Cystic nephroma

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(Redirected from Renal epithelial stromal tumor)

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Cystic nephroma
Cystic nephroma low mag.jpg
Synonyms Multilocular cystic nephroma
Pronounce N/A
Specialty N/A
Symptoms Abdominal pain, hematuria, palpable abdominal mass
Complications Hypertension, renal impairment
Onset Can occur at any age, but often seen in children and middle-aged adults
Duration Chronic
Types Benign
Causes Unknown
Risks Genetic predisposition, family history
Diagnosis Ultrasound, CT scan, MRI, histopathology
Differential diagnosis Wilms' tumor, multilocular cystic renal cell carcinoma
Prevention None known
Treatment Surgical resection
Medication None specific
Prognosis Excellent with surgical treatment
Frequency Rare
Deaths N/A


Cystic nephroma is a rare, benign kidney tumor that is characterized by multiple cysts of varying sizes. It is also known as multilocular cystic nephroma. This condition is usually diagnosed in children, but it can also occur in adults. The cause of cystic nephroma is unknown.

Symptoms[edit | edit source]

The symptoms of cystic nephroma may vary depending on the size and location of the tumor. Some people with this condition may not have any symptoms. When symptoms do occur, they may include:

Diagnosis[edit | edit source]

The diagnosis of cystic nephroma is usually made based on imaging studies such as ultrasound, computed tomography (CT) scan, or magnetic resonance imaging (MRI). A biopsy of the tumor may also be performed to confirm the diagnosis.

Treatment[edit | edit source]

The treatment for cystic nephroma is usually surgical removal of the tumor. In some cases, partial or total nephrectomy (removal of the kidney) may be necessary. After surgery, regular follow-up is important to monitor for any signs of recurrence.

Prognosis[edit | edit source]

The prognosis for cystic nephroma is generally good, as this tumor is benign and does not spread to other parts of the body. However, recurrence can occur, so regular follow-up is important.

Cystic nephroma gallery[edit | edit source]

See also[edit | edit source]

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Contributors: Prab R. Tumpati, MD