Tumors of the Pituitary Gland (Pages 750-754)
Tumors of the Thyroid Gland (Pages 763-768)
Tumors of the Adrenal Glands (Pages 792-795)
Necrosis and Inflammation:
Necrosis: Can occur due to shock or post-delivery events (e.g., Sheehan's syndrome)
Inflammations: Include tuberculosis (TBC), sarcoidosis
Adenomas:
Chromophobe (e.g., prolactinoma)
Eosinophilic (GH-secreting)
Basophilic (e.g., ACTH-, TSH-secreting)
Hyperpituitarism
Manifestations:
Growth Hormone (GH) → Gigantism/Acromegaly
ACTH → Cushing’s syndrome
TSH → Hyperthyroidism
FSH/LH → Hypogonadism
Prolactin → Galactorrhea, amenorrhea, infertility
Hypopituitarism
Causes: Tumors (destruction of the gland), congenital issues (e.g., dwarfism), effects of radiation, surgery, ischemia, and inflammation
Symptoms:
Visual field abnormalities (bitemporal hemianopsia)
Headache, nausea, vomiting (due to intracranial hypertension)
Seizures and obstructive hydrocephalus
Cranial nerve palsy
Pituitary apoplexy (bleeding)
Microadenomas: < 1 cm
Macroadenomas: ≥ 1 cm
Malformations: Aplasia, hypoplasia, ectopic thyroid gland, cysts
Inflammations:
Acute thyroiditis
Subacute thyroiditis (de Quervain, giant cells)
Chronic thyroiditis
Hashimoto thyroiditis
Riedel’s fibrous thyroiditis
Goiter Types:
Diffuse and nodular
Can be normo-, hypo-, or hyperfunctional
Endemic Goiter: Linked to iodine deficiency and TSH hypersecretion
Clinical Effects:
Compression effects (dysphonia, dysphagia, superior vena cava syndrome)
Hyperthyroidism Causes:
Basedow-Graves disease: Autoimmune
Toxic adenoma
Nodular goitre
Hypothyroidism Causes:
Congenital or acquired
Benign: Adenomas (with/without hyperfunction)
Malignant:
Papillary carcinoma
Follicular carcinoma
Medullary carcinoma
Undifferentiated carcinoma
Lymphoma, angiosarcoma
Hypofunction:
Causes include hemorrhages, tuberculosis, metastases
Waterhouse-Friderichsen syndrome
Addison disease
Hyperfunction:
Causes include hyperplasia (primary/secondary-ACTH), adenomas
Syndromes:
Cushing syndrome: Glucocorticoid excess
Conn syndrome: Aldosterone excess
Adrenogenital syndrome: Sex steroid excess
Cortex: Adenomas, carcinoma
Medulla:
Chromaffin cells (pheochromocytoma)
Neuroblastoma
Clinical Features:
Bilateral hemorrhagic necrosis of adrenal glands
Example:
41-year-old man with gynecomastia and advanced adrenal carcinoma
49-year-old woman with multiple endocrine neoplasia (MEN1) exhibiting various symptoms
Cushing Syndrome: Results from excessive cortisol; symptoms include hyperglycemia and hypertension.
Hyponatremia: Low sodium levels in the blood.
Paraneoplastic Syndromes: Disorders associated with cancer due to substances produced by tumors.
Cushing syndrome associated with small cell lung carcinoma.
Hypercalcemia (parathyroid hormone-like substance) from renal cell carcinoma.
Carcinoid syndrome (due to serotonin production).