- Case report
- Open Access
Mixed epithelial and stromal tumor of the kidney: report of eight cases and literature review
© Wang et al.; licensee BioMed Central Ltd. 2013
- Received: 10 February 2013
- Accepted: 7 August 2013
- Published: 20 August 2013
Mixed epithelial and stromal tumor of the kidney (MESTK) is the term given to a class of uncommon biphasic tumors of the kidney, with few reported cases. We describe eight cases of MESTK with detailed clinicopathological data and follow-up information. With this report, we hope to increase clinical awareness that MESTK should be considered as one of the possible diagnoses for cystic renal mass, especially in peri-menopausal women or those who receive hormone therapy. In addition, regular follow-up is necessary for the any cases with malignant potential.
- Mixed epithelial and stromal tumor
Mixed epithelial and stromal tumor of the kidney (MESTK), is a rare kidney tumor . The tumor was first identified by Michal and Syrucek in 1998  and has been ariously termed ‘cystic hamartoma of the renal pelvis,’ ‘adult mesoblastic nephroma,’ ‘cystic nephroma,’ ‘mature nephroblastic tumor’ or ‘cystic partially differentiated nephroblastoma.’ To date, approximately 100 cases have been reported , with most of these reports focusing on the pathological and radiological features of the tumors. In this paper, we report detailed clinicopathological findings and clinical outcomes of a series of MESTK cases, and review the related literature.
During the period 2005 to 2012, eight cases with a diagnosis of MESTK were identified from the surgical pathology files of the urology department at our hospital. The clinical information and pathological data were obtained from the medical records, and demographic information, presenting symptoms, treatment, tumor size, immunohistochemical staining profiles, and scheduled follow-up data were collected.
Clinicopathologic features of 8 patients with mixed epithelial and stromal tumor of the kidney
Tumor size, cm
Length of follow-up, months
Postive for ER and PR; negative for CD10
Positive for CK, PR, SMA, desmin, and vimentin
Positive for ER, PR, CK, vimentin, and CD10
Positive for CK, CD10, ER, PR, vimentin, and desmin; negative for Melan-A and HMB-45
Positive for ER and PR; negative for CD10
Positive for SMA, desmin, CD10, PR; negative for HMB-45
Positive for desmin, CD99, and S-100; negative for HMB-45, SMA, Myo-D1, CD31, and CD3
Positive for ER, PR, desmin, and CD10; negative for HMB-45
The patients were followed up for a mean duration of 28 months (4 to 50 months); at the end of which, all eight patients were alive without any evidence of recurrence or metastasis.
MESTK, which was included in the WHO 2004 renal tumor classification, is a rare and distinctive kidney tumor composed of both epithelium and stroma with solid and cystic architecture . As reported previously [5, 6], MESTK occurs predominantly in middle-aged peri-menopausal women and older women, especially those with a history of estrogen therapy, which indicates an underlying association between estrogen and MESTK. However, there are some rare male [5, 7–9] or pediatric [7, 10, 11] cases. In our series, most of the female patients were middle-aged peri-menopausal to older women. This implies that a disturbed hormonal environment contributes to the pathogenesis of MESTK; however, we did not observe any correlation between estrogen therapy and MESTK, as all the patients denied histories of hormonal therapy. Thus, whether estrogen therapy is indeed associated with MESTK warrants further study.
The most common clinical presentations of MESTK include palpable abdominal mass, flank pain, and hematuria. However, in our series, almost all the cases were asymptomatic, and wee detected only incidentally during regular investigation. Radiologically, MESTK appears as well-circumscribed multi-septate cystic mass with solid components and thick or thin septa on both CT and magnetic resonance imaging scans, and thus can mimic complex renal cyst or cystic nephroma [12–14]. Lack of any typical radiological features makes it difficult to establish a precise diagnosis of MESTK preoperatively , thus, most cases are confirmed postoperatively, as in our series.
Histologically, MESTK is a dimorphic tumor composed of cysts and tubules embedded in the spindle cell stroma. The histogenesis of MESTK is unknown, and it has been proposed that both components of the tumor, stromal and epithelial, are neoplastic  and probably arise from a common cell of origin . Miscroscopically, the stroma may resemble ovarian stroma, both morphologically and immunohistochemically (Figure 2B,C), and is composed of clusters of tubules or cystically dilated glands with variable lining . Immunohistochemically, the epithelial components are usually positive for epithelial membrane antigen and cytokeratin. Spindle cells usually show diffusely and strongly positive immunostaining with desmin (Figure 2D), smooth muscle actin, and vimentin (Figure 2E). In addition, there is a high frequency of estrogen and progesterone receptor present in the nuclei of the spindle cells (Figure 2F). The distinctive ER and PR expression pattern seems to support the hypothesis that hormonal hyperstimulation contributes to tumorigenesis of MESTK.
MESTK used to be categorized as a benign renal tumor without recurrence or metastasis. However, malignant transformation of MESTK has been recently recognized, and a small number of aggressive cases with varied transformation have been described in the literature [8, 9, 18–21]. All of these malignant cases were female patients with the exception of one male patient reported by Suzuki et al. [8, 22]. The prognosis for malignant MESTK varies from cases to cases, with half of the reported cases considered to have a dismal prognosis. There is no established predictor for prognosis, thus the histogenesis and clinical behavior of MESTK warrants further study.
MESTK is a rare clinical entity. It is generally considered to be a benign tumor with good prognosis, but there is malignant potential. MESTK should be considered as a possible diagnosis in cases of cystic renal mass, especially in peri-menopausal women or those who have received hormonal therapy.
Written informed consent was obtained from the patient for publication of this report and any accompanying images.
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