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Renal Cyst


Renal Cyst

Article Author:
David Sigmon
Article Author:
Rachel Shikhman
Article Editor:
Jeffery Nielson
Updated:
5/30/2020 9:05:25 AM
For CME on this topic:
Renal Cyst CME
PubMed Link:
Renal Cyst

Introduction

A renal cyst is the most common lesion of the kidney. Renal cysts are so ubiquitous that they are present in approximately 40% of the patients undergoing imaging. The cystic renal disease can be focal, multifocal, one-sided, or bilateral. Renal cysts can be a result of a congenital disease or acquired. The acquired form is the most common. Renal cysts can range from benign to malignant. A categorization system for adult renal cysts was introduced in the late 1980s known as the Bosniak classification. It was introduced in attempts to standardize characterization and management of renal cysts.[1][2][3]

The terminology of congenital renal cysts has changed throughout the years, with the current characterization known as the Potter classification. The Potter classifications have four categories: type I is infantile polycystic kidney disease, type II is multicystic dysplastic kidney disease, type III is adult polycystic kidney disease, and type IV is obstructive renal dysplasia. Infantile polycystic kidney disease is also known as autosomal recessive polycystic kidney disease. ARPKD demonstrates no gender predilection with a ratio of 1:1. The range of diagnosis is neonate to childhood, depending on the severity of the disease. Multicystic dysplastic kidney disease is a non-inherited kidney disease that develops in utero. It is most commonly unilateral with a higher incidence on the left-side. The diagnosis is often made while still in utero or very early in a neonate. Adult polycystic kidney disease is also known as autosomal dominant polycystic kidney disease. A patient with ADPKD has a normal appearance of the kidneys at birth and begins to develop multiple cysts bilaterally in their 20s to 30s. It is the most common inherited cause of end-stage renal failure with more than 50% of patients requiring dialysis by the age of 60 years. Obstructive cystic renal dysplasia results from an obstruction during development that causes scattered cysts throughout the affected kidney.[4][5]

Etiology

Autosomal recessive kidney disease is caused by a mutation in the PKHD1 gene located on chromosome 6 resulting in cyst formation in the collecting ducts. Multicystic dysplastic kidney disease is most commonly idiopathic. Autosomal dominant kidney disease is caused by a mutation in either the PKD1 gene on chromosome 16 or the PKD2 gene on chromosome 4.[6][7] Obstructive cystic renal dysplasia results from an obstruction of the ureter, bladder or urethra. Acquired renal cysts are most commonly idiopathic. Renal cysts can develop in the infectious setting, can be a result of multisystem diseases such as Von-Hippel-Lindau and tuberous sclerosis, or can form during end-stage renal disease.

Epidemiology

The presence of acquired renal cysts increases with increasing age. Simple renal cysts are the most common cystic renal lesions. They are thought to be present in up to 5% of the general population. This prevalence increases to more than 25% in people older than 50 years of age. In the elderly population, renal cysts can account for up to 65-70% of the renal mass. The prevalence of renal cysts was found to be higher in men compared to women in a retrospective magnetic resonance imaging study of 2000 patients. They also reported a higher prevalence in patients with hypertension and smoking history.[8]

Pathophysiology

Multicystic dysplastic kidney disease is caused by nonfunctioning kidney tissue in the affected area which develops into cysts. It can ultimately lead to renal agenesis of the affected side. Obstructive cystic renal dysplasia results from an obstruction of the ureter, bladder, or urethra that increases pressure to the kidney. This process creates cysts.

History and Physical

The presentation of a patient with cystic kidney disease varies with the underlying disease etiology. Physical examination is usually only pertinent to inherited renal disease, presenting as a palpable mass in a neonate or child. Patients with ADPKD commonly present with flank pain, renal failure, hypertension or palpable masses. Acquired cystic kidney disease rarely becomes large enough to become palpable on physical examination. Renal cysts are often found incidentally during an ultrasound or cross-sectional imaging for other causes. Taking a thorough family history is key to elucidating possible genetic factors in a patient with renal cysts.

Evaluation

Renal cysts can be diagnosed by ultrasound, computed tomography (CT), and magnetic resonance imaging scans (MRI).

Infantile polycystic kidney disease is usually first evaluated with ultrasound in utero. The mother usually has is usually present with oligohydramnios from the poor renal function. After birth, an ultrasound is performed that will show enlarged kidneys with numerous small renal cysts bilaterally. The kidneys can be further evaluated with MRI which normally shows a diffuse increase in T2 signal. Multicystic dysplastic kidney disease is usually evaluated in utero versus early in neonates and presents as multiple non-communicating renal cysts. Adult polycystic kidney disease is often evaluated with ultrasound or CT. The classification of more than two cysts per side by the age of 30 helps in the diagnosis. Obstructive cystic renal dysplasia is diagnosed in utero demonstrating a normal to small kidney size of the affected kidney with multiple scattered cysts.[9][10][11][12]

Ultrasound evaluation of a renal cyst can be described as simple, complex. A simple renal cyst has the following characteristics: a well-marginated anechoic lesion with possible posterior acoustic enhancement. A minimally complex cyst may demonstrate a few septations. A complex cyst will demonstrate thick septations or wall and can have a hypoechoic appearance or signs of internal debris. 

Acquired single or multifocal renal cysts are classified using the Bosniak classification on a contrast-enhanced CT and can be adjusted for MRI use. A Bosniak I lesion is a simple cyst with imperceptible walls and round. No follow-up is needed, and there is a less than 1% chance of malignancy. A Bosniak II lesion demonstrates minimal complexity: a few thin septations less than 1 mm in diameter, thin calcification, or a high attenuated lesion less than 3 cm in diameter without enhancement. Bosniak II lesions require no follow-up and have a less than 1% chance of malignancy. A Bosniak IIF lesion demonstrates minimal complexity —  an increased number of thin septations, with possible "perceived" enhancement with no true measurable enhancement — or a high attenuated lesion larger than 3 cm. These lesions require follow-up with CT or ultrasound. No definitive interval timeline is given, but most references say approximately 6 months after diagnosis and then annually for 5 years if there is no progression. A Bosniak IIF lesion has a 5% chance of malignancy. A Bosniak III lesion is indeterminant in appearance with thick septations with possible nodularity or measurable wall enhancement greater than ten Hounsfield units. The recommended treatment is the biopsy and partial nephrectomy versus ablation. A Bosniak III lesion has a 55% chance of being malignant. A Bosniak IV lesion describes a solid mass with cystic versus necrotic components. These are described as being unquestionably malignant. The recommended treatment is partial or total nephrectomy. The Bosniak lesion has a 100% chance of being malignant.

A simple cyst on MRI will demonstrate a low T1 signal, high T2 signal, with no evidence of enhancement post-contrast.

Treatment / Management

Infantile polycystic kidney disease treatment is mostly supportive, with dialysis and transplant, but overall patients tend to have a poor prognosis. Multicystic dysplastic kidney disease has a controversial treatment of nephrectomy of the affected side. If nephrectomy is not performed follow-up is recommended because there is a low risk of malignant transformation. The patients will have a normal life expectancy as long as the contralateral kidney has normal function. Adult polycystic kidney disease is the leading inherited cause of end-stage kidney disease and results in the requirement of dialysis and transplant is the vast majority of cases by middle age through the early 60s. Removal of the obstruction treats obstructive cystic renal dysplasia. Acquired lesions classified as Bosniak I and II require no further evaluation. A Bosniak IIF recommends follow-up with ultrasound or CT. A Bosniak III recommends surgical intervention with biopsy and partial nephrectomy or ablation. A Bosniak IV recommends partial or total nephrectomy.

Differential Diagnosis

If the patient presents with a symptomatic renal cyst, which may include abdominal pain or urinary obstruction, then the differential is broad. Given that the kidneys are bilateral structures almost every organ can be implicated in pain caused by a renal cyst. It is worth noting, however, that most renal cysts are asymptomatic and are most commonly found incidentally. The differential diagnosis for a symptomatic cyst includes but is not limited to:

  • Kidney stones
  • Pyelonephritis
  • Adrenal neoplasm
  • Renal neoplasm
  • Splenic infarction
  • Hernia
  • Trauma
  • Gallbladder disease

Prognosis

The prognosis of renal cysts varies widely with their etiology. Simple Bosniak Type I cysts have a less than 1% chance of malignancy whereas Bosniak Type IV cysts have a significant chance of harboring malignancy with a concomitantly worse prognosis. In recessive (pediatric) polycystic kidney disease approximately 30% of patients will not survive their first week of life and patients surviving beyond that will require life long dialysis or kidney transplant while also often having cystic liver disease. Dominant (adult) polycystic kidney disease has a variable onset but if it progresses to end-stage renal disease then the patient will require dialysis or kidney transplant.

Complications

As noted above in the prognosis of renal cysts the complications that can occur secondary to cysts and their treatment vary widely with the etiology of the cyst. Bosniak Type I cysts can be safely observed and thus pose no risk of complication whereas Bosniak Type IV cysts may require a radical surgery that is accompanied by a significant risk of complications such as damage to surrounding structures like the liver, spleen, or stomach. Patients with recessive (pediatric) polycystic kidney disease that survive their first few weeks of life will require life long dialysis or kidney transplant as do patients with dominant (adult) polycystic kidney disease who progress to end-stage renal disease. Dialysis can be complicated by infections or damage to vascular structures to name a few of the complications that accompany that treatment modality. Patients who receive transplants are at higher risk for infections due to immunosuppression as well as the complication profile that accompanies the major surgery entailed during a transplantation procedure.

Deterrence and Patient Education

While there is no way to deter the formation of renal cysts it is important to educate patients who develop or inherit them about the nature of their cysts. Patients will incidentally found Bosniak Type I or II cysts should be assured there is a minimal chance of malignancy and no scheduled follow-up is required. Patients with Bosniak Type IIF cysts should be educated about the need for them to attend their follow-up visits to ensure the cyst is not progressing. Patients with Bosniak Type II or IV cysts should be educated about their risk of malignancy and a long term care plan should be established both for the resection of their cyst and for their postoperative care. The parents of patients with recessive (pediatric) polycystic kidney disease should be educated on their child's lifelong need for dialysis as well as discussing the possibility of a kidney transplant in the future. Likewise, patients with dominant (adult) polycystic kidney disease who progress to end-stage renal disease should be educated about dialysis as well as the possibility of a future kidney transplant.

Pearls and Other Issues

The most common associated disease with infantile polycystic kidney disease is Caroli disease of the liver and hepatic fibrosis. There are many associated findings of adult polycystic kidney disease including berry aneurysms, hypertension, liver cysts, and cysts within different organs. There is an association of VACTERAL and congenital heart disease with obstructive cystic renal dysplasia.

Enhancing Healthcare Team Outcomes

The management of renal cysts is best done with an interprofessional team that includes a urologist, nephrologist, geneticist, and an internist with the assistance of a nurse practitioner or physician assistant. Hereditary cysts are progressive and may eventually affect renal function-thus these patients have to be monitored for life. For those without symptoms, the management is supportive. When renal function declines, end-stage renal disease is a possibility and the nephrologist should be involved early in the care of these patients. The nurse should educate the patient on options for dialysis and renal transplant. Unfortunately, patients with genetic disorders also have other organ involvement and their prognosis is guarded.[13][14][Level 5]


References

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