Case report highlights the diagnosis of perinephric myxoid pseudotumour in chronic kidney disease using CT imaging, suggesting importance of ancillary techniques to prevent misdiagnosis.
Perinephric myxoid pseudotumour of fat (PMPTF) is a recently defined rare entity with exact pathophysiology yet to be fully elucidated. 1-3 Thought to be non-neoplastic, the current literature demonstrates an association with chronic renal conditions, both non-neoplastic and neoplastic, and even vague regional insults. 3 Here, we describe a case of PMPTF in a male patient in the sixth decade of life, presenting with a perinephric mass found incidentally on CT imaging for renal transplant workup. Macroscopically, it was pedunculated and gelatinous. Microscopy demonstrated a myxoid lesion with interspersed adipocytes and no atypia, arising from perinephric fat. Well-differentiated liposarcoma was an important differential consideration, amongst others, and excluded following negative MDM2 fluorescence in-situ hybridisation. This case illustrates the diagnosis of PMPTF in the appropriate clinical context and the use of ancillary techniques to avoid misdiagnosis leading to over-treatment.
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Zafir et al. (2026) studied this question.
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