• JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator

ISSN (Print) 1013-9052
EISSN 1658-3558

The Saudi Dental Journal,
P.O. Box 52500,
Riyadh 11563,
Kingdom of Saudi Arabia
Tel.
966-1-467-7328
Fax.
933-1-467-7308 /
966-1-467-7534
Email
saudidj@ksu.edu.sa


Prevalence of recurrent aphthous ulceration in Gizan
 

Camil Salem, BDS, PhD*
* Dental Department, King Fahad Hospi­tal, P.O. Box 204, Gizan, Saudi Arabia.

Abstract 

 
Among present ulcers, recurrent aphthous ulceration (RAU) was found in 1.59% of 4,255 adult Saudi patients seen in the Dental Department, King Fahd Central Hospital, Gizan, between 1984-1989. Of all the patients examined including those with ulcers, 16.4% gave positive history of developing aphthus ulcers at least once during the two years previous to the time of examination. The highest prevalence for both present ulcers and history of ulcers was among the younger age-groups. No significant difference was found between the prevalence figures of RAU in the two sexes. None of the common triggering factors were contributary, nor there has been any correlation between smoking and RAU in this study.

Introduction

 
Recurrent aphthous ulceration (RAU) is the most common oral ulcerative disease affecting man, characterized by recurrent episodes of painful ulceration of the oral mucosa. Aphthous ulcers most commonly develop on the labial and buccal mucosa, tongue and less frequently on the mucobuccal folds, floor of mouth and soft palate.1-5 Involvement of keratinized mucosa bound to periosteum is generally considered uncommon.6,7
The ulcers are well demarcated; fibrin-covered and surrounded by a bright red inflammatory halo. The number of ulcers varies from a single lesion to 5-10 ulcers. The ulcers vary in diameter from 1-2 mm but rarely exceed 1 cm. The labial and buccal lesions are usually rounded, whereas in the sulci they tend to be oblong.4 The ulcers will most often heal within one to three weeks. Recurrence may take place at intervals of several years, whereas some patients had ulcerations almost constantly with healing times that exceeded one month.6
The disease has been classified in three different clinical forms: minor, major and herpetiform.1,5 The herpetiform type is characterized by recurrent crops of ulcers, 10 to 100 in number, involving the oral mucosa. The ulcers usually have a diameter of 1 to 2 mm. In these features, they resemble herpetic lesion.2 The major aphthous ulcers are larger in size, deep, crateriform, and may be accompanied by considerable induration, and characteristically heal with scar formation.2 The prevalence of RAU varied in different parts of the world and in different samples of population (Table 1). Donatsky12in a study of 512 dental students in Denmark, reported a prevalence of 56% for RAU. Fahmy14 reported a 5-year incidence of 27% among Arabs of various nationalities living in Kuwait, who also reported a low incidence of 5% in a sub group of Bedouins. Prevalence as high as 54% among health students8 and 66.2% among dental students has been reported in U.S.A. by Ship et al.10 Axell16 found a prevalence of 17.7% in the general Swedish population. No studies were done so far on the prevalence of RAU in Saudi Arabia.
The aim of the present investigation was to study the prevalence of RAU in an adult Saudi Arabian population from Gizan Region.

Materials and Methods

 
The material of this study comprised 4,257 Saudi patients (63% males and 39% females) aged 20 to 72 years, seen in the Dental Department, King Fahd Central Hospital, Gizan between 1984 and 1989. All patients were examined clinically for oral mucosal lesions, including RAU. The clinical criteria for the diagnosis of RAU1,2,5 were:
1. The presence of one or more well demarcated, painful ulcers on a nonkeratinized mucosa, fibrin covered and surrounded by an inflammatory halo.
2. Positive history of developing similar ulcers. The anatomic location of the ulcers was recorded for each patient with the aid of the diagram presented by Roed-Petersen and Renstrup16 for the topographic classification of the oral mucosa.
History of RAU was recorded as positive when the patient was able to identify the lesion of RAU on colored photographs helped by verbal explanation; and that he/she had experienced this lesion at least once during the past two years. The criteria used in this study for the diagnosis and in obtaining the history of RAU were those described in the early studies.8,10,15 All patients were inquired about the frequency of the ulcers, the healing period, consumption of drugs, triggering factors and tobacco habits. Healing period was assessed as days of symptoms associated with individual ulcers as referred to by the patient.

Results

 
The age and sex distribution of the individuals examined are shown in Table 2. The prevalence of RAU among patients with present ulcers was 1.59% as shown in Table 3. History of RAU was recorded among 14.8% of the population as shown in Table 4. Thus, the total prevalence of RAU, including present lesions and those with history of ulcers during the past 2 years was 16.4%. The frequency of ulcers as extracted from the history of RAU was more encountered in the age-groups 30-39 years and 20-29, respectively. As shown in Table 4, the prevalence then steadily decreased through the age strata. There was no significant difference in the prevalence of RAU between males and females in this study (P > 0.01). The anatomic distribution of the present lesions are shown in Table 5. The locations most often affected were the labial mucosa {upper and lower), the cheek mucosa, the vestibular mucosa, the tongue, and the floor of the mouth. No lesions were detected on the soft palate in this study.
Of the patients with present ulcers, 80% had lesions of the minor type [Fig. 11, 12% had lesions of the herpetiform type [Fig. 2], and 8% had lesions of the major type [Fig. 3J. No specific triggering factor or factors could be obtained in this study. No correlation was evident between smoking and RAU, since none of the females with RAU smoked. The frequency of the episodes of RAU is shown in Table 6. Most of the affected individuals had 2-4 episodes of RAU per year.
The healing period varied between 2 and 21 days. Symptoms lasting 3-8 days were reported by 79% of the individuals, Table 7.

Discussion

 
In the present study the diagnosis of "History of RAU" has included episodes during the past 2 years. This is in accordance with the criteria used by Ship eta!.10This delineation is considered more valid for screening RAU in the population than life­time experience with RAU, which would, of course, yield higher prevalence figures.
The prevalence of RAU in this study for both present ulcers and history of ulcers during the past 2 years was 16.4%. This value is in accordance with that given by Axell and Henricsson15 who used the same criteria and reported a prevalence of 17.7% for RAU among the general population in Sweden. Fahmy14 however, reported a 5-year incidence of 27% for RAU among Arabs of different nationalities living in Kuwait. No other studies on the prevalence of RAU in Saudi Arabia are available for comparison.
The variation in the prevalence figures of RAU in the different studies might be due to the fact that these studies have been carried out on various population   samples   which   differed   in   many respects (Table 1). Considering both type of population and age, Ship etal10 showed a prevalence of 66.2% among students and only 13.2% among hospitalized patients.
In the previous studies,8,10-12 the highest prevalence of RAU was found among students. The special features of student's life pattern may predispose the disease as suggested by Miller et al17 who pointed out the possibility of stress generated by the pressure of academic achievement as a triggering factor. In this study, 60% of the individuals examined were school teachers and Government officials, all being beyond school age. However, the prevalence of RAU in this study was higher among the younger age-groups (Tables 3 & 4) in accordance with earlier studies.5,9,13-15 A study sample including younger age-groups would have probably yielded different results.
The locations most often affected were the labial mucosa, the vestibular mucosa, the cheek mucosa, and the tip and margins of the tongue (Table 5). No lesions were detected on the soft palate in this study. With the exception of the absence of palatal lesions, the anatomic locations of present ulcers in this study were in accordance with those reported in earlier studies.13-16 How­ever, approximately 6% of the aphthous ulcers described by Ship et al8 were located on gingiva.
Among the triggering factors mentioned in the previous studies5,6,9-13,15 were catching cold, menstruation, trauma, and food allergy. In this study the triggering factors were not specified by the patients or expressed in vague terms as "fatigue". Obviously, the exacerbations of RAU are linked to general physiologic factors in the body. The mechanism behind such association is not known, but may be possibly mediated through the immunologic system. In such a case, oral epithelium or some cross-reacting antigen stimulates cell-mediated and humoral immune responses to induce epithelial damage.
Immunocytochemical studies using monoclonal antibodies against T-lymphocyte surface antigens showed consistent changes in the T4/T8 ratio extending from the preulcerative to the ulcerative and healing phases, which support an altered delayed hypersensitivity reaction.18'19
Further studies are needed, however, to elucidate the prevalence of RAl i in the general population of Saudi Arabia.


References

 

  1. World Health Organizations. Applications of the international classification of diseases to dentistry and stomatology. ICD, DA. Geneva, 1978.
  2. Pindborg Jj. Atlas of diseases of the oral mucosa. 3rd ed. Copenhagen: Munksgaard, 1980:138-41.
  3. Stanley HR. Aphthous lesions. Oral Surg 1972;33:407-16.
  4. Kramer IRH. Ulcerations of the mouth in children. Aust DentJ 1967;12:83-91.
  5. Sircus W, Church R, Kellcher j. Recurrent aphthous ulcerations of the mouth. A study of the natural history, etiology and treatment. Quebec J Med 1957;26:235-49.
  6. Antoon JW, Miller RL. Aphthous ulcers - a review of the literature etiology, pathogenesis, diagnosis, and treatment. J Am Dent Assoc 1980;10:803-08.
  7. Mintz GA, Smidansky ED. Aphthous stomatitis with involvement of attached gingiva. Oral Su rg Oral Med Oral Path 1985;60:122-24.
  8. Ship li, Morris AL, Durocher RT, Burket LW. Recurrent aphthous ulcerations and recurrent herpes labialis in a professional school student population. Oral Surg 1960; 13:119-120,1317-29,1438-44.
  9. Spoug ID, Diamond HF. Hypersensitivity reactions in mucous membranes. The relationship between hypersensitivity disease and recurrent oral ulcerations. Oral Surg 1963;16:412-21.
  10. Ship II, Brightman V), Laster LL. The patient with recurrent aphthous ulcerations and the patient with recurrent herpes labialis: A study of two population samples. J Am Dent Assoc 1967;74:645-53.
  11. Shapiro S, Olson DL, Chellemi SJ. The association between smoking and aphthous ulcers. Oral Surg 1970;30:624-30.
  12. Donatsky O. Epidemiologic study on recurrent aphthous ulceration among 512 Danish dental students, Comm Dent Oral Epidemiol 1973;1:37-40.
  13. Embil JA, Stephens RG, Manuel FR. Prevalence of recurrent herpes labialis and aphthous ulcers among young adults on six continents. Can Med Assoc J 1975; 113:627-30.
  14. Fahmy MS. Recurrent Aphthous ulcerations in a mixed Arab community. Comm Dent Oral Epidemiol 1976;4:160-4.
  15. AxellT, Henricsson V. The occurrence of recurrent aphthous ulcers is an adult Swedish population. Acta Odontol Scand 1985;43:121-25.
  16. Roed Petersen B, Renstrup CT. A topographical classification of the oral mucosa suitable for electronic data processing. Its application to 560 leukoplakias. Acta Odontol Scand 1962;27:681-95.
  17. Miller MF, Ship II, Ram C. A retrospective study of the prevalence and incidence of recurrent aphthous ulcers in a professional population 1958-1971. Oral Surg 1977;43:532-37.
  18. Lehner T. Auto immunity and management of recurrent aphthous ulceration. Br Dent J 1967;122:15-20.
  19. Dolby AE. Oral mucosa in health and disease. Oxford:Blackwell Scientific Publications, 1975:427-30.

Tables

 


  1992-3-107


1992-3-108-1


1992-3-108-2


1992-3-109-1


1992-3-109-2

1992-3-109-3

 
Website designed and maintained by DeltaCAS