Non Specific Interstitial Pneumonia: A Case Report
Autor: | Vinitha K Anirudhan, Arun Prasannan, Sahana Devadas |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: | |
Zdroj: | Journal of Clinical and Diagnostic Research, Vol 12, Iss 1, Pp SD10-SD12 (2018) |
Druh dokumentu: | article |
ISSN: | 2249-782X 0973-709X |
DOI: | 10.7860/JCDR/2018/26372.11127 |
Popis: | Idiopathic Non-Specific Interstitial Pneumonia (NSIP) is a rare entity in children and classified into cellular NSIP (c-NSIP) or fibrotic NSIP patterns. It comes under major idiopathic interstitial pneumonia. Both conditions are characterised by Ground Glass Opacities (GGO), irregular linear opacities and consolidations in a bilateral, symmetrical or sub pleural distribution. It’s a disease with diagnostic difficulty so a multidisciplinary diagnosis was approached for the diagnosis i.e., clinical, radiological and histopathological. The prognosis of this condition is variable; it is a reversible disease with risk of progression. Therefore, early diagnosis and disease stratification are important in this disease. Here we report the case of a three-year-old girl child who presented with atypical clinical and radiological features, but had been diagnosed to have c-NSIP. |
Databáze: | Directory of Open Access Journals |
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