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Review
. 2017 Dec;96(49):e8807.
doi: 10.1097/MD.0000000000008807.

Inflammatory myofibroblastic tumor of kidney together with ipsilateral perinephric and periureteric fibrosis: A case report and literature review

Affiliations
Review

Inflammatory myofibroblastic tumor of kidney together with ipsilateral perinephric and periureteric fibrosis: A case report and literature review

Zhuolun Sun et al. Medicine (Baltimore). 2017 Dec.

Abstract

Rationale: Both inflammatory myofibroblastic tumor (IMT) and retroperitoneal fibrosis are rare lesions, but kidney involvement is more rare. It is the first study about IMT of the kidney in a patient with perinephric and periureteric fibrosis and we hold that fibroblast proliferation may be an intermediate status in oncogenesis of IMT. But further investigation is necessary in order to better clarify the relationship between fibroblast proliferation and IMT.

Patient concerns: A 54-year-old female presented no positive signs except dull back pain after overwork.

Diagnoses: On the basis of the urinary ultrasonography and computed tomography (CT) scan, we strongly suspected a renal cell carcinoma.

Interventions: Considering the little remaining function of the right kidney and the possibility of malignancy, we performed a laparoscopic right radical nephrectomy.

Outcomes: According to the analysis of the postoperative paraffin section and immunohistochemistry assay, a final diagnosis of IMT and retroperitoneal fibrosis nodules was made.

Lessons: Both IMTs are rare lesions and its etiology and pathogeny are unclear. It is the first study about IMT of the kidney in a patient with perinephric and periureteric fibrosis. This report suggested that fibroblast proliferation may be an intermediate status in oncogenesis of IMT, but further investigation is necessary in order to better clarify the relationship between fibroblast proliferation and IMT. The preoperative diagnosis of renal IMT remains difficult. Preoperative fine-needle aspiration or percutaneous biopsy and intraoperative frozen section were applied to confirm the diagnosis to avoid unnecessary nephrectomy, especially in patients with renal insufficiency, bilateral masses, or a solitary kidney.

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Conflict of interest statement

The authors report no conflicts of interest.

Figures

Figure 1
Figure 1
Computed tomography image of inflammatory myofibroblastic tumor of the kidney showed the presence of a slightly enhanced mass.
Figure 2
Figure 2
Retrograde urography image showed an obvious stenosis at the upper segment of ureter and hydronephrosis.
Figure 3
Figure 3
Postoperative paraffin section showed inflammatory cells and fibroblasts and immunohistochemistry assay was positive for smooth muscle antigen.

References

    1. Bahadori M, Liebow AA. Plasma cell granulomas of the lung. Cancer 1973;31:191–208. - PubMed
    1. Nakamura Y, Urashima M, Nishihara R, et al. Inflammatory pseudotumor of the kidney with renal artery penetration. Radiat Med 2007;25:541–7. - PubMed
    1. Tazi K, Ehirchiou A, Karmouni T, et al. Inflammatory pseudotumors of the kidney: a case report. Annal Urol 2001;35:30–3. - PubMed
    1. Davides KC, Johnson SH3rd, Marshall M, Jr, et al. Plasma cell granuloma of the renal pelvis. J Urol 1972;107:938–9. - PubMed
    1. Aessopos A, Alatzoglou K, Korovesis K, et al. Renal pseudotumor simulating malignancy in a patient with Adamantiades-Behcet's disease: case report and review of the literature. Am J Nephrol 2000;20:217–21. - PubMed

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