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Case Reports
. 2019 Sep 30;12(9):e229293.
doi: 10.1136/bcr-2019-229293.

Metastasis in mixed epithelial stromal tumour of the kidney: a rare presentation

Affiliations
Case Reports

Metastasis in mixed epithelial stromal tumour of the kidney: a rare presentation

Pravin Sambhaji Holkar et al. BMJ Case Rep. .

Abstract

Mixed epithelial stromal tumour of the kidney (MESTK) is a rare genitourinary tract tumour. MESTK is typically seen in perimenopausal women and rarely reported in men and children. MESTK has been included in the WHO renal tumour classification since 2004. Here, we present a case of 50-year-old female patient who underwent left radical nephrectomy for left renal mass. Postoperative positron emission tomography (PET) scan also showed nodal metastasis, for which, she was started on chemotherapy.

Keywords: general surgery; urological cancer; urological surgery; urology.

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Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
A multicystic mass is seen arising on the anterior aspect of left kidney in the mid-region. Multiple enhancing septae are seen along with few areas along the margins.
Figure 2
Figure 2
Gross specimen of nephrectomy showing tumour with solid and cystic appearance.
Figure 3
Figure 3
Photomicrograph showing epithelial component in form of cysts and surrounding stroma resembling ovarian stroma (H&E, ×400).
Figure 4
Figure 4
PET–CT showing an FDG avid subcentimeter sized lymph node in the left para-aortic region near the operative site. Similar metabolically active lymph nodes were also seen in periportal and precaval regions (not shown).

References

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