scholarly journals Evaluation of clinical presentation and outcome of patients with respiratory bronchiolitis-associated interstitial lung disease

2015 ◽  
Vol 21 (1) ◽  
pp. 47-48
Author(s):  
M. Vaz ◽  
N. Melo ◽  
P.C. Mota ◽  
R. Cunha ◽  
J.M. Pereira
2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Gurveen Malhotra ◽  
Nitya Ramreddy ◽  
Serafin Chua ◽  
Mira Iliescu ◽  
Tanjeev Kaur

Antisynthetase (AS) syndrome is a major subgroup of inflammatory myopathies seen in a minority of patients with dermatomyositis and polymyositis. Although it is usually associated with elevated creatine phosphokinase level, some patients may have amyopathic dermatomyositis (ADM) like presentation with predominant skin involvement. Interstitial lung disease (ILD) is the main pulmonary manifestation and may be severe thereby determining the prognosis. It may rarely present with a very aggressive course resulting in acute respiratory distress syndrome (ARDS). We report a case of a 43-year-old male who presented with nonresolving pneumonia who was eventually diagnosed to have ADM through a skin biopsy without any muscle weakness. ADM may be associated with rapidly progressive course of interstitial lung disease (ADM-ILD) which is associated with high mortality. Differentiation between ADM-ILD and AS syndrome may be difficult in the absence of positive serology and clinical presentation may help in clinching the diagnosis.


Author(s):  
Vivien Somogyi ◽  
Monika Eichinger ◽  
Felix Lasitschka ◽  
Jutta Kappes ◽  
Michael Kreuter

CHEST Journal ◽  
2020 ◽  
Vol 158 (4) ◽  
pp. A1074-A1075
Author(s):  
Eleanor Phillips ◽  
Iazsmin Bauer Ventura ◽  
Cathryn Lee ◽  
Ayodeji Adegunsoye ◽  
Mary Strek ◽  
...  

2021 ◽  
Vol 2021 ◽  
pp. 1-7
Author(s):  
Matthew Koslow ◽  
Mehrnaz Maleki-Fischbach ◽  
Rebecca C. Keith

Interstitial lung disease (ILD) associated with connective tissue diseases (CTDs) is highly heterogeneous in its clinical presentation and course. The diagnosis and management of CTD-ILD require a multidisciplinary approach involving, at minimum, a rheumatologist, a pulmonologist, and a radiologist. Close monitoring of patients with CTD-ILD is important to enable early detection of disease progression and inform decisions regarding the initiation or escalation of pharmacotherapy. In the absence of guidelines regarding how CTD-ILDs should be treated, clinicians face difficult decisions on when to use immunosuppressant and anti-fibrotic therapies. The importance of a multidisciplinary and individualized approach to the diagnosis and management of CTD-ILD is highlighted in the three case studies that we describe in this article.


2004 ◽  
Vol 5 (2) ◽  
pp. 98-100 ◽  
Author(s):  
Brigitte Fauroux ◽  
Ralph Epaud ◽  
Annick Clément

Author(s):  
Tiyas Sen Dutt

Interstitial lung diseases (ILD) are a group of conditions with varied etiology, clinical presentation, management, outcome and complications. Although studies have described lung cancer as a sequel of ILD, the association of ILD with non-lung malignancies or ILD presenting as a paraneoplastic syndrome of an underlying occult malignancy deserves further study. In this case series, we describe eight patients with an ILD and an associated neoplasm and discuss the different questions raised by this association.


2022 ◽  
pp. 1-5
Author(s):  
Emily Molina ◽  
Lisa Christopher-Stine ◽  
Jemima Albayda

The clinical presentation of dermatomyositis (DM) is diverse, with varied phenotypes that may be correlated with specific autoantibodies. The anti-melanoma differentiation-associated gene 5 (MDA5) antibody in DM is associated with an amyopathic phenotype of DM, with several unusual cutaneous manifestation and increased risk for rapidly progressive interstitial lung disease. Initial presentation may be subtle, but early diagnosis is key to initiation of proper immunosuppressive therapy. In this report, we describe perinasal edema and erythema as a presenting complaint of anti-MDA5 DM in an otherwise healthy 40-year-old woman. The edema began shortly after heavy sun exposure and was followed by painful papules in her hands and arthritis within a few weeks. She was found to have high titer of anti-CCP and anti-MDA5, and thus was diagnosed with DM and rheumatoid arthritis overlap. A CT chest, abdomen, and pelvis showed patchy ground-glass and interstitial opacities in bilateral lower lobes consistent with mild interstitial lung disease without evidence of malignancy. Perinasal cutaneous findings and arthralgias improved with initiation of prednisone. To our knowledge, this is the first report of perinasal edema as a presenting symptom for DM and should raise suspicion for MDA-5 disease.


Pneumologie ◽  
2010 ◽  
Vol 64 (01) ◽  
Author(s):  
N Weichert ◽  
E Kaltenborn ◽  
A Hector ◽  
M Woischnik ◽  
S Moslavac ◽  
...  

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