Calcium deficiency and excess: main symptoms in children

1.General information

In the aspect of life, health, activity and normal functioning of the human body, the most important role of the so-called micro- and macroelements - chemical substances that are not nutritional in themselves, but in small concentrations are absolutely necessary in biochemical reactions and physiological processes.

Calcium is one of the key macroelements of this kind; Moreover, the specific content of calcium compounds (salts) in the human body exceeds the concentration of any other macronutrient. The absolute majority of calcium is found in bones and teeth, and only about 1% is found in blood plasma and intracellular spaces; in addition, the biochemical interaction of calcium and magnesium is one of the most important regulators of cardiovascular activity.

Thus, calcium deficiency has a detrimental effect on the condition and functioning of a number of systems. However, its excess content, or hypercalcemia, is pathological and leads to the development of a number of serious disorders.

According to modern epidemiological statistics, the incidence of hypercalcemia in the general population varies between 0.1-1.5%; in samples of inpatients, this proportion is much higher and reaches 0.5-3.5%, which is due to a complex of reasons and interrelated factors.

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Hypercalcemia

The first step in any unclear case of hypercalcemia is to measure PTH to confirm or rule out the diagnosis of pHPT. Along with the determination of iPTH, new measurement methods using specific amino-terminal antibodies have recently emerged. (Biointact-PTH, whole PTH). Application of PTH-Fragment-Assays obsolete. Other conditions that support the diagnosis of pHPT are hypophosphatemia, high-normal or elevated 1,25(OH)2D3 (with normal 25(OH)D3), elevated bone alkaline phosphatase, decreased to low-normal renal calcium excretion (as a result of increased renal PTH action and increased renal "calcium-Loads") and high renal excretion of phosphate (however, largely dependent on diet). Diagnosis of the localization of enlarged epithelial bodies before the first parathyroidectomy may be limited to ultrasonography of the neck, which in two thirds of cases determines the indicating condition. FHH (heterozygous inactivating mutation Calcium-sensing-Rezeptors) occurs with a frequency of 1: 15,000-20,000. Based on laboratory chemical results, it cannot be reliably distinguished from pHPT. The typical conditions for FHH are mild hypercalcemia and severe hypocalcemia; specificity is however limited. Family member screening for hypercalcemia and hypocalciuria can help make the diagnosis. The diagnosis can be made with confidence only at the present moment when the question is posed scientifically using Calcium-Sensing-Rezeptor-Gens sequencing. The distinction from pHPT is therefore important because FHH can generally be considered a non-therapeutic abnormality and unnecessary parathyroid surgery is not performed on affected patients.

It is assumed that about 70-80% of tumor-associated hypercalcemia are humorally mediated. The basis of most of these forms of hypercalcemia is the secretion of PTHrP from tumor tissue (often squamous cell carcinomas, such as renal carcinoma, bronchial carcinoma, and others). In the diagnosis of unclear hypercalcemia, one of the subsequent steps is also the measurement of PTHrP. Hematological malinomas (plasmacytoma, lymphoma), as a rule, do not produce PTHrP. In case of unclear hypercalcemia, using appropriate diagnostic measures (immunoelectrophoresis, as a mandatory study for any hypercalcemia, bone marrow puncture, radiological examination of the skeleton), plasmacytoma should be excluded. Plasmacytomas and lymphomas secrete cytokines (interleukin-1, tumor necrotizing factor a), which through the activation of osteoclasts lead to hypercalcemia. Systematic detection of these cytokines has no clinical significance.

If a tumor is suspected, a search program should be carried out with a thorough clinical examination (eg lymphoma, suspected skin changes, breast tumor, prostate enlargement), serological tumor markers, Haemoccult, chest X-ray (mass process), abdominal sonography (metastases) liver, kidney tumors) and radiological studies of the skeleton (scintiography, X-ray targeted images, detection of bone metastases, osteolysis, DD to pHPT, Morbus Paget). To diagnose unexplained hypercalcemia, a 1.25 (OH)2D3 measurement is performed. In rare cases, hypercalcemia may be caused by elevated levels of 1,25(OH)2D3. This most often indicates granulomatous diseases (most often sarcoidosis, less often tuberculosis and other diseases, see Table 2). Very rarely, ectopic lymphomas secernate 1,25 (OH)2D3.

2. Reasons

According to the published results of biochemical studies, up to 90% of cases of hypercalcemia are caused by oncological processes or pathology of the parathyroid glands: tumors of the lungs, intestines, kidneys, prostate in men and mammary glands in women; malignant diseases of the hematopoietic system.

Endocrine pathology in this predominant etiological structure is represented by hyperparathyroidism (abnormally high activity of the parathyroid glands), as well as thyrotoxicosis. Other, more rare causes include Paget's deforming osteopathy, some hereditary diseases (for example, familial hypocalciuric hypercalcemia, Jansen's chondrodysplasia, etc.), impaired absorption of calcium in the intestine, excess vitamin D, prolonged stay on bed rest (hence the large percentage of hypercalcemia in patients receiving long-term courses of inpatient treatment). Excess calcium is also caused by prolonged use of certain groups of drugs (lithium compounds, thiazide diuretics, theophylline, etc.), kidney and adrenal dysfunction.

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Characteristics

In the human body, a violation of calcium metabolism provokes the development of various diseases. Calcium is considered an important element in the process of regulating the nervous excitability of muscle tissue, the process of hemostasis, in the stabilization of cell tissue membranes, and in the transduction of intracellular signals.

In medicine, there are two forms of disturbance of mineral metabolism in the endocrine system:

• hypocalcemia (hypoparathyroidism);
• hypercalcemia (hyperparathyroidism).

The second type of disease is more dangerous and requires more complex treatment. In most cases, if the pathology is advanced, doctors resort to surgery.

In order to understand what could provoke a change in the production of calcium by the parathyroid glands into the blood, how to deal with this disorder and what the consequences may be, each pathology should be considered separately.

3. Symptoms and diagnosis

There are acute and chronic hypercalcemia. Acute is characterized by:

• general weakness, fatigue;
• unquenchable thirst (polydipsia) and increased volume of urination (polyuria);
• nausea, vomiting, digestive and stool disorders;
• high blood pressure;
• cardiac disorders, including life-threatening ones (arrhythmia, sudden cardiac arrest);
• epigastric pain associated with eating.

A hypercalcemic crisis is characterized by severe dyspeptic disorders, muscle weakness, sometimes epileptiform syndrome, a sharp increase in temperature, and an altered state of consciousness (up to coma). Considering the non-specificity of the symptoms, only reliable emergency diagnosis and urgent adequate intervention can save the patient’s life during such a crisis attack.

Chronic hypercalcemia leads to fibrous degeneration in the renal parenchyma, a number of progressive complications from the osteoarticular structures, central nervous system, heart, lungs, gastrointestinal tract - with the development of corresponding symptom complexes and syndromes.

If hypercalcemia is suspected, a number of specific blood and urine tests are prescribed, which must be repeated and taken under different conditions (for example, against the background of a special diet). Depending on the most likely causes of increased calcium concentration, instrumental diagnostic methods are additionally prescribed (densitometry, ultrasound of the kidneys, tests for tumor markers, ECG, etc.).

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A little more about the symptoms

The clinical picture in both cases is pronounced. The main area of ​​damage is the skeletal system, which contains more than 90% of the total calcium content in the body.

Symptoms of hypercalcemia, regarding bone tissue:

• pseudo- and simple form of gout;
• deformation;
• pain;
• muscle weakness and atrophy;
• fractures even with simple bruises;
• cystic bone formations.

In the severe stage, there is a sensation of “pins and needles”, numbness and burning in certain parts of the body, and temporary paralysis of the pelvic muscles may occur.

Hypocalcemia is characterized by seizures that can affect not only the limbs, but also the muscles of the chest. The danger comes from a hypocalcemic crisis, which causes serious complications.

4.Treatment

It is obvious that treating hypercalcemia itself is pointless: it is necessary to identify and eliminate the causes of excess calcium. Based on the results of the diagnostic examination, a decision is made on further actions - removal of the tumor and subsequent oncology therapy, specialized treatment by an endocrinologist, stopping taking medications and vitamin complexes containing vitamin D, etc. In severe cases, hospitalization with intensive therapy is required - intravenous administration of saline and calcium antagonists, hemodialysis, forced diuresis drugs, etc. For less threatening conditions, calcitonin, pamidronic acid are used, according to indications, glucocorticosteroids, gallium nitrate and other drugs prescribed based on the specific clinical situation .

Hypocalcemic crisis

An exacerbation of calcium deficiency is characterized by a decrease in plasma minerals to less than 2.25 mmol/l. A hypocalcemic crisis is also dangerous.

The attack can occur suddenly, but, as a rule, it is preceded by a number of symptoms:

• feeling of "goosebumps";
• tingling feeling throughout the body;
• limbs and part of the face go numb;
• severe muscle weakness;
• sudden muscle pain;
• depression;
• change in skin color.

Gradually, loss of sensitivity and other signs are replaced by muscle twitching. Initially, the patient feels only mild and isolated spasms, but quickly enough the condition develops into attacks of severe convulsions.

Muscle tone is expressed by characteristic manifestations:

• “the hand of the obstetrician”;
• "horse foot";
• "fish mouth";
• and others.

The danger arises when spasms affect the muscle tissue of internal organs: renal/liver colic, laryngospasm or bronchospasm. Impaired breathing can cause asphyxia.

At the moment of crisis, the patient feels unbearable pain, from which he loses consciousness and the ability to rationally perceive what is happening.

brief information

The most common causes of hypercalcemia are primary hyperparathyroidism and malignancies with paraneoplastic production of parathyroid hormone-related protein.

Symptoms of hypercalcemia include nephrolithiasis, bone pain, abdominal pain, and polyuria. Treatment tactics depend on the degree of calcium imbalance.

Mild and asymptomatic moderate hypercalcemia are treated with oral rehydration and low calcium intake, whereas symptomatic moderate and severe cases require intravenous rehydration and calcitonin.

Hypercalcemic crisis is a life-threatening complication that is manifested by dehydration, oliguria and changes in consciousness and requires immediate forced diuresis.