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      Metastatic Renal Cell Carcinoma to the Testis: A Clinicopathologic Analysis of Five Cases

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          Abstract

          The testicular spread of renal cell carcinoma is extremely rare. Five cases of renal cell carcinoma metastatic to the testis are described. The patients ranged from 45 to 81 years of age. Four of the five patients had known renal cell carcinoma. The time intervals between the partial and radical nephrectomies for the primary kidney tumors and the occurrence of testicular metastases ranged from 29 to 34 months. In one patient, the testicular mass was the initial presentation leading to a diagnosis of renal cell carcinoma. There were three ipsilateral metastases, one contralateral metastasis, and one bilateral metastasis. The metastatic deposits ranged in size from 2.0 to 5.7 cm. One case had multiple metastatic tumor nodules. All of the metastatic tumors had clear cell histological features, microscopically concordant with the primary renal cell carcinoma subtype. Three patients died of the disease 17 to 42 months after orchiectomy. One patient is alive with additional metastatic lesions 13 months after orchiectomy. One patient had been free of disease at 87 months after orchiectomy but is now on targeted therapy for an additional metastasis at 93 months after orchiectomy. To date, this report is one of the largest single series of patients with renal cell carcinoma metastatic to the testis, and it has the longest follow-up and survival among all the reported cases.

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          Most cited references29

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          Distant metastasis of renal adenocarcinoma.

          H Saitoh (1981)
          Renal adenocarcinoma in 1451 autopsy cases was classified according to the number of organs involved in distant metastasis, and the mode of metastasis. In cases with single-organ metastasis, lung and lymph node involvement was low (32% and 12%, respectively), but increased as the number of metastatically involved organs increased. Frequency of metastases to the pancreas, heart, and intestine rapidly increased as the number of involved organs increased, while the incidence of metastasis to the brain remained unchanged, regardless of the number of organs involved. A significant correlation was observed between metastases to the lung and organs involved. A significant correlation was observed between metastases to the lung and those to the pulmonary and tracheal lymph nodes, but not between those to the lung and those to the retroperitoneal lymph nodes. While the frequency of metastases to the contralateral kidney and brain was significantly higher in cases with recurrence after nephrectomy than in those who did not undergo nephrectomies, the frequencies of metastases to other organs was similar in these two groups. The number of metastatically involved organs is useful in analyzing the mode of metastasis.
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            Metastatic carcinoma involving the testis. Clinical and pathologic distinction from primary testicular neoplasms.

            Metastatic carcinoma to the testis is unusual. There are only seven previously reported cases in which a testicular mass was the first clinical manifestation of an underlying malignancy. The authors review 127 cases in which the testis was involved by metastatic carcinoma, and describe an additional two patients in whom a malignant testicular mass was the presenting sign of an underlying nontesticular carcinoma. The tumors most commonly reported to metastasize to the testis are: prostate (45 cases), lung (25 cases), melanoma (12 cases), colon (11 cases), kidney (10 cases), stomach (6 cases), and pancreas (5 cases). Neuroblastoma, retinoblastoma, carcinoid tumor, and cancers of the bile duct, ureter, bladder, salivary gland, and thyroid have also involved the testis secondarily. Nineteen patients (15%) had bilateral testicular metastases. Patients with secondary testicular neoplasms were older in general than those with germ cell tumors (mean, 55 years; median, 57 years). Histologically, the presence of extensive lymphatic and vascular invasion and an interstitial pattern, in which the seminiferous tubules are spared, is suggestive of a metastasis. In four of the nine cases (44%) in which testicular enlargement was the first manifestation of an underlying carcinoma the correct pathologic diagnosis was initially missed. Serum alpha-fetoprotein (AFP) and human chorionic gonadotropin (HCG) are occasionally elevated in patients with nontesticular primary tumors, but markedly elevated levels in young patients suggest a nonseminomatous germ cell tumor, as does positive immunoperoxidase staining for AFP and HCG.
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              Immunohistochemistry of germ cell and trophoblastic neoplasms.

              The immunoprofiles of 121 germ cell and trophoblastic neoplasms were defined, using a battery of antibodies against cytokeratin (CK), vimentin (VIM), epithelial membrane antigen (EMA), placental alkaline phosphatase (PLAP), S-100 protein, leukocyte common antigen (LCA), UCHL-1, LN-2, carcinoembryonic antigen (CEA), neuron-specific enolase (NSE), chromogranin A, Leu-7, alpha-fetoprotein (AFP), alpha-1-antitrypsin (AAT), and the beta subunit of human chorionic gonadotropin (BHCG). In addition to 85 neoplasms of testicular origin, the cases included eight ovarian germ cell tumors and 28 extragonadal neoplasms. All tissues had been subjected to formalin fixation and paraffin embedding. Similar immunoreactivity patterns were seen in gonadal and extragonadal neoplasms, gestational and nongestational choriocarcinomas, components of mixed germ cell tumors and their pure counterparts, and metastatic and primary lesions. Placental alkaline phosphatase was a sensitive marker of germ cell differentiation, and expression of this marker in the absence of EMA appeared to be a staining pattern unique to germ cell tumors. Both LCA and S100 were absent in neoplastic germ cells, and thus were useful in differentiating these tumors from malignant lymphoma and malignant melanoma, respectively. Cytokeratin was helpful in distinguishing seminomas/dysgerminomas from nonseminomatous germ cell tumors, although 10% of seminomas showed focal or diffuse cytokeratin reactivity. Finally, 75% of all germ cell neoplasms displayed NSE, calling the specificity of this determinant into question.
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                Author and article information

                Contributors
                Journal
                Case Rep Pathol
                Case Rep Pathol
                CRIPA
                Case Reports in Pathology
                Hindawi
                2090-6781
                2090-679X
                2020
                2 March 2020
                : 2020
                : 9394680
                Affiliations
                1Department of Pathology, BC Cancer Vancouver Centre, Vancouver, BC, Canada
                2Department of Urology, Vancouver General Hospital, Vancouver, BC, Canada
                3Department of Radiology, BC Cancer Vancouver Centre, Vancouver, BC, Canada
                4Department of Pathology, Vancouver General Hospital, Vancouver, BC, Canada
                Author notes

                Academic Editor: Piero Tosi

                Author information
                https://orcid.org/0000-0002-0225-4173
                Article
                10.1155/2020/9394680
                7073490
                32190396
                120939a3-c4e5-4e8c-af09-0edc5f98626e
                Copyright © 2020 Gang Wang et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 8 April 2019
                : 19 February 2020
                Categories
                Case Series

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