Adenocarcinoma of pituitary gland (Q85517): Difference between revisions

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Adenocarcinoma raro com prognóstico desfavorável, originando-se das células adenohipofisárias do lobo anterior da hipófise ou de adenomas pré-existentes. A maioria são neoplasias com função hormonal, geralmente produzindo prolactina ou ACTH. O diagnóstico é baseado na presença de metástases. As síndromes associadas aos carcinomas da glândula pituitária incluem hiperprolactinemia, doença de Cushing e acromegalia.
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A rare adenocarcinoma with poor prognosis, arising from the adenohypophysial cells of the anterior lobe of the pituitary gland or pre-existing adenomas. The majority are hormonally functioning neoplasms, usually producing prolactin or ACTH. The diagnosis is based on the presence of metastases. Syndromes associated with pituitary gland carcinomas include hyperprolactinemia, Cushing disease, and acromegaly.

Revision as of 10:52, 15 August 2026

A rare adenocarcinoma with poor prognosis, arising from the adenohypophysial cells of the anterior lobe of the pituitary gland or pre-existing adenomas. The majority are hormonally functioning neoplasms, usually producing prolactin or ACTH. The diagnosis is based on the presence of metastases. Syndromes associated with pituitary gland carcinomas include hyperprolactinemia, Cushing disease, and acromegaly.
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ID_123783203
    English
    Adenocarcinoma of pituitary gland
    A rare adenocarcinoma with poor prognosis, arising from the adenohypophysial cells of the anterior lobe of the pituitary gland or pre-existing adenomas. The majority are hormonally functioning neoplasms, usually producing prolactin or ACTH. The diagnosis is based on the presence of metastases. Syndromes associated with pituitary gland carcinomas include hyperprolactinemia, Cushing disease, and acromegaly.

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