Sleeping sickness

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Limited to the distribution in sub-Saharan of the Tsetse fly which is the intermediate host of the protozoa Trypanosoma brucei.

  • West African sleeping sickness (Gambiense trypanosomiasis) due to Trypanosoma brucei gambiense
    • Typical cause untreated 3 years
  • East African sleeping sickness (Rhodesiense trypanosomiasis) due to Trypanosoma brucei rhodesiense
    • Typical course untreated months
    • Tyyranosomal chancre in about 20%
  • Nagana in animals caused by Trypanosoma brucei brucei

Contents

Infection

  • Some mammals can harbour asymptomatic infection of the human Trypanosoma subspecies (so can some humans !)
  • Is related to contact time with the Tsetse fly. Thus tourists are far less likely to get the disease (but if they do get it tend to an acute presentation with high fever, chancre, rash)
  • Long incubation so many first manifest many years after exposure
  • Normal protection in man offered by trypansosome lytic factor, which has subunit components of apolipoprotein L1 and haptoglobin-related protein[1].

Clinical

  1. Haemolymphatic stage
    • Chronic intermittent fever
    • Headache
    • Puritis
    • Lymphadenopathy
    • Sometimes hepatosplenomegaly
    • Occasional myopericarditis (esp rhodesiense)
    • Occasional endocrine dysfuction (esp rhodesiense)
  2. Meningoencephalitic
    • Sleep disturbance
    • Other neuropsychiatric manifestations
      • Tremor
      • Palsies
      • Dyskinesias
      • Psychosis
    • Fever rare

Diagnosis

LogoKeyPointsBox.pngCSF examination is essential to differentiate between first and second stage
  • Card agglutination test (CATT) the usual practice in endemic regions[2]
  • Immunofluorescense
  • Blood/lymph node aspirate fresh films
  • PCR being developed[3]

Prevention

  • Surveillance and vector control
    • Almost eradicated disease in colonial era

Treatment

  1. Haemolymphatic stage
    • Pentamidine in West African sleeping sickness parentally once a week
    • Suramin in East African sleeping sickness (Take advice on regime as these vary)
  2. Meningoencephalitic

Possible treatments

Parfuramidine is too nephrotoxic to use. Fexinidazole is in phase 1 studies.

External link

References

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