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 |