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Copyright ©2013
Review Article
J Res Adv Dent 2014; 3:2:72-75.
An outline of existing clinical classification system for oral sub
mucous fibrosis
Nidhi Thakur1* Vishal Kumar2
1Senior Lecturer, Department of Oral Medicine and Radiology, Dr. B R Ambedkar Institute of Dental Sciences and Hospital, Patna, Bihar, India.
2Reader, Department of Orthodontics, Dr. B R Ambedkar Institute of Dental Sciences and Hospital, Patna, Bihar, India.
ABSTRACT
Objectives: Oral submucous fibrosis remains an enigma, with a poorly defined classification system and elusive
pathogenesis. Many attempts have been made to classify OSMF, some based on clinical criteria and some on
histopathological criteria. Some authors have classified it based on the functional aspects. But none of these
classification systems have a universal acceptance. Here is an attempt to compile the different systems of OSMF
classification for the ease and better understanding of the clinicians.
Keywords: Oral submucous fibrosis, potentially malignant disorder.
INTRODUCTION
Oral submucous fibrosis is a potentially
malignant disorder that is characterized by
blanching and stiffness of oral mucosa, trismus, and
burning sensation in the mouth. It also produces
hypomobility of the soft palate and tongue, and loss
of gustatory sensation. Occasionally there can be
mild hearing impairment due to blockade of the
eustachian tube. Although the etiology is not very
clear but a definitive association of the same with
areca nut (Areca catechu) consumption in variable
forms has been established by many studies1-5.
Some cases of oral submucous fibrosis have been
reported in patients without any habit of areca nut
consumption6. It affects people of all age groups and
both the sex but is more prevalent in males in
second and third decade. The malignant potential
for oral submucous fibrosis is considered high7.
Extensive studies done on the
etiopathogenesis of the disease have observed an
evidence of OSMF being a mucosal change
secondary to chronic iron and /or vitamin B
complex deficiency5.It has been suggested that the
disease is an Asian analogue of sideropenic
dysphagia. The biological basis for OSMF remains
unclear but cytotoxic, apoptotic and proliferative
effects from areca nut agents have been proposed
for it 8-11. Active oxygen species and reactive free
radicals mediate alterations that lead to mutations
and produce the genotypic and phenotypic
manifestations of the disease.
Both surgical and pharmacological
treatments have been tried in the management of
OSMF. Surgical treatment by excision of fibrous
tissues is effective but is often followed by relapse.
They are also inaccessible in certain backward
communities where OSMF is a common entity.
Conservative management has shown significant
improvement in mouth opening and providing
symptomatic relief to the patients14 to 16.
Physiotherapy along with micronutrients
supplements has also been reported to show
significant improvement in mouth opening in these
patients17, 18, 19.
Outline of the clinical classification systems:
73
Though oral submucus fibrosis has been classified
based on its clinical symptoms as well as
histopathological features but clinical staging is
gaining significance. This is because biopsy per se
for diagnosis has been largely abandoned as it is
seen to cause further fibrosis and scarring. The
existing clinical classification system has been
placed here arbitrarily in two groups (Table 1).
Classifications given before
year 2000
Classifications given
after year 2000
1. J V Desa(1957) 1. Rangnathan K et al
(2001)
2. Pindborg JJ(1989) 2. Rajendran et
al(2003)
3. S K Katharia(1992) 3. Nagesh and
Bailoor(2005)
4. Lai DR et al(1995) 4. Tinky Bose & Anita
Balan
5. R Maher(1996) 5. Kiran kumar et al
(2007)
6. Chandramani more
et al (2011)
Classification by J V Desa (1957)
 Stage I- stomatitis & vesiculations
 Stage II- Fibrosis
 Stage III- As its sequelae
Classification by Pindborg JJ (1989)
Stage I- Stomatitis includes erythematous mucosa,
vesicles, mucosal ulcers, melanotic mucosal
pigmentations and mucosal petechiae.
Stage II-Fibrosis occurring in the healing vesicles
and ulcers, is the hallmark of this stage.
 Early lesions demonstrate blanching of the
oral mucosa.
 Older lesions include vertical and circular
palpable fibrous bands in the buccal
mucosa and around the mouth opening or
lips. This results in a mottled marble like
appearance of the mucosa because of the
vertical thick fibrous bands in association
with a blanched mucosa.
Stage III- Sequelae of OSMF are as follows
 Leukoplakia as found in more than 25% of
individuals with OSMF
 Speech and hearing defects may occur
because of involvement of the tongue and
the Eustachian tubes.
SK Katharia classification et al (1992)
 Score 0- mouth opening is greater than 41 mm
 Score 1- mouth opening between 37 to 40 mm
 Score 2- mouth opening between 33 to 36 mm
 Score 3- mouth opening between 29 to 32 mm
 Score 4- mouth opening between 25 to 28 mm
 Score 5- mouth opening between 21 to 24 mm
 Score 6- mouth opening between17 to 20 mm
 Score 7- mouth opening between13 to 16 mm
 Score 8- mouth opening between 9 to 12 mm
 Score 9- mouth opening between 5 to 8 mm
 Score 10- mouth opening between 0 to 4mm
Lai DR conducted a study and dvided the patients
based on the interincisal distance as
 Group A- Mouth opening greater than 35mm
 Group B- Mouth opening between 30 to 35mm
 Group C – Mouth opening between 20 to 25mm
 Group D – Mouth opening less than 20mm
R Maher has given a classification based on area of
involvement of the oral cavity
 Involvement of 1/3rd or less of the oral cavity
74
 Involvement of 1/3rd to 2/3rd of the oral
cavity(if 4 to 6 intra oral sites are involved)
 Involvement of greater than 2/3rd of the oral
cavity.
Ranganathan K et al used a baseline study on the
mouth opening parameters of normal patients and
divided the OSMF patients as
 Group I- Only symptoms with no restriction of
mouth opening
 Group II- Limited mouth opening 2o mm and
above
 Group III- Mouth opening less than 20 mm
 Group IV – OSMF advanced with limited mouth
opening along with precancerous or cancerous
changes seen throughout the mucosa.
Rajendran R classification reported the clinical
features of OSMF as:
 Early OSMF- Burning sensation in the mouth.
Blisters especially on the palate, ulceration or
recurrent generalised inflammation of the oral
mucosa, excessive salivation, defective
gustatory sensation and dryness of mouth
present.
 Advanced OSMF- Blanched and slightly opaque
mucosa, fibrous bands in buccal mucosa
running in vertical direction. Palate and the
faucial pillars are the areas involved. Gradual
impairment of tongue movement and difficulty
in mouth opening.
Tinky Bose and Anita Balan classification of OSMF
 Group A – mild cases
 Group B – moderate cases
 Group C – severe cases
Kiran Kumar et al
 Stage I (Mouth opening greater than 45mm)
 Stage II (Restricted mouth opening 20 to
40mm)
 Stage III (Mouth opening less than 20mm)
Chandramani More et al classification20 (2011)
A. Clinical Staging:
Stage I (S1) –stomatitis and blanching
Stage II (S2) - Presence of palpable fibrous bands in
buccal mucosa and or oropharynx with or
without stomatitis.
Stage III- Involvement of other part.
Stage IV (S4)-
 Any of the above stage along with presence of
potentially malignant disorder.
 Presence of oral carcinomas.
Functional classification (Based on interincisal
distance)
M1- Interincisal mouth opening up to or > 35mm
M2- Interincisal distance between 25 to 35mm
M3- Interincisal distance between 15 to 25mm
M4- Interincisal distance of less than 15mm
CONCLUSION
The purpose of the present article is to outline the
existing clinical classification for the ease of
diagnosis and treatment of oral submucous fibrosis.
CONFLICT OF INTEREST
No potential conflict of interest relevant to this
article was reported.
REFERENCES
1. Lal D. Diffuse oral submucous fibrosis. All India
Dent Assoc 1953; 26:1-3.
2. Canniff J P, Harvey W. The aetiology of oral
submucous fibrosis: The stimulation of
collagen synthesis by extracts of areca nut. Int J
of Oral Surg 1981; 10(I):163-7.
3. Harvey W, Scutt A, Meghji S, Canniff J P.
Stimulation of human Buccal mucosa
fibroblasts in vitro by areca nut alkaloids. Arch
oral boil 1986; 31(1): 45-9.
75
4. Maher R, Lee A J, Warnakulasuriya KA, Lewis
JA. Role of areca nut in the causation of oral
submucous fibrosis: a case control study in
Pakistan. J of Oral Pathol Med1994; 23: 65-9.
5. Canniff JP, Harvey W, Harris M. Oral
submucous fibrosis: Its pathogenesis and
management. Br Dent J 1986; 160: 429-34.
6. Seedat HA, Van Wyk C. Submucous fibrosis in
non betel nut chewing subjects. J Biol
Buccale1988; 16: 3-6.
7. Pindborg JJ. Lesions of the oral mucosa to be
considered premalignant and their
epidemiology. Pg 2-12. In Mackenzie I C,
Dabelsteen E, Squier C A (eds). Oral
premalignancy. Iowa: University of Iowa press.
8. Tilakaratne WM, Klinikowski MF, Saku T,
Peters TJ, Waranakulasuriya S. Oral submucous
fibrosis: Review on aetiology and pathogenesis.
Oral Oncol 2006; 42: 561-8.
9. Chang MC, Wu HL, Lee JJ . The induction of
prostaglandin E2 production, cell cycle arrest
and cytotoxicity in primary oral keratinocytes
and KB cancer cells by areca nut ingredients is
differentially regulated by MEK/ERK
activation. J Biol Chem 2004; 279: 50676-83.
10. Jeng JH, Wang YJ, Chang WH. Reactive oxygen
species are crucial for hydroxychavicol toxicity
towards KB epithelial cells. Cell Mol Life Sci
2004; 61: 83-96.
11. Tsai C L,Kuo My, Hahn L J, Kuo YS, Yang PJ, Jeng
J H. Cytotoxic and cytoststic effects of arecoline
on oral mucosal fibroblasts. Proc Natl Sci Coun
Repub China B. 1997; 21: 161-7.
12. Le PV, Gornitsky M, Domanowski G. Oral stent
as treatment adjunct for oral submucous
fibrosis. Oral Surg Oral Med Oral Pathol Oral
Radiol Endod 1996; 81: 148-50.
13. Mokal NJ, Raje RS, Ranade SV Prasad JS, Thatte
RL. Release of oral submucous fibrosis and
reconstruction using superficial temporal
fascia flap and split skin graft- A new
technique. Br J Plast Surg 2005; 58: 1055-60.
14. R M Borle, S R Borle. Management of Oral
Submucous Fibrosis: A Conservative Approach.
J of Oral Maxillofac Surg 1991; 49: 788-91.
15. A Kumar, Anjana Bagewadi, Vaishali Keluskar.
Efficacy of lycopene in the management of oral
submucous fibrosis. Oral Surg Oral Med Oral
Pathol Oral Radiol Endod. 2007; 103: 207-13.
16. Maher R, Aga P, Johnson N W. Evaluation of
multiple micronutrient supplementations in
the management of oral submucous fibrosis in
Karachi, Pakistan. Nutr Cancer.1997; 27(1):
41-7.
17. Stephen Cox, Hans Zoellner. Physiotherapy
treatment improves oral opening in oral
submucous fibrosis. J of Oral Pathol Med 2009;
38: 220-226.
18. Nidhi Thakur, Vaishali Keluskar, Anjana
Bagewadi et al. Effectiveness of micronutrients
and physiotherapy in the management of oral
submucus fibrosis. Int J contem dentistry.2011
(1):101-105.
19. Richa Dhariwal, Sanjit Mukherjee, Sweta
Pattanayak. Zinc and Vitamin A can minimise
the severity of oral submucous fibrosis. BMJ
2010; doi: 10.1136/bcr.10.2009.2349.
20. Chandramani Bhagvan More, Swati Gupta, Jigar
Joshi et al. Classification system for oral
submucous fibrosis. JIOMR. 2012.24-29

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osmf classification,Review Article

  • 1. ___________________________________________________ ____________________ _______________________________________________________________________________________ Copyright ©2013 Review Article J Res Adv Dent 2014; 3:2:72-75. An outline of existing clinical classification system for oral sub mucous fibrosis Nidhi Thakur1* Vishal Kumar2 1Senior Lecturer, Department of Oral Medicine and Radiology, Dr. B R Ambedkar Institute of Dental Sciences and Hospital, Patna, Bihar, India. 2Reader, Department of Orthodontics, Dr. B R Ambedkar Institute of Dental Sciences and Hospital, Patna, Bihar, India. ABSTRACT Objectives: Oral submucous fibrosis remains an enigma, with a poorly defined classification system and elusive pathogenesis. Many attempts have been made to classify OSMF, some based on clinical criteria and some on histopathological criteria. Some authors have classified it based on the functional aspects. But none of these classification systems have a universal acceptance. Here is an attempt to compile the different systems of OSMF classification for the ease and better understanding of the clinicians. Keywords: Oral submucous fibrosis, potentially malignant disorder. INTRODUCTION Oral submucous fibrosis is a potentially malignant disorder that is characterized by blanching and stiffness of oral mucosa, trismus, and burning sensation in the mouth. It also produces hypomobility of the soft palate and tongue, and loss of gustatory sensation. Occasionally there can be mild hearing impairment due to blockade of the eustachian tube. Although the etiology is not very clear but a definitive association of the same with areca nut (Areca catechu) consumption in variable forms has been established by many studies1-5. Some cases of oral submucous fibrosis have been reported in patients without any habit of areca nut consumption6. It affects people of all age groups and both the sex but is more prevalent in males in second and third decade. The malignant potential for oral submucous fibrosis is considered high7. Extensive studies done on the etiopathogenesis of the disease have observed an evidence of OSMF being a mucosal change secondary to chronic iron and /or vitamin B complex deficiency5.It has been suggested that the disease is an Asian analogue of sideropenic dysphagia. The biological basis for OSMF remains unclear but cytotoxic, apoptotic and proliferative effects from areca nut agents have been proposed for it 8-11. Active oxygen species and reactive free radicals mediate alterations that lead to mutations and produce the genotypic and phenotypic manifestations of the disease. Both surgical and pharmacological treatments have been tried in the management of OSMF. Surgical treatment by excision of fibrous tissues is effective but is often followed by relapse. They are also inaccessible in certain backward communities where OSMF is a common entity. Conservative management has shown significant improvement in mouth opening and providing symptomatic relief to the patients14 to 16. Physiotherapy along with micronutrients supplements has also been reported to show significant improvement in mouth opening in these patients17, 18, 19. Outline of the clinical classification systems:
  • 2. 73 Though oral submucus fibrosis has been classified based on its clinical symptoms as well as histopathological features but clinical staging is gaining significance. This is because biopsy per se for diagnosis has been largely abandoned as it is seen to cause further fibrosis and scarring. The existing clinical classification system has been placed here arbitrarily in two groups (Table 1). Classifications given before year 2000 Classifications given after year 2000 1. J V Desa(1957) 1. Rangnathan K et al (2001) 2. Pindborg JJ(1989) 2. Rajendran et al(2003) 3. S K Katharia(1992) 3. Nagesh and Bailoor(2005) 4. Lai DR et al(1995) 4. Tinky Bose & Anita Balan 5. R Maher(1996) 5. Kiran kumar et al (2007) 6. Chandramani more et al (2011) Classification by J V Desa (1957)  Stage I- stomatitis & vesiculations  Stage II- Fibrosis  Stage III- As its sequelae Classification by Pindborg JJ (1989) Stage I- Stomatitis includes erythematous mucosa, vesicles, mucosal ulcers, melanotic mucosal pigmentations and mucosal petechiae. Stage II-Fibrosis occurring in the healing vesicles and ulcers, is the hallmark of this stage.  Early lesions demonstrate blanching of the oral mucosa.  Older lesions include vertical and circular palpable fibrous bands in the buccal mucosa and around the mouth opening or lips. This results in a mottled marble like appearance of the mucosa because of the vertical thick fibrous bands in association with a blanched mucosa. Stage III- Sequelae of OSMF are as follows  Leukoplakia as found in more than 25% of individuals with OSMF  Speech and hearing defects may occur because of involvement of the tongue and the Eustachian tubes. SK Katharia classification et al (1992)  Score 0- mouth opening is greater than 41 mm  Score 1- mouth opening between 37 to 40 mm  Score 2- mouth opening between 33 to 36 mm  Score 3- mouth opening between 29 to 32 mm  Score 4- mouth opening between 25 to 28 mm  Score 5- mouth opening between 21 to 24 mm  Score 6- mouth opening between17 to 20 mm  Score 7- mouth opening between13 to 16 mm  Score 8- mouth opening between 9 to 12 mm  Score 9- mouth opening between 5 to 8 mm  Score 10- mouth opening between 0 to 4mm Lai DR conducted a study and dvided the patients based on the interincisal distance as  Group A- Mouth opening greater than 35mm  Group B- Mouth opening between 30 to 35mm  Group C – Mouth opening between 20 to 25mm  Group D – Mouth opening less than 20mm R Maher has given a classification based on area of involvement of the oral cavity  Involvement of 1/3rd or less of the oral cavity
  • 3. 74  Involvement of 1/3rd to 2/3rd of the oral cavity(if 4 to 6 intra oral sites are involved)  Involvement of greater than 2/3rd of the oral cavity. Ranganathan K et al used a baseline study on the mouth opening parameters of normal patients and divided the OSMF patients as  Group I- Only symptoms with no restriction of mouth opening  Group II- Limited mouth opening 2o mm and above  Group III- Mouth opening less than 20 mm  Group IV – OSMF advanced with limited mouth opening along with precancerous or cancerous changes seen throughout the mucosa. Rajendran R classification reported the clinical features of OSMF as:  Early OSMF- Burning sensation in the mouth. Blisters especially on the palate, ulceration or recurrent generalised inflammation of the oral mucosa, excessive salivation, defective gustatory sensation and dryness of mouth present.  Advanced OSMF- Blanched and slightly opaque mucosa, fibrous bands in buccal mucosa running in vertical direction. Palate and the faucial pillars are the areas involved. Gradual impairment of tongue movement and difficulty in mouth opening. Tinky Bose and Anita Balan classification of OSMF  Group A – mild cases  Group B – moderate cases  Group C – severe cases Kiran Kumar et al  Stage I (Mouth opening greater than 45mm)  Stage II (Restricted mouth opening 20 to 40mm)  Stage III (Mouth opening less than 20mm) Chandramani More et al classification20 (2011) A. Clinical Staging: Stage I (S1) –stomatitis and blanching Stage II (S2) - Presence of palpable fibrous bands in buccal mucosa and or oropharynx with or without stomatitis. Stage III- Involvement of other part. Stage IV (S4)-  Any of the above stage along with presence of potentially malignant disorder.  Presence of oral carcinomas. Functional classification (Based on interincisal distance) M1- Interincisal mouth opening up to or > 35mm M2- Interincisal distance between 25 to 35mm M3- Interincisal distance between 15 to 25mm M4- Interincisal distance of less than 15mm CONCLUSION The purpose of the present article is to outline the existing clinical classification for the ease of diagnosis and treatment of oral submucous fibrosis. CONFLICT OF INTEREST No potential conflict of interest relevant to this article was reported. REFERENCES 1. Lal D. Diffuse oral submucous fibrosis. All India Dent Assoc 1953; 26:1-3. 2. Canniff J P, Harvey W. The aetiology of oral submucous fibrosis: The stimulation of collagen synthesis by extracts of areca nut. Int J of Oral Surg 1981; 10(I):163-7. 3. Harvey W, Scutt A, Meghji S, Canniff J P. Stimulation of human Buccal mucosa fibroblasts in vitro by areca nut alkaloids. Arch oral boil 1986; 31(1): 45-9.
  • 4. 75 4. Maher R, Lee A J, Warnakulasuriya KA, Lewis JA. Role of areca nut in the causation of oral submucous fibrosis: a case control study in Pakistan. J of Oral Pathol Med1994; 23: 65-9. 5. Canniff JP, Harvey W, Harris M. Oral submucous fibrosis: Its pathogenesis and management. Br Dent J 1986; 160: 429-34. 6. Seedat HA, Van Wyk C. Submucous fibrosis in non betel nut chewing subjects. J Biol Buccale1988; 16: 3-6. 7. Pindborg JJ. Lesions of the oral mucosa to be considered premalignant and their epidemiology. Pg 2-12. In Mackenzie I C, Dabelsteen E, Squier C A (eds). Oral premalignancy. Iowa: University of Iowa press. 8. Tilakaratne WM, Klinikowski MF, Saku T, Peters TJ, Waranakulasuriya S. Oral submucous fibrosis: Review on aetiology and pathogenesis. Oral Oncol 2006; 42: 561-8. 9. Chang MC, Wu HL, Lee JJ . The induction of prostaglandin E2 production, cell cycle arrest and cytotoxicity in primary oral keratinocytes and KB cancer cells by areca nut ingredients is differentially regulated by MEK/ERK activation. J Biol Chem 2004; 279: 50676-83. 10. Jeng JH, Wang YJ, Chang WH. Reactive oxygen species are crucial for hydroxychavicol toxicity towards KB epithelial cells. Cell Mol Life Sci 2004; 61: 83-96. 11. Tsai C L,Kuo My, Hahn L J, Kuo YS, Yang PJ, Jeng J H. Cytotoxic and cytoststic effects of arecoline on oral mucosal fibroblasts. Proc Natl Sci Coun Repub China B. 1997; 21: 161-7. 12. Le PV, Gornitsky M, Domanowski G. Oral stent as treatment adjunct for oral submucous fibrosis. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1996; 81: 148-50. 13. Mokal NJ, Raje RS, Ranade SV Prasad JS, Thatte RL. Release of oral submucous fibrosis and reconstruction using superficial temporal fascia flap and split skin graft- A new technique. Br J Plast Surg 2005; 58: 1055-60. 14. R M Borle, S R Borle. Management of Oral Submucous Fibrosis: A Conservative Approach. J of Oral Maxillofac Surg 1991; 49: 788-91. 15. A Kumar, Anjana Bagewadi, Vaishali Keluskar. Efficacy of lycopene in the management of oral submucous fibrosis. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007; 103: 207-13. 16. Maher R, Aga P, Johnson N W. Evaluation of multiple micronutrient supplementations in the management of oral submucous fibrosis in Karachi, Pakistan. Nutr Cancer.1997; 27(1): 41-7. 17. Stephen Cox, Hans Zoellner. Physiotherapy treatment improves oral opening in oral submucous fibrosis. J of Oral Pathol Med 2009; 38: 220-226. 18. Nidhi Thakur, Vaishali Keluskar, Anjana Bagewadi et al. Effectiveness of micronutrients and physiotherapy in the management of oral submucus fibrosis. Int J contem dentistry.2011 (1):101-105. 19. Richa Dhariwal, Sanjit Mukherjee, Sweta Pattanayak. Zinc and Vitamin A can minimise the severity of oral submucous fibrosis. BMJ 2010; doi: 10.1136/bcr.10.2009.2349. 20. Chandramani Bhagvan More, Swati Gupta, Jigar Joshi et al. Classification system for oral submucous fibrosis. JIOMR. 2012.24-29