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dc.contributor.authorOmoniyi-Esan, G.O-
dc.contributor.authorAdediran, I.A-
dc.contributor.authorFamurewa, O.C-
dc.contributor.authorBadmos, K.B-
dc.date.accessioned2025-03-25T12:37:10Z-
dc.date.available2025-03-25T12:37:10Z-
dc.date.issued2005-
dc.identifier.citationAfr .J. Med. Med. Sci. (2005) 34, 195-197en_US
dc.identifier.issn1116-4077-
dc.identifier.urihttp://adhlui.com.ui.edu.ng/jspui/handle/123456789/3676-
dc.descriptionArticleen_US
dc.description.abstractPulmonary alveolar microlithiasis (PAM) is a rare disease of unknown aetiology. It is characterized by the presence of calcific concretions (calcospherites) inside the alveoli [1]. We present a case of a 22year old sickle cell anaemia patient with an incidental finding of PAM. This report is to highlight the fact that though rare. PAM is not entirely unheard of in this environment and should be kept in mind as a cause of diffuse opacities of the lungs.en_US
dc.description.sponsorshipCOLLEGE OF MEDICINE, UNIVERSITY OF IBADAN, NIGERIAen_US
dc.language.isoenen_US
dc.publisherCOLLEGE OF MEDICINE, UNIVERSITY OF IBADAN, NIGERIAen_US
dc.subjectPulmonaryen_US
dc.subjectAlveolaren_US
dc.subjectMicrolithiasisen_US
dc.subjectA case reporten_US
dc.titlePulmonary alveolar microlithiasis — a case reporten_US
dc.typeArticleen_US
Appears in Collections:African Journal of Medicine and Medical Sciences

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