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dc.contributor.authorKitara, Lagoro David
dc.contributor.authorMwaka, Amos Deogratius
dc.contributor.authorWabinga, R Henry
dc.contributor.authorBwangamoi, Okot Paul
dc.date.accessioned2021-04-28T09:55:16Z
dc.date.available2021-04-28T09:55:16Z
dc.date.issued2013-10-23
dc.identifier.citationKitara, D.L., Mwaka, A.D., Wabinga, H.R. and Bwangamoi, P.O., 2014. Pyomyositis in Nodding Syndrome (NS) patient-a case report. Pan African Medical Journal, 16(1).en_US
dc.identifier.issn1937-8688
dc.identifier.urihttp://hdl.handle.net/20.500.12280/2765
dc.description.abstractWe report a case of Pyomyositis in a 13-year-old boy diagnosed using WHO surveillance definition of Probable Nodding syndrome. Complete blood count showed Leukocytosis with immature granulocytes and atypical lymphocytes. Except for the liver enzymes which were high the renal functions and serum electrolytes were within normal range values. Culture of a pus-swab grew Staphylococcus aureus. Abdominal ultrasound scan showed a focal mass on the internal and external oblique muscles of the right abdominal wall. Incision and drainage was performed. Histology of the muscle showed non-specific inflammation of the external and internal oblique muscles. This finding may highlight some of the other tropical diseases that occur in children with Nodding syndrome.en_US
dc.language.isoenen_US
dc.publisherAfrican Field Epidemiology Network (AFENET).en_US
dc.relation.ispartofseriesPan African Medical Journal;16(1)
dc.subjectNodding syndromeen_US
dc.subjectPyomyositisen_US
dc.subjectUgandaen_US
dc.titlePyomyositis in Nodding Syndrome (NS) Patient - A Case Reporten_US
dc.typeArticleen_US


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