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Interstitial lung disease in Indonesian adult with systemic sclerotic: A rare case

BACKGROUND: Systemic Sclerotic (SSc) with interstitial lung disease (ILD) is a rare autoimmune case. In Indonesia, SSc-ILD cases are still not widely reported. CASE PRESENTATION: A 43-year-old female complained fever, yellow phlegm, and shortness of breath for 1 week. The evaluation results based on...

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Detalles Bibliográficos
Autores principales: Anggoro, Adhitri, Hasan, Helmia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857448/
https://www.ncbi.nlm.nih.gov/pubmed/35242329
http://dx.doi.org/10.1016/j.amsu.2022.103386
Descripción
Sumario:BACKGROUND: Systemic Sclerotic (SSc) with interstitial lung disease (ILD) is a rare autoimmune case. In Indonesia, SSc-ILD cases are still not widely reported. CASE PRESENTATION: A 43-year-old female complained fever, yellow phlegm, and shortness of breath for 1 week. The evaluation results based on the American College of Rheumatology and European League Against Rheumatism (ACR EULAR) classification criteria for systemic sclerosis showed a score of 17. The patient received Methylprednisolone 8 mg tab/8 hours, Meropenem 1 gr/8 hours, Ranitidine 50 mg/12 hours, Metoclopramide 10 mg/8 hours, KSR 600 mg tab/8 hours, Paracetamol 500 mg tab/8 hours, VIP albumin 500 mg tab/8 hours, and Folic acid 400 mg tab/8 hours. The patient underwent high resolution computer tomography (HRCT). A chest scan obtained SSc-ILD. Sputum culture results did not reveal Mycobacterium tuberculosis. DISCUSSION: SSc-ILD patients in endemic tuberculosis need to be examined for GeneXpert and sputum culture. The HRCT scan is more helpful in diagnosing SSc-ILD than bronchoalveolar lavage (BAL). CONCLUSION: The HRCT is one of the gold standards in establishing the diagnosis of SSc-ILD.