Atraumatic Bilateral Renal Subcapsular Urinomas in a Young, Healthy Female.
J Emerg Med
; 63(3): e82-e86, 2022 09.
Article
en En
| MEDLINE
| ID: mdl-35279354
ABSTRACT
BACKGROUND:
Urinomas are rare and generally result from trauma to any part of the urinary collecting system. Appropriate imaging is crucial in the timely diagnosis and management of urinomas and for ruling out other etiologies such as subcapsular renal hematomas and perinephric abscesses. CASE REPORT A 31-year-old woman with no past medical history or known trauma presented to the Emergency Department (ED) with a week of right flank pain, abdominal pain, and intermittent fevers. On point-of-care ultrasound (POCUS), she was found to have a complex right perinephric collection, later confirmed with computed tomography (CT) imaging. She was treated with intravenous (IV) antibiotics and discharged after a 3-day hospital admission with instructions to follow up with Urology. A day later, she was readmitted with worsening bilateral flank pain and persistent fevers. Image-guided percutaneous aspirations of her bilateral perinephric fluid collections revealed both urine and blood. A right ureteral stent was then placed with ultimate resolution of her symptoms. Why Should an Emergency Physician Be Aware of This? Urinomas without history of trauma are rare and should be on the differential for patients presenting with flank pain and infectious symptoms. Urinomas or other expanding perinephric fluid collections can result in superimposed infection, rupture, secondary hypertension, and renal failure. Here, we present an atypical case of atraumatic bilateral renal subcapsular urinomas with hemorrhagic components in a young and healthy woman. Our case further outlines the utility of POCUS in the ED for the timely diagnosis and management of this disease process.Palabras clave
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Urinoma
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Enfermedades Renales
Tipo de estudio:
Diagnostic_studies
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Etiology_studies
Límite:
Adult
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Female
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Humans
Idioma:
En
Año:
2022
Tipo del documento:
Article