Rev Odontol UNESP
rounesp
Revista de Odontologia da UNESP
Rev. Odontol. UNESP
0101-1774
1807-2577
Universidade Estadual Paulista Júlio de Mesquita Filho
Resumo
Introdução
A queilite actínica e uma condição de natureza inflamatória que acomete o lábio inferior, e é causada pela exposição prolongada e crônica dos lábios à radiação ultravioleta proveniente dos raios solares.
Objetivo
Identificar as características clínicas e histopatológicas em uma série de 40 casos diagnosticados histopatologicamente como queilite actínica. Além disso, investigar possíveis associações entre estes aspectos.
Método
Caracterizado como um estudo observacional, transversal, retrospectivo e descritivo. Foram registrados dados a respeito da idade, gênero, ocupação, sintomatologia, histórico de exposição ao sol, uso de proteção solar, tabagismo, cor da pele, aspecto clínico e classificação histopatológica. Os dados foram submetidos ao teste de Qui-Quadrado de Pearson (p<0,05).
Resultado
Houve uma prevalência do gênero masculino, leucodermas, com faixa etária entre 50 e 60 anos e a ocupação mais presente foi a de agricultor. Da amostra, 85% apresentou histórico de exposição crônica ao sol, onde 50% relatou uso de algum tipo de proteção solar e apenas 25% era tabagista. A principal apresentação clínica foi leucoplasia não ulcerada, e no estudo histopatológico as hiperceratoses foram as mais presentes. Não foi possível correlacionar o grau de alteração tecidual verificada no diagnóstico histopatológico com as variáveis clínicas estudadas (p=0,112).
Conclusão
Não foi possível correlacionar o grau de alteração tecidual verificada no diagnóstico histopatológico com os aspectos clínicos observados. O aspecto clínico da lesão pode mascarar alterações teciduais em diversos estágios, o que enaltece a importância do diagnóstico precoce.
INTRODUCTION
Actinic cheilitis (AC) is an inflammatory, potentially malignant condition. It affects mainly the lower lip and is caused by long-term, chronic sun exposure1,2.
AC affects mainly fair-skinned men, over 30 years of age, with chronic sun exposure1,3. The lesions are usually asymptomatic, and may be leukoplakia, erythroplakia or erythroleukoplakia, with or without the presence of ulcers2. These lesions may be clinically characterized as acute or chronic. Acute lesions are characterized by erythematous lips, swelling, formation of blisters followed by crusts. Regression of the lesion occurs when the etiologic agent is interrupted. Chronic AC is clinically characterized by atrophy of the red lower part of the lip, with loss of elasticity and the presence of rough, scaly, keratotic plaques, unevenly overlapping the erythematous areas. In addition, the presence of ulcers and fissures is common3-5.
Considering the well-established association between AC and the development of squamous cell carcinoma in the lower lip (SCC), biopsy of the lesion is indicated to improve the diagnostic accuracy of this lesion3,4,6. Histopathologically, tissue changes can range from mild to severe in the epithelial and conjunctive components. In the epithelial tissue, the changes include thickening of the epithelium and the keratinized layer, ulcers, acanthosis and dysplasias that can range from mild to severe. The connective component can present solar elastosis, vasodilation and a mononuclear inflammatory infiltrate ranging from moderate to intense1,6-9. Based on the current knowledge of AC and its potential to become malignant, early diagnosis and follow-up of the lesions is extremely important. Thus, the present study aimed to identify and associate the clinical and histopathological characteristics in a series of cases, in order to obtain subsidies for better diagnosis and to establish the prognosis of the lesions.
METHOD
The present study was characterized as an observational, cross-sectional descriptive study, based on retrospective data. All the cases of patients diagnosed with actinic cheilitis, through a clinical and histopathological exam, who were treated at the Liga Interdisciplinar de Combate ao Câncer Oral (Interdisciplinary League Against Oral Cancer) clinic of the State University of Paraíba, from October 2008 to August 2012,were evaluated (approval number 0002.0.133.000-09).
The sample was composed of 40 cases, with data on gender, age, skin color, occupation, smoking, sun exposure, painful symptoms and the clinical aspects of the lesions. To evaluate the histopathological data, a single, previously calibrated examiner, using light microscopy (Leica DM 500, Leica Microsystems Vertrieb GmbH, Wetzlar),assessed the specimens with clinical diagnosis compatible with AC. The lesion was classified as hyperkeratosis, mild, moderate or severe dysplasia or carcinoma in situ, according to the criteria for diagnosis of dysplasia described by Cavalcante et al.8.
The results were submitted to descriptive and inferential statistical analysis using the Statistical Package for the Social Sciences (version 17.0, IBM SPSS Inc., Armonk, NY, USA) applying Pearson’s Chi-square hypothesis tests. All tests were conducted at a significance level of 5% (p < 0.05).
RESULT
Sample Characterization
Table 1 shows the data obtained from the analysis of the clinical characteristics of the sample submitted. It can be observed that 82.5% of the patients were male, 75% were leucodermic, 37.5% were farmers, and only 25% were smokers. The mean age was 54.5 years, with a standard deviation of ±15.75 years and 85% of the sample reported chronic sun exposure and 50% reported using sunscreen.
Table 1
Sample distribution by individual characteristics
Individual Characteristics
N
%
Sex
Male
33
82.5
Female
7
17.5
Total
40
100
Skin color
Leukoderm
30
75
Pheoderm
10
25
Total
40
100
Occupation
Farmer
15
37.5
Driver
5
12.5
Electrician
2
5
Construction worker
3
7.5
Fisherman
1
2.5
Tire repair man
1
2.5
Student
1
2.5
Retiree
6
15
Other
6
15
Total
40
100
Smoking
Yes
10
25
No
30
75
Total
40
100
Sun exposure
Yes
34
85
No
6
15
Total
40
100
Sun protection
Yes
20
50
No
20
50
Total
40
100
Clinical Analysis
Upon clinical examination, the lesions studied presented aspects of leukoplakia, erythroplakia and mixed aspect. They were symptomatic in 32.5% of the sample, as shown in Table 2. All cases affected the lower lip. Other features such as blurred demarcation of the vermilion border of the lip, erythema, atrophy, keratosis, erosion, crusts and fissures were observed.
Table 2
Sample distribution by clinical and pathological features
Characteristic
n
%
Painful symptomatology
Yes
13
32.5
No
27
67.5
Total
40
100
Clinical aspect of the lesion
No-ulcerated leukoplakia
19
47.5
No-ulcerated Erythroplakia
10
25
Erosion/ulceration
1
2.5
Mixed aspects
10
25
Total
40
100
Histopathological Diagnosis
Hyperkeratosis
20
50
Mild Dysplasia
8
20
Moderate Dysplasia
10
25
Severe Dysplasia
2
5
Total
40
100
Histopathological Analysis
Typical characteristics of this type of lesion such as hyperplasia of the epithelial layer of the vermilion of the lip, disorderly maturation, cellular atypia, varying degrees of mitotic activity and hyper-keratinization were observed. Basophilic degeneration of the collagen fibers in the connective tissue (solar elastosis), common in AC, was also observed, as well as the presence of predominantly mononuclear inflammatory infiltrate.
The sample was classified according to the histopathological diagnosis as hyperkeratosis, mild, moderate and severe dysplasia, as shown in Table 2. The no-ulcerated aspect of leukoplakia was present in 10 cases of hyperkeratosis, while no-ulcerated erythroplakia and mixed aspects were present in five cases each, displaying equal frequency of mild dysplasia. Moderate dysplasia was present in five lesions with the clinical aspect of no-ulcerated leukoplakia. Only one lesion with mixed clinical aspect and one with erosion/ulceration were histopathologically classified as severe dysplasia. It was not possible to establish a statistically significant correlation between the clinical aspect and the histopathological classification of the ACs (p = 0.112) (Table 3).
Table 3
Correlation between clinical aspects and histopathological classification in number of cases
CLINICAL ASPECT
HISTOPATHOLOGICAL CLASSIFICATION
Hyperkeratosis
Mild dysplasia
Moderate dysplasia
Severe dysplasia
No-ulcerated leukoplakia
10 (52.6%)
4 (21%)
5 (26.3%)
-
No-ulcerated Erythroplakia
5 (50%)
2 (20%)
2 (20%)
1 (10%)
Mixed aspect
5 (50%)
2 (20%)
3 (30%)
-
Erosion/ulceration
-
-
-
1 (100%)
DISCUSSION
Leukoplakia, erythroplakia, oral lichen planus and AC are the oral lesions with the greatest potential for becoming malignant10. AC is considered a potentially malignant disorder, characterized by a variety of clinical aspects that may not correspond with its real severity6. The primary etiological agent is chronic exposure to solar radiation. The malignant transformation can occur, causing SCC, which develops slowly and causes late metastasis2.
AC predominantly affects men and is more common in individuals with fair skin2,3,10. In the present study, the data align with the literature, since leucoderma males composed most of the sample. According to previous studies, individuals over 50 years of age are the most affected, reinforcing the finding of cumulative damage coming from solar radiation1,4,11. However, Souza Lucena et al.3 observed that fair-skinned men, average age of 37 years, were the most affected by AC. According to these authors, this association can be justified by the prevalence of men in activities involving chronic exposure to the sun, in addition to lack of self-care which can result in more lesions.
Therefore, the occupational issue is closely related to the lesion. This can be associated with the fact that workers who are chronically exposed to the sun are more affected, especially farmers, fishermen, couriers and traffic cops3,8. Corroborating previous studies, most of the sample of the present study was composed of farmers with a history of chronic sun exposure.
In relation to location, the literature shows that the lower lip is the most affected area, due to greater exposure to direct solar radiation1,4,11. For the present study, all specimens were removed from the lower lip for biopsy, corroborating the relevant literature.
The appearance of potentially malignant oral lesions, such as AC, have been related to exposure to risk factors such as smoking, alcohol and excessive sun exposure12,13. In this context, smoking, like alcohol, can be a confounding variable since it facilitates the appearance of leukoplakias which have a differential diagnosis from AC. Thus, for such cases, it is important that patients report their history of chronic exposure to the sun. There is controversy in the literature regarding the association of smoking with the development of AC. While Souza Lucena et al.3 observed that only 18.9% of patients with AC were smokers, Markopoulos et al.1 reported that 60% of individuals with AC were smokers. The data used in the present study showed that 25% of patients with AC were smokers.
Among the main clinical characteristics, AC can be characterized by the presence of eukoplakia and ulcerated1 lesions and lip dryness8. For Piñera-Marques et al.4, the main clinical alterations of AC are erythema, keratosis, atrophy, erosion and fissures. However, in the present study, an increased frequency of no-ulcerated leukoplakia aspects was observed. According to Gonzaga et al.5, there is no correlation between the clinical appearance and the degree of histopathological damage, as there are no specific clinical aspects to distinguish AC from CSS, which enhances the importance of histopathological analysis.
The histopathological aspects of AC can range from hyperkeratosis to epithelial dysplasia. Dysplastic changes can occur in the deeper layers of the epithelium4. The existence of epithelial dysplasia, even if mild, indicates increased risk and subsequent development of cancer. At the level of the epithelium, the first microscopic changes are hyperkeratosis, in addition to atrophy or epithelial hyperplasia. At a more advanced stage, these findings are amplified and the thorny layer becomes thicker. Keratin pearls, as well as areas of cellular atypia, can also be found. In the connective tissue, some important changes such as the basophilic degeneration of collagen fibers, known as solar elastosis, can also be observed. In this change, it has been ascertained that the elastic and collagen fibers are replaced by a granular, basophilic, amorphous and acellular material that usually contains dilated blood vessels. An inflammatory infiltrate, ranging from moderate to intense, can be observed1,8,14.
In the present study, hyperkeratosis was the histopathological aspect most commonly observed, followed by moderate, mild and severe epithelial dysplasia. The greatest frequency of hyperkeratosis was seen in lesions with no-ulcerated leukoplakia aspect, despite having also been the most observed histopathological classification in lesions with mixed and no-ulcerated erythroplakia aspect. Moderate epithelial dysplasias were also commonly seen in lesions clinically classified as no-ulcerated leukoplakia. Only two lesions were histopathologically classified as severe dysplasia, having been observed specifically in lesions with no-ulcerated erythroplakia and erosion/ulceration aspect. Therefore, it was not possible to establish a correlation between the clinical characterization and histopathological classification of the lesions in the studied sample.
CONCLUSION
It was not possible to correlate the degree of tissue change found in the histopathological diagnostic with the clinical aspects observed. Thus, it can be concluded that the clinical aspect of the lesion can mask tissue changes at various stages, including the most advanced and of greatest risk to the patient. This fact highlights the importance of early diagnosis. Therefore, it is imperative that the dental surgeon have knowledge of CA in order to be able to make a correct diagnosis and detect the clinically visible changes in the lip epithelium in the initial stages.
How to cite: Brito LNS, Bonfim ACEA, Gomes DQC, Alves PM, Nonaka CFW, Godoy GP. Clinical and histopathological study of actinic cheilitis. Rev Odontol UNESP. 2019;48:e20190005. https://doi.org/10.1590/1807-2577.00519
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Autoria
Lívia Natália Sales BRITO
UFPE – Universidade Federal de Pernambuco, Programa de Pós-graduação em Odontologia, Recife, PE, BrasilUniversidade Federal de PernambucoBrasilRecife, PE, BrasilUFPE – Universidade Federal de Pernambuco, Programa de Pós-graduação em Odontologia, Recife, PE, Brasil
UEPB – Universidade Estadual da Paraíba, Campina Grande, PB, BrasilUniversidade Estadual da ParaíbaBrasilCampina Grande, PB, BrasilUEPB – Universidade Estadual da Paraíba, Campina Grande, PB, Brasil
UEPB – Universidade Estadual da Paraíba, Programa de Pós-graduação em Odontologia, Campina Grande, PB, BrasilUniversidade Estadual da ParaíbaBrasilCampina Grande, PB, BrasilUEPB – Universidade Estadual da Paraíba, Programa de Pós-graduação em Odontologia, Campina Grande, PB, Brasil
UEPB – Universidade Estadual da Paraíba, Programa de Pós-graduação em Odontologia, Campina Grande, PB, BrasilUniversidade Estadual da ParaíbaBrasilCampina Grande, PB, BrasilUEPB – Universidade Estadual da Paraíba, Programa de Pós-graduação em Odontologia, Campina Grande, PB, Brasil
UEPB – Universidade Estadual da Paraíba, Programa de Pós-graduação em Odontologia, Campina Grande, PB, BrasilUniversidade Estadual da ParaíbaBrasilCampina Grande, PB, BrasilUEPB – Universidade Estadual da Paraíba, Programa de Pós-graduação em Odontologia, Campina Grande, PB, Brasil
Gustavo Pina GODOY
*
*Gustavo Pina Godoy, UFPE – Universidade Federal de Pernambuco, Departamento de Patologia, Avenida Professor Moraes Rêgo, 1235, Cidade Universitária, 50670-901 Recife - PE, Brasil, e-mail: gruiga@hotmail.com
UFPE – Universidade Federal de Pernambuco, Departamento de Patologia, Recife, PE, BrasilUniversidade Federal de PernambucoBrasilRecife, PE, BrasilUFPE – Universidade Federal de Pernambuco, Departamento de Patologia, Recife, PE, Brasil
CONFLICTS OF INTERESTS The authors declare no conflicts of interest.
*Gustavo Pina Godoy, UFPE – Universidade Federal de Pernambuco, Departamento de Patologia, Avenida Professor Moraes Rêgo, 1235, Cidade Universitária, 50670-901 Recife - PE, Brasil, e-mail: gruiga@hotmail.com
SCIMAGO INSTITUTIONS RANKINGS
UFPE – Universidade Federal de Pernambuco, Programa de Pós-graduação em Odontologia, Recife, PE, BrasilUniversidade Federal de PernambucoBrasilRecife, PE, BrasilUFPE – Universidade Federal de Pernambuco, Programa de Pós-graduação em Odontologia, Recife, PE, Brasil
UEPB – Universidade Estadual da Paraíba, Campina Grande, PB, BrasilUniversidade Estadual da ParaíbaBrasilCampina Grande, PB, BrasilUEPB – Universidade Estadual da Paraíba, Campina Grande, PB, Brasil
UEPB – Universidade Estadual da Paraíba, Programa de Pós-graduação em Odontologia, Campina Grande, PB, BrasilUniversidade Estadual da ParaíbaBrasilCampina Grande, PB, BrasilUEPB – Universidade Estadual da Paraíba, Programa de Pós-graduação em Odontologia, Campina Grande, PB, Brasil
UFPE – Universidade Federal de Pernambuco, Departamento de Patologia, Recife, PE, BrasilUniversidade Federal de PernambucoBrasilRecife, PE, BrasilUFPE – Universidade Federal de Pernambuco, Departamento de Patologia, Recife, PE, Brasil
Table 3
Correlation between clinical aspects and histopathological classification in number of cases
table_chartTable 1
Sample distribution by individual characteristics
Individual Characteristics
N
%
Sex
Male
33
82.5
Female
7
17.5
Total
40
100
Skin color
Leukoderm
30
75
Pheoderm
10
25
Total
40
100
Occupation
Farmer
15
37.5
Driver
5
12.5
Electrician
2
5
Construction worker
3
7.5
Fisherman
1
2.5
Tire repair man
1
2.5
Student
1
2.5
Retiree
6
15
Other
6
15
Total
40
100
Smoking
Yes
10
25
No
30
75
Total
40
100
Sun exposure
Yes
34
85
No
6
15
Total
40
100
Sun protection
Yes
20
50
No
20
50
Total
40
100
table_chartTable 2
Sample distribution by clinical and pathological features
Characteristic
n
%
Painful symptomatology
Yes
13
32.5
No
27
67.5
Total
40
100
Clinical aspect of the lesion
No-ulcerated leukoplakia
19
47.5
No-ulcerated Erythroplakia
10
25
Erosion/ulceration
1
2.5
Mixed aspects
10
25
Total
40
100
Histopathological Diagnosis
Hyperkeratosis
20
50
Mild Dysplasia
8
20
Moderate Dysplasia
10
25
Severe Dysplasia
2
5
Total
40
100
table_chartTable 3
Correlation between clinical aspects and histopathological classification in number of cases
CLINICAL ASPECT
HISTOPATHOLOGICAL CLASSIFICATION
Hyperkeratosis
Mild dysplasia
Moderate dysplasia
Severe dysplasia
No-ulcerated leukoplakia
10 (52.6%)
4 (21%)
5 (26.3%)
-
No-ulcerated Erythroplakia
5 (50%)
2 (20%)
2 (20%)
1 (10%)
Mixed aspect
5 (50%)
2 (20%)
3 (30%)
-
Erosion/ulceration
-
-
-
1 (100%)
Como citar
BRITO, Lívia Natália Sales et al. Estudo clínico e histopatológico das queilites actínicas. Revista de Odontologia da UNESP [online]. 2019, v. 48 [Acessado 17 Abril 2025], e20190005. Disponível em: <https://doi.org/10.1590/1807-2577.00519>. Epub 03 Out 2019. ISSN 1807-2577. https://doi.org/10.1590/1807-2577.00519.
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