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Artykuły w czasopismach na temat „Hypersensitive pneumonitis”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Demko, I. V., N. V. Gordeeva, I. A. Solovyeva, et al. "Hypersensitive pneumonitis: clinical case." Profilakticheskaya meditsina 26, no. 7 (2023): 88. http://dx.doi.org/10.17116/profmed20232607188.

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Gordeeva, N. V., I. V. Demko, M. G. Mamaeva, et al. "HYPERSENSITIVE PNEUMONITIS (DIFFICULT CLINICAL CASE)." Siberian Medical Review, no. 5 (2015): 92–95. http://dx.doi.org/10.20333/25000136-2015-5-92-95.

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Sergienko, D. F. Sergienko, O. A. Bashkina Bashkina, and T. M. Kuznetsova Kuznetsova. "Hypersensitive pneumonitis in children. Clinical experience." Pharmateca 3_2024 (July 22, 2024): 83–88. http://dx.doi.org/10.18565/pharmateca.2024.3.83-88.

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Moysan, Ph, P. Attali, and D. Valeyre. "Hypersensitive pneumonitis: CT findings (In French)." Clinical Imaging 20, no. 2 (1996): 149. http://dx.doi.org/10.1016/0899-7071(96)84514-1.

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Spichak, Т. V., L. A. Razina, A. A. Dyomushkina, O. V. Kustova, and O. F. Lukina. "Difficulties in differential diagnosis of lingering dry cough in children: from typical to rare causes." Medical Council, no. 11 (July 18, 2019): 74–81. http://dx.doi.org/10.21518/2079-701x-2019-11-74-81.

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This article deals with difficulties in differential diagnosis of lingering dry cough in children. The focus of the article is on the rare reason for lingering cough: hypersensitive pneumonitis. A brief review of the literature on this rare form of pathology is presented. The authors described two own clinical observations that demonstrate the difficulties in diagnosis, features of the course and management of patients with acute / subacute form of hypersensitive pneumonitis in prolonged observation.

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Tyagi, Kajal. "Role of HRCT in evaluation of Interstitial Lung Disease." International Journal for Research in Applied Science and Engineering Technology 9, no. 12 (2021): 2049–51. http://dx.doi.org/10.22214/ijraset.2021.39683.

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Abstract: In this study, HRCT is the examination technique of choice as it is quickly accomplished, readily available and does not require ancillary studies using other imaging technologies in most cases. In this given study, A total of 40 patients were included in which 16 patients were found to be having ILDs , there were 10 male patients (62.5%) and 6 were female patients i.e., (37.5%) of total number of patients .Idiopathic pulmonary fibrosis were found in 3 (18.75%) patients, Usual interstitial pneumonia in 2 (12.5%) patients, Chronic Hypersensitive pneumonitis in 1 (6.25%) patient , Fibr

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LEV, N. S., S. E. DIAKOVA, M. V. KOSTYUCHENKO, Y. L. MIZERNITSKY, N. N. ROZINOVA, and L. V. SOKOLOVA. "PEDIATRIC HYPERSENSITIVE PNEUMONITIS POSITIVE EXPERIENCE IN MANAGEMENT." Medical Council, no. 9 (July 18, 2017): 131–35. http://dx.doi.org/10.21518/2079-701x-2017-9-131-135.

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Hypersensitive pneumonitis (HP) is an interstitial lung disease occuring in childhood. This article demonstrates own long-running monitoring of a girl with HP at the age of 8. The development of the disease is linked to the home ecology. The diagnosis was based on data from the history, clinical symptoms with respiratory deficiency and crepitating wheezing in the lungs, characteristicfunctional and X-ray manifestations; it was proved by detection in the plasma of the blood of specific immunoglobulins of class G to cause-significant allergens. Elimination interventions and adequate treatment ha

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8

Babu, Sarath Balaji, Chetan Kumar Sohanraj, and Thangaraj Chellakutti. "Hypersensitive Pneumonitis Masquerading as Acute Severe Asthma." Journal of Pediatric Pulmonology 3, no. 3 (2024): 83–84. https://doi.org/10.4103/jopp.jopp_20_24.

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Abstract Hypersensitive pneumonitis (HP) is an uncommon cause of interstitial lung diseases in children and is often misdiagnosed as a case of asthma and treated with inhaled corticosteroids. Prompt identification of exposure in children can reduce unnecessary investigations and step-up therapy. Early identification of HP can bring better outcomes in children. We present the case of an 8-year-old boy with a recent onset of poorly controlled asthma, who presented with cyanosis, and was found to have been exposed to pigeons; his serum specific protein level for pigeon exposure was positive with

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9

Vasilieva, O. S., A. G. Chuchalin, A. L. Chernyaev, M. V. Samsonova, and E. A. Kulemina. "Hypersensitive pneumonitis caused by exposure of metal allergens." PULMONOLOGIYA, no. 4 (August 28, 2008): 116–18. http://dx.doi.org/10.18093/0869-0189-2008-0-4-116-118.

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Patra, PratapKumar, Priyanka Priyanka, Pakkiresh Reddy, Nutan Sharma, and MF Giridhar. "Hypersensitive pneumonitis in a young infant: A diagnostic imbroglio!" Journal of Pediatric Pulmonology 1, no. 2 (2022): 67. http://dx.doi.org/10.4103/jopp.jopp_10_22.

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11

Gupta, Sushan, Avani Mohta, and Danish Thameem. "Vasoreactive pulmonary artery hypertension in non-fibrotic hypersensitive pneumonitis." BMJ Case Reports 17, no. 1 (2024): e255921. http://dx.doi.org/10.1136/bcr-2023-255921.

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Group III pulmonary hypertension (PH) is common in patients with hypersensitivity pneumonitis (HSP). Group I PH and vasoreactivity in HSP have not been reported. We describe a case of an elderly veterinarian woman who presented with progressive shortness of breath and desaturation on exertion. The patient was diagnosed with non-fibrotic HSP after consistent findings on chest CT, transbronchial biopsy and a positive HSP serological panel. The patient relocated her birds, and prednisone was started. Due to persistent symptoms, she underwent a right heart catheterisation, which showed PH with vas

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12

Kuklina, Galina M., Aminat Z. Akhmedova, and Natalia N. Makariants. "Clinical observation of the course of new coronavirus infection in a patient with subacute form of hypersensitive pneumonitis." Consilium Medicum 23, no. 9 (2021): 477–79. http://dx.doi.org/10.26442/20751753.2021.9.201021.

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We present a case of difficult differential diagnostics of subacute form of hypersensitive pneumonitis in a patient with radiological symptom of "frosted glass" in the conditions of new coronavirus infection pandemic, and also the combined course of this disease and coronavirus in one patient.

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Chernyak, B. A. Chernyak, I. I. Vorzheva Vorzheva, and I. N. Trofimenko Trofimenko. "Hypersensitive pneumonitis: from etiology and pathogenesis to diagnosis and treatment." Pharmateca 5_2021 (May 26, 2021): 17–31. http://dx.doi.org/10.18565/pharmateca.2021.5.17-31.

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14

Burmistrova, T. B. "Computed tomography in the differential diagnosis of interstitial lung diseases in occupational health." Russian Journal of Occupational Health and Industrial Ecology, no. 9 (March 19, 2020): 572. http://dx.doi.org/10.31089/1026-9428-2019-59-9-572-573.

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High-resolution computed tomography made it possible to assess changes in the lungs from the effects of industrial aerosols in the development of interstitial pulmonary diseases of professional and non-professional Genesis in 342 patients: pneumoconiosis, hypersensitive pneumonitis, allergic and fibrosing alveolitis, sarcoidosis, pulmonary tuberculosis. High-resolution computed tomography was an additional method in the diagnosis of various forms of lung diseases.

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15

MOHTA, AVANI, SUSHAN GUPTA, and DANISH THAMEEM. "COMPLETE RESOLUTION OF VASOREACTIVE PULMONARY ARTERY HYPERTENSION IN CHRONIC HYPERSENSITIVE PNEUMONITIS." Chest 162, no. 4 (2022): A2012. http://dx.doi.org/10.1016/j.chest.2022.08.1658.

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16

Akbar, Muhammad Rizki, and Putu Ristyaning Ayu Sangging. "Diagnosis dan Tatalaksana Pneumonitis Hipersensitif." Wellness And Healthy Magazine 2, no. 1 (2020): 13–22. http://dx.doi.org/10.30604/well.55212020.

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Hypersensitive pneumonitis (HP), also known as extrinsic allergic alveolitis, is a complex pulmonary syndrome mediated by the immune system and caused by inhalation of various antigens that have previously been sensitized by the individual. The pathobiology of this disease is not fully understood, but in addition to the triggers that initiate the disease, genetic factors tend to be necessary, because only a small proportion of people are exposed to HP. Because of the lack of standard diagnostic standards, the diagnosis of HP is not directly established and depends on several factors, including

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17

Lev, N. S., N. N. Rozinova, Yu L. Mizernickiy, et al. "Hypersensitive pneumonitis (exogenous allergic alveolitis) in children (diagnosis and treatment). Clinical recommendations." Pediatrics (Suppl Consilium Medicum), no. 4 (2017): 10–17. http://dx.doi.org/10.26442/2413-8460_2018.4.10-17.

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18

YAMAKIDO, MICHIO. "Advanced on medical care of autoimmune disease and allergosis. Allergosis. Hypersensitive pneumonitis." Nihon Naika Gakkai Zasshi 87, no. 3 (1998): 441–45. http://dx.doi.org/10.2169/naika.87.441.

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SLAVIN, JAMES D., RATHNAKARA M. SHERIGAR, RICHARD P. SPENCER, and M. NATHAN LASSMAN. "In-111 Octreotide Lung Uptake in Hypersensitive Pneumonitis Caused by Fungal Infection." Clinical Nuclear Medicine 23, no. 12 (1998): 847–48. http://dx.doi.org/10.1097/00003072-199812000-00016.

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20

Liu, Hui, Haiming Yang, Huimin Li, Jinrong Liu, and Shunying Zhao. "Hypersensitive Pneumonitis: an Initial Presentation of Chronic Granulomatous Disease in a Child." Journal of Clinical Immunology 38, no. 2 (2018): 155–58. http://dx.doi.org/10.1007/s10875-017-0473-8.

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21

Yakushin, S. S. "Clinical thinking and instrumental diagnostics in the late stage of hypersensitive pneumonitis." Clinical Medicine (Russian Journal) 102, no. 2 (2024): 172–77. http://dx.doi.org/10.30629/0023-2149-2024-102-2-172-177.

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The existing inertia of clinical thinking in establishing a diagnosis, even in the presence of instrumental and valid diagnostic criteria, does not always allow for a reconsideration of the diagnosis given to the patient, especially several years ago. Existing clinical recommendations for certain nosological forms, which currently play a decisive role in diagnostics, treatment, and quality assessment of medical services, may not be fully applicable to all patients with a specifi c disease. As an illustration of the above, a clinical example of a patient diagnosed with “bronchial asthma” about

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22

Gorblyansky, Yuri Y., Tatyana E. Pictushanskaya, Marina A. Panova, Elena P. Kontorovich, and Oksana P. Ponamareva. "Burden of occupational lung disease." Russian Journal of Occupational Health and Industrial Ecology 61, no. 4 (2021): 243–52. http://dx.doi.org/10.31089/1026-9428-2021-61-4-243-252.

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The article presents the basic concepts of the burden of occupational diseases, the modern concept of burden assessment is considered. The burden of occupational respiratory diseases (bronchial asthma, COPD, lung cancer, pneumoconiosis, hypersensitive pneumonitis) is analyzed. In connection with the significant socio-economic damage caused by occupational diseases of the respiratory system, attention is drawn to the need to improve the effectiveness of preventive measures in the field of respiratory health protection of employees of harmful (dangerous) industries.

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23

Karoli, N. A., V. E. Kharlamov, and O. T. Zarmanbetova. "Clinical observation of interstitial lung injury caused by the use of humidifier." South Russian Journal of Therapeutic Practice 2, no. 4 (2021): 96–100. http://dx.doi.org/10.21886/2712-8156-2021-2-4-96-100.

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Humidifier lung syndrome is a rare phenotype of hypersensitive pneumonitis (HP) caused by inhalation of fumes from contaminated climate appliances such as a humidifier and air conditioner. Since the described syndrome is rarely found in the Russian Federation, the practitioner should be wary of this pathology, carefully collect an anamnesis from the patient, and also carry out differential diagnostics with lung lesions of autoimmune, drug, infectious genesis. HP therapy includes exclusion of contact with the etiological factor and the appointment of systemic hormonal therapy.

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24

Basanets, A. V., T. A. Ostapenko, and O. V. Yermakova. "Hypersensitive pneumonitis as a problem of occupational pathology of allergic origin (a clinical case)." Ukrainian Journal of Occupational Health 2019, no. 1 (2019): 67–72. http://dx.doi.org/10.33573/ujoh2019.01.067.

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Christy, Alap, Flavia Almeida, Madhuri Bhosle, Raj Jatale, and Shibani Ramchandran. "Prevalence of hypersensitive pneumonitis specific IgG antibodies in the Indian population: A retrospective study." IP Indian Journal of Immunology and Respiratory Medicine 8, no. 3 (2023): 87–94. http://dx.doi.org/10.18231/j.ijirm.2023.019.

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Identifying the underlying antigen responsible for Hypersensitivity Pneumonitis (HP) in patients poses a significant challenge within the confines of a typical clinical environment. Our primary objective in this study was to investigate the distribution and prevalence of G antibodies among individuals diagnosed with HP, taking into account factors such as age, gender, and geographical location.A retrospective study spanning 5 years (from January 2018 to June 2023) was conducted, involving patients over the age of 18 who had undergone screening for HP. Data collected from 1087 patients was anal

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Djuric, Mirna, Djordje Povazan, Svetozar Secen, and Jelena Jovic. "Differential diagnosis problem of pulmonary changes in ulcerative colitis." Vojnosanitetski pregled 67, no. 6 (2010): 511–14. http://dx.doi.org/10.2298/vsp1006511d.

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Introduction. Inflammatory intestinal diseases are often accompanied with extraintestinal and even pulmonary manifestations. The treatment of these intestinal diseases includes sulphasalazine and mesalazine, which may have undesirable allergic and other side effects, including hypersensitive pneumonitis. Case report. Having performed colonoscopy due to abdominal pains and mushy stools, the diagnosis of ulcerous colitis was established in a 20-year old female patient and the treatment with mesalazine initiated. However, the patient developed slimy and bloody stools, slightly increased body temp

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Gorblyansky, Yuriy Yu, Elmira R. Ramazanova, Elena P. Kontorovich, and Oksana P. Ponamareva. "Current views on diagnosis, treatment and prevention of occupational hypersensitivity pneumonitis." Russian Journal of Occupational Health and Industrial Ecology 63, no. 3 (2023): 171–78. http://dx.doi.org/10.31089/1026-9428-2023-63-3-171-178.

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In the structure of interstitial lung diseases (ILD), hypersensitive pneumonitis (HP) is quite common in the world. However, to date, the disease is often diagnosed at a late stage (fibrosis), which requires improving the methods of early diagnosis of the disease and timely examination of the connection of the disease with the profession. The analysis of domestic and foreign literature devoted to the peculiarities of the formation of a professional GP in modern socio-economic conditions is given. The authors have described the evolution of ideas about the disease, modern classification, occupa

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Hernandez-Gonzalez, Fernanda, Antoni Xaubet, and Jacobo Sellarés. "Keratinolytic Fungi in the Feather Stuffing of a Sofa: A Rare Cause of Hypersensitive Pneumonitis." Archivos de Bronconeumología (English Edition) 51, no. 9 (2015): 474–75. http://dx.doi.org/10.1016/j.arbr.2014.11.026.

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Kuleshov, D. A., and S. Yu Chikina. "Possibilities of computed tomography of lungs in diagnosis and differential diagnosis of hypersensitive pneumonitis (literature review)." Journal of Respiratory Medicine 1, no. 1 (2025): 23. https://doi.org/10.17116/respmed2025101123.

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Hypersensitive pneumonitis (HP) is a disease that occurs in inhalational exposure of environmental antigens and develops an immune-mediated inflammatory reaction in terminal bronchioles, alveoli and pulmonary interstitium. Classification of HP has changed many times, nevertheless emphasis on the selection of fibrotic and non-fibrotic HP phenotypes is made in recent years. Despite the modern achievements in high-resolution computed tomography (HRCT) of the lungs, significant difficulties in differential diagnosis of fibrotic HP with other pulmonary fibrosis variants, especially with idiopathic

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Vladimirova, E. B., E. I. Shmelev, I. E. Stepanyan, et al. "Interstitial lung disease: search for the cause (a clinical case)." Russian Pulmonology 28, no. 4 (2018): 490–95. http://dx.doi.org/10.18093/0869-0189-2017-28-4-490-495.

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Interstitial changes in the lungs could be caused by vast majority of diseases including tuberculosis, sarcoidosis, hypersensitive pneumonitis, metastatic injury of the lungs, etc. Differential diagnosis of pulmonary dissemination remains an urgent and challenging clinical task. This article is a review of published literature and presentation of a clinical case of a patient with interstitial lung disease. The case demonstrates diagnostic difficulties in identification the cause of interstitial lung injuries. Interstitial lung injury was incidentally found in this patient and initially was con

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Suvorova, Olga A., Natalia V. Trushenko, Maria V. Samsonova, et al. "Hypersensitivity pneumonitis: the current state of the problem." Russian Journal of Occupational Health and Industrial Ecology 63, no. 6 (2024): 408–19. http://dx.doi.org/10.31089/1026-9428-2024-64-6-408-419.

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Hypersensitive pneumonitis (HP) is an inflammatory interstitial lung disease (ILD) that occurs in predisposed individuals in response to repeated exposure to various aerosol antigens. In 2020 and 2021, specialists made changes to the latest clinical recommendations, to the classification of HP, allowing to distinguish between fibrous and non-fibrous types of HP. The fibrous type is associated with the progression of the disease and an unfavorable prognosis. The diagnosis of HP and its division into types are based on a combination of clinical and anamnestic data, a high-resolution computed tom

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Vladimirovich, Medvedev Alexander. "Some Peculiarities of Non-Specific Interstitial Pneumonia, Lung Sarcoidosis and Hypersensitive Pneumonitis Associated with the Ischemic Heart Disease." Revista Gestão Inovação e Tecnologias 11, no. 2 (2021): 39–49. http://dx.doi.org/10.47059/revistageintec.v11i2.1642.

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Introduction. Modern aspects of the diagnostics and treatment of interstitial lung diseases are closely connected with the comorbidity, which is based on the study of the associations between cardiovascular diseases and interstitial lung diseases. Material and Methods. The study included 65 patients with non-specific interstitial pneumonia, 78 patients with hypersensitive pneumonitis, and 68 patients with lung sarcoidosis. Results. An association between the character of morphological alterations in the lung tissue and clinical-functional disorders was established. More expressed fibrous and i

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International, Journal of Medical Science and Innovative Research (IJMSIR). "A Rare Case Report of End Stage Occupational Lung Disease- A Single-Centre Experience From South India." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 6 (2024): 69–72. https://doi.org/10.5281/zenodo.15449484.

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<strong>Abstract</strong> <strong> </strong> Byssinosis, also known as "brown lung disease," is a respiratory condition caused by prolonged inhalation of cotton, flax, and other textile fibers. It predominantly affects workers in India's textile industry. Classified as hypersensitivity pneumonitis (HP), byssinosis manifests symptoms such as chest tightness, cough, and wheezing, particularly on Mondays. While its exact pathogenesis remains unclear, it shares similarities with HP. Although byssinosis can lead to chronic lung diseases, fibrosis is rare, Byssinosis is primarily linked to cott

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Arkhangelskaya, E. E., S. V. Lyamina, E. O. Kozhevnikova, I. V. Kozlova, T. G. Shapovalova, and G. L. Yurenev. "Idiopathic Pulmonary Fibrosis and Hypersensitive Pneumonitis: A Fresh View on The Role of Genetic and Epigenetic Factors in The Development and Course of Diseases." Russian Archives of Internal Medicine 14, no. 6 (2024): 405–18. http://dx.doi.org/10.20514/2226-6704-2024-14-6-405-418.

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Given their ubiquitous progressive nature and unfavorable prognosis, interstitial lung diseases (ILD), especially such common variants as idiopathic pulmonary fibrosis (IPF) and hypersensitivity pneumonitis (HP), rightly attract considerable attention from clinicians and scientists worldwide. In recent years, the need for an in-depth study of the clinical and pathogenetic features of ILD, improvement of existing approaches and development of effective personalized approaches to the management of this category of patients, based on the most promising targets of action, among which genetic and e

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Medvedev, A. V., A. F. Abubikirov, L. A. Mazaeva, N. G. Demyanenko, E. I. Shmelev, and N. M. Shmeleva. "Chronic Heart Failure in Patients with Hypersensitivity Pneumonitis and Ischemic Heart Disease (Clinical and Functional Parallels)." Doctor.Ru 24, no. 2 (2025): 29–39. https://doi.org/10.31550/1727-2378-2025-24-2-29-39.

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Aim. Study of clinical and functional parameters in patients with hypersensitive pneumonitis (GSP) associated with chronic heart failure (CHF) and identification of predictors of CHF development in patients with GSP. Design. Open-label comparative one-time study. Materials and methods. A total of 207 SHG patients were enrolled in the two parallel groups. The main group consisted of 109 people with SHP combined with coronary heart disease (CHD), the comparison group included 98 patients without CHD. Anamnestic data, radiation and functional parameters, echocardiography parameters for various cl

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Lobanov, Mikhail N., Oleg Y. Bronov, Yuliya A. Abovich, et al. "Differential Diagnosis of Lungs Lesions in a New Coronavirus Infection COVID-19 and Diseases of Non-Viral Etiology on the Clinical Cases by Computed Tomography Scans in Outpatient CT Centers." Annals of the Russian academy of medical sciences 75, no. 5S (2020): 395–405. http://dx.doi.org/10.15690/vramn1429.

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New coronavirus infection (COVID-19) viral pneumonia diagnosed by a complex assessment of the epidemiological history, clinical symptoms, radiological and laboratory tests. Radiologists often play a leading role in diagnosis of viral pneumonia, since they may encounter suspicious changes according to radiological studies before clinicians. However, in a number of diseases, including diseases of non-infectious non-viral etiology with a corresponding similar clinical symptoms, it may be difficult to correctly assess the changes detected by computed tomography. This study uses clinical cases to s

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Ray, Roshmi, and V. V. Venkatachalam. "Epigallocatechin Gallate Adjuvant Immunomodulatory Therapy for Hypersensitivity Pneumonitis." UTTAR PRADESH JOURNAL OF ZOOLOGY 44, no. 18 (2023): 53–63. http://dx.doi.org/10.56557/upjoz/2023/v44i183606.

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The current research aims to investigate the management of Hypersensitivity Pneumonitis (HP), a respiratory ailment affecting the lung parenchyma, particularly the alveoli, terminal bronchioli, and alveolar interstitium, due to a delayed allergic response. Various factors, such as microbial agents, animal and plant proteins, organic and inorganic compounds, and environmental substances, can contribute to respiratory issues. The inflammatory reaction in the alveolar mucosa is a hypersensitive response of type-3 (immune-complex-mediated) or type-4 (T-lymphocytes-mediated) that plays a role in th

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Rosyid, Alfian Nur, and Isnin Anang Marhana. "Faal Paru Difusi." Jurnal Respirasi 4, no. 2 (2018): 61. http://dx.doi.org/10.20473/jr.v4-i.2.2018.61-70.

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Diffusion capacity is useful for measuring ability of pulmonary microcirculation to transfer oxygen and carbon dioxide from alveoli to capillaries. Physiological examination of diffusion is a continuation of physiological examination of ventilation. Diffusion capacity is measured by DLCO (Diffusing capacity for Carbon Monoxide). Measurement of oxygen diffusion capacity directly is very difficult so that indirect methods are used using carbonmonoxide (DLCO). Diffusion capacity of oxygen is equivalent to DLCO multiplied by 1.23. Normal value of DLCO is 20-30 ml/minute mmHg. Some factors that aff

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Balaji, Mounnish, Parmarth Chandane, Avantika Chauhan, Atul Rane, and Alpa Bhosale. "Clinical profile of interstitial lung disease in children from Western India." International Journal of Contemporary Pediatrics 12, no. 2 (2025): 246–53. https://doi.org/10.18203/2349-3291.ijcp20250092.

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Background: The epidemiology of interstitial lung disease in children (chILD) remains largely unknown, particularly in developing countries. This study aims to estimate the spectrum of ILD in children in India Methods: We retrospectively analysed data from consecutive subjects aged 0 to 18 years with interstitial lung diseases (ILD) recorded in the hospital registry at the Paediatric Respiratory Unit of Bai Jerbai Wadia Institute of Child Health from January 2018 to December 2023. We determined the proportion of each ILD subtype among children. Results: Out of 30 enrolled children, 60% were ma

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Brovko, M. Yu, L. A. Strizhakov, V. I. Sholomova, et al. "Lipoid pneumonia in an employee of the petrochemical laboratory." Russian Journal of Occupational Health and Industrial Ecology, no. 4 (May 22, 2019): 223–26. http://dx.doi.org/10.31089/1026-9428-2019-59-4-223-226.

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Th e most common pathologies of the respiratory organs caused by harmful production factors include dust diseases, bronchial asthma, various variants of toxic lesions and hypersensitive pneumonitis. However, there are also more rare diseases, the awareness of doctors about which is insuffi cient. Th ese include, in addition to alveolar proteinosis, rare forms of interstitial pneumonia, including lipoid pneumonia. Lipoid pneumonia is a rare lung disease characterized by the accumulation of lipid substances in the alveoli. Cases of development of lipoid pneumonia as a result of inhalation or asp

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Shudueva, A. R., Yu L. Mizernitskiy, O. S. Groznova, and L. I. Agapitov. "Pulmonary hypertension in children with chronic bronchopulmonary pathology: a pulmonologist’s perspective to the problem." Meditsinskiy sovet = Medical Council, no. 17 (November 1, 2021): 300–309. http://dx.doi.org/10.21518/2079-701x-2021-17-300-309.

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The respiratory diseases are consistently ranked first in the morbidity pattern among children and adolescents in the Russian Federation. Registry data show that 10-12% of children with pulmonary hypertension have PH-associated chronic lung pathology. Pulmonary hypertension as a life-threatening complication of such chronic lung diseases as hypersensitive pneumonitis, bronchiectasis, bronchial asthma, etc. aggravates the severity of their clinical course and has a great impact on the outcome of the disease. The article summarizes modern data on pulmonary hypertension in children of various age

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Kuzubova, N. A., O. N. Titova, and D. B. Skliarova. "Interstitial lung diseases with progressive pulmonary fibrosis: pathogenetic features and approaches to therapy." Meditsinskiy sovet = Medical Council, no. 17 (November 22, 2020): 99–106. http://dx.doi.org/10.21518/2079-701x-2020-17-99-106.

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A number of patients with interstitial lung diseases (ILD) of various etiologies, including hypersensitive pneumonitis, diffuse connective tissue diseases (rheumatoid arthritis, systemic scleroderma, dermatomyositis), sarcoidosis, idiopathic non-specific interstitial pneumonia (NSIP) and unclassified ILD develop rapid deterioration of lung ventilation function due to the progression of fibrotic changes, accompanied by a decrease in physical performance and quality of life. It is proposed to distinguish a progressive fibrotic phenotype from those with similar pathogenetic mechanisms, radiologic

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MEDVEDEV, ALEXANDER V., ANVER F. ABUBIKIROV, ANNA S. ZAITSEVA, LARISA A. MAZAEVA, NATALIA N. MAKARYANTS та EVGENY I. SHMELEV. "КАЧЕСТВЕННАЯ И КОЛИЧЕСТВЕННАЯ ХАРАКТЕРИСТИКА ОДЫШКИ У БОЛЬНЫХ ПРОГРЕССИРУЮЩИМ ФИБРОТИЧЕСКИМ ФЕНОТИПОМ ИНТЕРСТИЦИАЛЬНЫХ БОЛЕЗНЕЙ ЛЕГКИХ, АССОЦИИРОВАННЫХ С СЕРДЕЧНО-СОСУДИСТЫМИ ЗАБОЛЕВАНИЯМИ". Bulletin of Contemporary Clinical Medicine 14, № 5 (2021): 34–42. http://dx.doi.org/10.20969/vskm.2021.14(5).34-42.

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Aim. Analysis of quantitative and qualitative parameters of dyspnea in patients with the fibrotic phenotype of interstitial lung disease associated with coronary artery disease. Material and methods. We examined 49 patients. Among those were 9 patients with idiopathic pulmonary fibrosis, 25 patients with chronic variant of hypersensitive pneumonitis, and 14 patients with nonspecific interstitial pneumonia. The main group consisted of 25 patients with interstitial lung diseases and coronary heart disease; comparison group consisted of 24 patients without ischemic heart disease. Clinical symptom

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Kuzubova, N. A., O. N. Titova, and D. B. Skliarova. "Prognostic biomarkers of progressive pulmonary fibrosis in patients with interstitial lung diseases." Meditsinskiy sovet = Medical Council, no. 4 (April 13, 2023): 86–91. http://dx.doi.org/10.21518/ms2023-013.

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A high proportion of patients with various interstitial lung diseases (ILD) develop progressive pulmonary fibrosis (PLF) associated with a deterioration in the quality of life, a decrease in functional status and early mortality. PLF is diagnosed in patients with ILD of known or unknown etiology other than idiopathic pulmonary fibrosis (ILF), who have radiological signs of pulmonary fibrosis, and at least two of the three criteria for progression, including clinical, functional and radiological indicators that have arisen over the past year in the absence of alternative causes of deterioration

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Bukhtiyarov, Igor V., Galina P. Orlova, Oleg N. Andreenko, and Svetlana S. Zemlyakova. "The epidemiology of occupational interstitial lung diseases in Russia." Russian Journal of Occupational Health and Industrial Ecology 62, no. 7 (2022): 430–36. http://dx.doi.org/10.31089/1026-9428-2022-62-7-430-436.

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Introduction. Occupational interstitial lung diseases (ILD) include exogenous allergic alveolitis (EAA), exogenous toxic alveolitis (ETA), pneumoconiosis. The scientists have established the fact of exposure to external factors in 35% of patients with ILD. We have confirmed the association of the disease with the profession in 10% of cases. The study aims to assess the prevalence and clarify the reasons for the unsatisfactory diagnosis of occupational diseases (ILD) in Russia. Materials and methods. The researchers have conducted the analysis of officially registered occupational morbidity in

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Самаль, Т. Н. "Infantile Interstitial Lung Diseases." Педиатрия. Восточная Европа, no. 1 (March 3, 2021): 79–93. http://dx.doi.org/10.34883/pi.2021.9.1.007.

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Интерстициальные болезни легких (ИБЛ) у детей первых лет жизни, как и ИБЛ у взрослых, относятся к редкой патологии. Несмотря на схожесть клинической и рентгенологической картины, младенческие ИБЛ имеют значительные отличия от данной патологии у старших детей и взрослых, поскольку развиваются на фоне активно растущих легких и особенностей иммунитета. У детей важную роль в развитии ИБЛ играют наследственные и неонатальные причины (наследственная патология сурфактанта, нейроэндокринная гиперплазия, пневмопатии недоношенных и т. д.), в то время как аутоиммунные реакции, доминирующие у взрослых, не

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Kobzar, V. "Allergy to Cannabis Pollen in a Changing World." Bulletin of Science and Practice, no. 9 (September 15, 2023): 58–68. http://dx.doi.org/10.33619/2414-2948/94/06.

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Globally, the family of Cannabaceae (hemp) — dicotyledonous plants of the order Rosaceae Rosales (formerly the order Urticales nettle) includes two allergenic genera, namely: hemp and hops. It is estimated that only one male cannabis flower produces about 350,000 pollen grains, and if the plant includes hundreds of flowers, then it gives a lot of pollen in the air, carried far enough. Given that marijuana is legalized as a light drug in many countries, the effects of Cannabis on health, including allergies, are coming to the forefront of medical research and interest. As an aeroallergen, hemp

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Medvedev, A. V., A. F. Abubikirov, A. S. Zaitseva, L. A. Mazaeva, N. N. Makaryants, and E. I. Shmelev. "Shortness of Breath in Patients with Progressive Fibrous Interstitial Lung Disease Associated with Cardio Ischemia." Doctor.Ru 20, no. 7 (2021): 58–65. http://dx.doi.org/10.31550/1727-2378-2021-20-7-58-65.

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Study Objective: To compare the quantitative aspects of shortness of breath in patients with fibrous interstitial lung disease (ILD) associated with cardio ischemia; to compare analysis results of the data obtained during functional and instrumental examinations. Study Design: Open comparative study in parallel groups. Materials and Methods. The study included 47 patients with fibrous ILD: 8 patients had idiopathic pulmonary fibrosis; 25 patients had chronic hypersensitive pneumonitis, and 14 patients had fibrous non-specific interstitial pneumonia. The patients were divided into two groups: s

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Tarasov, R. V., L. N. Lepekha, S. S. Sadovnikova, et al. "The complexities of complex treatment of a patient with widespread destructive pulmonary tuberculosis against the background of severe pulmonary bullous dystrophy after exogenous exposure to fine particles of coal dust in the anamnesis." Bulletin of the Medical Institute "REAVIZ" (REHABILITATION, DOCTOR AND HEALTH) 13, no. 5 (2023): 142–52. http://dx.doi.org/10.20340/vmi-rvz.2023.5.case.5.

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An observation from practice is given – a staged surgical treatment of a patient with widespread destructive pulmonary tuberculosis with preXDR MBT against the background of severe bullous lung dystrophy after prolonged exogenous exposure to fine particles of coal dust in the anamnesis. Patient M., 42 years old, smoker, has been working as a loader at a railway station since the age of 20, unloading wagons with bags of coal at high temperatures without using personal protective equipment. He was ill with pulmonary tuberculosis 12 years ago, the original form: infiltrative tuberculosis of the u

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Raikova, Svetlana Vladimirovna, Natalia Evgenievna Komleva, Marina Valerianovna Potapova, Olga Viktorovna Livkina, Oksana Tamerlanovna Mishankina, and Svyatoslav Igorevich Mazilov. "Hypersensitive pneumonitis: diagnostic difficulties (Clinical case)." Medical news of the North Caucasus 18, no. 3 (2023). http://dx.doi.org/10.14300/mnnc.2023.18077.

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