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Biomedical subjects

P V Iushkov

Publications and source records attributed to P V Iushkov.

At least 19 recordsLinked to original sources

[Diagnostics and treatment of the functional autonomy of the thyroid gland].

Functional autonomy of the thyroid gland (FATG) remains an important problem due to iodine deficiency over the whole territory of Russian Federation and the fact that iodine prophylaxis has not been conducted for a long period of time. Since iodine deficiency affects the thyroid gland (TG) as a whole, the formation of nodules is not limited to a single lobe, but leads to the development of multinodular goiter, the main feature of which is morphological and functional heterogeneity of TG tissue. Active cell proliferation in the iodine deficiency related goiter is associated with an elevated risk of somatic mutations, including activating mutations leading to thyrocyte functional autonomy. Diagnosis is often late due to the absence of any specific complaints in most patients. Hence, the pathology is often an accidental finding and is mostly revealed in patients with cardial diseases. For a long time, TG scintigraphy has been the only method allowing the diagnosis of FATG, while other techniques, such as ultrasonography and the measurement of the hormone levels in blood, only make it possible to assume the presence of this pathology. Nowadays, fine needle biopsy plays an important role since it gives a possibility to obtain direct cell-level findings concerning the morphological structure of TG nodules and, in some cases, the functional condition of cells. Of late, great importance to clinical practice has been attached to new developments in FATG diagnostics, immunomorphological (immunocytochemical and immunohistochemical) techniques in particular. Most probably, new techniques of FATG verification will be based upon the study of TSHR as the specific marker of this pathology, and it will be possible to use immunocytochemical assay as an additional diagnostic method for the verification of autonomic nodular formations as early as right after the puncture.

Biopsy↗

[Target thin-needle puncture biopsy in diagnosis of thyroid cancer].

One hundred medical histories of patients with thyroid cancer (TC) were analyzed. Patients were divided into two groups depending on the variant of thin-needle biopsy technique (TNB). In group 1TNB was performed with "blind" method (with palpation control)--43 cases, in group 2 target TNB (ultrasound-guided) was carried out--57 cases. Patients of each group were divided depending on cytological presurgical diagnosis. Statistical analysis was carried out with two-sided Fisher's criterion. It is demonstrated that detection of TC in group 2 (84.2%) was higher than in group 1 (62.8%) where "blind" method of puncture was used (p = 0.020). It is recommended to perform target TNB in all cases of nodular goiter that improves quality of TC diagnosis.

Adenocarcinoma, Follicular↗

[Diagnostic criteria of pyloric helicobacter infection in peptic ulcer].

Helicobacter pylori (HP) in 41 patients (10 with stomach ulcer and 31 with duodenum ulcer) was found in gastro-biopsies from the stomach antrum before and after the treatment. The following methods to reveal HP were used: Giemsa staining, immunoperoxidase reaction with polyclonal monospecific antibodies against HP, urease rapid test. HP was also revealed in the blood serum by antibodies against HP by means of enzyme immunoassay. Electron microscopy was performed in 5 patients and bacteriologic study in 10 patients. Immunohistochemical method allows one to judge about real HP colonization of the gastric mucosa. Bacterioscopy with Giemsa staining gives good results but they are not true markers of HP presence this being explained by other methods. Serologic enzyme immunoassay gives an idea about the patient contamination, but not about HP eliminations as a result of treatment. Urease-test is adjuvant.

Azure Stains↗

[Extracellular matrix in various forms of ulcerated stomach cancer, their differential diagnosis and morphogenesis].

Immunohistochemical study of the extracellular matrix in ulcerated stomach carcinoma has been performed. Material is taken from 70 patients having either ulcerated or non-ulcerated carcinoma, and from 10 patients with chronic stomach ulcer. Results of the study revealed additional criteria for a differential diagnosis of various forms of ulcerated stomach carcinoma and gave a description of their morphogenesis.

Diagnosis, Differential↗

[Lung carcinosarcoma].

Lung carcinoma in a 72-year-old man smoker is described. Tumour, 12x8x8 sm in size, was located in the middle lobe of the right lung. Metastases were in the regional lymph nodes, soft tissue of the anterior abdominal wall, gastric mucosa and left adrenal. Epithelial component had signs of the undifferentiated carcinoma and adenocarcinoma, mesenchymal component consisted of leiomyosarcoma. Electron-microscopically, tumour cells with squamous, glandular, smooth muscle and fibroblastic features were found.

Aged↗

[The immunohistochemistry of cellular oncogenes in precancer and cancer of the lung].

Operative material obtained from patients with lung cancer and precancer, carcinoids, secondary tuberculosis, chronic nonspecific diseases and pulmonary lymphosarcoma was examined immunohistochemically. Expression of the oncogenes was higher in lung carcinoma than in the foci of lung epithelium regeneration, metaplasia and dysplasia. All the oncogenes in precancer and cancer may be divided into two groups by the degree of their expression: oncogenes the activation of which occurs in the same way at certain stages of tumour progression regardless of the lung carcinoma histogenesis and oncogenes expressed at certain stages depending upon the carcinoma histogenesis. The majority of oncogenes studied may be included into the second group (C-myc, ras, sis, src) and only one c-fos into the first group. The oncogenes expression may occur at the precancerous stage and precede the morphological changes in cells and tissues. The expression of some oncogenes (C-myc, sis) takes place not only in the tumour parenchyma but in the cancer stroma as well thus making the immunohistochemical method most reliable that permits one to study a true expression of oncogenes by cancer cells.

Chronic Disease↗

[Functional morphology of the hypophyseal-adrenal-gonad system in different variants of prostatic hyperplasia].

Two forms of prostatic hyperplasia are distinguished: fibro-glandular (FGH) and glandular-fibrous (GFH). An increase in the number of adenohypophysis cells producing gonadotrophic hormone, hyperplasia of the adrenal reticular zone, hyperplasia and hypertrophy of Leydig and Sertoli cells in the testis were observed in FGH. Signs of enhanced functional activity were observed in all cases of hyperplasia. In GFH there was an increase in the number of adenohypophyseal cells producing adrenocorticotrophic hormone, hyperplasia of the fascicular layer in the adrenals, atrophy of Leydig cells in the presence of Sertoli cell hyperplasia. The variant of prostatic hyperplasia is determined by the hormonal changes and this may help in choosing of approaches to therapeutic correction of prostatic hyperplasia and its early diagnosis.

Adult↗

[Functional morphology and prognosis of hormonally-active pituitary adenomas].

This paper is a review of literature on the etiology, pathogenesis and morphogenesis (electron microscopy, immunocytochemistry) of pituitary adenomas (PA). Clinical manifestations of PA are considered depending on their structure. Approaches to the clinico-morphological classification of PA and factors of their prognosis are discussed.

Adenoma↗

[Clinical morphology of hormonally-inactive adrenal neoplasms].

94 patients with primary diagnosis "adrenal incidentaloma" were operated. Ultrasound investigation, MR-tomography, computed tomography, hormonal tests were made in examination of these patients. The results were compared with morphology and histochemistry of the removed adrenals. True hormonally inactive tumors were detected in 11 cases only. The conclusion is made that the term "adrenal incidentaloma" is a collective term which does not reflect the essence of the processes in the adrenals. Verification of morphofunctional features of adrenal tumors is possible only after clinical and morphobiochemical examinations.

Adolescent↗

[Pathogenesis and clinical morphology of congenital disorders of sex differentiation].

Bisexual structure of genitalia presents difficulties for clinical diagnosis. Therefore, knowledge of pathogenesis and clinical morphology of congenital disturbances of sexual differentiation helps to establish earlier hermaphroditism variant, appropriate surgery for complete social-psychological adaptation of this group of patients.

Disorders of Sex Development↗

[Clinical and morphological characteristics of thyroid adenomatosis].

Surgical (374 cases) and puncture (6148 cases) material from patients with multinodular goiter was studied. Definitions and a working classification characterizing morphological and cytological signs of adenomatous goiter were formulated. Prognostic significance of thyroid adenomatosis and approaches to its treatment in multinodular goiter are shown.

Adenoma↗

[Osteopathy in diabetic foot syndrome].

Morphological characteristics of bone tissues were studied in the feet of patients with diabetes mellitus type 1 and 2 (DM1 and DM2). Osteoblasts and osteoclasts prevalence, the presence of collagen type III in the composition of newly formed bone were characteristic for DM1. Osteocytes prevalence and abundant granulation tissue in newly formed bone was a feature of DM2. The analysis of bone tissue resorption suggests that lacunar osteoclastic resorpsion is the main type in DM1 while periosteocytic osteolysis and smooth resorption are typical for DM2. Thus, osteolysis genesis and synthesis of bone tissue in DM1 and DM2 may be different.

Adult↗

[Galectin-3 in differential diagnosis and prognosis of follicular tumors of the thyroid gland].

Differential diagnosis between follicular thyroid tumours (FTT) is difficult both at cytological and histological levels. Infiltrative growth is authentic criterion of malignancy. Immunohistochemical reaction (PAP-method) with galectin-3 antibodies was used. The results allow to make differential diagnosis of thyroid tumours before the surgery. Immunohistochemical identification of galectin-3 in the tissue of follicular adenomas with grave dysplasia and follicular carcinoma is an unfavourable prognostic sign.

Adenocarcinoma, Follicular↗

[Clinico-morphologic criteria for prognosis of stomach cancer].

New criteria of prognosis are established on the basis of study of 265 surgically removed stomach carcinomas. The factors of an unfavourable prognosis are as follows: young age, dysproteinemia, low blood coagulability, high leucocytosis and reaction of erythrocyte sedimentation, endocrine diseases, eosinophilic infiltration of stroma with high content of collagen type V and fibronectin, high expression of pepsinogen C, gastrin and carcino-embryonic antigen in the tumour parenchyma.

Age Factors↗

[Possible markers of the progression and ulcerogenesis of stomach cancer].

The stomachs from 40 patients operated on for gastric cancer and chronic ulcer were studied immunohistochemically using antibodies to CEA, galactosyl transferase, pepsinogens A and C, gastrin, alpha 1-antitrypsin. CEA and galactosyl transferase of the cancer parenchyma are shown to mark tumor progression. The ratio of alpha 1-antitrypsin to pepsinogens in gastric epithelium and cancer cells probably plays a role in ulcerogenesis of normal mucosa and tumor tissue. Gastrin in carcinoma tissue is both an ulcerogenesis factor and a marker of tumor progression, an unfavourable prognosis of gastric cancer.

Adenocarcinoma↗

[Duodenal gastrinoma with the development of Zollinger-Ellison syndrome].

Gastrinoma consisting of eosinophilic gastrin--producing cells (this was proven electron--microscopically and immunohistochemically) was found in a 32-year-old female. The tumour, 1 x 1 x 1.5 cm in size, was located in the submucosa of the horizontal part of the duodenum. This was the cause of Zollinger--Ellison syndrome in the above patient.

Adult↗