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  • 1
    Online Resource
    Online Resource
    MDPI AG ; 2010
    In:  Advances in Respiratory Medicine Vol. 79, No. 1 ( 2010-12-28), p. 6-15
    In: Advances in Respiratory Medicine, MDPI AG, Vol. 79, No. 1 ( 2010-12-28), p. 6-15
    Abstract: Introduction: Although induced sputum (IS) has recently been used in studies of interstitial lung disease (ILD), there havebeen few reports on studies investigating the usefulness of this method in the differential diagnosis of ILD. The aim of ourstudy was to determine the diagnostic value of differential cell counts and CD4+/CD8+ ratio in induced sputum frompatients with sarcoidosis and other ILDs. Material and methods: We enrolled 59 patients in the study (36 with sarcoidosis, 16 with hypersensitivity pneumonitis[HP] and seven with idiopathic pulmonary fibrosis [IPF] ). Sputum was induced a minimum of seven days following BAL byinhalation of 5% NaCl solution for five minutes and repeated four times. Differential cell count was determined in Giemsastained cytospins by counting 400 mononuclear cells for specific cell types per slide. The analysis of T-cell subtypes wascarried out by flow cytometry. The potential for differentiating sarcoidosis from the other ILDs was checked by determiningthe predictive value for CD4+/CD8+ ratio or by using the object classification method based on the k-nearest neighbour(k-NN) rule. The variables used in the k-NN rule were the following parameters of IS: cell viability, total cell count,percentages of macrophages, lymphocytes, neutrophils, eosinophils, CD4+ lymphocytes and CD8+ lymphocytes, and theCD4+/CD8+ ratio. Results: Evaluation of IS was possible in 33 patients (15 with sarcoidosis, 11 with HP and seven with IPF). A CD4+/CD8+ratio in IS exceeding 2.6 had a sensitivity of 100%, and a specificity of 72% with the likelihood of establishing the correctdiagnosis while differentiating sarcoidosis from HP and IPF. On the other hand, when we used the k-NN rule, the likelihood ofestablishing the correct diagnosis was 79% (with an estimated classification error of 21%). Conclusion: Using the object classification method based on the k-NN rule in the differential diagnosis of sarcoidosis, HPand IPF on the basis of all the IS parameters is not associated with a higher likelihood of establishing the correct diagnosisthan the analysis of CD4+/CD8+ ratio alone.
    Type of Medium: Online Resource
    ISSN: 2543-6031
    Language: English
    Publisher: MDPI AG
    Publication Date: 2010
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  • 2
    In: Advances in Respiratory Medicine, MDPI AG, Vol. 88, No. 1 ( 2020-02-28), p. 42-94
    Abstract: Introduction: This document presents the Guideliness of the Polish Respiratory Society (PTChP, Polskie Towarzystwo Chorób Płuc) for diagnosis and treatment of idiopathic pulmonary fibrosis (IPF), developed by agroup of Polish experts. Material and methods: The recommendations were developed in the form of answers to previously formulated questions concer-ning everyday diagnostic and therapeutic challenges. They were developed based on acurrent literature review using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) methodology. Results: We formulated 28 recommendations for diagnosis (8), pharmacological treatment (12) as well as non-pharma-cological and palliative therapy (8). The experts suggest that surgical lung biopsy (SLB) not be performed in patients with the probable usual interstitial pneumonia (UIP) pattern, with an appropriate clinical context and unanimous opinion of a multidisciplinary team. The experts recommend using antifibrotic agents in IPF patients and suggest their use irrespective of the degree of functional impairment. As regards non-pharmacological and palliative treatment, strong re-commendations were formulated regarding pulmonary rehabilitation, oxygen therapy (in patients with chronic respiratory failure), preventive vaccinations as well as referring IPF patients to transplant centres. Table 1 presents an aggregate list of recommendations. Conclusions: The Polish Respiratory Society Working Group developed Guideliness for IPF diagnosis and treatment.
    Type of Medium: Online Resource
    ISSN: 2543-6031
    Language: English
    Publisher: MDPI AG
    Publication Date: 2020
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  • 3
    In: Advances in Respiratory Medicine, MDPI AG, Vol. 90, No. 5 ( 2022-10-04), p. 425-450
    Abstract: The recommendations were developed as answers to previously formulated questions concerning everyday diagnostic and therapeutic challenges. They were developed based on a review of the current literature using the GRADE methodology. The experts suggest that PF-ILD be diagnosed based on a combination of different criteria, such as the aggravation of symptoms, progression of radiological lesions, and worsening of lung function test parameters. The experts recommend a precise diagnosis of an underlying disease, with serological testing for an autoimmune disease always being included. The final diagnosis should be worked out by a multidisciplinary team (MDT). Patients with an interstitial lung disease other than IPF who do not meet the criteria for the progressive fibrosis phenotype should be monitored for progression, and those with systemic autoimmune diseases should be regularly monitored for signs of interstitial lung disease. In managing patients with interstitial lung disease associated with autoimmune diseases, an opinion of an MDT should be considered. Nintedanib rather than pirfenidon should be introduced in the event of the ineffectiveness of the therapy recommended for the treatment of the underlying disease, but in some instances, it is possible to start antifibrotic treatment without earlier immunomodulatory therapy. It is also admissible to use immunomodulatory and antifibrotic drugs simultaneously. No recommendations were made for or against termination of anti-fibrotic therapy in the case of noted progression during treatment of a PF-ILD other than IPF. The experts recommend that the same principles of non-pharmacological and palliative treatment and eligibility for lung transplantation should be applied to patients with an interstitial lung disease other than IPF with progressive fibrosis as in patients with IPF.
    Type of Medium: Online Resource
    ISSN: 2543-6031
    Language: English
    Publisher: MDPI AG
    Publication Date: 2022
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  • 4
    In: Advances in Respiratory Medicine, MDPI AG, Vol. 86, No. 2 ( 2018-04-30), p. 92-96
    Abstract: Differentiation between pulmonary tuberculosis and lung cancer is often challenging for clinicians, especially that both conditions can coexist. This is due to the fact that the clinical and radiological symptoms of both diseases can be similar. Our Case Report presents a patient who was treated for advanced lung cancer 10 years earlier and currently has been hospitalized again because of a strong clinical and radiological suspicion of the cancer progression, but whose final diagnosis was tuberculosis.
    Type of Medium: Online Resource
    ISSN: 2543-6031
    Language: English
    Publisher: MDPI AG
    Publication Date: 2018
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  • 5
    In: Advances in Respiratory Medicine, MDPI AG, Vol. 81, No. 6 ( 2013-10-21), p. 550-555
    Abstract: Rak płuca jest najczęstszym nowotworem złośliwym u mężczyzn, który w stadium zaawansowanym może dawać przerzuty do tkanki podskórnej lub naciekać ścianę klatki piersiowej. Przedstawiono przypadek chorego, który został skierowany do kliniki z podejrzeniem raka płuca naciekającego boczną ścianę klatki piersiowej. Dodatkowo u pacjenta stwierdzono liczne przerzuty do kości płaskich (żeber, kręgów, czaszki). Szeroko zakrojona diagnostyka przyniosła zaskakujące rozpoznanie raka przewodowego piersi, nowotworu, który u mężczyzn występuje niezwykle rzadko i najczęściej prezentuje się jako dobrze odgraniczony guzek w okolicy brodawki sutkowej. Prezentowany przypadek pokazuje, jak istotną rolę odgrywa wnikliwa ocena mikroskopowa zmiany zlokalizowanej w ścianie klatki piersiowej.
    Type of Medium: Online Resource
    ISSN: 2543-6031
    Language: English
    Publisher: MDPI AG
    Publication Date: 2013
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  • 6
    In: Advances in Respiratory Medicine, MDPI AG, Vol. 83, No. 6 ( 2015-11-10), p. 453-456
    Abstract: Pulmonary alveolar proteinosis is a very rare interstitial lung disease caused by abnormal intra-alveolar surfactant accumulation. Usually, it appears as a “crazy-paving” pattern on high-resolution computed tomography. The image is so typical, that together with the characteristic bronchoalveolar lavage examination with presence of Periodic Acid Schiff positive substance is sufficient for establishing diagnosis, without histological confirmation. We present the case of the young woman with severe dyspnoea suspected of acute hypersensitivity pneumonia. The computed tomography showed numerous intralobular nodules uniformly distributed troughout the lungs. Treatment by corticosteroids had no clinical effect and next computed tomography showed progression. Despite the high risk of complications (patient had a respiratory failure), a surgical lung biopsy was performed and the histopathological diagnosis of pulmonary alveolar proteinosis was made. The whole lung lavage procedure performed twice caused regression of radiological lesions and respiratory failure.
    Type of Medium: Online Resource
    ISSN: 2543-6031
    Language: English
    Publisher: MDPI AG
    Publication Date: 2015
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  • 7
    In: Advances in Respiratory Medicine, MDPI AG, Vol. 89, No. 5 ( 2021-07-16), p. 532-537
    Abstract: Actinomycosis is a rare disease caused by Actinomyces spp. The clinical and radiological picture of the disease is uncharacter-istic, which delays the diagnosis and can lead to complications. We present a case of pulmonary actinomycosis complicated by a chest wall fistula in a 43-year-old man with advanced tooth decay. The patient was admitted to our Department due to a chest wall fistula with bloody discharge. A few months earlier, he was treated with antibiotics for pneumonia. Since then, weakness, exertional dyspnoea, and weight loss had been observed. On admission, increased inflammatory markers were found in laboratory tests. Chest computed tomography (CT) revealed right-sided encapsulated pleural fluid collection containing gas bubbles, pleural thickening, anterior thoracic wall soft tissues thickening and subcutaneous fat stranding. CT suggested an empyema or a breast either pleural malignancy. The picture suggested a breast or pleural tumour to differentiate with an empyema. Videothoracoscopy was performed, the histological examination of the collected samples revealed granulation tissue and bacterial colony of a morphology corresponding to Actinomyces spp. Pulmonary actinomycosis was diagnosed. Antibiotic therapy according to the Guideliness was initiated and dental treatment was recommended. Healing of the fistula and significant regression of lesions in the right lung were achieved. Although it is a rare disease, actinomycosis should be considered in the differential diagnosis of any chronic infiltrative lung lesions.
    Type of Medium: Online Resource
    ISSN: 2543-6031
    Language: English
    Publisher: MDPI AG
    Publication Date: 2021
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  • 8
    In: Advances in Respiratory Medicine, MDPI AG, Vol. 77, No. 5 ( 2009-08-12), p. 446-452
    Abstract: Introduction: Th1 response is known to play a dominant role in the resistance to tuberculosis. Nevertheless, IFN gamma levels are frequently increased in tuberculous patients, especially at the site of the disease. It is also possible that the shift toward Th2 response is responsible for the loss of resistance. The aim of this study was to compare the Th1 function of peripheral blood cells and the levels of antimycobacterial antibodies in the serum of culture positive tuberculosis patients and healthy tuberculosis (Tb) contacts. The correlation between the levels of antimycobacterial antibodies and Th1 function of blood cells was also evaluated. Material and Methods: The material consisted of 51 tuberculous patients and 20 healthy persons, close contacts of tuberculosis patients. The ability of peripheral blood cells to secrete IFN gamma and IL-2 was estimated in whole blood cultures with PHA, PWM and tuberculin. The levels of IFN gamma and IL-2 in the supernatants of cultures was estimated via a commercial ELISA test. The levels of antimycobacterial antibodies was measured with commercial immunoenzymatic kits detecting IgG antibodies against 38 kDa+16 kDa and IgG, IgA and IgM antibodies to 38 kDa + lipoarabinomannan (LAM). Results: No difference was found in the secretion of IFN gamma and IL-2 after stimulation with PHA and PWM between the patients and contacts. The secretion of IFN gamma after stimulation with tuberculin was even greater in tuberculous patients than in contacts. The levels of IgG and IgA (38 kDa+LAM) were higher in tuberculous patients than in contacts. There was a negative correlation between the level of IgG anti 38 kDa+LAM and the ability of peripheral blood cells to secrete IFN gamma after non-specific stimulation in patients with tuberculosis. Conclusions: Our study confirms the hypothesis that it is not the diminished production of Th1 cytokines, but rather the parallel overproduction of Th2 cytokines, which are essential in the development of tuberculosis.
    Type of Medium: Online Resource
    ISSN: 2543-6031
    Language: English
    Publisher: MDPI AG
    Publication Date: 2009
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  • 9
    In: Advances in Respiratory Medicine, MDPI AG, Vol. 86, No. 102 ( 2018-08-18), p. 4-9
    Abstract: Różnicowanie pomiędzy gruźlicą płuc a rakiem płuca stanowi często prawdziwe wyzwanie dla klinicystów, szczególnie że oba schorzenia mogą występować równocześnie. Jest to spowodowane tym, że zarówno objawy kliniczne, jak i radiologiczne obu chorób są podobne. Prezentowany opis przypadku przedstawia pacjentkę leczoną 10 lat wcześniej na zaawansowanego raka płuca, która z powodu pojawienia się nowych objawów klinicznych i zmian radiologicznych trafiła ponownie do szpitala z powodu podejrzenia progresji raka, a u której ostatecznie rozpoznano gruźlicę.
    Type of Medium: Online Resource
    ISSN: 2543-6031
    Language: English
    Publisher: MDPI AG
    Publication Date: 2018
    detail.hit.zdb_id: 2893877-X
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  • 10
    In: Endoscopic Ultrasound, Medknow, Vol. 5, No. 3 ( 2016), p. 173-
    Type of Medium: Online Resource
    ISSN: 2303-9027
    Language: English
    Publisher: Medknow
    Publication Date: 2016
    detail.hit.zdb_id: 2998317-4
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