Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add filters








Language
Year range
1.
Indian J Chest Dis Allied Sci ; 2006 Jul-Sep; 48(3): 209-11
Article in English | IMSEAR | ID: sea-29420
2.
Indian J Chest Dis Allied Sci ; 2006 Jan-Mar; 48(1): 75-7
Article in English | IMSEAR | ID: sea-29833

ABSTRACT

Idiopathic pulmonary haemosiderosis (IPH) is a rare disorder and is characterised by the occurrence of episodes of diffuse alveolar haemorrhage (DAH). The patients usually present with a history of recurrent haemoptysis, anaemia and alveolar opacities on chest radiograph. The radiographic features are very characteristic and reveal alveolar opacities in middle and lower zones with selective sparing of the upper zones. An extensive diagnostic work-up is needed to exclude other causes of DAH. We report two cases of idiopathic pulmonary haemosiderosis who responded well to treatment with oral glucocorticoids.


Subject(s)
Adolescent , Adult , Biopsy , Glucocorticoids/therapeutic use , Hemorrhage/etiology , Hemosiderosis/complications , Humans , Lung/pathology , Lung Diseases/drug therapy , Male , Prednisolone/therapeutic use
3.
J Postgrad Med ; 2005 Oct-Dec; 51(4): 322-3
Article in English | IMSEAR | ID: sea-117357

ABSTRACT

A virus belonging to the Flaviviridae group causes dengue haemorrhagic fever. Dengue presenting as acute liver failure is rare. Dengue is endemic in India. The last epidemic of dengue occurred in Delhi in 2003. During this epidemic, 2185 confirmed cases of dengue were reported. Dengue virus serotypes 2 and 3 were responsible for this epidemic. A 19-yr-old male presented to our hospital with the complaints of fever for 12 days, during this epidemic. He was diagnosed as having dengue shock syndrome, stage IV with acute liver failure. He had primary dengue infection. He made complete recovery with supportive management.


Subject(s)
Adult , Severe Dengue/diagnosis , Humans , Male
4.
Indian J Chest Dis Allied Sci ; 2004 Jul-Sep; 46(3): 205-8
Article in English | IMSEAR | ID: sea-30130

ABSTRACT

A 24-year-old female presented with complaints of cough with scanty expectoration, breathlessness on exertion and chest pain for the last three years. These symptoms had appeared during the 12th week of her third pregnancy. She was given anti-tuberculosis treatment at another hospital for nine months without any improvement in symptoms. Four years ago she had been diagnosed to have leprosy of borderline variety for which she had received treatment. On examination, she was tachypnoeic with a respiratory rate of 33 breaths per minute. She had clubbing and small, discrete and firm lymph nodes in the anterior cervical region. Chest examination revealed wheezing with bibasilar end-inspiratory crepitations.


Subject(s)
Adult , Dyspnea/etiology , Female , Humans , Lung Neoplasms/complications , Lymphangioleiomyomatosis/complications
SELECTION OF CITATIONS
SEARCH DETAIL