Onco Wiki / Krankheit

Adenom der Hypophyse

Deterministische Ansicht der Quelle YAML Entität. Klinische Autorität bleibt mit den zitierten Quell-IDs und Rezensenten Sign-off Zustand.

IDDIS-PITUITARY-ADENOMA
ArtErkrankung
Aliase
Kortikotrophes AdenomMEN1-assoziiertes HypophyseadenomNonfunctioning pituitary adenomaPitNETHirntumor der neuroendokrinen HautProlaktinomSomatotroph AdenomАденома гіпофіза
Statusreviewed 2026-05-18 | pending_clinical_signoff
ErkrankungenNone declared
QuellenSRC-NCCN-CNS-2025 SRC-NCCN-NET-2025

Informational support. All recommendations must be verified by a qualified oncologist. Engineering checks are not clinical validation or treatment approval.

Quelle: YAML

icd_o_3_morphology8272/0
icd_o_3_topography["C75.1"]
icd_10D35.2
who_classificationWHO Endokrine und Neuroendokrine Tumore 5 ed (2022) + ZNS 5 end (2021): Klassifikation auf der Grundlage der Linie des pituitären Neuroendocrinen Tumors (PitNET) — Lactotroph / Somatotroph/Corticotroph / Thyrotroph / Gonadotroph / null-Zell

Fähigkeiten

Anmerkungen

Functional adenomas classified by lineage / hormone hypersecretion; treatment is endocrine-cohort-specific: prolactinoma — dopamine agonists (cabergoline > bromocriptine) first-line, surgery for resistant / intolerant; somatotroph (acromegaly) — transsphenoidal surgery first-line, somatostatin analogs (octreotide LAR, lanreotide, pasireotide LAR), GH-receptor antagonist (pegvisomant) for residual; corticotroph (Cushing disease) — surgery, pasireotide, ketoconazole / metyrapone / osilodrostat for cortisol control; nonfunctioning — surgery for mass effect / visual compromise. MEN1 carriers: cascade screening from age 5 (prolactin + IGF-1 + serum Ca + intact PTH + fasting gastrin + pituitary MRI per protocol).

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Therapieschema