Inflammatory pseudotumor of the Kidney
© Selvan et al; licensee BioMed Central Ltd. 2007
Received: 23 January 2007
Accepted: 24 September 2007
Published: 24 September 2007
Inflammatory pseudotumor of the kidney or inflammatory myofibroblastic tumor (IMT) is composed of spindle cells admixed with variable amount of proliferating myofibroblasts, fibroblasts, extracellular collagen, lymphocytes and plasma cells. This mainly affects the urinary bladder or prostate. Renal involvement is rare.
A 56 year-old man was diagnosed with asymptomatic left sided hydronephrosis while being investigated for rheumatoid arthritis. CT scan imaging showed ill defined fascial plains around the kidney and thickening around the renal hilum suggestive of localized inflammatory change. Worsening intermittent left loin pain with increasing hydronephrosis, significant cortical thinning and marked deterioration of renal function necessitated nephrectomy. Macroscopy showed a hydronephrotic fibrotic kidney with microscopy and immunohistochemistry consistent with a histological diagnosis of IMT.
We report a case of an inflammatory pseudotumor of the kidney. It is unique in that the patient presented with painless hydronephrosis followed two years later with progressive deterioration in renal function and worsening loin pain.
Inflammatory myofibroblastic tumor (IMT) or pseudotumor is a rare benign tumor that can be seen in various organs. It is of unknown etiology and difficult to differentiate from malignancy. Histologically, there is evidence of marked proliferation of myofibroblasts, fibroblasts, histiocytes, and plasma cells. There have been no reports of recurrence.
We report a unique case of inflammatory pseudotumor of the kidney; the patient presented with painless hydronephrosis followed two years later with progressive deterioration in renal function and worsening loin pain.
Inflammatory pseudotumour of the kidney or IMT is a disease of young people and unknown etiology, affecting females more than males . Differential diagnoses include malignant tumors such as renal cell carcinoma, sarcomatoid renal cell carcinoma, inflammatory fibrosarcoma, malignant fibrous histiocytoma, low grade neurogenic tumor, myxoid leimyosarcoma  and non-malignant tumors such as angiomyolipoma, xanthogranuloma pyelonephritis and plasma cell granuloma . Patients usually present with haematuria and/or abdominal pain. Clinical examination and radiological investigations are often inconclusive. It is difficult to obtain enough tissue by CT-guided fine needle aspiration to make a definitive histological diagnosis [3, 4] and most diagnoses have been made at the time of surgical intervention.
Histologically, they consist of proliferation of spindle cells admixed with various amounts of lymphocyplasmacytic infiltrate with consistent expression of vimentin and smooth muscle actin [5, 6]. These tumors are strongly positive for CD 34 reactivity. ALK is only positive in 50% and it generally tends to be positive in younger patients . The architectural appearances vary and have been described as a patternless pattern .
IMT generally tend to lack severe cytologic atypia and less mitosis than sarcomas and also generally tend to be negative for p53 which is positive in sarcomas .
We report a rare case of an inflammatory pseudotumour of the kidney. It is unique in that the patient presented with painless hydronephrosis and progressive deterioration in renal function while developing worsening loin pain. We suspect that the inflammatory reaction could have occurred as a consequence of chronic pelvi-ureteric junction obstruction.
We report a rare case of an inflammatory pseudotumor of the kidney. It is unique in that the patient presented with painless hydronephrosis and progressive deterioration in renal function while developing worsening loin pain. We suspect that the inflammatory reaction could have occurred as a consequence of chronic pelvi-ureteric junction obstruction.
Written consent of patient was obtained for publication of this case report
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