Reliable cell and tissue morphology-based diagnosis of endemic Burkitt lymphoma in resource-constrained settings in Ghana

dc.contributor.authorSmith-Togobo, C.
dc.contributor.authorPedersen, M.
dc.contributor.authorJensen, S.G.
dc.contributor.authorDuduyemi, B.
dc.contributor.authorGyasi, R.K.
dc.contributor.authorOfori, M.F.
dc.contributor.authorPaintsil, V.
dc.contributor.authorRenner, L.
dc.contributor.authorNørgaard, P.
dc.contributor.authorHviid, L.
dc.date.accessioned2020-01-17T08:49:39Z
dc.date.available2020-01-17T08:49:39Z
dc.date.issued2019-12-30
dc.descriptionResearch Articleen_US
dc.description.abstractBackground: Endemic Burkitt lymphoma (eBL) is an aggressive B-cell lymphoma, which is a common childhood cancer in areas with intense transmission of Plasmodium falciparum parasites. Early and accurate diagnosis is a prerequisite for successful therapy, but it optimally involves advanced laboratory investigations. These are technologically demanding, expensive, and often difficult to implement in settings where eBL is prevalent. Diagnosis is thus generally based on clinical assessment and morphological examination of tumour biopsies or fine-needle aspirates (FNAs). Methods: The purpose of the present study was to assess the accuracy of eBL diagnosis at two tertiary hospitals in Ghana. To that end, we studied FNAs from 29 eBL patients and 21 non-eBL lymphoma patients originally diagnosed in 2018. In addition, we examined 111 archival formalin-fixed and paraffin-embedded (FFPE) biopsies from Ghanaian patients originally diagnosed as eBL (N = 55) or non-eBL (N = 56) between 2010 and 2017. Availability-based subsets of samples were subjected to haematoxylin-eosin or Giemsa staining, C-MYC immunohistochemistry, and fluorescence in situ hybridisation (FISH) analysis of c-myc rearrangements. Results: We found a good correlation between original diagnosis and subsequent retrospective assessment, particularly for FNA samples. However, evidence of intact c-myc genes and normal C-MYC expression in samples from some patients originally diagnosed as eBL indicates that morphological assessment alone can lead to eBL over-diagnosis in our study area. In addition, several FFPE samples could not be assessed retrospectively, due to poor sample quality. Therefore, the simpler FNA method of obtaining tumour material is preferable, particularly when careful processing of biopsy specimens cannot be guaranteed. Conclusion: We conclude that the accuracy of eBL diagnostic tools available in Ghana is generally adequate, but could be improved by implementation of additional pathology laboratory investigations. Improved attention to adequate preservation of archival samples is recommendeden_US
dc.description.sponsorshipBuilding Stronger Universities (BSU-II) collaboration between Universities Denmark and University of Ghana (grant BSU2-UG). BSU-II is sponsored by the Ministry of Foreign Affairs of Denmark and administered by Danida Fellowship Centreen_US
dc.identifier.otherhttps://doi.org/10.1186/s12885-019-6488-1
dc.identifier.urihttp://ugspace.ug.edu.gh/handle/123456789/34419
dc.language.isoenen_US
dc.publisherBMC Canceren_US
dc.relation.ispartofseries19;1270
dc.subjectEndemic Burkitt lymphomaen_US
dc.subjectDiagnostic accuracyen_US
dc.subjectMorphologyen_US
dc.subjectC-MYC immunohistochemistryen_US
dc.subjectc-myc FISHen_US
dc.titleReliable cell and tissue morphology-based diagnosis of endemic Burkitt lymphoma in resource-constrained settings in Ghanaen_US
dc.typeArticleen_US

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