Renal cysts
Alerts and Notices
Synopsis

Renal cysts are abnormal fluid-filled sacs within the kidney that can occur at any age. Approximately 1 in every 3 adults over the age of 50 has a renal cyst, with a higher prevalence in males. Renal cysts can be characterized by morphology (simple versus complex), malignant potential (Bosniak classification), or etiology of cysts (congenital or acquired).
Simple renal cysts are common renal lesions (70%); the majority are benign, and further imaging is not required.
The most common form of cystic renal disease is due to autosomal dominant polycystic kidney disease (PKD) and accounts for 8%-10% of all causes of end-stage renal disease. The develoment of renal cysts has also been associated with diuretic use as well as some medications.
The presentation of renal cysts varies based on the cause, and physical examination may reveal a palpable flank or abdominal mass. Radiographic findings of a thick irregular wall, thick septations, or multilocular findings are concerning for malignancy.
Simple renal cysts are common renal lesions (70%); the majority are benign, and further imaging is not required.
The most common form of cystic renal disease is due to autosomal dominant polycystic kidney disease (PKD) and accounts for 8%-10% of all causes of end-stage renal disease. The develoment of renal cysts has also been associated with diuretic use as well as some medications.
The presentation of renal cysts varies based on the cause, and physical examination may reveal a palpable flank or abdominal mass. Radiographic findings of a thick irregular wall, thick septations, or multilocular findings are concerning for malignancy.
Codes
ICD10CM:
N28.1 – Cyst of kidney, acquired
Q61.00 – Congenital renal cyst, unspecified
SNOMEDCT:
722223000 – Cyst of kidney
N28.1 – Cyst of kidney, acquired
Q61.00 – Congenital renal cyst, unspecified
SNOMEDCT:
722223000 – Cyst of kidney
Look For
Subscription Required
Diagnostic Pearls
Subscription Required
Differential Diagnosis & Pitfalls
Categories of renal cysts are:
- Developmental – Multicystic dysplastic kidney, uniformly diagnosed on prenatal ultrasound; medullary sponge kidney
- Genetic – Autosomal dominant PKD, autosomal recessive PKD, medullary cystic kidney disease, glomerulocystic kidney disease, and juvenile nephronophthisis
- Associated with systemic disease – von Hippel-Lindau syndrome and tuberous sclerosis
- Acquired – Simple cysts, acquired cystic renal disease, lithium-induced renal disease (microcysts in the medulla and cortex), angiomyolipoma, metanephric adenoma, cystic oncocytoma
- Malignancy-associated – Cystic renal cell carcinoma, lymphoma
Best Tests
Subscription Required
Management Pearls
Subscription Required
Therapy
Subscription Required
Drug Reaction Data
Below is a list of drugs with literature evidence indicating an adverse association with this diagnosis. The list is continually updated through ongoing research and new medication approvals. Click on Citations to sort by number of citations or click on Medication to sort the medications alphabetically.
Subscription Required
References
Subscription Required
Last Reviewed:03/06/2018
Last Updated:04/18/2018
Last Updated:04/18/2018