Literature DB >> 9116705

Diagnosis of alveolitis in interstitial lung manifestation in connective tissue diseases: importance of late inspiratory crackles, 67 gallium scan and bronchoalveolar lavage.

C Witt1, T Dörner, F Hiepe, A C Borges, I Fietze, G Baumann.   

Abstract

The diagnostic relevance of bronchoalveolar lavage (BAL) and associated non-invasive findings in connective tissue diseases (CTD) has not been established regarding alveolitis so far. The goal of the study was to determine the relations between BAL cell differential count and findings of non-invasive diagnostic procedures for alveolitis to predict the clinical value of BAL in CTD. One hundred-five patients (92 non-smokers; 13 smokers) with CTD (73 patients with systemic sclerosis, 19 with systemic lupus erythematosus, 13 with primary Sjögren's syndrome) had symptoms or signs of lung involvement and were further examined (lung function test, chest radiography, thoracic computed tomography, 67 gallium scintigraphy and BAL). The relations between BAL in middle lobe and cell count differentiation to non-invasive investigations were analyzed by logistic regression. In all CTD patients investigated a pulmonal involvement occurred based on non-invasive methods. Regarding non-invasive methods, alveolitis determined by BAL cell differential count was significantly associated with an increased 67-gallium uptake and late inspiratory crackles (P < 0.01), and to a lesser extent with an abnormal interstitial pattern in CT (P < 0.055). Parameters of lung function and laboratory parameters were related to alveolitis using multivariate testing. Considering the alveolitis subtype (granulo- or lymphocytosis), only a reduced FEV1 showed a relationship to granulocytic alveolitis (P < 0.01). Late inspiratory crackles and increased 67 gallium uptake as non-invasive diagnostic findings point out alveolitis in CTD remarkably. Therapeutic and prognostic aspects necessitate BAL to specify the type of alveolitis (lymphocytosis or granulocytosis or mixed forms) in CTD patients with lung manifestation. Non-invasive diagnostic procedures cannot predict the type of alveolitis sufficiently.

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Year:  1996        PMID: 9116705     DOI: 10.1177/096120339600500609

Source DB:  PubMed          Journal:  Lupus        ISSN: 0961-2033            Impact factor:   2.911


  5 in total

1.  Pulmonary involvement in diffuse cutaneous systemic sclerosis: broncheoalveolar fluid granulocytosis predicts progression of fibrosing alveolitis.

Authors:  C Witt; A C Borges; M John; I Fietze; G Baumann; A Krause
Journal:  Ann Rheum Dis       Date:  1999-10       Impact factor: 19.103

2.  Systemic lupus erythematosus presenting as acute lupus pneumonitis in a young female.

Authors:  B Chattopadhyay; A Chatterjee; A Maiti; N B Debnath
Journal:  J Postgrad Med       Date:  2015 Apr-Jun       Impact factor: 1.476

3.  Exhaled IL-8 in systemic lupus erythematosus with and without pulmonary fibrosis.

Authors:  Agnieszka Nielepkowicz-Goździńska; Wojciech Fendler; Ewa Robak; Lilianna Kulczycka-Siennicka; Paweł Górski; Tadeusz Pietras; Ewa Brzeziańska; Adam Antczak
Journal:  Arch Immunol Ther Exp (Warsz)       Date:  2014-02-04       Impact factor: 4.291

4.  Pulmonary Systemic Lupus Erythematosus Mimicking a Pneumonia in a Postpartum Female.

Authors:  Varun Jain; Maryann Aziz; Mina G Banoub; Jeremy T Neuman; Richard Sidlow
Journal:  Case Rep Rheumatol       Date:  2018-07-24

Review 5.  Respiratory Manifestations in Systemic Lupus Erythematosus.

Authors:  Salvatore Di Bartolomeo; Alessia Alunno; Francesco Carubbi
Journal:  Pharmaceuticals (Basel)       Date:  2021-03-18
  5 in total

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