Infectious Agents and Cancer (Nov 2018)

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

  • Nader Kim El-Mallawany,
  • Jimmy Villiera,
  • William Kamiyango,
  • Erin C. Peckham-Gregory,
  • Michael E. Scheurer,
  • Carl E. Allen,
  • Casey L. McAtee,
  • Alejandra Legarreta,
  • Dirk P. Dittmer,
  • Carrie L. Kovarik,
  • Elizabeth Y. Chiao,
  • Stephen C. Martin,
  • Nmazuo W. Ozuah,
  • Parth S. Mehta,
  • Peter N. Kazembe

DOI
https://doi.org/10.1186/s13027-018-0207-4
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 7

Abstract

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Abstract Background Endemic 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. Methods We describe clinical characteristics of 20 HIV-negative children with endemic KS over a six-year period and compare findings with a historical control—an HIV-related pediatric KS cohort from Lilongwe, Malawi. Results The HIV-negative endemic KS cohort was 70% male with a median age of 9.3 years. 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 < 8 g/dL) and thrombocytopenia (platelet count < 100 × 109/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). Conclusions These 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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