TY - JOUR KW - Adolescent KW - Adult KW - Age Factors KW - Aged KW - Antigens, Bacterial KW - Cross-Sectional Studies KW - Female KW - Glycolipids KW - Humans KW - leprosy KW - Male KW - Middle Aged KW - Mycobacterium leprae KW - Nasal Mucosa KW - polymerase chain reaction KW - Prospective Studies KW - Rhinitis KW - Sex Factors KW - Young Adult AU - Martins ACC AU - Miranda A AU - Oliveira MLWD AU - Bührer-Sékula S AU - Martinez AN AB -

UNLABELLED: Leprosy is a chronic infectious disease caused by Mycobacterium leprae. The disease more frequently affects the nasal mucosa and can occur independently of its clinical form or even before lesions on the skin or on other parts of the body. It is necessary to employ epidemiological surveillance of household contacts with new leprosy cases for early disease diagnosis.

AIM: identify specific and early leprosy lesions through endoscopic, baciloscopy, histopathology exams, and real time polymerase chain reaction of the nasal cavity mucosa on household and peridomiciliary contacts with positive serology for the phenolic glycolipid 1 antigen.

METHODOLOGY: Between 2003 at 2006 there was a prospective cross-sectional clinical study with 31 contacts with patients with leprosy with positive serology against PGL-1, 05 negative controls and 01 positive control.

RESULTS: Between seropositive contacts, real-time PCR was positive for M. leprae DNA in 06 (19.35%) of them and the higher number of genome copies were found in contacts who became sick.

CONCLUSION: Nasal mucosa tests alone did not enable the early diagnosis of Leprosy. However, through the combination of various methods, tests on the contacts can help identify subclinical infection and monitor the contacts that could be responsible for spreading the disease.

BT - Brazilian journal of otorhinolaryngology C1 - http://www.ncbi.nlm.nih.gov/pubmed/20963340?dopt=Abstract DA - 2010 Sep-Oct DO - 10.2340/16501977-0625 IS - 5 J2 - Braz J Otorhinolaryngol LA - eng N2 -

UNLABELLED: Leprosy is a chronic infectious disease caused by Mycobacterium leprae. The disease more frequently affects the nasal mucosa and can occur independently of its clinical form or even before lesions on the skin or on other parts of the body. It is necessary to employ epidemiological surveillance of household contacts with new leprosy cases for early disease diagnosis.

AIM: identify specific and early leprosy lesions through endoscopic, baciloscopy, histopathology exams, and real time polymerase chain reaction of the nasal cavity mucosa on household and peridomiciliary contacts with positive serology for the phenolic glycolipid 1 antigen.

METHODOLOGY: Between 2003 at 2006 there was a prospective cross-sectional clinical study with 31 contacts with patients with leprosy with positive serology against PGL-1, 05 negative controls and 01 positive control.

RESULTS: Between seropositive contacts, real-time PCR was positive for M. leprae DNA in 06 (19.35%) of them and the higher number of genome copies were found in contacts who became sick.

CONCLUSION: Nasal mucosa tests alone did not enable the early diagnosis of Leprosy. However, through the combination of various methods, tests on the contacts can help identify subclinical infection and monitor the contacts that could be responsible for spreading the disease.

PY - 2010 SP - 579 EP - 87 T2 - Brazilian journal of otorhinolaryngology TI - Nasal mucosa study of leprosy contacts with positive serology for the phenolic glycolipid 1 antigen. UR - http://www.scielo.br/pdf/bjorl/v76n5/en_v76n5a08.pdf VL - 76 SN - 1808-8686 ER -