Wegener’s granulomatosis: Is it rare?

dc.contributor.authorSantara
dc.contributor.authorZaw Lynn Aung
dc.date.accessioned2015-11-18T09:00:07Z
dc.date.available2015-11-18T09:00:07Z
dc.date.issued2015-09-01
dc.description.abstractA 52 year old lady was admitted with fever, productive cough and breathlessness for one month. She had past history of recurrent sinusitis. Clinically, she had bilateral sensorineural hearing impairment, nasal crusts and peripheral neuropathy apart from signs of consolidation. Vasculitic lesions appeared a day after admission. Investigations revealed multiple nodular like lesions scattered in both lungs on CXR. Blood tests revealed positive cANCA (Cytoplasmic fluorescence Antineutrophil Cytoplasmic Antibodies) and raised infl ammatory markers. She was treated with immunosuppressant and antibiotic. Clinical and radiological improvement was noted 2 weeks later.en_US
dc.format.extent76p.en_US
dc.identifier.citationSantara, Zaw Lynn Aung. Wegener’s granulomatosis: Is it rare? Myanmar Medical Journal. 2015 September; 57 (3): 60-63..en_US
dc.identifier.issn0007-6295
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/165961
dc.language.isoenen_US
dc.publisherMyanmar Medical Associationen_US
dc.rightsMyanmar Medical Associationen_US
dc.source.uriwww.mmacentral.org/myanmarmedicaljournalen_US
dc.subjectCase presentationen_US
dc.subjectInvestigationsen_US
dc.subjectTreatmenten_US
dc.subjectBackgrounden_US
dc.subject.meshGranulomatosis with Polyangiitisen_US
dc.subject.meshMyeloblastinen_US
dc.titleWegener’s granulomatosis: Is it rare?en_US
dc.typeArticleen_US
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