This rare type of cancer appears as a tumor surrounded by a fibrous capsule. The inside of the tumor is made up of cysts and tissue. The tissue contains clear epithelial cells.
This article will provide an overview of multilocular cystic renal cell carcinoma and outline treatment options.
Types of Renal Cell Carcinoma
Multilocular cystic renal cell carcinoma is a very rare type of cancer. In addition, there are several other types of renal cell carcinoma, including:
Clear cell renal cell carcinoma: This is the most common subtype of renal cell carcinoma and makes up about 70% of all cases. Under a microscope, these cells appear pale or clear. Papillary renal cell carcinoma: This is the second most common subtype and makes up about 10% of all renal cell carcinoma cases. It causes finger-like projections to grow in the small tubes in the kidneys. Chromophobe renal cell carcinoma: This type makes up about 5% of renal cell carcinoma cases, and its cells appear pale or clear under a microscope. Collecting duct renal cell carcinomaMultilocular cystic renal cell carcinomaMedullary carcinomaMucinous tubular and spindle cell carcinomaNeuroblastoma-associated renal cell carcinoma
Multilocular Cystic Renal Cell Carcinoma Symptoms
Many people with multilocular cystic renal cell carcinoma have no symptoms at all. Possible symptoms of multilocular cystic renal cell carcinoma include:
Blood in the urineA lump in the side abdomenAbdominal or back painFatigueFeverUnintended weight loss
Causes
Multilocular cystic renal cell carcinoma usually occurs randomly without a known cause.
It’s important to note that clear cell renal cell carcinoma, the type of kidney cancer that includes multilocular cystic renal cell carcinoma, is believed to run in families. If you have a family history of Hippel-Lindau disease, you may be at higher risk. This is due to a mutation in the VHL gene.
The average age at diagnosis for multilocular cystic renal cell carcinoma is 51 years, and men are more likely to experience this type of cancer by a ratio of 3:1.
Other risk factors for all types of renal cell carcinoma include:
Smoking Misusing certain pain medications Obesity High blood pressure (hypertension) Family history of kidney cancer Hereditary papillary renal cell carcinoma
Diagnosis
Multilocular cystic renal cell carcinoma can be difficult to diagnose because it often appears as a benign cyst on imaging studies. Tests to diagnose this rare cancer include:
Computed tomography (CT) scan: A CT scan takes detailed pictures of the body and can show where cancerous tumors are growing, as well as how big they are. Magnetic resonance imaging (MRI): An MRI may be recommended to help determine if and where cancer has spread. This is known as metastasis. Biopsy: A kidney biopsy will likely be performed by placing a thin needle into the kidney and taking a tissue sample to examine under a microscope for cancer cells.
Treatment
Multilocular cystic renal cell carcinoma is considered slow-growing cancer with a positive prognosis. This type of cancer rarely if ever spreads or metastasizes. It behaves more like a benign tumor and is thus easier to treat than other types of kidney cancer.
Treatment plans usually involve surgery to remove the cancerous growth. If cancer is in an early stage, your surgeon will likely recommend removing the part of the kidney with the tumor. If the tumor is large or located in the middle of the kidney, the entire kidney may need to be removed.
The two types of surgery include:
Simple nephrectomy: Removal of the entire kidney Nephron-sparing surgery: Removal of part of a kidney, also known as partial nephrectomy
Rarely, other treatment options may include immunotherapy, targeted therapy, and radiation therapy.
Prognosis
Fortunately, the prognosis for multilocular cystic renal cell carcinoma is positive. Cancer cells are usually found only in the kidney and do not tend to spread. Multilocular cystic renal cell carcinoma has the most positive prognosis of all the subtypes of renal cell carcinoma.
Multilocular cystic renal cell carcinoma is known as a low-grade neoplasm. This means that the cells appear almost normal under a microscope. This type of cancer usually has an excellent prognosis because the cells tend to grow and spread slowly.
Coping
Undergoing cancer treatment is an overwhelming experience, and finding ways to cope is essential. Talk with your medical team about your prognosis and what to expect from surgery. Ask about support groups or online communities, as well as financial assistance programs.
The following organizations may be able to help as well:
Action to Cure Kidney Cancer (ACKC): Gives education and support to those being treated for kidney cancer Patient Access Network (PAN) Foundation: Provides additional assistance to low-income patients who have health insurance Social Security Administration: Includes renal cell carcinoma in their Compassionate Allowances Initiative to speed up the processing of disability claims The Assistance Fund: Offers education and financial aid to individuals with chronic diseases
Summary
Multilocular cystic renal cell carcinoma is a very rare type of kidney cancer and is a subtype of clear cell renal cell carcinoma. This low-grade neoplasm usually does not spread beyond the kidney and tends to have a positive diagnosis. Surgery to remove the cancerous area of the kidney or the entire kidney is generally recommended.
A Word From Verywell
Learning that you have cancer may be one of the most stressful moments of your life. It is helpful to remember that while multilocular cystic renal cell carcinoma is rare, it has an excellent prognosis when treated with surgery. Talk with your medical team about your treatment options and available support services.
SmokingMisusing certain pain medications ObesityHigh blood pressure (hypertension) Family history of kidney cancer Hippel-Lindau diseaseHereditary papillary renal cell carcinoma
