dc.contributorUniversidade de São Paulo (USP)
dc.date.accessioned2022-04-29T08:42:23Z
dc.date.accessioned2022-12-20T03:08:56Z
dc.date.available2022-04-29T08:42:23Z
dc.date.available2022-12-20T03:08:56Z
dc.date.created2022-04-29T08:42:23Z
dc.date.issued1990-01-01
dc.identifierArchives of Pathology and Laboratory Medicine, v. 114, n. 8, p. 899-901, 1990.
dc.identifier0003-9985
dc.identifierhttp://hdl.handle.net/11449/230858
dc.identifier2-s2.0-0025372025
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5410992
dc.description.abstractWe describe a case of paraganglioma arising in the spermatic cord, which is an extremely rare location. Immunohistochemical studies characterized two types of cells: (1) polygonal cells expressing neuron-specific enolase, chromogranin A, and synaptophysin and (2) S100 protein-positive sustentacular cells. Electron microscopy revealed that within the cytoplasm of the polygonal cells, there were electron-dense granules whose morphological appearance was consistent with that of neurosecretory granules. Paraganglioma of the spermatic cord may originate from embryonic chromaffin cells that have followed the testis into the scrotum.
dc.languageeng
dc.relationArchives of Pathology and Laboratory Medicine
dc.sourceScopus
dc.titleParaganglioma of the spermatic cord. Report of a case with immunohistochemical and ultrastructural studies
dc.typeArtículos de revistas


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