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Updated: May 7, 2026

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Mechanistic Insight into the Development of TNBS-Mediated Intestinal Fibrosis and Evaluating the Inhibitory Effects of Rapamycin
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Renal inflammatory myofibroblastic tumor: a case report
Zhentao Zhang1, Dawei Wang2, Feihu Tang1
1School of Clinical Medicine, Shandong Second Medical University, Weifang, Shandong, China.
Frontiers in Oncology
|May 6, 2026
Summary
Renal inflammatory myofibroblastic tumors (IMT) are rare and diagnosed via histopathology. Surgical resection is the primary treatment, with targeted therapies for advanced cases.
Area of Science:
- Oncology
- Nephrology
- Pathology
Background:
- Renal inflammatory myofibroblastic tumors (IMT) are rare mesenchymal neoplasms.
- These tumors have intermediate malignant potential within the urinary system.
- Clinical and imaging features of renal IMT are nonspecific, making histopathology crucial for diagnosis.
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