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Wunderlich Syndrome: A Rare Case Associated with Bleeding Renal Angiomyolipoma (AML)
Nidha Gaffoor1, Vijaya V Mysorekar1, Shankar Gunadal2
1Department of Pathology, Dr. Chandramma Dayananda Sagar Institute of Medical Education and Research, Dayananda Sagar University, Ramanagara, Karnataka, India.
Indian Journal of Nephrology
|August 8, 2024
Summary
Renal angiomyolipoma (AML), a benign kidney tumor, can cause severe bleeding and flank pain, mimicking aggressive cancers. Prompt diagnosis and surgical intervention are crucial for patient survival and reduced complications.
Area of Science:
- Urology
- Oncology
- Pathology
Background:
- Renal angiomyolipoma (AML) is a rare benign mesenchymal tumor of the kidney.
- AMLs constitute 1-3% of all solid renal tumors.
- Despite being benign, AML can exhibit aggressive behavior and locoregional extension.
Observation:
- A 60-year-old female presented with left flank pain and unstable blood pressure.
- CT imaging revealed a renal mass with hemorrhagic densities.
- Intraoperative findings confirmed significant bleeding from the renal mass.
Findings:
- The patient underwent radical nephrectomy due to the symptomatic presentation.
- Histopathologic examination confirmed renal AML with secondary changes.
- The clinical presentation and findings were consistent with Wunderlich syndrome, often associated with AML.
Implications:
- This case highlights the importance of considering AML in the differential diagnosis of acute flank pain and renal masses.
- Early detection and prompt surgical management of symptomatic renal AML are critical for preventing life-threatening hemorrhage.
- Increased clinical awareness can improve the timely diagnosis and treatment of renal AML, reducing patient morbidity and mortality.
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