USMLE® Step 1 style questions USMLE
A 24-year-old woman comes to the office because of a 5-day history of left flank pain. Her medical history is relevant for mitral regurgitation, mild intellectual disability, and facial hypomelanotic macules. Upon further interrogation, the patient denies pain, burning, or discomfort during urination. Physical exam shows generalized pallor and tenderness in her left flank. Her temperature is 37.9ºC (100.2ºF), pulse is 101/min, respirations are 22/min, blood pressure is 90/66 mmHg. An abdominal CT scan reveals a well-circumscribed hypoattenuating left kidney mass with a small and confined retroperitoneal hematoma. A mutation in which of the following genes is the most likely cause of the findings in this patient?
Content Reviewers:Rishi Desai, MD, MPH
Contributors:Vincent Waldman, PhD
Angiomyolipomas are the most common benign tumors found in the kidneys, although they can be found in other tissues like the liver and on rare occasions in some reproductive structures.
Angiomyolipomas are often described as hamartomas, which means that they are focal, abnormal growth of cells which are normally found at that site, but are disorganized.
It’s a bit like a house with a front door that can’t be reached, it’s the right part for the structure, but it’s not organized in the right way.
Angiomyolipomas also belong to the perivascular epithelioid cell tumor family, or PEComa family, meaning that they are made of epithelial-like cells that are found around blood vessels.
Now, it’s worth mentioning that normally there are no perivascular epithelioid cells that exist; the name just refers to the way that the tumor cells look under the microscope.
The actual cell type from which PEComas, including angiomyolipomas arise, is not known.
The majority of angiomyolipomas will pop up sporadically - which means they are not a part of a syndrome - as isolated lesions.
Interestingly, the tumors develop more often in the right kidney than in the left.
Individuals with tuberous sclerosis often have multiple angiomyolipomas along the surface of both kidneys, and they can be larger in size than the sporadic ones.
Regardless of whether the angiomyolipoma occurs sporadically or as a consequence of tuberous sclerosis, there is usually an underlying mutation in one of the tuberous sclerosis genes - TSC1 or TSC2 - which code for the tuberous sclerosis complex proteins hamartin and tuberin, respectively.
- "Robbins Basic Pathology" Elsevier (2017)
- "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
- "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
- "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
- "The Differential Imaging Features of Fat-Containing Tumors in the Peritoneal Cavity and Retroperitoneum: the Radiologic-Pathologic Correlation" Korean Journal of Radiology (2010)
- "Tuberous Sclerosis Complex Diagnostic Criteria Update: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference" Pediatric Neurology (2013)