EOD Primary Tumor
This input is used for staging
Notes
**Note:** This is a new schema for pheochromocytomas (PHs) and paragangliomas (PGs), which are rare neuroendocrine tumors originating in the paraganglia. Pheochromocytomas originate in the adrenal medulla and sympathetic tumors. Paragangliomas originate either in the parasympathetic or sympathetic autonomous nervous system ganglia, which is outside the adrenal medulla.Default
999NAACCR Item
NAACCR #772Code | Description | SS2018 T |
---|---|---|
000 | In situ: Noninvasive; intraepithelial | IS |
100 | Any size pheochromocytoma (PH) tumor, no extra-adrenal invasion Confined to adrenal gland Localized, NOS | L |
200 | Any size paraganglioma (PG) tumor, no extra-adrenal invasion | L |
300 | Adjacent connective tissue Gerota’s fascia Invasion of adjacent organs - Blood vessels (large) + Renal vein + Vena cava - Kidney - Retroperitoneal structures including + Great vessels * Aorta * Inferior vena cava | RE |
700 | Diaphragm Liver Pancreas Spleen Further contiguous extension | D |
800 | No evidence of primary tumor | U |
999 | Unknown; extension not stated Primary tumor cannot be assessed Not documented in patient record Death Certificate Only | U |