Diseases of thyroid gland occupy 2nd place after saccharine diabetes.
Thyroid gland (TG) – one of major organs of incretion. Alage of TG takes place on 4th week of gestation. Thyroid tissue appears on 2th month. On 16th week TG is differentiated. There are 2 periods of stormy growth of TG (5-7 and 12-15 years). Hormones of TG are: thyroxin (T4) and triiodo-thyronine (T3). T4 has 65 % iodine. Initial product of biosynthesis of thyroid hormones is AA – tyrosine and iodine.
Physiology of hormones of TG
Main factor of regulation of function of TG is TTH. Regulation takes place on principle of feedback between hypophysis and TG. Secretion of thyrotropin of adenohypophysis takes place under influence a hypothalamus (thyrotropin-releasing factor).
Physiological action of thyroid hormones:
influence on all types of metabolism;
important role in development of fetus, processes of growth and differentiation of tissues (especially brain);
assist normal physical and mental development of child;
strengthen lypolysis and metabolisn of carbonhydratess, decrease maintenance of glycogen in liver;
actively influence on a mineral and water metabolism;
in ordinary doses have an anabolic effect, in high – catastatic.
Hypothyroidism
Hypothyroidism – endocrine-metabolitic disease in origin of which there is a decline or nonfunction of thyroid gland.
Classification:
I. By the time of origin:
-congenital
-acquired
ІІ. By form:
-primary
-secondary
-tertiary
ІІІ. By degree of severity:
-easy
-intermedius
-severe
Hypothyroidism
Primary – it is arisen up as a result of primary defeat of thyroid gland.
Secondary – at the defeat of hypophysis (as a result of hypopituitarism, isolated lack of TTH or secretion of nonactive TTH). More frequent meets at the tumours of hypophysis.
Tertiary – related to the defeat a hypothalamus and synthesis of thyroliberine.
Hypothyroidism
I. Congenital hypothyroidism.
Etiology:
-90 % - defeat the precusor of thyroid gland on 4-9 week of gestation (dysgenesis and ectopia);
-thyrostatic medicinal therapy (mercasolil, iodine, bromide, salts of lithium, tranquilizers);
-autoimmune thyroiditis at mother;
-influence of different chemical substances, irradiation on fetus;
-intrauterine infections.
In 10 % of cases Congenital hypothyroidism arises up because of genetical deficit of synthesis of thyroid hormones.
In basis of pathogenesis is violation of metabolism of albumens, fats and carbonhydrates. Through the decline of synthesis of hormones of TG there is diminishing of amount of neurons, violation of differentiation of brain, suppression of function of CNS. Decline of metabolic processes causes delay of growth and forming of skeleton, processes of metabolism are violated (hyperketonemia and lipidemia).
For congenital hypothyroidism very important is early diagnostics of disease (pathological changes of CNS are reverse only to 4th week).
bradycardia, deafness of cardiac tones, cardiomegalia
Clinical symptoms of congenital hypothyroidism
At late diagnostic:
-delay of psychomotoric development (cretinism);
-considerable delay of growth (bone age);
-violation of sexual development;
-severe anaemia.
Easy forms of innate thyroprivia
Can be manifestated in 2-5 years or even during sexual development. Is characterized by the delay of growth and sexual development, decline of intellect, the symptoms of myocardial dystrophy, constipations, xerosis.
Diagnostic criterias of congenital hypothyroidism
-decreased concentarion of T4 in blood (N=110-225 nmole/l) and Т3 (N=2-4 nmole/l);
-increased concentration of TTH (N=1,5-20 MCED/ml);
-delay of bone age;
-scannography of TG (agenesia, ectopia, enzyme disorders.)
Acquired hypothyroidism
Is manifestated after 1 year of life. More frequent meets at girls.
-at examination: edema of face, rough lines, flattened bridge of the nose, xerosis, dry and fragile hair.
Laboratory diagnostics of acquired hypothyroidism
-decreasing of concentration of T3 and T4;
-increasing of TTH;
-expressed delay of bone age;
-determining of antithyroid antibodies;
-scanography of TG.
Treatment of hypothyroidism
L-tyroxine (thyreocomb). Initial dose – 3-5 mcg/kg, with a gradual increase each 3-5 days on 10-15 mcg to 10 mcg/kg. Treatment of congenital hypothroidism continues to 1-3 years.
Criteria of adequacy of choice of endocrinotherapy dose:
-pulse
-AP
-weight
-activity of child
-level of TTH, T3 and T4
-estimation of growth and bone age
Euthyroid goiter
Euthyrosis (diffuse non-toxic goitre) is euthyroid hyperplasy of TG, which is manifestated as its enlargement without parafunction. Enlargement of TG is scray reaction which is directed on providing of synthesis of enough quantity of thyroid hormones in the conditions of iodic deficit.
Theories of origin:
inherited defects of delight and organization of iodine;
disbalance of oligoelementss (surplus of Cu and Co);
influence of small doses of radionuclides;
hasty growth of organism.
Classification of euthyrosis
I. Endemic goitre – it is arisen up as a result of deficit of endogen iodides and other oligoelementss in soil.
ІІ. Sporadic goitre – arises up in endemic districts, is provoked by the protracted use of goitriferous preparations and influence of ecological situation.
ІІІ. Juvenile hyperplasy of TG – provoked by increased requirement in iodine and thyroid hormones during sexual development.
Determining of level of thyroid hormones in blood.
Determining of antibodies to tissue of thyroid gland.
Determining of level of day iodineuria.
By prescriptions - punctional biopsy.
Prophylaxis of iodine-deficit
Mass – substances with iodine are artificially plugged in feed (salt, bread, dairy products).
Group - preparations which contain physiological dose of iodine are used the origin in the groups of iodine deficit risk (to put, teenagers, pregnant).
Individual - use of products with increased maintenance of iodine (seafood, oarweed) and use of medications (antistrumin, potassium iodide 200).
Requirement in J in different age (WHO)
Adults – 150 mcg/day
Pregant – 200 mcg/day
Mature newborns – 15 mcg/kg/day
Premature newborns – 30 mcg/kg/day
First year children – 50 mcg/day
Children of 1-6 years – 90 mcg/day
Children of 7-12 years – 120 mcg/day
Treatment of euthyrosis
Always begins with prescribing of iodinated preparations: KJ - 100 mcg/day. If on background of treatment with preparations of iodine there is not normalization of sizes of TG during 6 month –L-тироксин (initial dose – 3 mcg/day, in future chosing of dose takes place under control of determination of TTH in blood of patient) is prescribed.
Hyperthyroidism
Diffuse toxic goitre (thyrotoxicosis, Basedow’s disease, Graves disease) – endocrine-exchange disease in basis of which there are hyperproduction of hormones of TG. On the modern stage a toxic goitre is determined as autoimmune disease at which LATS-factor is increased (longitude action stimulator of synthesis of thyroid hormones).
Etiology:
infections;
stresses;
psychical and physical traumas;
overheat in the sunshine
Clinical manifestations of hyperthyroidism
enlargement of TG;
violation of activity of CNS (crossness, fussiness, enhanceable motive activity, rapid fatigueability, emotional lability, sleep disturbance, headache, tremor of extremities);
violation of activity of CVS (tachycardia, arhythmia, systolic murmur, increased voltage of indents on ECG);
cachexia;
eye symptoms (exophthalmus; Graves oculopathy - lymphoid infiltration of conjunctiva, its hyperemia and edema; Dalrimil’s symptom - wide opening eye crack; Ellinec’s - strengthening of pigmentation of eyelids; Zinger’s - an edema of eyelids; Rosenbach's symptom – tremor of eyelids; Kraus’ symptom - increased brilliance of eyes; Stellwag’s is the infrequent blinking and retraction of overhead eyelid; Möbius's symptom - violation of convergence; Graefe's sign - lag of overhead eyelid at a look downward.
Laboratory changes at hyperthyroidism
-increasing of concentration Т3, Т4;
-decreasing of concentration of ТТH;
-bone age prevails factical on 2-5 years;
-decreasing of cholesterol in blood serum;
-CBA: leucopenia, lymphocytosis, increasing of ESR.
Organospecific autoimmune disease, which is accompanied by formation of autoantibodies to tissue of TG. More frequent meets at children and juvenile age. Girls are ill twice more frequent boys.
Is characterised by lymphocytic infiltration of TG, there can be only hyperplasia of TG on the early stages. Disease is inherited with the system HLA.
Clinical manifestations of Hashimoto’s disease
disease begins during 3 first years of life, after 6 frequency is increased (max – in teens);
goitre develops gradually and without symptoms (diffuse enlargement of TG, a surface is uneven by touch, in course of time becomes solid with nodes);
children are irritable, easily excitative, hiperhydrosis, hyperactive (it is possible to suspect hyperthyroidism, but not confirmed laboratory);
clinical course is various (spontaneous diminishing and disappearance or remain without changes during many years);
stages of disease: hyperthyroidism (transitory stage) – euthyrosis –hypothyroidism.
Diagnostics of Hashimoto’s disease
high titer of autoantibodies in blood serum (more frequent AB to thyroglobuline 1:100 and AG of microsomes >1:32);
level of T4 and TTH in blood is normal, or increased concentration of TTH at normal level of T4 (“compensated” hypothyroidism), or decline of level of T4 at increased concentration of TTH (hypothyroidism);