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Metanephric adenosarcoma: a rare case with immunohistochemistry and molecular analysis

Abstract

Background

Metanephric neoplasms comprised a spectrum of kidney tumors containing renal epithelial or stromal cells or both, including metanephric adenoma, metanephric stromal tumor, and metanephric adenofibroma. The majority of cases were benign; only one case of "metanephric adenosarcoma" had been reported in the English literature.

History

We present the case of a 69-year-old man who developed a neoplasm composed of renal epithelial component identical to metanephric adenoma combined with malignant spindle-cell stroma. The epithelial component was positive for CD57, AE1/AE3, but negative for WT-1, CD56, SYN, and CgA; whereas the sarcomatous component was negative for epithelial markers, SMA, Caldesmon, MyoD1, Myogenin, and S-100; and positive for vimentin, CD10, and WT1 focally. No specific sarcoma differentiation was apparent in the stroma by immunohistochemistry, and no SYT-SS18 rearrangement or BRAF mutation was detected by molecular analysis.

A diagnosis of metanephric adenosarcoma was made because of the morphological features and immunohitochemistry and molecular pathology analysis.

Clinical significance

We believe that metanephric adenosarcoma should be in the expanded spectrum of metanephric neoplasia as a malignant stromal variant.

Conclusions

We report a rare case of metanephric adenosarcoma with immunohistochemistry and molecular analysis and emphasize the histopathologic features and differential diagnosis of the rare lesion to promote a better and broader understanding of this less understood subject.

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Background

Metanephric neoplasms, as uncommon renal tumors [1], have so far been reported to encompass metanephric adenoma (purely epithelial neoplasm), metanephric stromal tumor (purely stromal tumor), and metanephric adenofibroma (biphasic tumor). Most of these tumors have been known for their benign behavior. Before present report, only one case of "metanephric adenosarcoma" was described by M. M. Picken et al. as a metanephric tumor with malignant stroma [2]. Our case represents the second report of this lesion in the literature with immunohistochemistry and molecular pathologic analysis. The study was approved by the Ethics Committee of Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. Written informed consent was obtained from the patient prior to death.

Case report

A 69-year-old, previously healthy Chinese man underwent a routine physical examination three months ago, and a mass was discovered in his left kidney with ultrasound examination and computed tomography (Figure 1 A and B). Based on these findings, a clinical diagnosis of a malignant tumor of uncertain type with invasion of splenic hilum and adjacent peritoneum indicated a need for total left nephrectomy. The patient was taken up for surgery. Left kidney resection was performed subsequently as well as spleen and part of peritoneum.

Figure 1
figure 1

Radiological features of the tumor. (A) Ultrasound examination showed a space-occupying mass of low echogenicity within irregular margin. (B) Computed tomography showed a large mass in the left kidney.

Grossly, there was an 11 cm × 8 cm grey white, hard solid mass in the renal parenchyma cross section without cysts (Figure 2). Several hard nodes could be touched in adipose tissue of hilum of spleen and peritoneum. Histopathological examination of the mass showed a biphasic tumor composed of benign epithelium and malignant spindle shaped mesenchymal cells. Similar morphological features were found in the soft tissue in hilum of spleen and peritoneum.

Figure 2
figure 2

Macroscopic features of the kidney. There was an 11 cm × 8 cm grey white, hard solid mass in the renal parenchyma cross section without cysts.

The patient died of infection and multisysterm organ failure approximately two weeks after the surgery.

Methods

Surgical specimen was fixed in 10% buffered neutral formalin and paraffin sections were stained with hematoxylin and eosin.

Immunostaining was performed by an enhancement method based on repetitive microwave heating of slides that were placed into 0.01 M citrate buffer at pH 6.0. A panel of antibodies (Table 1) was used. Binding of primary antibodies was visualized with an Envision two-step method. Diaminobenzidine was used as the chromogen. Nuclei were stained with Mayer's hematoxylin. Appropriate positive and negative controls were included.

Table 1 Antibodies and dilutions used in the evaluation of metanephric adenosarcoma of the kidney

For fluorescence in situ hybridization (FISH), paraffin-embedded 5-μm sections were deparaffinized and the locus-specific probe (Vysis LSI SYT [18q11.2] Dual-Color, Break-Apart Rearrangement Probe) was used according to the manufacturer's protocol. The fluorescence signals were analyzed using an Olympus BX51 fluorescence microscope (Olympus, Tokyo, Japan) equipped with appropriate filters and imaged using Vysis software. At least 100 cells were scored.

For BRAF mutation analysis, paraffin-embedded tissue samples were macrodissected to remove stromal contamination and to ensure tumor cellularity of ≥80%. Briefly, DNA extracted from the case was amplified and sequenced, using the BRAF Pyro Kit (QIAGEN) designed to detect mutations in codon 600. The kit was used according to the manufacturer's instructions. GTCTCAGTCGTATGTAGTCTAG was used as the nucleotide dispensation order.

Results

Microscopically, the unencapsulated tumor consisted of epithelium and stroma components (Figure 3A and B). The relative proportion of stroma to epithelium in the sections varied over a wide range. The two components were frequently intimately associated with each other in the tumor with sharp border. Some areas were almost entirely composed of epithelium identical to MA (Figure 3C). Others were predominantly stromal, identical to high-grade sarcomatous tumor (Figure 3D).

Figure 3
figure 3

Histopathological features of the tumor. The unencapsulated tumor consisted of epithelium and stroma components. (A) Some areas were predominantly composed of epithelium identical to metanephric adenoma (H & E, ×200); (B) some areas were predominantly stromal, identical to high-grade sarcomatous tumor (H & E, ×200); (C) there were hypercellular uniform cells in solid-acini pattern, and the cells were small, round and tightly packed in MA area (H & E, ×400). (D) There were highly cellular, consisting of polymorphic spindle cells with obvious nuclear atypia and frequent mitosis in sarcomatous area (H & E, ×400).

In benign epithelium area, there were hypercellular uniform cells in solid-acini pattern, Papillary architecture could be seen focally, and no Ductal and glomeruloid structures could be seen. No psammoma bodies or osseous metaplasia were observed either. Tumors cells were small, round and tightly packed. Motitic figures were rare and absent. There were no atypical ones either. In malignant stroma area, there were highly cellular, consisting of polymorphic spindle cells with obvious nuclear atypia and frequent mitosis (16/10 high power fields).

Immunohistochemical results showed that the epithelial component was positive for CD57 (Figure 4A), AE1/AE3 (Figure 4G), cytokeratin (CK) 7, epithelial membrane antigen (EMA) (Figure 4C) and CD117 (Figure 4F); other markers including WT-1 (Figure 4B), CD10, CD56, synaptophysin (Syn), Chromogranin A (CgA), CD34 and α-inhibin were negative. The stromal spindle cells were positive for Vimentin (Figure 4D) and CD10 (Figure 4E), and scattered WT-1 staining (Figure 4B), but negative for smooth muscle actin (SMA), Caldesmon, Desmin, MyoD1, Myogenin, S-100, HMB45, MelanA, CD99 and TFE3. The Ki-67 labeling indices were up to 60% in sarcomatous element and <1% in epithelial element (Figure 4H), respectively.

Figure 4
figure 4

Immunohistochemical findings of the biphasic tumor: (A) CD57; (B) WT1; (C) EMA; (D) Vimentin; (E) CD10; (F) CD117; (G) AE1/AE3; (H) Ki67. (A-H, ×200).

FISH analysis for synovial sarcoma showed negative result since more than 90% of the counted cells didn't show separated green and orange signals indicative of rearrangement of the SYT gene. Mutation analysis showed that no BRAF V600E mutations were detected in this case.

Discussion

Metanephric neoplasms comprised a spectrum of kidney tumors containing renal epithelial or stromal cells or both [1],[3]. The majority of cases are usually benign without atypical histological features in not only epithelial component but also stromal one; Metanephric adenoma (MA) is a common subtype in previous reports [4]-[6]. Rare malignant or metastatic diseases have been reported [7]-[9]. As we known by checking previous references, only one case of metanephric neoplasm with malignant stroma, named as "metanephric adenosarcoma", was reported in 2001 [2]. Here we believe that this biphasic tumor we present is the second case of metanephric adenosarcoma.

Microscopically, the biphasic tumor has two components, one is epithelial element, which composed of solid or tightly packed small, monotonous, and round acini and focal papillary structures; tumor cells possessed scant cytoplasm, usually pale or light pink, with small uniform nuclei, delicate chromatin, and absent or inconspicuous nucleoli. These morphological features favor the diagnosis of MA. The epithelial component positive for CD57 also gave a valuable implication of MA although there was no immunohistochemical profile specific for metanephric neoplasia [10]-[12]. However, the epithelial component was negative for WT-1 immunohistochemically [10],[13]. It was different from a majority of reports of MA with WT-1positive staining. According to Oligac's report, 30% of MA cases he reviewed shown WT-1 negative staining because of different WT-1 antibodies application [12]. We believe that the histological features and immunohistochemical profile of epithelial components were identical to MA in our case.

To date, there is no special molecular pathology analysis used as diagnostic one for MA [14],[15]. Recently Choueiri TK et al. confirmed BRAF V600E mutations were present in approximately 90% of all MA cases [16], serving as a potential valuable diagnostic tool in the differential diagnosis, but there was no BRAF mutation in our case.

The stromal element was composed of spindle cells with sarcomatous features. The cells were elongated with abundant cytoplasm and irregular nuclei, hyperchromatic chromatin, and plenty of atypical mitotic figures, and necrosis was not identified. The histological features of stroma were identical to high-grade sarcoma. Immunohistochemistry showed that the malignant stroma revealed no specific differentiation direction with Vimentin and CD10 positive staining, but others including SMA, Caldesmon, Desmin, MyoD1, Myogenin, S-100, HMB45, MelanA and CD99, were negative.

Because the mass was a morphologically biphasic tumor in kidney, we considered the following as differential diagnoses of this tumor base on gross and microscopic resemblance: mixed epithelial and stromal tumor (MEST) with malignant transformation, adult nephroblastoma, and renal synovial sarcoma (SS) and sarcomatoid renal cell carcinoma.

MEST is a rare adult renal neoplasm and microscopic analog of our case. The tumor is ordinary benign one, although some malignant transformation has been reported [17],[18]. Our case differs from MEST with malignant transformation by the absence of multiple cysts macroscopically and microscopically and lack of hobnail appearance of the epithelial cells. A cystic renal tumor consisting of benign epithelial and malignant stromal components named "adenosarcoma" was reported recently, and the author believed that it was a novel entity [19]. We thought our case was a different one because it had no cystic change. Diagnosis of adult nephroblastoma could not be made because the tumor had no typical triphasic pattern morphologically and negative WT1 staining either. Primary synovial sarcoma (SS) in kidney is a rare distinct entity which is potentially a true biphasic tumor [20]. The epithelial component in current tumor lacked the cellular atypia associated with biphasic SS, and the stromal elements were highly pleomorphic with distinct nucleoli in contrast to the rather monomorphic spindle cells with inconspicuous nucleoli in typical SS. Immunohistochemistry results also contradicted the diagnosis of SS. FISH analysis showed no rearrangement of the SYT gene, which did not support the diagnosis of synovial sarcoma either. Sarcomatoid Renal Cell Carcinoma can be ruled out since there was no carcinomatous component and CD10-/CD57 + profile of epithelial element.

Conclusions

In summary, we believe the macroscopic, histopathologic features of our case most closely resemble the metanephric adenosarcoma as M. M. Picken et al. named in 2001, and metanephric adenosarcoma should be in the expanded spectrum of metanephric neoplasia as a malignant stromal variant. The diagnosis of metanephric adenosarcoma, an extremely rare malignant renal tumor, required the incorporation of clinical information, histopathologic features, related markers IHC staining and molecular pathology analysis.

Consent

Written informed consent was obtained from the patient for the publication of this report and any accompanying images.

Authors' contributions

TFS carried out the molecular experiments, TFS, PCZ performed image observation, TFS, PCZ analyzed the data, and FY participated in providing the clinical information and histological observation. TFS, PCZ drafted the manuscript. All authors read and approved the final manuscript.

References

  1. Argani P: Metanephric neoplasms: the hyperdifferentiated, benign end of the Wilms tumor spectrum?. Clinics in laboratory medicine. 2005, 25: 379-392. 10.1016/j.cll.2005.01.002.

    Article  PubMed  Google Scholar 

  2. Picken MM, Curry JL, Lindgren V, Clark JI, Eble JN: Metanephric adenosarcoma in a young adult: morphologic, immunophenotypic, ultrastructural, and fluorescence in situ hybridization analyses: a case report and review of the literature. The American journal of surgical pathology. 2001, 25: 1451-1457. 10.1097/00000478-200111000-00016.

    Article  PubMed  CAS  Google Scholar 

  3. Kuroda N, Tol M, Hiroi M, Enzan H: Review of metanephric adenoma of the kidney with focus on clinical and pathobiological aspects. Histology and histopathology. 2003, 18: 253-257.

    PubMed  CAS  Google Scholar 

  4. Jones EC, Pins M, Dickersin GR, Young RH: Metanephric adenoma of the kidney. A clinicopathological, immunohistochemical, flow cytometric, cytogenetic, and electron microscopic study of seven cases. The American journal of surgical pathology. 1995, 19: 615-626. 10.1097/00000478-199506000-00001.

    Article  PubMed  CAS  Google Scholar 

  5. Granter SR, Fletcher JA, Renshaw AA: Cytologic and cytogenetic analysis of metanephric adenoma of the kidney: a report of two cases. American journal of clinical pathology. 1997, 108: 544-549.

    PubMed  CAS  Google Scholar 

  6. Galmiche L, Vasiliu V, Poiree S, Helenon O, Casanova JM, Brousse N: Diagnosis of renal metanephric adenoma: relevance of immunohistochemistry and biopsy. Annales de pathologie. 2007, 27: 365-368. 10.1016/S0242-6498(07)78275-5.

    Article  PubMed  Google Scholar 

  7. Renshaw AA, Freyer DR, Hammers YA: Metastatic metanephric adenoma in a child. The American journal of surgical pathology. 2000, 24: 570-574. 10.1097/00000478-200004000-00012.

    Article  PubMed  CAS  Google Scholar 

  8. Drut R, Drut RM, Ortolani C: Metastatic metanephric adenoma with foci of papillary carcinoma in a child: a combined histologic, immunohistochemical, and FISH study. International journal of surgical pathology. 2001, 9: 241-247. 10.1177/106689690100900313.

    Article  PubMed  CAS  Google Scholar 

  9. Pins MR, Jones EC, Martul EV, Kamat BR, Umlas J, Renshaw AA: Metanephric adenoma-like tumors of the kidney: report of 3 malignancies with emphasis on discriminating features. Archives of pathology & laboratory medicine. 1999, 123: 415-420.

    CAS  Google Scholar 

  10. Muir TE, Cheville JC, Lager DJ: Metanephric adenoma, nephrogenic rests, and Wilms' tumor: a histologic and immunophenotypic comparison. The American journal of surgical pathology. 2001, 25: 1290-1296. 10.1097/00000478-200110000-00010.

    Article  PubMed  CAS  Google Scholar 

  11. Fischer EG, Carney JA, Anderson SR, Klatt EC, Lager DJ: An immunophenotypic comparison of metanephric metaplasia of Bowman capsular epithelium with metanephric adenoma, Wilms tumor, and renal development: a case report and review of the literature. American journal of clinical pathology. 2004, 121: 850-856. 10.1309/RCT9FVUMVN2UC2HB.

    Article  PubMed  Google Scholar 

  12. Olgac S, Hutchinson B, Tickoo SK, Reuter VE: Alpha-methylacyl-CoA racemase as a marker in the differential diagnosis of metanephric adenoma. Modern pathology: an official journal of the United States and Canadian Academy of Pathology, Inc. 2006, 19: 218-224. 10.1038/modpathol.3800520.

    Article  CAS  Google Scholar 

  13. Gatalica Z, Grujic S, Kovatich A, Petersen RO: Metanephric adenoma: histology, immunophenotype, cytogenetics, ultrastructure. Modern pathology: an official journal of the United States and Canadian Academy of Pathology, Inc. 1996, 9: 329-333.

    CAS  Google Scholar 

  14. Brunelli M, Eble JN, Zhang S, Martignoni G, Cheng L: Metanephric adenoma lacks the gains of chromosomes 7 and 17 and loss of Y that are typical of papillary renal cell carcinoma and papillary adenoma. Modern pathology: an official journal of the United States and Canadian Academy of Pathology, Inc. 2003, 16: 1060-1063. 10.1097/01.MP.0000090923.50509.55.

    Article  Google Scholar 

  15. Pesti T, Sukosd F, Jones EC, Kovacs G: Mapping a tumor suppressor gene to chromosome 2p13 in metanephric adenoma by microsatellite allelotyping. Human pathology. 2001, 32: 101-104. 10.1053/hupa.2001.21132.

    Article  PubMed  CAS  Google Scholar 

  16. Choueiri TK, Cheville J, Palescandolo E, Fay AP, Kantoff PW, Atkins MB, McKenney JK, Brown V, Lampron ME, Zhou M, Hirsch MS, Signoretti S: BRAF Mutations in Metanephric Adenoma of the Kidney. European urology. 2012, 62: 917-922. 10.1016/j.eururo.2012.05.051.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  17. Adsay NV, Eble JN, Srigley JR, Jones EC, Grignon DJ: Mixed epithelial and stromal tumor of the kidney. The American journal of surgical pathology. 2000, 24: 958-970. 10.1097/00000478-200007000-00007.

    Article  PubMed  CAS  Google Scholar 

  18. Jung SJ, Shen SS, Tran T, Jun SY, Truong L, Ayala AG, Ro JY: Mixed epithelial and stromal tumor of kidney with malignant transformation: report of two cases and review of literature. Human pathology. 2008, 39: 463-468. 10.1016/j.humpath.2007.08.008.

    Article  PubMed  CAS  Google Scholar 

  19. Sameshima N, Marutsuka K, Tsukino H, Kamoto T, Kono S, Asada Y: So-called `adenosarcoma' of the kidney a novel adult renal tumor with a cystic appearance. Pathology international. 2011, 61: 313-318. 10.1111/j.1440-1827.2011.02653.x.

    Article  PubMed  Google Scholar 

  20. Kim DH, Sohn JH, Lee MC, Lee G, Yoon GS, Hashimoto H, Sonobe H, Ro JY: Primary synovial sarcoma of the kidney. The American journal of surgical pathology. 2000, 24: 1097-1104. 10.1097/00000478-200008000-00007.

    Article  PubMed  CAS  Google Scholar 

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Su, T., Yan, F. & Zhu, P. Metanephric adenosarcoma: a rare case with immunohistochemistry and molecular analysis. Diagn Pathol 9, 179 (2014). https://doi.org/10.1186/s13000-014-0179-7

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