Non Specific Interstitial Pneumonia: A Case Report

Autor: Vinitha K Anirudhan, Arun Prasannan, Sahana Devadas
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