Presentation A 27-year-old male presented to the Emergency Department with acute severe left flank pain following ingestion of 5 pints of beer. Approximately 20 bouts of similar episodes over the past year, in the setting of alcohol ingestion. Despite attending GP, no diagnosis reached yet. Diagnosis "Pelvo-ureteric junction (PUJ) obstruction Syndrome". Bedside ultrasound in the Emergency Department during the acute pain crisis: massive hydronephrosis left kidney. Finding confirmed on CT scan. Subsequent 99m-Tec renogram showed markedly decreased renal function on the left. Treatment Interval Pyeloplasty two months later. Conclusion Delayed recognition is the norm for PUJ obstruction syndrome, as CT/MRI/US studies often do not display hydronephrosis if the patient is asymptomatic. We could not find any reports in the literature of diagnosing PUJ obstruction syndrome using bedside ultrasound in the Emergency Department. We advise acquiring rapid bedside ultrasound imaging in suspected cases of PUJ obstruction syndrome, enabling earlier diagnosis.
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J Surg Case Rep
December 2024
Accident and Emergency Department, Provincial Hospital Malangwa, Balmandir Chowk, Malangwa, Sarlahi 45800, Nepal.
A 16-year-old male presented to OPD with right-sided flank pain associated with lower urinary tract symptoms. CT scan and ultrasound findings demonstrated a 12.9 mm renal stone in the lower calyx and moderate hydronephrosis, respectively.
View Article and Find Full Text PDFJ Minim Access Surg
November 2024
Department of Urology, All India Institute of Medical Sciences, New Delhi, India.
Introduction: To evaluate the feasibility, safety, and effectiveness of different pyeloplasty procedure approaches for pelvicureteric junction (PUJ) obstruction in kidney anomalies. The presence of difficult, unfamiliar and anomalous anatomy makes pyeloplasty challenging in these conditions.
Patients And Methods: We conducted a retrospective review of pyeloplasty in patients with congenital anomalous kidneys at our national tertiary referral centre.
J Indian Assoc Pediatr Surg
August 2024
Department of Pediatric Surgery, Mazumder Shaw Medical Center, Bengaluru, Karnataka, India.
Inflammatory myofibroblastic tumor (IMT) is a very rare tumor with still rare occurrence in the genitourinary system, presenting as a pelvic-ureteric junction (PUJ) obstruction (PUJO). We report a case of IMT at the PUJ mimicking congenital PUJO and review the relevant literature.
View Article and Find Full Text PDFArch Ital Urol Androl
June 2024
Urologic Department, Sisters of Charity Hospital and Urologic Praxis, Wien.
Children (Basel)
March 2024
Pediatric Surgery Unit, Salesi Children's Hospital, 60123 Ancona, Italy.
Introduction: In children, the association of ipsilateral pyeloureteral junction obstruction (PUJO) and ureterovesical junction obstruction (UVJO) is a rare malformation with a non-standardized treatment. We report a case of PUJO and UVJO treated by a combined minimally invasive surgical treatment to resolve the double urinary obstruction. The current literature was also reviewed.
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