4.3 Article

Endemic Kaposi sarcoma in HIV-negative children and adolescents: an evaluation of overlapping and distinct clinical features in comparison with HIV-related disease

Journal

INFECTIOUS AGENTS AND CANCER
Volume 13, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s13027-018-0207-4

Keywords

Kaposi sarcoma; Human herpesvirus-8; KS; KSHV; HHV-8; Endemic; HIV-negative; Pediatric oncology; Africa; Global health

Funding

  1. United States Agency for International Development through the Tingathe Program [674-A-00-10-00093-00]
  2. [R21CA217137]
  3. [CA019014]
  4. [CA190152]
  5. [CA192744]

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BackgroundEndemic Kaposi sarcoma (KS) was first described in African children over fifty years ago, but has recently been overshadowed by HIV-related disease. We aimed to evaluate the similarities and differences between endemic HIV-negative and epidemic HIV-positive pediatric KS in a KS-associated herpesvirus-endemic region of Africa.MethodsWe describe clinical characteristics of 20 HIV-negative children with endemic KS over a six-year period and compare findings with a historical controlan HIV-related pediatric KS cohort from Lilongwe, Malawi.ResultsThe HIV-negative endemic KS cohort was 70% male with a median age of 9.3years. Lymph node involvement was present in 50%, hyperpigmented skin lesions in 45%, and woody edema in 40%. One patient (5%) presented with oral KS involvement and no patients presented initially with visceral KS. Significant anemia (hemoglobin <8g/dL) and thrombocytopenia (platelet count <100x10(9)/L) were found at time of original KS diagnosis in 45 and 40% respectively. In both HIV-negative and HIV-positive cohorts, lymphadenopathy was the most common presentation, prototypical skin lesions were often absent, severe cytopenias were a common clinical feature, and treatment outcomes were similar. Patients with endemic KS demonstrated less frequent oral involvement (5% versus 29%, P=0.03) and a lower proportion of patients with visceral involvement (0% versus 16%, P=0.06).ConclusionsThese data suggest clinical overlap between epidemiological variants. Treatment protocols for pediatric KS in sub-Saharan Africa should be devised to include both endemic HIV-negative and epidemic HIV-related disease to better define the clinical and biological comparison.

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