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Updated: Feb 9, 2026

Modeling Spontaneous Metastatic Renal Cell Carcinoma mRCC in Mice Following Nephrectomy
Published on: April 29, 2014
New onset hyperglycemia attributed to renal cell carcinoma
Jonathan Gapp1, Muhammad Fazeel Anwar1, Jai Parekh1
1Department of Internal Medicine, Creighton University Medical Center, Omaha, NE, USA.
Severe hyperglycemia in a 61-year-old male resolved after surgical removal of papillary renal cell carcinoma (RCC). This rare paraneoplastic syndrome highlights the importance of investigating new-onset hyperglycemia alongside renal masses.
Area of Science:
- Endocrinology
- Oncology
- Nephrology
Background:
- Severe hyperglycemia, indicated by a rise in hemoglobin A1c from 5 to 11.3 mmol/mol, necessitated insulin therapy.
- A 61-year-old male presented with new-onset severe hyperglycemia, unresponsive to initial management.
- Pre-existing chronic kidney disease workup revealed bilateral renal masses on ultrasound.
Observation:
- Magnetic resonance imaging (MRI) confirmed renal masses suspicious for renal cell carcinoma (RCC).
- The patient underwent partial nephrectomy and cryoablation for papillary type RCC.
- Post-surgical pathology confirmed papillary RCC.
Findings:
- Hyperglycemia resolved completely after tumor resection, allowing discontinuation of insulin therapy.
- The patient required only an oral hypoglycemic agent post-operatively.
- This case suggests a rare paraneoplastic syndrome associated with RCC.
Implications:
- Severe hyperglycemia, in the absence of typical causes and concurrent with a renal mass, may indicate an uncommon paraneoplastic syndrome secondary to RCC.
- Understanding the mechanisms, such as ectopic glucagon production or IL-6 pathways, is crucial for managing such rare presentations.
- This case underscores the importance of a multidisciplinary approach in diagnosing and treating complex endocrine-oncologic conditions.
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