TY - JOUR
T1 - Clinical investigation of carbon dioxide laser treatment for lingual leukoplakia
AU - Matsumoto, Kousuke
AU - Suzuki, Hiroaki
AU - Asai, Tomoko
AU - Wakabayashi, Reina
AU - Enomoto, Yui
AU - Kitayama, Midori
AU - Shigeoka, Manabu
AU - Kimoto, Akira
AU - Takeuchi, Junichiro
AU - Yutori, Hirokazu
AU - Komori, Takahide
N1 - Publisher Copyright:
© 2015 Asian AOMS, ASOMP, JSOP, JSOMS, JSOM, and JAMI.
PY - 2015/7/1
Y1 - 2015/7/1
N2 - Objective: Previous studies have described the clinical statistics and treatment outcomes of leukoplakia of the oral cavity. However, because leukoplakia is often clinically diagnosed without any histopathological examination, current opinion regarding treatment methods and preoperative pathological diagnosis is inconsistent and no standard site-specific treatment guidelines exist for oral leukoplakia. The purpose of this study is to clinically evaluate carbon dioxide (CO2) laser treatment for leukoplakia of the tongue. Methods: We examined 38 lesions in 35 patients of lingual leukoplakia who underwent CO2 laser treatment with using Lugol staining at our department over a 10-year period, i.e., from 2001 to 2010. We investigated gender-related differences, age distribution, left and right differences, clinical classification, histopathological diagnosis (presence or absence of epithelial dysplasia), treatment technique (excision or evaporation), recurrence rate, residual rate, and malignant transformation among these cases. Results: Of the 38 lesions that fulfilled the inclusion requirements, 35 were excised and 3 were evaporated. After CO2 laser treatment, the recurrence and residual rates for lingual leukoplakia were 10.5% and 7.9%, respectively. The recurrence rate of cases examined in this study was lower than that reported by our hospital previously (2004) and many other hospitals. None of the lesions exhibited malignant transformation. Conclusions: Our results suggest that the CO2 laser excision method with using Lugol staining, as performed at our hospital, is useful for the treatment of lingual leukoplakia.
AB - Objective: Previous studies have described the clinical statistics and treatment outcomes of leukoplakia of the oral cavity. However, because leukoplakia is often clinically diagnosed without any histopathological examination, current opinion regarding treatment methods and preoperative pathological diagnosis is inconsistent and no standard site-specific treatment guidelines exist for oral leukoplakia. The purpose of this study is to clinically evaluate carbon dioxide (CO2) laser treatment for leukoplakia of the tongue. Methods: We examined 38 lesions in 35 patients of lingual leukoplakia who underwent CO2 laser treatment with using Lugol staining at our department over a 10-year period, i.e., from 2001 to 2010. We investigated gender-related differences, age distribution, left and right differences, clinical classification, histopathological diagnosis (presence or absence of epithelial dysplasia), treatment technique (excision or evaporation), recurrence rate, residual rate, and malignant transformation among these cases. Results: Of the 38 lesions that fulfilled the inclusion requirements, 35 were excised and 3 were evaporated. After CO2 laser treatment, the recurrence and residual rates for lingual leukoplakia were 10.5% and 7.9%, respectively. The recurrence rate of cases examined in this study was lower than that reported by our hospital previously (2004) and many other hospitals. None of the lesions exhibited malignant transformation. Conclusions: Our results suggest that the CO2 laser excision method with using Lugol staining, as performed at our hospital, is useful for the treatment of lingual leukoplakia.
KW - CO laser
KW - Lingual leukoplakia
KW - Local biopsy
KW - Lugol staining
KW - Recurrence
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U2 - 10.1016/j.ajoms.2015.01.001
DO - 10.1016/j.ajoms.2015.01.001
M3 - Article
AN - SCOPUS:84933673477
SN - 2212-5558
VL - 27
SP - 493
EP - 497
JO - Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology
JF - Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology
IS - 4
ER -