté de Médecine, Tunis, Tunisia; Faculty of Medicine of Tunis, University of Tunis El Manar, R534+F9H, Rue de la Faculté de Médecine, Tunis, Tunisia.
  • Belhadj A; General Surgery Department, Mahmoud El Matri Hospital, R534+F9H, Rue de la Faculté de Médecine, Tunis, Tunisia; Faculty of Medicine of Tunis, University of Tunis El Manar, R534+F9H, Rue de la Faculté de Médecine, Tunis, Tunisia.
  • Saidani A; General Surgery Department, Mahmoud El Matri Hospital, R534+F9H, Rue de la Faculté de Médecine, Tunis, Tunisia; Faculty of Medicine of Tunis, University of Tunis El Manar, R534+F9H, Rue de la Faculté de Médecine, Tunis, Tunisia.
  • Chebbi F; General Surgery Department, Mahmoud El Matri Hospital, R534+F9H, Rue de la Faculté de Médecine, Tunis, Tunisia; Faculty of Medicine of Tunis, University of Tunis El Manar, R534+F9H, Rue de la Faculté de Médecine, Tunis, Tunisia.
Int J Surg Case Rep ; 118: 109679, 2024 May.
Article en En | MEDLINE | ID: mdl-38663289
ABSTRACT
INTRODUCTION AND IMPORTANCE Renal ectopia, a rare congenital anomaly, can occur in various body regions and may be associated with other abnormalities. It is often asymptomatic, commonly found incidentally, as in our 70-year-old patient during appendicitis exploration. This case highlights the importance of recognizing renal ectopia and associated anomalies, such as vascular abnormalities and renal malrotation, which may predispose patients to potential complications and require vigilant monitoring for urinary tract infections and lithiasis events, as well as potential challenges during laparoscopic surgical procedures, as in our appendectomy case. CASE PRESENTATION A 70-year-old female presented with right iliac fossa pain and elevated inflammatory markers. Abdominopelvic CT scan confirmed uncomplicated appendicitis and revealed a right ectopic and malrotated kidney. Laparoscopic appendectomy was performed without complications. Postoperative recovery was uneventful, and discharge occurred one day post-procedure. A four-week follow-up was scheduled to monitor for urinary infection and stone formation, with initiation of hygienic and dietary measures. CLINICAL

DISCUSSION:

Renal ectopia, a congenital anomaly, frequently positions the kidneys in the pelvic region. Iliac ectopias are often confused with pelvic or abdominal ectopias. Ectopic kidneys can result in complications like vesicoureteral reflux, urinary tract infections, or kidney stones. Despite being typically left-sided, our patient presented with right-sided renal ectopia with malrotation. Despite lacking urinary symptoms, a urological consultation was advised due to the potential risk of infection or kidney stones. Surgical intervention is reserved for complication management.

CONCLUSION:

Renal ectopia, a rare congenital anomaly, can be asymptomatic but often coincides with other renal or vascular issues. Early detection and accurate imaging are essential, emphasizing clinical vigilance and interdisciplinary collaboration for better patient care.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Int J Surg Case Rep Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Int J Surg Case Rep Año: 2024 Tipo del documento: Article