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close this bookStandard Treatment Guidelines (STG) and The National Essential Drug List for Tanzania (NEDLIT) (WHO; 1997; 210 pages)
View the documentFOREWORD
View the documentACKNOWLEDGMENTS
View the documentINTRODUCTION
close this folderStandard Treatment Guidelines (STG)
Open this folder and view contents1. GASTROINTESTINAL CONDITIONS
Open this folder and view contents2. RESPIRATORY DISEASES
Open this folder and view contents3. OBSTETRIC AND GYNAECOLOGICAL CONDITIONS AND CONTRACEPTION
Open this folder and view contents4. CARDIOVASCULAR DISEASES
Open this folder and view contents5. MALARIA
Open this folder and view contents6. SKIN DISEASES
Open this folder and view contents7. SEXUALLY TRANSMITTED INFECTIONS / DISEASES (STD)
Open this folder and view contents8. DENTAL AND ORAL CONDITIONS
Open this folder and view contents9. GENITO-URINARY DISEASES: KIDNEY CONDITIONS
Open this folder and view contents10. EAR, NOSE AND THROAT CONDITIONS
Open this folder and view contents11. EYE CONDITIONS
close this folder12. TUBERCULOSIS AND LEPROSY
Open this folder and view contents12.1 Tuberculosis
close this folder12.2 Leprosy
Open this folder and view contents12.2.1 General Information about Leprosy
close this folder12.2.2 Classification of Leprosy
View the document12.2.2.1 Tuberculoid Leprosy
View the document12.2.2.2 Borderline Leprosy
View the document12.2.2.3 Borderline Tuberculoid (BT) Leprosy
View the document12.2.2.4 Borderline Lepromatous (BL) Leprosy
View the document12.2.2.5 Lepromatous (LL) leprosy
Open this folder and view contents12.3 Treatment of Leprosy
View the document12.4 Prevention of Disabilities and rehabilitation
Open this folder and view contents12.5 Signs and Treatment of Severe Reversal Reaction (RR)
View the document12.6 Responsibilities
View the document12.7 How to Look After Ulcers
View the document12.8 Surveillance of Patients After Release from MDT
View the document12.9 Referral Criteria of Leprosy Patients
Open this folder and view contents13. MUSCULOSKELETAL CONDITIONS AND JOINT DISEASES
Open this folder and view contents14. METABOLIC AND ENDOCRINE SYSTEM CONDITIONS
Open this folder and view contents15. CENTRAL NERVOUS SYSTEM DISEASE CONDITIONS
Open this folder and view contents16. OTHER DISEASE CONDITIONS
Open this folder and view contents17. VIRAL INFECTIONS
Open this folder and view contents18. ALLERGIC REACTIONS
Open this folder and view contents19. NUTRITIONAL AND HAEMATOLOGIC CONDITIONS
Open this folder and view contents20. MALIGNANT DISEASE CONDITIONS
Open this folder and view contents21. INJURIES AND TRAUMA
View the document22. FOREIGN BODIES
View the document23. PAIN
View the document24. POISONING
View the document25. NORMAL LABORATORY VALUES
Open this folder and view contentsNATIONAL ESSENTIAL DRUG LIST
View the documentABBREVIATIONS AND SYMBOLS
 
12.2.2.5 Lepromatous (LL) leprosy

In contrast with tuberculoid cases, lepromatous patients show very low or no resistance at all and therefore have very large numbers of M. Leprae in the skin, peripheral nerves and various organs.

Skin lesions

innumerable macule, papules, nodules, infiltration; sometimes “histoid nodules” shiny firm nodules usually found in relapse; slight or no hypopigmentation; no loss of sensation.

Nerves

nerve trunk damage occurs late, usually years after the onset of the disease and is extensive

Eyes

eye involvement as a result of the presence of M. leprae in the eye: nodules may grow on the conjunctiva, in the sclera and cornea; sensory fibres in the cornea may be damaged leading to further damages of the insensitive cornea, resulting in opacities (scar tissue); the iris may be involved, causing an acute or chronic iridocyclitis.

Skin smears

are always highly positive for AFB

Other organs

nose, mouth, throat and in women breasts and testes in mencan also be affected.

The classification of leprosy and the distinction between multi bacillary and paucibacillary are important because there are differences in infectiousness, treatment duration and in the problems of reactions and complications.

For the choice of MDT regimen, patients should be allocated either to the PB or to the MB group. If there is doubt about the classification, the patient should be classified as MB and treated accordingly. This in particular applies to patients who have been treated with dapsone before MDT, and for whom the available records or clinical findings give insufficient evidence for the original classification.

PB patients: are patients who are clinically TT or BT and who have negative skin smears. All clinically PB. patients who have a positive skin smear result (B1 = 1 or more) should be allocated to the MB regimen.

MB patients: are patients who are clinically BL or LL and all PB cases with a positive skin smear result (B1 = 1 or more).

If clinical classification cannot be confirmed by bacteriology, then all patients who are clinically MB and have negative skin smear results should be allocated to the MB regimen

In case of doubt, for reasons of unreliable or inconsistent results of the skin smear, any leprosy patient with more then 10 lesions should be allocated to the MB regimen.

In this way as few MB leprosy patients as possible will be wrongly allocated to the PB category.

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