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Dyskeratosis congenita associated non-specific interstitial pneumonia
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نویسنده
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desai u.d. ,joshi j.m.
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منبع
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journal of krishna institute of medical sciences university - 2017 - دوره : 6 - شماره : 1 - صفحه:99 -103
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چکیده
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Dyskeratosis congenita (dc) is a rare inherited disorder of ectodermal dysplasia. it consists of a classical mucocutaneous triad of abnormal skin pigmentation,nail dystrophy and leukoplakia. pulmonary disease is seen in 10-15%. it is characterized by idiopathic pulmonary fibrosis (ipf),or idiopathic familial pulmonary fibrosis (ifpf). non-specific interstitial pneumonia (nsip) has been reported rarely in children with dc and in an isolated adult patient. our patient had classical clinical presentation of dc with pancytopenia and portal hypertension and clinic-radiological features of nsip which is a rare association. � journal of krishna institute of medical sciences university.
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کلیدواژه
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Dyskeratosis Congenita; Familial Pulmonary Fibrosis; Idiopathic Pulmonary Fibrosis
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آدرس
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department of pulmonary medicine,tnmc & byl nair hospital,al nair road,mumbai central,mumbai,maharashtra, India, department of pulmonary medicine,tnmc & byl nair hospital,al nair road,mumbai central,mumbai,maharashtra, India
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Authors
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