Contents

SynopsisCodesDifferential Diagnosis & PitfallsBest TestsDrug Reaction DataReferences
Nonspecific interstitial pneumonia
Other Resources UpToDate PubMed

Nonspecific interstitial pneumonia

Contributors: Christine Osborne MD, Mary Anne Morgan MD
Other Resources UpToDate PubMed

Synopsis

Part of the family of idiopathic interstitial pneumonias, but lacks the histopathologic features to specifically classify the disease. Patients typically present with the subacute development of dyspnea and cough. Other presenting symptoms such as Raynaud phenomenon, dry mouth or eyes, or rash or skin changes may point to an underlying collagen-vascular disease. Physical examination typically reveals bibasilar crackles.

While there is no definitive cause, there are associations with collagen-vascular diseases including polymyositis-dermatomyositis, rheumatoid arthritis, Sjögren syndrome, and systemic sclerosis, infections such as human immunodeficiency virus (HIV), and medications such as flecainide, amiodarone, methotrexate, carmustine, nitrofurantoin, statins, and chlorambucil.

Codes

ICD10CM:
J84.113 – Idiopathic non-specific interstitial pneumonitis

SNOMEDCT:
129452008 – Nonspecific interstitial pneumonia

Differential Diagnosis & Pitfalls

To perform a comparison, select diagnoses from the classic differential

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Best Tests

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Drug Reaction Data

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References

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Last Updated:01/21/2016
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Nonspecific interstitial pneumonia
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A medical illustration showing key findings of Nonspecific interstitial pneumonia : Exertional dyspnea, Dry cough, Bibasilar crackles
Copyright © 2024 VisualDx®. All rights reserved.