Life threatening exacerbation in idiopathic pulmonary hemosiderosis salvaged by cyclophosphamide infusion
Identifieur interne : 000041 ( PascalFrancis/Corpus ); précédent : 000040; suivant : 000042Life threatening exacerbation in idiopathic pulmonary hemosiderosis salvaged by cyclophosphamide infusion
Auteurs : Rahul Naithani ; Jagdish Chandra ; Varinder Singh ; Veerendra Kumar ; N. K. DubeySource :
- Indian journal of chest diseases & allied sciences [ 0377-9343 ] ; 2006.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
A seven-year-old girl presented with frequent fever, cough and shortness of breath of three months duration. On the basis of her clinical features, peripheral blood and sputum findings, she was diagnosed as a case of idiopathic pulmonary hemosiderosis. After initial stabilisation with steroids and chloroquine, she presented four years later with massive pulmonary hemorrhage and respiratory failure, which responded dramatically to cyclophosphamide infusion. The rare occurrence of pulmonary hemosiderosis and different treatment regimens is discussed.
Notice en format standard (ISO 2709)
Pour connaître la documentation sur le format Inist Standard.
pA |
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Format Inist (serveur)
NO : | PASCAL 06-0415378 INIST |
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ET : | Life threatening exacerbation in idiopathic pulmonary hemosiderosis salvaged by cyclophosphamide infusion |
AU : | NAITHANI (Rahul); CHANDRA (Jagdish); SINGH (Varinder); KUMAR (Veerendra); DUBEY (N. K.) |
AF : | Pulmonary and Critical Care Division, Kalawati Saran Children's Hospital and Lady Hardinge Medical College/New Delhi/Inde (1 aut., 2 aut., 3 aut., 4 aut., 5 aut.) |
DT : | Publication en série; Etude de cas, cas et faits cliniques; Niveau analytique |
SO : | Indian journal of chest diseases & allied sciences; ISSN 0377-9343; Coden ICDSD6; Inde; Da. 2006; Vol. 48; No. 4; Pp. 287-289; Bibl. 11 ref. |
LA : | Anglais |
EA : | A seven-year-old girl presented with frequent fever, cough and shortness of breath of three months duration. On the basis of her clinical features, peripheral blood and sputum findings, she was diagnosed as a case of idiopathic pulmonary hemosiderosis. After initial stabilisation with steroids and chloroquine, she presented four years later with massive pulmonary hemorrhage and respiratory failure, which responded dramatically to cyclophosphamide infusion. The rare occurrence of pulmonary hemosiderosis and different treatment regimens is discussed. |
CC : | 002B22E03 |
FD : | Hémosidérose; Cyclophosphamide; Idiopathique; Poumon; Perfusion; Immunodépression; Fer; Anticancéreux |
FG : | Métabolisme pathologie; Agent alkylant; Moutarde à l'azote; Oxazaphosphinane dérivé |
ED : | Hemosiderosis; Cyclophosphamide; Idiopathic; Lung; Perfusion; Immunosuppression; Iron; Antineoplastic agent |
EG : | Metabolic diseases; Alkylating agent; Nitrogen mustard; Oxazaphosphinane derivatives |
SD : | Hemosiderosis; Ciclofosfamida; Idiopático; Pulmón; Perfusión; Inmunodepresión; Hierro; Anticanceroso |
LO : | INIST-19759.354000156933860100 |
ID : | 06-0415378 |
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Pascal:06-0415378Le document en format XML
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<front><div type="abstract" xml:lang="en">A seven-year-old girl presented with frequent fever, cough and shortness of breath of three months duration. On the basis of her clinical features, peripheral blood and sputum findings, she was diagnosed as a case of idiopathic pulmonary hemosiderosis. After initial stabilisation with steroids and chloroquine, she presented four years later with massive pulmonary hemorrhage and respiratory failure, which responded dramatically to cyclophosphamide infusion. The rare occurrence of pulmonary hemosiderosis and different treatment regimens is discussed.</div>
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<ET>Life threatening exacerbation in idiopathic pulmonary hemosiderosis salvaged by cyclophosphamide infusion</ET>
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<EA>A seven-year-old girl presented with frequent fever, cough and shortness of breath of three months duration. On the basis of her clinical features, peripheral blood and sputum findings, she was diagnosed as a case of idiopathic pulmonary hemosiderosis. After initial stabilisation with steroids and chloroquine, she presented four years later with massive pulmonary hemorrhage and respiratory failure, which responded dramatically to cyclophosphamide infusion. The rare occurrence of pulmonary hemosiderosis and different treatment regimens is discussed.</EA>
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