Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/133269
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dc.titleFatal aplastic anaemia complicating infectious mononucleosis. A case report with brief review of literature
dc.contributor.authorQuak, S.H.
dc.contributor.authorYip, W.C.L.
dc.date.accessioned2016-12-19T06:48:54Z
dc.date.available2016-12-19T06:48:54Z
dc.date.issued1979
dc.identifier.citationQuak, S.H., Yip, W.C.L. (1979). Fatal aplastic anaemia complicating infectious mononucleosis. A case report with brief review of literature. Journal of the Singapore Paediatric Society 21 (3-4) : 132-139. ScholarBank@NUS Repository.
dc.identifier.issn00375683
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/133269
dc.description.abstractA 9-year old girl suffering from infectious mononucleosis with fatal aplastic anaemia was reported. It was the second Chinese patient in Singapore with a positive heterophil antibody response. A review of the literature showed that aplastic anaemia was a very rare complication of infectious mononucleosis. Up to 1978, only 9 other cases were found in the English Literature. Amongst these 10 cases, there were 7 males and 3 females. The age distribution ranged from 7 to 30 years old. Not all cases had clinical features typical of infectious mononucleosis. These cases were diagnosed by the presence of atypical mononuclear cells in the peripheral blood films with or without a positive heterophil antibody response. In other words, infectious mononucleosis should be considered in any case of unexplained aplastic anaemia. The presence of pancytopenia is prognostically bad for patients with infectious mononucleosis. Amongst these 10 cases, only 6 survived. Overwhelming septicaemia was the cause of death in 4 patients.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPAEDIATRICS
dc.description.sourcetitleJournal of the Singapore Paediatric Society
dc.description.volume21
dc.description.issue3-4
dc.description.page132-139
dc.description.codenSPSJB
dc.identifier.isiutNOT_IN_WOS
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