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Published on: March 30, 2015
Perinephric Myxoid Pseudotumor of Fat: A Series of 29 Cases Demonstrating Inconsistent Associations With Underlying
Azfar Neyaz1, John S A Chrisinger2, Dimitrios Korentzelos1
1Department of Pathology, University of Pittsburgh, Pittsburgh, PA.
Abstract:
Perinephric myxoid pseudotumor of fat (PMPTF) is a recently characterized lesion typically associated with non-neoplastic renal disease. Its pathogenesis is thought to result from chronic renal "irritation," either due to mass effect from renal carcinoma or inflammation related to benign renal conditions. Prompted by several cases arising in the absence of underlying renal pathology, we conducted a multi-institutional study of 29 mass-forming cases with detailed clinical, histologic, and molecular characterization. We also reviewed 79 published cases to place our findings in a broader context. Histologic slides were reviewed for morphologic and immunohistochemical features. Clinical and follow-up data were obtained through retrospective chart review. The mean age was 67 years (range: 35 to 82), with a strong male predominance (M:F=13.5:1). The average tumor size was 10.3 cm. Liposarcoma was the most common initial diagnosis (n=20). Twelve patients (42%) had non-neoplastic renal disease, 7 (24%) had both non-neoplastic disease and renal cell carcinoma, one (3%) had renal cell carcinoma only, and 9 (31%) had no renal pathology. Histologically, lesions showed mature fat with scattered bland spindle to stellate cells, chronic inflammation, lymphoid aggregates, myxoid change, fat necrosis, hemosiderin, and prominent vasculature; extramedullary hematopoiesis was rare. All tested 28 cases were negative for MDM2 amplification by FISH. Comprehensive targeted NGS (Oncomine) and whole transcriptome sequencing (n=4) did not reveal any pathogenic alterations. Follow-up (n=28; mean, 20 months) showed stable or no disease in 24 cases; 3 patients died of unrelated causes, and one from postoperative complications. PMPTF is a benign, mass-forming lesion that mimics malignancy, particularly well-differentiated liposarcoma. Its occurrence in patients without identifiable renal pathology suggests alternative etiologies. Lack of genomic alterations supports its non-neoplastic nature. Accurate recognition is critical to prevent overtreatment. PMPTF may represent an early-stage reactive process within a broader spectrum of adipose tissue remodeling that includes renal replacement lipomatosis.
Insights
Perinephric myxoid pseudotumor of fat (PMPTF) is a benign lesion mimicking liposarcoma. This study found PMPTF can occur without kidney disease, suggesting alternative causes and supporting its non-neoplastic nature.
Area of Science:
- Pathology
- Oncology
- Genitourinary pathology
Background:
- Perinephric myxoid pseudotumor of fat (PMPTF) is a rare lesion often linked to renal disease.
- Its exact cause and relationship to renal pathology remain unclear.
- Previous studies suggest chronic renal irritation may play a role.
Purpose of the Study:
- To investigate the clinical, histologic, and molecular features of mass-forming PMPTF.
- To determine the association of PMPTF with underlying renal pathology.
- To evaluate the genomic profile of PMPTF and its implications for diagnosis.
Main Methods:
- Multi-institutional retrospective study of 29 PMPTF cases.
- Review of 79 published cases for broader context.
- Histologic and immunohistochemical analysis.
- FISH for MDM2 amplification.
- Next-generation sequencing (NGS) and whole transcriptome sequencing.
Main Results:
- PMPTF occurred in patients with and without renal pathology (31% had no renal pathology).
- Histology showed mature fat with bland spindle cells, inflammation, and myxoid changes.
- No MDM2 amplification or pathogenic genomic alterations were detected.
- Most cases showed stable disease post-diagnosis, with no evidence of recurrence.
Conclusions:
- PMPTF is a benign entity that can mimic malignancy, particularly liposarcoma.
- Its occurrence without renal pathology suggests alternative etiologies.
- The lack of genomic alterations supports a non-neoplastic, possibly reactive, nature.
- Accurate diagnosis is crucial to avoid overtreatment.
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