Show simple item record

dc.contributor.authorLawrence, Stephen
dc.contributor.authorKhammissa, R.A.G.
dc.contributor.authorFourie, J.
dc.contributor.authorMasilana, A.
dc.contributor.authorLemmer, J.
dc.contributor.authorFeller, L.
dc.date.accessioned2019-08-12T13:57:17Z
dc.date.available2019-08-12T13:57:17Z
dc.date.issued2018
dc.identifier.citationKhammissa, R., Fourie, J., Masilana, A., Lawrence, S., Lemmer, J., & Feller, L. (2018). Oral manifestations of thrombocytopaenia. The Saudi Dental Journal, 30(1), 19-25. doi:10.1016/j.sdentj.2017.08.004en_US
dc.identifier.issn1013-9052
dc.identifier.urihttps://doi.org/10.1016/j.sdentj.2017.08.004
dc.identifier.urihttp://hdl.handle.net/10566/4774
dc.description.abstractThe appearance in the mouth of haemorrhagic petechiae, ecchymoses or blood blisters with spontaneous bleeding is suggestive of a haemorrhagic disorder that may be caused either by functional impairment of platelets or of blood vessel walls, by an abnormal decrease in the number of circulating platelets (thrombocytopaenia), or by defects in the blood clotting mechanism. Thrombocytopaenia from decreased production or increased destruction of platelets may be caused by multiple factors including immune mediated mechanisms, drugs or infections. A diagnosis of thrombocytopaenic purpura can be made when any other disease entity that might be causing the purpura is excluded on the basis of the medical history, the physical examination, a complete blood count and a peripheral blood smear. In this paper, we outline the clinical features of oral thrombocytopaenic purpura and briefly discuss some aspects of its aetiopathogenesis and treatment.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectEcchymosisen_US
dc.subjectPetechiaeen_US
dc.subjectHaemorrhagic blisteren_US
dc.subjectImmune mediated thrombocytopaeniaen_US
dc.titleOral manifestations of thrombocytopaeniaen_US
dc.typeArticleen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record