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Texte intégral de l'article
 
  Version imprimable

Human West African trypanosomiasis with chancre presentation


European Journal of Dermatology. Volume 10, Numéro 7, 561-2, October - November 2000, Votre diagnostic !


Summary  

Auteur(s) : D. Malvy, F. Djossou, M. Longy-Boursier, M. Le Bras, F.X. Weill, P. Chapuis, Department of Internal Medicine, Infectious and Tropical Diseases, Hôpital St-André, Bordeaux, France..

Illustrations

ARTICLE

In this case, evaluation of a peripherical blood smear confirmed the diagnosis and showed trypanosomes. Indeed, the patient had two trypanosomal chancres and examination of blood specimens revealed West African trypanosomiasis due to Trypanosoma brucei. Diagnosis of West African trypanosomiasis at the very early hemolymphatic stage was retained, and the patient received a regimen of five doses of iv pentamidine isethionate (4 mg/kg) over 10 days. The symptoms and blood parasitic involvement improved within two days. The immunological evaluation by immunofluorescence antibodies test (IFAT) showed an elevated serum specific IgM and IgG antibody titer level accounting at 1/50, 1/2500 respectively.

Our observation is remarkable as chancres to T. brucei gambiense are rarely reported, with frequency varying from 25 to 40% in a few small size series of European patients. Lesions have rarely been described as unique erythematous or violaceous circumscribed indurated nodules, measuring 5-15 cm in diameter, with or without local adenopathy [1, 2].

Unlikely trypanosomal chancres occur frequently in infections due to Trypanosoma rhodensiense suggesting a higher virulence of the parasite and consist of rubbery inflammatory nodules, measuring 2-5 cm in diameter, usually desquamating and resolving in 2 or 3 weeks [3].

Indeed, West African trypanosomiasis must be suspected among patients with lymphadenopathy and fever and living in a recognized endemic area, or even occurring in potential emergent conditions, and similarly be recognized at the early stage of the disease when the trypanosomal chancre is present, and a convenient and efficient therapeutic approach is possible before the stage of CNS involvement.

Article accepted on 5/6/00

REFERENCES

1. Iborra C, Danis M, Bricaire F, Caumes E. A traveller returning from Central Africa with fever and skin lesion. Clin Inf Dis 1999; 28: 679-80.

2. Duggan AJ, Hutchinson MP. Sleeping sickness in Europeans: a review of 109 cases. J Trop Med Hyg 1966; 69: 124-31.

3. Dumas M, Bisser J. Clinical aspects of human African trypanosomiasis (Chapter 13). In: Dumas M, Bouteille B, Buquet A. Progress in huma African trypanosomiasis, sleeping sickness. Paris: Springer-Verlag ed., 1999; 215-33.

4. Doua F, Mieza TW, Sanon Singaro JR, et al. The efficacy of pentamidine in the treatment of early-late. Trypanosoma brucei gambiense trypanosomiasis. Am J Trop Med Hyg 1996; 55: 586-8.

5. Van Nieuwenhave S. Present strategies in the treatment of human African trypanosomiasis (Chapter 15). In: Dumas M, Bouteille B, Buguet A. Progress in human African trypanosomiasis, sleeping sickness. Paris: Springer-Verlag ed., 1999; 253-80.


 

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