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Physical signs of most common endocrine diseases Dr. Szathmári Miklós Semmelweis University First Department of Medicine 05. December 2011. Subjects of the lecture • Thyroid diseases – hyperthyroidism – hypothyroidism • Diseases of adrenal cortex – Cushing’s syndrome – Addison’s disease • Gynecomastia • Acromegaly Enlargement of thyroid gland=goiter nodular diffuse Palpation of the thyroid gland • Place the fingers of both hands on the patient’s neck so that your index fingers are just below the cricoid cartilage • The patient’s neck should be extended, but not far enough to tighten the muscles • Ask the patient to sip and swallow water. Feel for the thyroid gland rising up under your fingerpads • Displace the trachea to the right with your left fingers. With the right hand fingers, palpate laterally for the right lobe in the space between the displaced trachea and the relaxed sternomastoid. Find the lateral margin. Palpation of the thyroid gland • Normal size of a lateral lobe is approximately the size of the distal phalanx of the thumb. – Enlarged in Graves’ disease (diffuse), malignancy (nodular), in thyroiditis. • Normal consistancy: feels somewhat rubbery. – Soft in Graves’ disease – Firm in Hashimoto’s thyroiditis, malignancy • Normally not painful – Tenderness in thyroiditis • Localized systolic or continuous bruit (noncardiac origin) may be heard in hyperthyroidism Graves’ disease Stimulatory antibody to the thyroidal TSH receptors swelling in the neck Mucinous infiltration of the dermal and subdermal layers: pretibial myxedema showing the coarsened, nodular, infiltrated, pigmented lesions on the lower extremities. Graves’ disease Ocular involvement is mediated by one or more distinct but still poorly characterised orbital-stimulating immunoglobulins:Proptosis, due to increased volume and edema of retrobulbar fat. Shortened extraocular muscles, because of the muscle infiltration and fibrosis result in upper lid retraction. Conjunctival erythema, and periorbital edema are evident. Facial expression The stare in hyperthyroidism Hyperthyroidism - clinical features • Associated directly with thyroid hormone excess: – Weight loss, heat intolerance due to hypermetabolism – Patients tend to be physically and mentally hyperactive – Supraventricular arrhythmias and precipitation of cardiac failure – Osteoporosis (increased bone turnover) – Amenorrhoea (suppressed gonadotrophins) Hyperthyroidism- clinical features • Sympathetic potentiation – Tachycardia – Sweating – Tremor – Intestinal hypermotility – Anxiety • Extrathyroid manifestations Graves’ disease - investigations Isotopic uptake of tracer doses of radioactive iodine or technetium is increased Detection of thyroid antibodies directed against microsomal thyroid cell antigens Measurements TSH and serum free T4 and T3 Hypothyroidism • The most common cause is the Hashimoto’s thyroiditis, affects appr. 1% of adult population This woman demonstrates the typical hypothyroid facies. She also had a slow, hoarse, deep voice and lassitude (state of feeling very tired in mind or body). • Dull, puffy facies. Edema does not pit with pressure. The lateral eyebrows are thin. Hypothyroidism –clinical features • Generalized tiredness and lethargy • Bradycardy, congestive cardiomyopathy, occasionally pericardial effusion. ECG: low voltage • Muscle weackness, muscle cramps • Depression, organic psychosis • Dry and flaky skin, hair loss • Weight gain • The voice is deep and husky Hypothyroidism The treatment of patient with hypothyroidism is one of the most fruitful task for the physician. A: before treatment, B: with adequate hormone supplementation The adrenal cortex • It secretes steroids which: – Control either salt and water balance – mineralocorticoids – Regulate metabolic processes – glucocorticoids – Androgens and estrogens • The adult adrenal cortex consists three relatively distinct bands of cells – The outermost layer – zone glomerulosa, expresses 18-hydroxylase and 18-dehydrogenase activity – aldosteron production – The middle zone – zone fasciculata, expresses the enzyme 17hydroxylase – cortisol and corticosterone production – The innermost zone – zone reticularis – androgen (preandrogens) production Adrenal steroid biosynthesis Cholesterol Pregnenolon 17OH-Pregnenolon DHEA Progesterone 17OH-Progesterone Androstenedione DOC 11-desoxycortisol ALDOSTERONE CORTISOL P450scc- side chain cleaving 21-hydroxilase 3β-hydroxysteroid dehydrogenase 17-hydroxilase and 17,20 liase 11β-hydroxilase, 18-hydroxylase and 18-hydroxydehydrogenase Metabolic effects of glucocorticoids • Carbohydrate metabolism – Stimulates hepatic gluconeogenesis – Increases deposition of glycogen in the liver – Antagonizes the peripheral action of insulin on glucose uptake • Protein metabolism – Inhibits amino acid uptake and protein synthesis in extrahepatic tissues – Potent protein catabolic agent in peripheral tissues such as muscle, skin, and bone – Stimulates amino acid uptake of the liver which are gluconeogenesis precursors • Fat metabolism – Increases mobilisation of fatty acids – Stimulates the lypolysis in adipose tissue – Increases the deposition of fat in the facial and truncal areas Other effects of glucocorticoids • Mineralocorticoid activity – Mostly in case of cortisol excess • Water metabolism – Increases glomerular filtration rate, and negative feedback effect on vasopressin • Cardiovascular effect – Potentiating the vasoconstrictor effect of other vasoactive molecules such as catecholamins and even vasopressin • Growth – Inhibitory effect on somatotrophin release and direct inhibitory action on insulin-like growth factor I production • Response to stress – Various stressors are associated with dramatic increase in the blood concentrations of corticotrophin and cortisol Cushing’s syndrome, prevalence Cushing’ syndrome is a rare disease predominantly affecting women in the age group 30 to 50 years (The ectopic ACTH production occurs more frequently in male patients because of the higher prevalence of lung cancer) • Incidence: 3.5/million/year • Prevalence: 39/million Causes of Cushing’s syndrome Corticotrophin-dependent Cushing’s syndrome • Cushing’s disease 64% • Ectopic Cushing’s syndrome 13% • Ectopic CRH syndrome 1% Corticotrophin-independent Cushing’s syndrome • Adrenal adenoma 10% • Adrenal carcinoma 8% • Adrenal hyperplasia 2% Pseudo-Cushing’s syndrome • Depression 1% • Alcoholism 1% Cushing’s syndrome – clinical features • • • • • • Proximal muscle weackness (steroid myopathy) Back pain (osteoporosis) Gain of weight Excessive hair growth Acne Amenorrhea (suppression by cortisol of the pitutary-ovarian axis) • Hypertension (sodium and water retention) • Hyperglykaemia (steroid induced gluconeogenesis, peripheral insulin insensitivity) • Increased proneness to bacterial infections (immunosuppressive effects of steroids) Cushing syndrome – purple striae The purple striae are found on lower abdomen, upper arms and thighs, which reflect the catabolic effects on protein structures in the skin. The thinness and easy bruising of the skin are additional manifestations of this process Adrenocortical hypofunction Primary deficiency due to disease of adrenal gland itself → a decrease in the mineralocorticoid as well as glucocorticoid hormone concentrations. Incidence: 5/million/year ; Prevalence: 80/million. Female/male: 1:0.7; between 30-60 years of age. Addison’s disease with hyperpigmentation Courtesy of David N Orth MD. www. uptodate Adrenocortical hypofunction Clinical features • Extreme muscular weakness and fatigue (characteristically at the night) due to electrolyte abnormalities and hypoglykaemia • Weight loss (anorexia, dehydration) • Gastrointestinal symptoms: diarrhea, vomiting, abdominal pain • Increased pigmentation (points of friction, palmar creases, buccal mucosa) • Depigmentation reflecting an associated immunological abnormality • Diziness (because of the orthostatic hypotension and hypoglykaemia) • Depression, confusion even coma • Salt-hunger • Amenorrhea, decreased libido, impotency • Anaemia • Loss of body hair (because of androgen deficiency) • Severe hyponatraemia – rhabdomyolysis, severe hyperkalaemia – tetraparesis • Additional symptoms according to the underlying disease Primary hyperaldosteronism Clinical symptoms of classical aldosterone-producing adenoma • Hypertension (sodium and water retention and increased vascular resistance). • The treatments generally used in hypertensive patients are ineffective. • Serious hypertensive complications. • Headache (due to the hypervolaemia) • Hypokalaemia is usually but not obligatory dominant feature of the clinical presentation, giving rise to symptoms such as muscle weakness and polyuria, psychiatric changes and cardiac arrythmias. • Metabolic alkalosis • Impaired glucose tolerance (direct effect of hypokalaemia on insulin secretion or/and increased glucocorticoid effect) • Mild hypernatraemia • Oedema is characteristically rare due to the renal escape phenomenon Polycystic ovary syndrome • Approximately 10% of women have polycystic ovary syndrome (PCOS). Women with PCOS experience increased body hair (hirsutism), increased weight and infertility due to both lack of ovulation and recurrent miscarriage. In addition, women with PCOS are subject to a markedly increased risk of heart disease, endometrial cancer and possibly breast cancer. If you have menstrual irregularities, you may have PCOS. Hirsutism- acanthosis nigricans PCOS Young woman with PCOS showing facial hirsutism (A) and axillary acanthosis nigricans (B). The latter is associated with severe insulin resistance and hyperinsulinaemia and is an occasional finding in PCOS Gynecomastia Excessive development of the mammary glands, even to the functional state, in children or males. Gynecomastia The feminine type enlargement of male breast The mean reason is higher estrogen/androgen ratio. Physiological gynecomastia 1. in newborns 2. during the puberty 3. in elderly men (prevalence is more than 40%) Pathological gynecomastia 1. Estrogen-producing adrenal and testis tumor 2. Increased aromatase activity (obesity, congenital) 3. hCG-producing testis, lung or liver tumor 4. Exogenous estrogen (prostatic carcinoma) 5. Hypogonadism (Klinefelter’s syndrome) 6. Systemic diseases: renal and,hepatic disorders, hyperthyroidism 7. Drugs (hormones, drugs with antiandrogen effect, sedativs, 8. Idiopathic (15%) Inspection of the breast • Examination of the breast includes careful inspection for skin changes, symmetry, contours, and retraction in four views: – Arm at sides (skin color, symmetry, contour) – Arm over head (dimpling or retraction of the breast in this position suggest an underlying cancer) – Arm pressed against hips (to contract the pectoral muscles) – Leaning forward (provocation of retraction nipple and areola that suggest underlying cancer) Acromegaly Characteristic clinical appearance manifest by coarsening of facial features due to an increase of connective tissue Acromegaly Alveolar bone growth causes the teeth to separate The enlargement of the frontal and maxillary sinuses results in an prominent brow and long face Growth of mandible leads to a jutting jaw (prognathism). Acromegaly Macroglossia. There is also generalized visceral enlargement Broadening and enlargement of the hands and feet due to increased periosteal growth as well as thickening of the skin Acromegaly- clinical features • Hypertension (related to sodium and water retention) • Anatomical effects of the pituitary tumor on neighbouring structures • Joint pain (due to associated synovial hypertrophy and degenerative arthritis) • Excessive sweating (direct effect of growth hormone) • Paraesthesiae of hands and feet because of the nerve entrapment by thickened bone and subcutaneous tissue • Headache (sensory nerve entrapment)