2006
DOI: 10.1007/s12022-006-0004-2
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Histopathology and immunohistochemistry of adrenal medullary tumors and paragangliomas

Abstract: Paragangliomas arise from sympathetic or parasympathetic paraganglia and should now be defined by their site and type. The term pheochromocytoma is reserved for intra-adrenal tumors. This short review discusses the gross and microscopic features, the immunohistochemical profile, the problem of recognizing malignant potential, and the rare instances where a differential diagnosis has to be considered.

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Cited by 32 publications
(41 citation statements)
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“…Immunohistochemistry is commonly used to differentiate adrenal medullary tumors from cortical or extra-adrenal tumors (McNicol, 2006). Markers commonly used to differentiate pheochromocytomas include CGA, SYN and neuron-specific enolase (NSE) (Feldman and Eiden, 2003;McNicol, 2006).…”
Section: Discussionmentioning
confidence: 99%
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“…Immunohistochemistry is commonly used to differentiate adrenal medullary tumors from cortical or extra-adrenal tumors (McNicol, 2006). Markers commonly used to differentiate pheochromocytomas include CGA, SYN and neuron-specific enolase (NSE) (Feldman and Eiden, 2003;McNicol, 2006).…”
Section: Discussionmentioning
confidence: 99%
“…Markers commonly used to differentiate pheochromocytomas include CGA, SYN and neuron-specific enolase (NSE) (Feldman and Eiden, 2003;McNicol, 2006). Neuroendocrine markers like CGA, NSE and SYN are typically positive in cases of pheochromocytoma, particularly with CGA, which is reported to stain 100% of pheochromocytomas (McNicol, 2006). CGA is the major secreted protein of the adrenal medulla and play an important role in binding and aggregating intracellular calcium (Feldman and Eiden, 2003).…”
Section: Discussionmentioning
confidence: 99%
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“…Zellatypien, hoher Mitose-Index, Gefäß-einbrüche oder lokale Infiltration des retroperitonealen Fettgewebes können zwar Hinweise für Malignität sein, sind jedoch nicht als sichere Malignitätskriterien anerkannt [22,36] [19,48]. Symptomfreie Phäochromozytome sind selten und v. a. bei Verwandten von Patienten mit familiärem Phäochromo-zytom zu beobachten.…”
Section: Epidemiologieunclassified
“…[8][9][10] The distant metastases are usually of hematologic origin, mostly involving bone, liver and lung. Since metastasis represents the only accepted criterion for malignancy, it is important to distinguish between metastasis and multifocality which may occur, especially in inherited disorders.…”
mentioning
confidence: 99%