Adenocarcinoma of parathyroid gland (Q85520): Difference between revisions
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| description / pt-br | description / pt-br | ||
Tumor maligno originado das células parenquimatosas da glândula paratireoide. Está associado aos sintomas de hiperparatireoidismo primário, resultante da produção excessiva do hormônio da paratireoide. Morfologicamente, o diagnóstico diferencial com o adenoma da glândula paratireoide pode ser difícil. Um diagnóstico definitivo de carcinoma é feito apenas na presença de invasão capsular, invasão vascular e / ou invasão perineural. | |||
| description / en | description / en | ||
A malignant tumour arising from the parenchymal cells of the parathyroid gland. It is associated with the symptoms of primary hyperparathyroidism, resulting from the excessive production of parathyroid hormone. Morphologically, the differential diagnosis from parathyroid gland adenoma may be difficult. A definitive diagnosis of carcinoma is made only in the presence of capsular invasion, vascular invasion, and/or perineural invasion. | |||
Revision as of 10:52, 15 August 2026
A malignant tumour arising from the parenchymal cells of the parathyroid gland. It is associated with the symptoms of primary hyperparathyroidism, resulting from the excessive production of parathyroid hormone. Morphologically, the differential diagnosis from parathyroid gland adenoma may be difficult. A definitive diagnosis of carcinoma is made only in the presence of capsular invasion, vascular invasion, and/or perineural invasion.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_821291357 |
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| English | Adenocarcinoma of parathyroid gland |
A malignant tumour arising from the parenchymal cells of the parathyroid gland. It is associated with the symptoms of primary hyperparathyroidism, resulting from the excessive production of parathyroid hormone. Morphologically, the differential diagnosis from parathyroid gland adenoma may be difficult. A definitive diagnosis of carcinoma is made only in the presence of capsular invasion, vascular invasion, and/or perineural invasion. |
