| Literature DB >> 29211243 |
Fred Bernardes1, Natália Aparecida de Paula1, Marcel Nani Leite1, Thania Loyola Cordeiro Abi-Rached1, Sebastian Vernal1, Moises Batista da Silva2, Josafá Gonçalves Barreto2,3, John Stewart Spencer4, Marco Andrey Cipriani Frade1.
Abstract
OBJECTIVES: Show that hidden endemic leprosy exists in a municipality of inner São Paulo state (Brazil) with active surveillance actions based on clinical and immunological evaluations.Entities:
Mesh:
Substances:
Year: 2017 PMID: 29211243 PMCID: PMC5719551 DOI: 10.1590/0074-02760170173
Source DB: PubMed Journal: Mem Inst Oswaldo Cruz ISSN: 0074-0276 Impact factor: 2.743
Epidemiologic characteristics of the new cases detected
| Category | Subcategory | Leprosy cases | ||
|---|---|---|---|---|
| (n) | (%) | |||
| Gender | Male | 11 | 45.8 | |
| Female | 13 | 54.2 | ||
| Age group | < 15 years old | 2 | 8.3 | |
| ≥ 15 years old | 22 | 91.7 | ||
| Place of birth | ||||
| Jardinópolis (SP) | 14 | 58.3 | ||
| São Joaquim da Barra (SP) | 1 | 4.2 | ||
| Brodowski (SP) | 1 | 4.2 | ||
| Other states | 8 | 33.3 | ||
| Dwelling time in Jardinópolis | ||||
| Average | 28.7 years | |||
| 1st quartile | 15 years | |||
| Median | 27 years | |||
| 3rd quartile | 41 years | |||
| Classification | I/TT/N | 0 | 0 | |
| BT | 3 | 12.5 | ||
| BB | 19 | 79.2 | ||
| BL | 0 | 0 | ||
| LL | 2 | 8.3 | ||
| Degree of disability | 0 | 6 | 25 | |
| 1 | 10 | 41.7 | ||
| 2 | 8 | 33.3 | ||
| BCG scar | 0 | 8 | 33.3 | |
| 1 | 16 | 66.7 | ||
| ≥ 2 | 0 | 0 | ||
| Anti-PGL-I | Seronegative | 18 | 75 | |
| Seropositive | 6 | 25 | ||
SP: São Paulo state; I: indeterminate; TT: tuberculoid leprosy; BT: borderline tuberculoid leprosy; BB: borderline borderline leprosy; BL: borderline lepromatous leprosy; LL: lepromatous leprosy; N: pure neural manifestations.
Fig. 1(A) anesthetic hypochromic macule on the right hemiface; (B) points with altered sensitivity (hypoesthetic and anesthetic) inside the area of hypopigmented spot; (C) absence of secondary erythema reflex on leprosy hypochromic lesion as compared to peripheral areas after strong scrawl through the lesion in the endogenous histamine test in hypochromiant dimorphous leprosy patient; (D) anesthetic hypochromic macule with alopecia on the right knee; (E) hypochromic macula with pain anesthesia showed with a needle tip test; (F) hypochromic hypoesthetic and anesthetic macule on the right leg; (G) distal third of the left leg with alopecia, hypoesthesia and anesthesia; (H) hypochromic macule with alopecia on the proximal dorsal half of the left leg; (I) hypochromic macule on the right forearm; (J) multiple hypochromic macules with altered sensitivity, with alopecia, on both legs. Auxiliary clinical tests: “+” normoesthesia (preserved sensitivity); “0” anesthesia (lack of sensitivity); “-” hypoesthesia (perception preserved but less intense than in normoesthetics areas); blue point: tactile sensitivity tested; red point: pain sensitivity tested.
Fig. 2(A, B) lepromatous patient with multiple papules and nodules on back and face; (C, D) patient with Lucio's phenomenon - necrotising lesions over the legs, buttocks and dorsum.
Fig. 3spatial distribution of newly detected cases and of subclinical infection. A hotspot of new cases was localised within the northwestern census tracts, accounting for 19 out of 24 new cases detected (79.16%). Additionally, 12 subjects with no clinical signs or symptoms of leprosy displayed Enzime-linked immunosorbent assay (ELISA) indexes to IgM anti-PGL-I over 2.0, that is comparable to multibacillary (MB) cases exhibiting a high bacillary index, indicating higher risk of leprosy in the future.