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In Vivo, Percutaneous, Needle Based, Optical Coherence Tomography of Renal Masses
Published on: March 30, 2015
Multilocular cystic renal cell carcinoma: a rare entity
Atin Singhai1, Suresh Babu, Nidhi Verma
1Department of Pathology, King George's Medical University, Lucknow, Uttar Pradesh, India. atinsinghai@yahoo.com
BMJ Case Reports
|April 6, 2013
Summary
Multilocular cystic renal cell carcinoma (MCRCC), a rare kidney cancer subtype, typically shows a favorable prognosis. This case report details a patient with MCRCC who recovered well after nephrectomy.
Area of Science:
- Nephrology
- Oncology
- Pathology
Background:
- Multilocular cystic renal cell carcinoma (MCRCC) is a rare subtype of clear cell renal cell carcinoma.
- MCRCC accounts for only 1-2% of renal neoplasms and is associated with a favorable prognosis.
Observation:
- A 60-year-old male presented with an abdominal lump, leading to a suspicion of renal malignancy.
- Diagnostic criteria for MCRCC include an encapsulated expansile mass, entirely cystic interior with septa, and septa containing clear epithelial cells.
Findings:
- The patient underwent a nephrectomy for suspected renal malignancy.
- Postoperative follow-up at 3 months showed the patient was well, consistent with a favorable outcome.
Implications:
- This case highlights the importance of recognizing MCRCC's distinct pathological features and favorable prognosis.
- Early diagnosis and surgical management, such as nephrectomy, appear effective for MCRCC.
- Further research into MCRCC can refine diagnostic criteria and treatment strategies.
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