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Giant renal angiomyolipoma: A case report
Peijie Chen1,2, Lu Jin1,3, Yu Yang1
1Department of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Molecular and Clinical Oncology
|August 8, 2017
Summary
A rare giant renal angiomyolipoma (AML), a benign kidney tumor, was surgically removed from a 34-year-old female. This case highlights the importance of reporting large AMLs for diagnosis and treatment strategies.
Area of Science:
- Oncology
- Urology
- Pathology
Background:
- Renal angiomyolipoma (AML) is a rare, benign solid kidney tumor.
- Inherited in an autosomal dominant pattern, AMLs can cause complications if they grow significantly.
- Giant AMLs, defined as >20 cm, are exceptionally uncommon.
Purpose of the Study:
- To report a unique case of a giant renal AML.
- To emphasize the diagnostic and therapeutic considerations for large renal tumors.
Main Methods:
- A 34-year-old female presented with abdominal bloating.
- Diagnostic imaging included abdominal ultrasound and computed tomography.
- Surgical intervention involved a total left nephrectomy.
Main Results:
- A massive renal mass measuring 29×20x10 cm was resected.
- Histopathological examination confirmed the diagnosis of renal angiomyolipoma.
- The patient's symptoms were attributed to the large tumor size.
Conclusions:
- Giant renal AML is a rare entity requiring surgical management.
- Reporting such cases aids in understanding diagnosis and treatment.
- Prompt identification and intervention are crucial for managing symptomatic large AMLs.
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