ReviewSao Paulo medical journal = Revista paulista de medicina2012
Paraganglioma of seminal vesicle and chromophobe renal cell carcinoma: a case report and literature review.
Review in Sao Paulo medical journal = Revista paulista de medicina, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
5 citing papers in PubMed, 15 citations in OpenAlex.
- Primary Paraganglioma of Seminal Vesicle.Chinese medical journal · 2016Article
- [Succinate dehydrogenase (SDH)-deficient renal cell carcinoma].Der Pathologe · 2016Article
- Paraganglioma of the Seminal Vesicle Case Report and Review of the Literature.Journal of endourology case reports · 2016Article
- Paraganglioma of the vagina: a case report and review of the literature.OncoTargets and therapy · 2014Article
- Primary paraganglioma of seminal vesicle.International journal of surgery case reports · 2013Article
Corrections and comments
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Authors and funding
9 authors at 1 institution in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
contextExtra-adrenal paragangliomas are rare tumors that have been reported in many locations, including the kidney, urethra, urinary bladder, prostate, spermatic cord, gallbladder, uterus and vagina. CASE REPORT: This report describes, for the first time to the best of our knowledge, a primary paraganglioma of the seminal vesicle occurring in a 61-year-old male. The patient presented persistent arterial hypertension and a previous diagnosis of chromophobe renal cell carcinoma. It was hypothesized that the seminal vesicle tumor could be a metastasis from the chromophobe renal cell carcinoma. Immunohistochemical characterization revealed expression of synaptophysin and chromogranin in tumor cell nests and peripheral S100 protein expression in sustentacular cells. Succinate dehydrogenase A and B-related (SDHA and SDHB) expression was present in both tumors.
conclusionsNo genetic alterations to the VHL and SDHB genes were detected in either the tumor tissue or tissues adjacent to the tumor, which led us to rule out a hereditary syndrome that could explain the association between paraganglioma and chromophobe renal cell carcinoma in a patient with arterial hypertension.
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