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Review

Pediatric Kaposi sarcoma in context of the HIV epidemic in sub-Saharan Africa: current perspectives

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Pages 35-46 | Published online: 19 Apr 2018

Figures & data

Figure 1 Photographic representations of lymphadenopathic Kaposi sarcoma.

Notes: The typical bulging, massive lymphadenopathy characteristic of lymphadenopathic Kaposi sarcoma is demonstrated in these photographs. Reprinted by permission from Springer Nature: Springer Nature, Br J Cancer. 4Childhood Kaposi’s sarcoma: clinical features and therapy, Olweny CL, Kaddumukasa A, Atine I, Owor R, Magrath I, Ziegler JL, ©1976;33(5):555–560.
Figure 1 Photographic representations of lymphadenopathic Kaposi sarcoma.

Table 1 Comparison of clinical features among pediatric KS cohorts in Africa

Table 2 Comparison of treatment outcomes among pediatric KS cohorts in Africa

Figure 2 The modified Lilongwe pediatric Kaposi sarcoma staging classification.

Notes: *See “Clinical characteristics” section for descriptions of clinical pulmonary or abdominal visceral involvement in resource-limited settings in the absence of bronchoscopy and endoscopy. Data from El-Mallawany et al.Citation55
Abbreviation: KS, Kaposi sarcoma.
Figure 2 The modified Lilongwe pediatric Kaposi sarcoma staging classification.

Figure 3 Treatment design schema for a risk-stratified and response-adapted therapeutic approach to pediatric Kaposi sarcoma.

Notes: *Subjective determination of percent decrease in size of all lesions; # stage 4 patients achieving complete remission who have a persistently low CD4 count <350 or unsuppressed HIV viral load are at high risk for relapse and should be monitored closely (ideally every 2 weeks for 3 months). Please note that, for patients with endemic (HIV-unrelated KS), ART is not included in the therapeutic approach, and therefore patients with stage 1A disease would be treated the same as patients with stage 1B KS. Data from El-Mallawany et al.Citation23,Citation55
Abbreviations: KS, Kaposi sarcoma; ART, antiretroviral therapy; progressive disease is defined as an increase in the size of existing lesions or the appearance of new lesions; BV, = bleomycin and vincristine; induction BV includes four cycles of BV given every 2 weeks, consolidation BV includes four cycles of BV given every 4 weeks; ABV, doxorubicin, bleomycin, and vincristine, QoL, quality-of-life; complete remission is defined as no clinical evidence of KS lesions; HIV, human immunodeficiency virus.
Figure 3 Treatment design schema for a risk-stratified and response-adapted therapeutic approach to pediatric Kaposi sarcoma.