Idiopathic Pulmonary Hemosiderosis in a Young Adult Patient: A Rare Case

التفاصيل البيبلوغرافية
العنوان:	Idiopathic Pulmonary Hemosiderosis in a Young Adult Patient: A Rare Case
المؤلفون:	Abhishek Agarwal, Rahul Kumar, Anand Jaiswal, Vikram Vohra, Poulomi Chatterjee
المصدر:	The Journal of Association of Chest Physicians, Vol 6, Iss 1, Pp 38-40 (2018)
بيانات النشر:	Wolters Kluwer Medknow Publications, 2018.
سنة النشر:	2018
المجموعة:	LCC:Diseases of the respiratory system
مصطلحات موضوعية:	Corticosteroid, diffuse alveolar hemorrhage, idiopathic pulmonary hemosiderosis, Diseases of the respiratory system, RC705-779
الوصف:	Idiopathic pulmonary hemosiderosis (IPH) is often an ignored and rare cause of diffuse alveolar hemorrhage (DAH). It is characterized by triad of hemoptysis, anemia, and alveolar opacity on radiology. It is a diagnosis of exclusion, established after ruling out other causes of DAH such as Goodpasture’s syndrome, large vessel vasculitis, small vessel vasculitis associated with anti-neutrophil cytoplasmic antibody (ANCA) (Wegener’s granulomatosis, Churg–Strauss syndrome, microscopic polyangiitis), immune complex-related vasculitis (collagen vascular diseases, Henoch–Schönlein purpura, mixed cryoglobulinemia) drug reactions, anticoagulation and thrombocytopenia. Though it is a disease primarily affecting children, we hereby report a case of IPH in an adult patient who responded dramatically to oral corticosteroid.
نوع الوثيقة:	article
وصف الملف:	electronic resource
اللغة:	English
تدمد:	2320-8775 2320-9089
Relation:	http://www.jacpjournal.org/article.asp?issn=2320-8775;year=2018;volume=6;issue=1;spage=38;epage=40;aulast=Agarwal; https://doaj.org/toc/2320-8775; https://doaj.org/toc/2320-9089
DOI:	10.4103/jacp.jacp_12_17
URL الوصول:	https://doaj.org/article/05b3c23a762b4e87994566043a0c8bc8
رقم الأكسشن:	edsdoj.05b3c23a762b4e87994566043a0c8bc8
قاعدة البيانات:	Directory of Open Access Journals

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الوصف
تدمد:	23208775 23209089
DOI:	10.4103/jacp.jacp_12_17