Endocrine Flashcards
Hyperthyroidism causes
Primary: Graves, toxic multinodular goitre, toxic neoplasm
Secondary: pituitary hyperfunction
Hypothyroidism causes
Primary: Hashimoto (most common in SG), iatrogenic, cretinism, dietary iodine deficiency
Secondary: Pituitary failure
Signs of hyperthyroidism and hypothyroidism
Hyperthyroidism: thin, staring gaze, lid lag, exophthalmos (graves), warm sweaty skin, tachycardia and atrial fibrillation, proximal myopathy, pretibial myxoedema
Hypothyroidism: mildly obese, swollen and puffy face, dry cool skin, bradycardia, pericardial effusion, proximal myopathy
Symptoms of hyperthyroidism and hypothyroidism
Hyperthyroidism: Weight loss, heat intolerance, oligomenorrhea, diarrhoea, irritable mental state and increased appetite
Hypothyroidism: Weight gain, cold intolerance, menorrhagia, oligomenorrhea, constipation, mental slowness, may have poor appetite
Biochemical symptoms of hyperthyroidism and hypothyroidism
Hyperthyroidism: High T4, T3, low TSH (primary hyper), Graves’ autoantibodies
Hypothyroidism: Low T4, T3, high TSH (primary hypo) or low TSH (secondary hypo), Hashimoto autoantibodies
What is Graves disease
Autoantibodies bind to and activate TSH receptors, releasing T3 and T4, and increases cellularity and causes hyperplasia of the thyroid gland (goitre)
What is Hashimoto thyroiditis
Immune mediated cytotoxic destruction of follicular epithelial cells
Gross features of Graves thyroid
Diffuse enlargement
Reddish meaty cut surface with high cell density
Smooth and soft gland with intact capsule
Histologically, follicular cells are tall, columnar and crowded, forming pseudopapillae with inflammatory cells
What are the thyroid cancers
Follicular adenoma
Anaplastic carcinoma
Medullary carcinoma (MEN syndrome, FMTC if hereditary)
Follicular carcinoma (capsular/vascular invasion, metastasis to lungs, bone, liver via blood)
Papillary carcinoma (metastasis to lymph nodes, diagnosis based on nuclear features: finely dispersed chromatin, nuclear grooves, pseudo inclusions, classical features: papillae with fibrovascular cores, psammoma bodies)
Gene mutations in MEN
MEN 1: MENIN gene
MEN 2: RET gene
MEN 1 clinical features
Prolactinoma: excess breast milk formation
Hyperparathyroidism: hypercalcemia
Adrenal adenoma: cushing’s syndrome
Insulinoma: hypoglycemia
Gastrinoma: gastric ulceration
MEN 2B clinical features
Mucosal neuroma syndrome: growth around nerves of mucous membranes
Marfanoid habitus: long limbs, loose joints, curved spine
Causes of hyperparathyroidism
Primary:
Parathyroid adenoma, most common
Parathyroid carcinoma
Parathyroid hyperplasia (more than 1 gland enlarged)
Secondary:
Renal failure (kidney reabsorbs too much phosphate, forming insoluble CaPO4, reducing Ca ion levels, stimulating increased PTH)
Effects of hyperparathyroidism
Renal and urinary calculi
Osteitis fibrous cystica
Hypertension
Pancreatitis
Peptic ulcers
Metastatic calcification
Causes of adrenal hyperfunction
Primary:
Adrenal adenoma/carcinoma
Adrenal hyperplasia
Secondary:
Pituitary adenoma (increased ACTH causing increased cortisol)
Others:
Iatrogenic: steroids
Paraneoplastic: SCLC producing ACTH