| Literature DB >> 26894111 |
Ajay Raj Mallela1, Shetty Hariprasad2, Rohini Koya1, Vasudev Acharya3, Shastry Barkur Anantha Krishna3.
Abstract
Malaria is an endemic disease in tropical countries and disease of universal importance. Central Nervous System (CNS) complications of malaria are severe and associated with significant mortality. Thrombocytopaenia in malaria causing haemorrhagic CNS complications is rare. We report a case of 35-year-old male patient presented with headache, vomiting and was diagnosed to have subdural haemorrhage (SDH). On examination patient was found to be febrile with peripheral smear showing evidence of Plasmodium vivax (P.vivax) infection with severe thrombocytopaenia. In endemic regions with malaria, SDH being rare presentation of malaria should be considered as a differential diagnosis in febrile patients with neurological manifestations. Rarity of spontaneous SDH in malaria and raising awareness amongst treating physicians about the same is the driving factor for reporting this case.Entities:
Keywords: Cerebral malaria; Falciparum; Thrombocytopaenia
Year: 2016 PMID: 26894111 PMCID: PMC4740639 DOI: 10.7860/JCDR/2016/15418.7098
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X