|
| Code | Diagnosis | Comment | Score |
| anonymous | Adrenal cortical carcinoma (100%) | nil | 90 |
| anonymous | Adrenal cortical carcinoma | nil | 90 |
| anonymous | ADRENOCORTICAL NEOPLASM, favour benign | To look for features of Beckwith-Wiedemann syndrome, e.g. macroglossia, macrosomia, midline abdominal wall defects (e.g. umbilical hernia) and neonatal hypoglycemia | 80 |
| anonymous | Adrenocortical carcinoma | nil | 90 |
| anonymous | Poorly differentiated malignant neoplasm consistent with ADRENOCORTICAL CARCINOMA. 100% | More sampling for eg. vascular invasion and necrosis to establish the malignant category for adrenocortical neoplasm. Correlate with clinical findings eg. virilisation. To exclude remote differential eg pheochromocytoma melan A-, chromogranin+; rhabdomyosarcoma actin+ desmin+. Adrenocortical ca is usually melan A+, chromogranin-. | 90 |
| anonymous | Adrenal cortical carcinoma, to exclude Li-Fraumeni syndrome.(100%) | nil | 100 |
| anonymous | Adrenal - Adrenocortical carcinoma 100% | nil | 90 |
| anonymous | Phaeochromocytoma (100%) | nil | 50 |
| anonymous | Adrenal cortical carcinoma. 100% | nil | 90 |
| anonymous | Pediatric Adrenal gland tumor, 1) More suggestive of Adrenal cortical neoplasm. 2) Pheochromocytoma, need to exclude. | Confirm with Immunohistochemistry, clinical and laboratorial correlation. Long time follow up to exclude malignant behavior. | 60 |
| anonymous | Left adrenal gland, tumour excision - Adrenal cortical neoplasm. | Please correlate with clinical features to rule out carcinoma. | 80 |
| anonymous | Adrenal cortical tumor, uncertain malignant potential | nil | 80 |
| anonymous | Adrenal cortical tumour, favour carcinoma (100% probability) | nil | 90 |
| anonymous | Adrenal cortical carcinoma (100%) | nil | 90 |
| anonymous | ADRENAL - Adrenal cortical neoplasm, favour adrenal cortical carcinoma (100%) | Take more blocks and correlate with clinical findings. | 90 |