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1.
Urologiia ; (3): 114-116, 2023 Jul.
Article in Russian | MEDLINE | ID: mdl-37417420

ABSTRACT

This paper analyzes the etymology of the Russian names of the organs of the urinary system (kidney, ureter, urinary bladder, urethra) and their separate parts (renal pelvis). It is shown that Russian anatomical terms originate from the root morphemes of the Indo-European language group, which convey morphological, physiological or anatomical features of this or that organ. At the moment Russian terminology is widely used in the study of anatomy and other fundamental and medical sciences in universities and clinical practice along with common Latin names and eponyms of names of these or other structures.


Subject(s)
Language , Ureter , Humans , Urethra , Kidney , Russia
2.
Probl Endokrinol (Mosk) ; 70(2): 37-45, 2023 Oct 04.
Article in Russian | MEDLINE | ID: mdl-38796759

ABSTRACT

Currently, all pheochromocytoma/paraganglioma (PPGLs) are considered malignant due to metastatic potential. Consequently, PPGLs are divided into «metastatic¼ and «non-metastatic¼. Metastatic PPGLs can be with synchronous metastasis (metastases appear simultaneously with the identified primary tumor) or metachronous (metastases develop after removal of the primary tumor). The term metastatic PPGLs is not used in the presence of tumor invasion into surrounding organs and tissues, without the presence of distant metastases of lymphogenic or hematogenic origin. It is generally believed that about 10% of pheochromocytomas and about 40% of sympathetic paragangliomas have metastatic potential. On average, the prevalence of PPGLs with the presence of metastases is 15-20%. Risk factors for metastatic PPGLs are widely discussed in the literature, the most significant of which are groups of clinical, morphological and genetic characteristics. The review presents a discussion of such risk factors for metastatic PPGLs as age, localization and type of hormonal secretion of the tumor, the size and growth pattern of the adrenal lesion, the presence of necrosis and invasion into the vessels, the tumor capsule surrounding adipose tissue, high cellular and mitotic activity, Ki-67 index, expression of chromogranin B and S100 protein, the presence of genetic mutations of three main clusters (pseudohypoxia, kinase signaling and Wnt signaling).Over the past two decades, a number of authors have proposed various predictor factors and scales for assessing a probability of metastatic PPGLs. The review contains detailed description and comparison of sensitivity and specificity of such predictor scales as PASS, GAPP, M-GAPP, ASES and COPPS.


Subject(s)
Adrenal Gland Neoplasms , Paraganglioma , Pheochromocytoma , Humans , Pheochromocytoma/pathology , Pheochromocytoma/epidemiology , Adrenal Gland Neoplasms/pathology , Adrenal Gland Neoplasms/epidemiology , Risk Factors , Paraganglioma/pathology , Paraganglioma/genetics , Paraganglioma/epidemiology , Neoplasm Metastasis
3.
Probl Endokrinol (Mosk) ; 68(1): 8-17, 2021 11 15.
Article in Russian | MEDLINE | ID: mdl-35262293

ABSTRACT

The widespread introduction of genetic testing in recent years has made it possible to determine that more than a third of cases of pheochromocytomas and paragangliomas (PPPGs) are caused by germline mutations. Despite the variety of catecholamine-producing tumors manifestations, there is a sufficient number of clinical and laboratory landmarks that suggest a hereditary genesis of the disease and even a specific syndrome. These include a family history, age of patient, presence of concomitant conditions, and symptoms of the disease. Considering that each of the mutations is associated with certain diseases that often determine tactics of treatment and examination of a patient, e.g. high risk of various malignancies. Awareness of the practitioner on the peculiarities of the course of family forms of PPPGs will allow improving the tactics of managing these patients.The article provides up-to-date information on the prevalence of hereditary PPPGs. The modern views on the pathogenesis of the disease induced by different mutations are presented. The main hereditary syndromes associated with PPPGs are described, including multiple endocrine neoplasia syndrome type 2A and 2B, type 1 neurofibromatosis, von Hippel-Lindau syndrome, hereditary paraganglioma syndrome, as well as clinical and laboratory features of the tumor in these conditions. The main positions on the necessity of genetic screening in patients with PPPGs are given.


Subject(s)
Adrenal Gland Neoplasms , Multiple Endocrine Neoplasia Type 2a , Paraganglioma , Pheochromocytoma , von Hippel-Lindau Disease , Adrenal Gland Neoplasms/diagnosis , Adrenal Gland Neoplasms/genetics , Humans , Multiple Endocrine Neoplasia Type 2a/diagnosis , Multiple Endocrine Neoplasia Type 2a/genetics , Paraganglioma/diagnosis , Paraganglioma/genetics , Pheochromocytoma/genetics , von Hippel-Lindau Disease/diagnosis , von Hippel-Lindau Disease/genetics
4.
Med Parazitol (Mosk) ; (4): 22-5, 2015.
Article in Russian | MEDLINE | ID: mdl-26827581

ABSTRACT

This paper is dedicated to moth flies, a new medical disinsection object in our country. These insects are common in urban areas, generally in the premises with poor sanitary conditions. Moth fly larvae may cause accidental human urinary miasmata; imagoes, if many, become a worrisome factor; a source of allergy, and potential mechanical vectors of human diseases. In this connection, it is necessary to implement measures to control the number of the moth flies when the latter are detected on the objects particularly in therapeutic and preventive facilities and public catering esablishments.


Subject(s)
Insect Vectors/pathogenicity , Psychodidae/pathogenicity , Urinary Tract Infections/parasitology , Animals , Humans , Larva/pathogenicity , Psychodidae/physiology , Urinary Tract Infections/epidemiology
5.
Kardiologiia ; 53(6): 66-70, 2013.
Article in Russian | MEDLINE | ID: mdl-23953048

ABSTRACT

Contemporary data on mechanisms of development, types, and clinical picture of hypertensive crisis (HC) are presented. Algorithms of rational therapy of uncomplicated and complicated HC are considered. Appropriateness of the use in HC of antihypertensive drugs with multifactorial action is stressed. These drugs include urapidil - an antihypertensive agent with complex mechanism of action. Blocking mainly the postsynaptic 1-adrenoreceptors urapidil attenuates vasoconstrictor effect of catecholamines and decreases total peripheral resistance. Stimulation of 5HT1-receptors of medullary vasculomotor center promotes lowering of elevated vascular tone and prevents development of reflex tachycardia.


Subject(s)
Antihypertensive Agents , Aortic Aneurysm , Aortic Dissection , Heart Failure , Hypertension, Malignant , Hypertensive Encephalopathy , Algorithms , Aortic Dissection/etiology , Aortic Dissection/prevention & control , Antihypertensive Agents/classification , Antihypertensive Agents/pharmacology , Antihypertensive Agents/therapeutic use , Blood Pressure/drug effects , Disease Management , Emergencies , Emergency Treatment/methods , Heart Failure/etiology , Heart Failure/prevention & control , Humans , Hypertension, Malignant/complications , Hypertension, Malignant/diagnosis , Hypertension, Malignant/etiology , Hypertension, Malignant/physiopathology , Hypertension, Malignant/therapy , Hypertensive Encephalopathy/etiology , Hypertensive Encephalopathy/prevention & control , Piperazines/pharmacology , Piperazines/therapeutic use
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