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Early aggressive intra-venous pulse cyclophosphamide therapy for interstitial lung disease in a patient with systemic sclerosis. A case report

Identifieur interne : 001874 ( Main/Exploration ); précédent : 001873; suivant : 001875

Early aggressive intra-venous pulse cyclophosphamide therapy for interstitial lung disease in a patient with systemic sclerosis. A case report

Auteurs : R. Peshin [Irlande (pays)] ; L. O Eill [Irlande (pays)] ; P. Browne [Irlande (pays)] ; P. O Onnell [Irlande (pays)] ; G. Kearns [Irlande (pays)]

Source :

RBID : ISTEX:C9D8EA3A9C7B2AB164773F3D1EDA6D905FBBE054

English descriptors

Abstract

Abstract: Interstitial lung disease is an important cause of mortality and morbidity in patients with systemic sclerosis (SSc). There are currently no recommended guidelines for management of these patients. This is probably due to the rarity of this condition, as well as clinical trials with only a small number of cases. There are published case report and case series along with the two main trials, viz. Scleroderma Lung Study and the Fibrosing Alveolitis Study, but again, there is no consensus on treatment protocols. In this report, we present a case of aggressive interstitial lung disease in a patient with SSc, which improved dramatically on treatment with intra-venous cyclophosphamide and high dose prednisolone therapy.

Url:
DOI: 10.1007/s10067-009-1098-y


Affiliations:


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<div type="abstract" xml:lang="en">Abstract: Interstitial lung disease is an important cause of mortality and morbidity in patients with systemic sclerosis (SSc). There are currently no recommended guidelines for management of these patients. This is probably due to the rarity of this condition, as well as clinical trials with only a small number of cases. There are published case report and case series along with the two main trials, viz. Scleroderma Lung Study and the Fibrosing Alveolitis Study, but again, there is no consensus on treatment protocols. In this report, we present a case of aggressive interstitial lung disease in a patient with SSc, which improved dramatically on treatment with intra-venous cyclophosphamide and high dose prednisolone therapy.</div>
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