Interstitial Pneumonia with Autoimmune Features (IPAF)
Presentation, diagnosis and clinical course of the spectrum of progressive-fibrosing interstitial lung diseases
... with interstitial pneumonia with autoimmune features ...However, IPAF is not an established diagnostic entity: IPAF criteria were constructed by the European Respiratory Society ...
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State of the art in interstitial pneumonia with autoimmune features: a systematic review on retrospective studies and suggestions for further advances
... “ interstitial pneumonia with autoimmune features ” and “ IPAF ” to identify all descriptive works on IPAF patients subsequent to publishing specific criteria, between January ...
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Interstitial pneumonia with autoimmune features: an additional risk factor for ARDS?
... between IPAF patients and control population Table 3 shows the comparison of baseline characteristics and clinical outcome among the three patient ...parameters. IPAF patients tended to have a higher median ...
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Interstitial pneumonia with autoimmune features show better survival and less exacerbations compared to idiopathic pulmonary fibrosis
... the IPAF group to groups of other ILD types with different levels of autoimmune ...of IPAF were first recommended by ATS/ERS, they focused on ILD with autoimmunity, not meeting established cri- teria ...
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Serological and morphological prognostic factors in patients with interstitial pneumonia with autoimmune features
... and interstitial lung disease were reported to be the poor prognostic survival factors of SSc patients ...in IPAF patients, and the prognosis might be more strongly affected by lung manifestation itself ...
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Mycophenolate therapy in interstitial pneumonia with autoimmune features: a cohort study
... of autoimmune disease (scleroderma, systemic lupus erythematosus, Sjögren’s syndrome/sicca, dermatomyositis, polymyositis, CTD, undifferentiated CTD) and 2) a diagnosis of ILD, nonspecific IP (NSIP), usual IP ...
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Interstitial lung disease
... organising pneumonia component and may suggest CTD; honeycombing is sparse or absent at presentation but may increase in prevalence and extent during follow-up ...
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PNEUMOCYSTIS CARINII PNEUMONIA
... sis of interstitial plasma cell pneumonia due to Pneumocystis carinii was confirmed by. Dr[r] ...
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Lung fibrotic tenascin-C upregulation is associated with other extracellular matrix proteins and induced by TGFβ1
... flammatory interstitial (saHP) and normal lungs, but this protein profile is similar to other lung fibrotic disorders such as ...different interstitial lung diseases; usual interstitial ...
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Desquamative Interstitial Pneumonia Presenting With Clubbing
... Desquamative interstitial pneumonia (DIP) is one of the rarest of the idiopathic interstitial ...with interstitial inflammation and/or ...
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Can chest x-ray predict pneumonia severity and its outcome in children aged 2 months - 5 years?
... to pneumonia every ...the pneumonia especially in developing country like in ...proven pneumonia and to see the correlation between x-rays findings and clinical severity of pneumonia, so as to ...
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Idiopathic Interstitial Pneumonias (IIPs): Review of Clinical, Radiographic and High Resolution Computed Tomography (HRCT)
... of interstitial pneumonia which is severe and sudden onset with rapid ...rapid interstitial disease after observing similar cases which had priorly ...
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Epimorphin expression in interstitial pneumonia
... izing pneumonia pattern, are frequently observed in non- specific interstitial pneumonia (NSIP); NSIP usually has a better prognosis than does usual interstitial pneumonia (UIP), which ...
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Overlaps and uncertainties of smoking-related idiopathic interstitial pneumonias
... idiopathic interstitial pneumonias (IIPs) in the revision of the 2013 American Thoracic Society/European Respiratory Society (ATS/ERS) IIP statement, represent a histologi- cal spectrum of macrophage accumulation ...
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Interstitial granulomatous dermatitis: a rare case report of dermatological manifestation of rheumatoid arthritis
... histiocytic interstitial infiltration seen on immunohistochemistry and absence of significant mucin deposition on alcian blue staining in areas of granulomatous inflammation will help in further confirmation of ...
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Characterization of lymphocyte populations in nonspecific interstitial pneumonia*
... studies on UIP suggested a Th2 type response with very low levels of INF γ , and higher levels of IL-4 [9,10]. Our study indicates that there is a substantial increase in IFN γ production in NSIP when compared to both ...
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Nonspecific interstitial pneumonia: clinical associations and outcomes
... 16. Travis WD, Hunninghake G, King TE Jr, Lynch DA, Colby TV, Galvin JR, Brown KK, Chung MP, Cordier JF, du Bois RM, Flaherty KR, Franks TJ, Hansell DM, Hartman TE, Kazerooni EA, Kim DS, Kitaichi M, Koyama T, Martinez ...
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Diagnosing fibrotic lung disease: When is high resolution computed tomography sufficient to make a diagnosis of idiopathic pulmonary fibrosis?
... Several studies have shown that in a prescribed clini- cal setting, high-resolution computed tomography (HRCT) of the chest with certain features can be used as a surrogate to recognize the pathological pattern of ...
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Pilot experience of multidisciplinary team discussion dedicated to inherited pulmonary fibrosis
... During the geneMDD, clinical data, chest CT scan and lung histological pattern were reviewed and classified ac- cording to the 2018 ATS/ERS/JRS/ALAT statement for IPF and the 2013 ATS/ERS classification of idiopathic ...
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Management of acute respiratory failure in interstitial lung diseases: overview and clinical insights
... Results: In managing ARF, it is important to establish an adequate diagnostic and therapeutic management depending on whether the patient has an underlying known chronic ILD or ARF is presenting in an unknown or de novo ...
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