Abstract:Inflammatory pseudotumor (IPT) is a quasineoplastic lesion that most commonly involves the lung and the orbit; kidney involvement is rare. We report a case of inflammatory pseudotumor of the kidney. The patient was a 61-year-old man who presented with no symptoms. Nonenhanced computed tomography (CT) demonstrated an ill-defined, isodensity mass measuring 3.5 cm in the lower portion of the left kidney. Contrast-enhanced CT showed that branches of the renal artery without encasement penetrated the tumor; there w… Show more
“…2,6,7 The clinical findings of renal IMT include flank pain, hematuria, fever, growth retardation, weight loss, microcytic hypochromic anemia, and thrombocytosis. However, it may be asymptomatic without any signs.…”
Renal inflammatory myofibroblastic tumor (IMT) is an extremely rare lesion especially in children. This report describes a case of renal IMT accompanied by multiple lung nodules mimicking Wilms tumor with lung metastasis in a 3-year-old boy. To our knowledge, this is a unique case of IMT which has not been reported in the literature previously.
“…2,6,7 The clinical findings of renal IMT include flank pain, hematuria, fever, growth retardation, weight loss, microcytic hypochromic anemia, and thrombocytosis. However, it may be asymptomatic without any signs.…”
Renal inflammatory myofibroblastic tumor (IMT) is an extremely rare lesion especially in children. This report describes a case of renal IMT accompanied by multiple lung nodules mimicking Wilms tumor with lung metastasis in a 3-year-old boy. To our knowledge, this is a unique case of IMT which has not been reported in the literature previously.
“…Although we did not proceed with magnetic resonance imaging (MRI), this modality is similar to contrast-enhanced CT. IMTs typically appear as low signal intensity on T2-weighted images and highly variable on T1-weighted images [10]. This modality is less attractive in the setting of any renal dysfunction given the gadolinium-associated nephrogenic systemic fibrosis [11].…”
“…US of IPT in other locations has demonstrated a variable pattern of echogenicity with illdefined or well-circumscribed margins. On CT scanning, renal IPT can appear as a mass showing low attenuation, and delayed enhancement has been observed, probably because of the accumulation of extravascular contrast media in the fibrotic component of the lesion [21]. However, there is considerable heterogeneity in the CT appearance of these lesions.…”
Section: Discussionmentioning
confidence: 99%
“…However, there is considerable heterogeneity in the CT appearance of these lesions. Renal IPT on MRI usually displays itself as a variable signal intensity lesion on T1-weighted images and low signal intensity on T2-weighted images [21]. The preoperative recognition of renal IPT is important to avoid unnecessary nephrectomy especially in the setting of bilateral involvement where nephrectomies would render the patient anephric and dialysis dependent.…”
Section: Discussionmentioning
confidence: 99%
“…Differential diagnosis of renal IPT may include renal cell carcinoma (RCC), transitional cell carcinoma of the renal pelvis, malignant lymphoma, xanthogranulomatous pyelonephritis and angiomyolipoma with minimal fat [21]. Current radiological modalities will detect a mass lesion or an enlarged kidney but have limited utility in differentiating between IPT and other malignant tumours.…”
Inflammatory pseudotumour (IPT) is a rare disease of unknown cause that most commonly involves the lung but can occur in almost any site in the body. Occurrence in the kidneys is very rare and bilateral renal involvement even rarer. There are 34 previously reported cases in the English-language medical literature between 1966 and 2008. Herein we report a case of IPT infiltrating both kidneys. We have also reviewed the clinical features, radiological findings, treatment and outcome of renal IPT. Clinical features at presentation are commonly non-specific. Features on imaging are inadequate to make a diagnosis of IPT or to clearly distinguish it from malignancy. Consequently diagnosis has frequently been made after nephrectomy and on a few occasions with the aid of percutaneous or open biopsies. The majority of renal IPT (83%) have been treated with nephrectomy and those cases with bilateral IPT have received corticosteroids.
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