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Artykuły w czasopismach na temat „Non-specific interstitial pneumonia”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Negmatullaevna, Makhmatmuradova Nargiza. "RADIOLOGICAL SIGNS NON-SPECIFIC INTERSTITIAL PNEUMONIA." American Journal of Medical Sciences and Pharmaceutical Research 04, no. 02 (2022): 7–11. http://dx.doi.org/10.37547/tajmspr/volume04issue02-03.

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The retrospective analysis of case histories of 82 patients with nonspecific interstitial pneumonia, treated as inpatients at the Pulmonology Department of Samarkand City Medical Association during the period from 2010 to 2020 has been carried out. All patients were examined by means of X-ray and computed tomography with high resolution. In the cellular subtype predominance of "frosted glass" and absence of "honeycomb lung" and in fibrous or mixed subtype all four main X-ray syndromes as well as the sign of "honeycomb lung" were noted to a different extent [1]

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Belloli, Elizabeth A., Rosemarie Beckford, Ryan Hadley, and Kevin R. Flaherty. "Idiopathic non‐specific interstitial pneumonia." Respirology 21, no. 2 (2015): 259–68. http://dx.doi.org/10.1111/resp.12674.

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Fujita, Jiro, Yuji Ohtsuki, Takeo Yoshinouchi, et al. "Idiopathic non-specific interstitial pneumonia: as an “autoimmune interstitial pneumonia”." Respiratory Medicine 99, no. 2 (2005): 234–40. http://dx.doi.org/10.1016/j.rmed.2004.07.001.

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Makhmatmuradova, Nargiza, Olga Ibadova, and Parvina Zikriyaeva. "DIFFERENTIAL DIAGNOSTICS OF NON-SPECIFIC INTERSTITIAL PNEUMONIA." JOURNAL OF CARDIORESPIRATORY RESEARCH 2, no. 1 (2020): 50–52. http://dx.doi.org/10.26739/2181-0974-2020-2-7.

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A retrospective analysis of case histories of 82 patients with nonspecific interstitial pneumonia, 24 patients with idiopathic pulmonary fibrosis, 8 with exogenous allergic alveolitis, 12 with systemic scleroderma and 6 with drug pneumonia was carried out in hospital treatment in the pulmonology department of the Samarkand city medical hospital in 2010-2019 years. It has been established that in the differential diagnosis of nonspecific interstitial pneumonia and other lung diseases, particular attention should be paid to the anamnesis, clinical presentation and CT signs

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Aralov, Nematillo, Nargiza Makhmatmuradova, and Parvina Zakiryaeva. "CURRENT FEATURES OF NON-SPECIFIC INTERSTITIAL PNEUMONIA." Doctor's Herald/ Доктор ахборотномаси /Вестник врача 93, no. 1 (2020): 11–13. http://dx.doi.org/10.38095/2181-466x-2020931-11-13.

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In order to study the frequency of occurrence, clinical characteristics, and diagnosis of interstitial pneumonia in the pulmonary department of hospitals, a retrospective analysis of case histories of 22 patients with nonspecific interstitial pneumonia who were hospitalized in the pulmonology department of the Samarkand city medical association in 2018-2019 was performed. An increase was found in patients with interstitial lung diseases, which are observed more often in women of working age, with prevalence of dyspnea, weakness, cough in the clinic, and the importance of the use of imaging tec

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Havlucu, Yavuz, Levent Ozdemir, Suat Durkaya, and Erkan Sahin. "Non-specific Interstitial Pneumonia with Unusual Symptoms." Archivos de Bronconeumología ((English Edition)) 46, no. 7 (2010): 393–94. http://dx.doi.org/10.1016/s1579-2129(10)70091-4.

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Fujita, J., I. Yamadori, I. Suemitsu, et al. "Clinical features of non-specific interstitial pneumonia." Respiratory Medicine 93, no. 2 (1999): 113–18. http://dx.doi.org/10.1016/s0954-6111(99)90300-1.

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Makhmatmuradova, Nargiza Negmatulllaevna. "Radiological Characteristics Of Non-Specific Interstitial Pneumonia." American Journal Of Advanced Scientific Research 2, no. 9 (2025): 30–32. https://doi.org/10.5281/zenodo.14619282.

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Sawata, Tetsuro, Masashi Bando, Masayuki Nakayama, Naoko Mato, Hideaki Yamasawa, and Yukihiko Sugiyama. "Influence of Smoking in Interstitial Pneumonia Presenting with a Non-Specific Interstitial Pneumonia Pattern." Internal Medicine 55, no. 20 (2016): 2939–44. http://dx.doi.org/10.2169/internalmedicine.55.6890.

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HARADA, TAISHI, KENTARO WATANABE, KAZUKI NABESHIMA, MAKOTO HAMASAKI, and HIROSHI IWASAKI. "Prognostic significance of fibroblastic foci in usual interstitial pneumonia and non-specific interstitial pneumonia." Respirology 18, no. 2 (2013): 278–83. http://dx.doi.org/10.1111/j.1440-1843.2012.02272.x.

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Gupta, Saurabh, S. K. Verma, and Ashutosh Soni. "Idiopathic non-specific interstitial pneumonia: a brief review." International Journal Of Community Medicine And Public Health 12, no. 2 (2025): 1141–46. https://doi.org/10.18203/2394-6040.ijcmph20250336.

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Non-specific interstitial pneumonia (NSIP) is one of the better variants of interstitial lung disease in terms of outcomes. Timely diagnosis with early treatment has excellent 5-year survival figures. Typical clinical symptoms and radiologic findings makes diagnosis easy. Ruling out various associated connective tissue disease (CTD) is of paramount importance as they are amenable to immunosuppressant therapies. Majority of cases still remain idiopathic which forms the major chunk of NSIP pool. This article highlights the natural history, epidemiology and key differentiating features of NSIP an

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Bhat, Rama, Navaneeth S. Kamath, Raghavendra Rao, and S. Sneha. "Varicella pneumonia masquerading as interstitial lung disease: Non-specific interstitial pneumonitis." SAGE Open Medical Case Reports 9 (January 2021): 2050313X2110592. http://dx.doi.org/10.1177/2050313x211059293.

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Varicella-zoster virus infection also known as chickenpox is a common clinical entity especially among unvaccinated children and adults. It is said that severity increases as the age increases. Approximately 5%–15% of adult varicella can produce pulmonary manifestations. Varicella pneumonitis occurs especially in at-risk individuals like pregnant, smokers, chronic lung diseases like chronic obstructive pulmonary disease, and immunosuppression. The authors describe a case of severe varicella pneumonitis in a healthy immunocompetent middle-aged woman which posed a great diagnostic challenge. The

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Meryem, Sqalli Houssaini, Yahya Mourabiti Abdelaali, El Bouardi Nizar, Youssef Alaoui Lamrani Moulay, Maaroufi Mustapha, and Alami Badreedine. "Clinical, radiological and evolutionary aspects of non-specific interstitial Pneumonia." World Journal of Advanced Research and Reviews 19, no. 2 (2023): 872–83. https://doi.org/10.5281/zenodo.10846680.

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<strong>Introduction: </strong>Non-specific interstitial pneumonia (NSIP) is an interstitial lung disease that may be idiopathic or secondary to connective tissue disease, toxins or numerous other causes. <strong>Materials and methods: </strong>This is a retrospective study of 30 cases of non-specific interstitial lung disease collected in the radiology and pneumology departments of the Hassan II University Hospital of Fez, spread over a period of 4 years. <strong>Results: </strong>We collected 30 cases followed for NSIP. The mean age was 49.5 years, with extremes ranging from 2

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14

KATOH, Toshiyuki, Takayuki ANDOH, Kenichiro MIKAWA, et al. "Computed tomographic findings in non-specific interstitial pneumonia/fibrosis." Respirology 3, no. 2 (1998): 69–75. http://dx.doi.org/10.1111/j.1440-1843.1998.tb00099.x.

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Jeong, Yeon Joo, Kyung Soo Lee, Nestor L. Müller, et al. "Usual Interstitial Pneumonia and Non-Specific Interstitial Pneumonia: Serial Thin-Section CT Findings Correlated with Pulmonary Function." Korean Journal of Radiology 6, no. 3 (2005): 143. http://dx.doi.org/10.3348/kjr.2005.6.3.143.

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Ishii, H. "High serum concentrations of surfactant protein A in usual interstitial pneumonia compared with non-specific interstitial pneumonia." Thorax 58, no. 1 (2003): 52–57. http://dx.doi.org/10.1136/thorax.58.1.52.

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Tomoo, Kishaba, Fukuoka Junya, Nei Yuichiro, Nagano Hiroaki, Yamashiro Shin, and Kunishima Fumihito. "Fibrotic Sarcoidosis Mimics Non-specific Interstitial Pneumonia: A Case Report." British Journal of Medicine & Medical Research 21, no. 11 (2017): 1–6. https://doi.org/10.9734/BJMMR/2017/33805.

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<strong>Aims: </strong>Fibrotic sarcoidosis is not common presentation and it is not easy to diagnose for many differential diagnosis. We herein report an interesting fibrotic sarcoidosis who shows atypical presentation such as progressive dyspnea with fibrotic imaging findings. <strong>Presentation of Case: </strong>A 75-year-old Japanese lady visited our hospital with fifteen months duration of non-productive cough and one month exertional dyspnea. Physical examination revealed bilateral fine crackles and squawk at left lung base. Laboratory findings showed elevation of lactate dehydrogenase

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18

Biswas, Muhammad Asaduzzaman, Muhammad Nazrul Islam, Khalifa Mahmud Walid, and Zhilam Zia Rassel. "Case Report of Diffuse Parenchymal Lung Disease with Non-Specific Interstitial Pneumonia Pattern and Good Response to Treatment." Faridpur Medical College Journal 13, no. 2 (2019): 101–3. http://dx.doi.org/10.3329/fmcj.v13i2.43646.

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The diffuse parenchymal lung diseases (DPLDs) are a heterogeneous group of conditions affecting the pulmonary parenchyma (interstitial) and/or alveolar lumen. IPF (Idiopathic Pulmonary Fibrosis) is a chronic interstitial pneumonia of unknown causes. It is commonest form of DPLD but its treatment response is very poor. On the other hand, NSIP (Non-Specific Interstitial Pneumonia) can still be a variant of DPLD with better treatment response and prognosis. Here we discussed a young female with NSIP with good response to steroid. Faridpur Med. Coll. J. Jul 2018;13(2): 101-103

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Kishaba, Tomoo, Junya Fukuoka, Yuichiro Nei, Hiroaki Nagano, Shin Yamashiro, and Fumihito Kunishima. "Fibrotic Sarcoidosis Mimics Non-specific Interstitial Pneumonia: A Case Report." British Journal of Medicine and Medical Research 21, no. 11 (2017): 1–6. http://dx.doi.org/10.9734/bjmmr/2017/33805.

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Fujita, J. "Non-specific interstitial pneumonia as pulmonary involvement of systemic sclerosis." Annals of the Rheumatic Diseases 60, no. 3 (2001): 281–83. http://dx.doi.org/10.1136/ard.60.3.281.

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Saraya, T., S. Takata, M. Fujiwara, and H. Takei. "Cellular non-specific interstitial pneumonia masquerading as congestive heart failure." Case Reports 2013, sep03 1 (2013): bcr2013010502. http://dx.doi.org/10.1136/bcr-2013-010502.

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Marten, Katharina, David Milne, Katerina M. Antoniou, et al. "Non-specific interstitial pneumonia in cigarette smokers: a CT study." European Radiology 19, no. 7 (2009): 1679–85. http://dx.doi.org/10.1007/s00330-009-1308-7.

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Pataka, Athanasia, Argyris Tzouvelekis, and Demosthenes Bouros. "Infliximab-induced non-specific interstitial pneumonia and lupus-like eruption." European Journal of Internal Medicine 17, no. 7 (2006): 520. http://dx.doi.org/10.1016/j.ejim.2006.02.010.

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Meryem Sqalli Houssaini, Abdelaali Yahya Mourabiti, Nizar El Bouardi, Moulay Youssef Alaoui Lamrani, Mustapha Maaroufi, and Badreedine Alami. "Clinical, radiological and evolutionary aspects of non-specific interstitial Pneumonia." World Journal of Advanced Research and Reviews 19, no. 2 (2023): 872–82. http://dx.doi.org/10.30574/wjarr.2023.19.2.1630.

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Introduction: Non-specific interstitial pneumonia (NSIP) is an interstitial lung disease that may be idiopathic or secondary to connective tissue disease, toxins or numerous other causes. Materials and methods: This is a retrospective study of 30 cases of non-specific interstitial lung disease collected in the radiology and pneumology departments of the Hassan II University Hospital of Fez, spread over a period of 4 years. Results: We collected 30 cases followed for NSIP. The mean age was 49.5 years, with extremes ranging from 26 to 70 years. A clear female predominance was noted (83%). Smokin

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Zhang, Lei, Tian Xie, Yaqing Li, et al. "Diagnostic value and safety of medical thoracoscopy under local anesthesia for unexplained diffuse interstitial lung disease: A retrospective study." Chronic Respiratory Disease 19 (January 2022): 147997312211333. http://dx.doi.org/10.1177/14799731221133389.

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Objective We aimed to explore the safety and diagnostic value of medical thoracoscopic lung biopsy in patients with unexplained diffuse interstitial lung disease (ILD) in a single center pilot study. Method We retrospectively analyzed clinical and pathological diagnostic data from 52 patients with diffuse ILD undergoing medical thoracoscopic lung biopsy. Results Forty-four cases of diffuse ILD were confirmed pathologically, giving a diagnostic rate of 84.6%. Among these 44 patients, 11 patients were diagnosed with cancer, including eight patients with lung adenocarcinoma, three patients with m

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Fujita, Jiro, Shuji Bandoh, Michiaki Tokuda, et al. "Non-Specific Interstitial Pneumonia and <i>Chlamydia pneumoniae</i> Infection." Japanese Journal of Infectious Diseases 54, no. 6 (2002): 225–28. https://doi.org/10.7883/yoken.jjid.2001.225.

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Desai, Nikunj C., Nilesh P. Parkar, and Asutosh N. Dave. "A Cross-Sectional Study of Radiological Profile of Interstitial Lung Disease Using High Resolution Computed Tomography of Patients Attending Medical College at Ahmedabad." Journal of Evidence Based Medicine and Healthcare 8, no. 17 (2021): 1127–32. http://dx.doi.org/10.18410/jebmh/2021/218.

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BACKGROUND Interstitial lung disease (ILD) is an unpredictable diffuse parenchymal lung disease, which involves interstitium of lung (tissue around the alveoli of the lungs). High resolution computed tomography (HRCT) is one of the confirmatory, easily accessible methodology for the conclusion and follow up assessment of interstitial lung disease. We wanted to study the normal HRCT patterns found with interstitial lung disease and contrastingly different HRCT designs and clinical information in differential determination of pulmonary fibrosis. We also wanted to study the different patterns of

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de Carvalho, E. F., E. R. Parra, R. de Souza, A. M. A’b Saber, J. de Carvalho Machado, and V. L. Capelozzi. "Arterial and interstitial remodelling processes in non-specific interstitial pneumonia: systemic sclerosis versus idiopathic." Histopathology 53, no. 2 (2008): 195–204. http://dx.doi.org/10.1111/j.1365-2559.2008.03072.x.

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Samarelli, Anna Valeria, Roberto Tonelli, Alessandro Marchioni, et al. "Fibrotic Idiopathic Interstitial Lung Disease: The Molecular and Cellular Key Players." International Journal of Molecular Sciences 22, no. 16 (2021): 8952. http://dx.doi.org/10.3390/ijms22168952.

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Interstitial lung diseases (ILDs) that are known as diffuse parenchymal lung diseases (DPLDs) lead to the damage of alveolar epithelium and lung parenchyma, culminating in inflammation and widespread fibrosis. ILDs that account for more than 200 different pathologies can be divided into two groups: ILDs that have a known cause and those where the cause is unknown, classified as idiopathic interstitial pneumonia (IIP). IIPs include idiopathic pulmonary fibrosis (IPF), non-specific interstitial pneumonia (NSIP), cryptogenic organizing pneumonia (COP) known also as bronchiolitis obliterans organi

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Aryal, Prakash, Srijan Pantha, Kum Bahadur Gurung, et al. "Amiodarone Induced Interstitial Lung Disease: An Enigma." Nepalese Respiratory Journal 3, no. 1 (2024): 24–26. http://dx.doi.org/10.3126/nrj.v3i1.69216.

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Amiodarone is an anti-arrhythmic drug that has potential to cause Interstitial Lung Disease (ILD) commonly non-specific Interistitial pneumonia. We present a 75-year male presenting with gradual onset progressive shortness of breath and dry cough after undergoing coronary artery bypass grafting (CABG) and was kept on amiodarone therapy post-surgery to control arrhythmias. The patient was diagnosed as amiodarone induced Non-Specific Interstitial Pneumonia (NSIP) after excluding alternative diagnosis. Early recognition and stoppage of amiodarone, prompt treatment with corticosteroid and respirat

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Todd, Nevins W., Ellen T. Marciniak, Ashutosh Sachdeva, et al. "Organizing pneumonia/non-specific interstitial pneumonia overlap is associated with unfavorable lung disease progression." Respiratory Medicine 109, no. 11 (2015): 1460–68. http://dx.doi.org/10.1016/j.rmed.2015.09.015.

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Atkins, S. R. "Morphological and quantitative assessment of mast cells in rheumatoid arthritis associated non-specific interstitial pneumonia and usual interstitial pneumonia." Annals of the Rheumatic Diseases 65, no. 5 (2006): 677–80. http://dx.doi.org/10.1136/ard.2005.043877.

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FUJITA, Jiro, Ichiro YAMADORI, Shuji BANDOH, et al. "Clinical Features of Three Fatal Cases of Non-specific Interstitial Pneumonia." Internal Medicine 39, no. 5 (2000): 407–11. http://dx.doi.org/10.2169/internalmedicine.39.407.

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., Abolfazl Barkhordari, R. W. Stoddart ., and Sheena F. Mclureand . "Immuno Histochemistry of Cholesterol Cleft Granulomas in Non-specific Interstitial Pneumonia." Pakistan Journal of Biological Sciences 8, no. 10 (2005): 1383–86. http://dx.doi.org/10.3923/pjbs.2005.1383.1386.

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Chakaravarthy, Pradeep, Divanshee Sharma, Manjunath Totaganti, Jithesh G, Mukesh Bairwa, and Ravikant. "Non-Specific Interstitial Pneumonia Overlapping Tuberculosis: A Diagnostic Challenge in Elderly." American Journal of Infectious Diseases 17, no. 4 (2021): 161–64. http://dx.doi.org/10.3844/ajidsp.2021.161.164.

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Churg, Andrew, and AnaMaria Bilawich. "Confluent fibrosis and fibroblast foci in fibrotic non-specific interstitial pneumonia." Histopathology 69, no. 1 (2016): 128–35. http://dx.doi.org/10.1111/his.12950.

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Abella, Ana, Marcela Homez, and Isabel Conejo. "Electrical Impedance Tomography in a Patient With Non-Specific Interstitial Pneumonia." Archivos de Bronconeumología (English Edition) 53, no. 3 (2017): 160. http://dx.doi.org/10.1016/j.arbr.2016.12.008.

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Ledda, Roberta Eufrasia, and Corrado Campochiaro. "High resolution computed tomography in systemic sclerosis: From diagnosis to follow-up." Rheumatology and Immunology Research 5, no. 3 (2024): 166–74. http://dx.doi.org/10.2478/rir-2024-0023.

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Abstract Early diagnosis of interstitial lung disease (ILD) and pulmonary hypertension (PH) is crucial in systemic sclerosis (SSc) for both management and treatment. However, diagnosing SSc-ILD can be challenging because symptoms of lung involvement are often non-specific at the early stages of disease. High-resolution computed tomography (HRCT) of the chest is recognized as the most accurate imaging modality for baseline and follow-up evaluation of SSc-ILD. Key features of SSc-ILD on HRCT include a non-specific interstitial pneumonia (NSIP) pattern, with peripheral ground-glass opacities and

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Tafti, S. F., A. Cheraghvandi, B. Mokri, and F. Talischi. "Cases non-specific interstitial pneumonia and hypersensitivity pneumonia: A new pathologic diagnosis or overlap syndrome." Respiratory Medicine Case Reports 5 (2012): 45–48. http://dx.doi.org/10.1016/j.rmedc.2011.09.003.

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Dr., Mahreen Siddique Dr. Muhammad Khalid Abbas Dr. Sadia Rehman. "ANALYSIS OF GENE EXPRESSION PROFILING AND OVERLAPPING TRANSCRIPTIONAL PROFILES IN NON-SPECIFIC INTERSTITIAL PNEUMONIA." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 10 (2018): 10772–76. https://doi.org/10.5281/zenodo.1470641.

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<strong><em>Introduction: </em></strong><em>Idiopathic pulmonary fibrosis, identified histologically as usual interstitial pneumonia, accounts for most cases of </em><em>idiopathic interstitial pneumonia</em><em>. IPF affects men and women > 50 in a ratio of 2:1, with a markedly increased incidence with each decade of age.</em><strong><em> Aims and objectives: </em></strong><em>The basic aim of the study is to analyze gene expression profiling and overlapping transcriptional profiles in non-specific interstitial pneumonia.<strong> Material and methods: </strong>This study was conducted

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Senger, Krishna Pratap Singh, and Ankita Singh. "High-resolution computed tomography as a non-invasive imaging biomarker for interstitial lung diseases: a tertiary center study." International Journal of Advances in Medicine 8, no. 2 (2021): 207. http://dx.doi.org/10.18203/2349-3933.ijam20210265.

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Background: Interstitial lung diseases (ILD) are a heterogeneous group of non-neoplastic disorders resulting from damage to the lung parenchyma by varying patterns of inflammation and fibrosis. With high-resolution computed tomography (HRCT) the pattern of lung damage can be mapped accurately which may help to identify specific ILD.Methods: 65 diagnosed cases of ILD by HRCT who were admitted to a tertiary care chest hospital, formed the study group. All these patients also underwent histopathological confirmation as per hospital protocol. The study was done over a period from August 2016 to Ju

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Camelo, Ingrid Y., Rachel Pieciak, Ilse castro-aragon, Bindu Setty, Lauren Etter, and Christopher Gill. "156. Correlation Between WHO (World Health Organization) Case Definition of Severe Pneumonia and Lung POCUS (Point of Care Ultrasound) vs Chest X-ray (CXR) Findings to Diagnose Pediatric Community-Acquired Pneumonia (CAP) in Limited Resource Settings." Open Forum Infectious Diseases 8, Supplement_1 (2021): S94—S95. http://dx.doi.org/10.1093/ofid/ofab466.156.

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Abstract Background Childhood pneumonia is one of the leading causes of death in low-income countries. The diagnosis of pediatric pneumonia is a critical epidemiological duty for treatment effectiveness and vaccine surveillance. Previous studies have demonstrated an important lack in correlation between CXR findings and the clinical WHO case definition of severe pneumonia. Lung Point of Care Ultrasound (POCUS) has demonstrated in multiple studies to be more sensitive and specific for diagnosing pneumonia in the pediatric population. With no exposure to radiation, extensive availability in limi

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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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van den Bosch, Laura, Fabrizio Luppi, Giovanni Ferrara, and Marco Mura. "Immunomodulatory treatment of interstitial lung disease." Therapeutic Advances in Respiratory Disease 16 (January 2022): 175346662211170. http://dx.doi.org/10.1177/17534666221117002.

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Interstitial lung diseases (ILDs) other than idiopathic pulmonary fibrosis (IPF) have an array of immunomodulatory treatment options compared with IPF, due to their inflammatory component. However, there is a relative paucity of guidance on the management of this heterogeneous group of diseases. In ILDs other than IPF, immunosuppression is the cornerstone of therapy, with varying levels of evidence for different immunomodulatory agents and for each specific ILD. Classification of ILDs is important for guiding treatment decisions. Immunomodulatory agents mainly include corticosteroids, mycophen

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Oldham, Justin M., Ayodeji Adegunsoye, Eleanor Valenzi, et al. "Characterisation of patients with interstitial pneumonia with autoimmune features." European Respiratory Journal 47, no. 6 (2016): 1767–75. http://dx.doi.org/10.1183/13993003.01565-2015.

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Patients with interstitial lung disease (ILD) may have features of connective tissue disease (CTD), but lack findings diagnostic of a specific CTD. A recent European Respiratory Society/American Thoracic Society research statement proposed criteria for patients with interstitial pneumonia with autoimmune features (IPAF).We applied IPAF criteria to patients with idiopathic interstitial pneumonia and undifferentiated CTD-ILD (UCTD). We then characterised the clinical, serological and morphological features of the IPAF cohort, compared outcomes to other ILD cohorts and validated individual IPAF d

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SATO, Toshio, Ichiro YAMADORI, Jiro FUJITA, et al. "Three Cases of Non-specific Interstitial Pneumonia Associated with Primary Lung Cancer." Internal Medicine 43, no. 8 (2004): 721–26. http://dx.doi.org/10.2169/internalmedicine.43.721.

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Sim, Yun Su, Jin Hwa Lee, Yon Ju Ryu, et al. "A Case of Non-Specific Interstitial Pneumonia Associated with Primary Lung Adenocarcinoma." Tuberculosis and Respiratory Diseases 63, no. 1 (2007): 83. http://dx.doi.org/10.4046/trd.2007.63.1.83.

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Akira, M. "Non-specific interstitial pneumonia: findings on sequential CT scans of nine patients." Thorax 55, no. 10 (2000): 854–59. http://dx.doi.org/10.1136/thorax.55.10.854.

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Cho, Dong Hui, Ji Hwan An, Yu Mi Kang, Eun Jin Chae, Joon Seon Song, and Jin Woo Song. "A Case of IgG4-Related Lung Disease Mimicking Non-Specific Interstitial Pneumonia." Korean Journal of Medicine 88, no. 3 (2015): 308. http://dx.doi.org/10.3904/kjm.2015.88.3.308.

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Knipscheer, Barbara J., Coline H. M. van Moorsel, and Jan C. Grutters. "Non-specific and Usual Interstitial Pneumonia, Short-Term Survival After Surgical Biopsy." Lung 193, no. 3 (2015): 449–50. http://dx.doi.org/10.1007/s00408-015-9721-y.

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