02233nas a2200289 4500000000100000008004100001260001300042653001500055653001000070653002100080653001100101653001100112653001000123653001100133653001200144653000900156653001500165653002400180100001500204700001700219245004600236300001000282490000700292050001500299520161500314022001401929 1993 d c1993 Mar10aAdolescent10aChild10aChild, Preschool10aFemale10aHumans10aIndia10aInfant10aleprosy10aMale10aPrevalence10aProspective Studies1 aSehgal V N1 aChaudhry A K00aLeprosy in children: a prospective study. a194-70 v32 aSEHGAL19933 a
BACKGROUND: Leprosy has been identified as an important health problem in the pediatric age group. The study of leprosy in children is imperative as it may unravel the missing links in the natural evolution of the disease and dispel the uncertainty of the precise incubation period.
METHODS: The study was undertaken on patients attending the Urban Leprosy Centre. There were 161 children in the age group of 0 to 14 years, amongst 3184 cases of leprosy, detected between 1981 and 1991. The diagnosis in each was formed after meticulously recording the clinical features, slit-skin smear examination, and histopathologic characteristics. In addition, a detailed history of duration of the disease was elicited by complement recall method.
RESULTS: The study revealed an incidence of 5.06% amongst leprosy patients, in an urban setting. The boys:girls ratio was 2.6:1. The mean duration of the disease was 1.2 years in paucibacillary and 2.8 years in multibacillary. History of intra- or extrafamilial contact was elicited in 8.7%. The typical lesion was a "hypopigmented macule," either of indeterminate, tuberculoid, borderline tuberculoid, or borderline borderline leprosy. Borderline lepromatous, lepromatous, and polyneuritic leprosy were uncommon.
CONCLUSIONS: Leprosy in children is a well-established distinct entity. Any hypopigmented macule in pediatric age group should arouse suspicion of leprosy. The diagnosis is clinical. Other investigative parameters, namely slit-skin smear, and histopathology may supplement but not supplant the diagnosis.
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