This document provides an overview of oral submucous fibrosis (OSF), including its definition, epidemiology, classification, etiology, pathogenesis, clinical features, and histopathology. OSF is a chronic disease characterized by inflammation and fibrosis of the submucosal tissues caused by chewing areca nut. It predominantly affects people from South Asia and is associated with significantly increased risk of oral cancer. The areca nut alkaloid arecoline is the main causative agent, inducing fibrosis through oxidative damage, upregulation of growth factors and cytokines, and inhibition of collagen degradation. Clinically, OSF presents with burning sensation and scarring that results in restricted mouth opening and tongue movement.
Odontogenic keratocyst (OKC) is the cyst arising from the cell rests of dental lamina. It can occur anywhere in the jaw, but commonly seen in the posterior part of the mandible. Radiographically, most OKCs are unilocular when presented at the periapex and can be mistaken for radicular or lateral periodontal cyst.
ORN is an inflammatory condition of bone that occurs after the bone has been exposed to therapeutic doses of radiation usually given for a malignancies.
Fibro-osseous lesions of the jaws
Fibrous dysplasia
Cemento-osseous dysplasia
Focal cemento-osseous dysplasia
Periapical cemento-osseous dysplasia
Florid cemento-osseous dysplasia
Ossifying fibroma
Juvenile aggressive ossifying fibroma
Cherubism
Fibro-osseous lesions (FOL) are characterized by replacement of normal bone architecture by collagen fibers and fibroblasts containing calcified tissue.
They include a wide variety of lesions of developmental, dysplastic and neoplastic origins with clinical and radiographic presentation and behavior.
Because of the histological similarities between diverse diseases, proper diagnosis requires correlation of history, clinical and radiographic findings.Fibrous Dysplasia
2. Reactive (dysplastic lesions arising in the tooth-bearing area (presumably of periodontal origin).
a. Periapical cemento-osseous dysplasia
b. Focal cemento-osseous dysplasia
c. Florid cemento-osseous dysplasia
3. Fibro-osseous neoplasms (widely designated as cementifying fibroma, ossifying fibroma or cemento-ossifying fibroma.Bone dysplasias
a. Fibrous dyspla i. Monostoticii. Polyostotic
iii. Polyostotic with endocrinopathy (McCune-Albright)
iv Osteofibrous dysplasia
b. Osteitis deformansc. Pagetoid heritable bone dysplasias of childhood
d. Segmental odontomaxillary dysplasia
2. Cemento-osseous dysplasias
a. Focal cemento-osseous dysplasia b. Florid cemento-osseous dysplasia
3.Inflammatory/reactive processes
a. Focal sclerosing osteomyelitisb. Diffuse sclerosing osteomyelitis
c. Proliferative periostitis
4. Metabolic Disease: hyperparathyroidism
5. Neoplastic lesions (Ossifying fibromas)
a. Ossifying fibromab. Hyperparathyroidism jaw lesion syndrome
c. Juvenile ossifying fibroma i. Trabecular typeii. Psammomatoid type
d. Gigantiform cementomas
Odontogenic keratocyst (OKC) is the cyst arising from the cell rests of dental lamina. It can occur anywhere in the jaw, but commonly seen in the posterior part of the mandible. Radiographically, most OKCs are unilocular when presented at the periapex and can be mistaken for radicular or lateral periodontal cyst.
ORN is an inflammatory condition of bone that occurs after the bone has been exposed to therapeutic doses of radiation usually given for a malignancies.
Fibro-osseous lesions of the jaws
Fibrous dysplasia
Cemento-osseous dysplasia
Focal cemento-osseous dysplasia
Periapical cemento-osseous dysplasia
Florid cemento-osseous dysplasia
Ossifying fibroma
Juvenile aggressive ossifying fibroma
Cherubism
Fibro-osseous lesions (FOL) are characterized by replacement of normal bone architecture by collagen fibers and fibroblasts containing calcified tissue.
They include a wide variety of lesions of developmental, dysplastic and neoplastic origins with clinical and radiographic presentation and behavior.
Because of the histological similarities between diverse diseases, proper diagnosis requires correlation of history, clinical and radiographic findings.Fibrous Dysplasia
2. Reactive (dysplastic lesions arising in the tooth-bearing area (presumably of periodontal origin).
a. Periapical cemento-osseous dysplasia
b. Focal cemento-osseous dysplasia
c. Florid cemento-osseous dysplasia
3. Fibro-osseous neoplasms (widely designated as cementifying fibroma, ossifying fibroma or cemento-ossifying fibroma.Bone dysplasias
a. Fibrous dyspla i. Monostoticii. Polyostotic
iii. Polyostotic with endocrinopathy (McCune-Albright)
iv Osteofibrous dysplasia
b. Osteitis deformansc. Pagetoid heritable bone dysplasias of childhood
d. Segmental odontomaxillary dysplasia
2. Cemento-osseous dysplasias
a. Focal cemento-osseous dysplasia b. Florid cemento-osseous dysplasia
3.Inflammatory/reactive processes
a. Focal sclerosing osteomyelitisb. Diffuse sclerosing osteomyelitis
c. Proliferative periostitis
4. Metabolic Disease: hyperparathyroidism
5. Neoplastic lesions (Ossifying fibromas)
a. Ossifying fibromab. Hyperparathyroidism jaw lesion syndrome
c. Juvenile ossifying fibroma i. Trabecular typeii. Psammomatoid type
d. Gigantiform cementomas
ROLE OF NEUTROPHILS IN HEALTH & DISEASE.pptxjasmine918783
The slide contains information about neutrophils, its basic structure, formation, trafficking, functions, the role of neutrophils in acute inflammation, various disorders of neutrophils, etc.
Oral Submucous fibrosis and the role of curcumin in its treatment: A reviewinventionjournals
International Journal of Pharmaceutical Science Invention (IJPSI) is an international journal intended for professionals and researchers in all fields of Pahrmaceutical Science. IJPSI publishes research articles and reviews within the whole field Pharmacy and Pharmaceutical Science, new teaching methods, assessment, validation and the impact of new technologies and it will continue to provide information on the latest trends and developments in this ever-expanding subject. The publications of papers are selected through double peer reviewed to ensure originality, relevance, and readability. The articles published in our journal can be accessed online.
Leprosy is a chronic infectious disease caused by
Mycobacterium leprae, discovered by Norwegian physician
in 1873.
The first known written reference to the disease was found
on Egyptian papyrus in about 1550 B.C. The disease was
well recognized in ancient China, Egypt, and India.
According to the WHO research, India continues to
record the highest number of new leprosy cases in
the world.
It currently has about 54% of all the new leprosy
cases in that 48,000 women and 13,610 children are
newly detected with leprosy
The maximum incubation period reported is as
long as 30 years
The average incubation period is between three
and ten years
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
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Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
3. INTRODUCTION
Oral mucous membrane is a unique area of the body, which
is continuously exposed to various kinds of stresses such as
heat, cold, microorganisms, chemicals and mechanical
irritations.
In response to these stresses, both epithelium and
connective tissue layers of the oral mucosa exhibit acute and
chronic reactive changes.
4. One such reaction of the collagen of oral mucosa to arecanut
is oral submucous fibrosis.
Oral Submucous Fibrosis (OSMF) is a chronic disease of
insidious onset and a prevailing potentially malignant disorder
characterized by juxta-epithelial inflammatory reaction along
with mucosal fibrosis.
OSMF is characterized by deposition of dense collagen in the
connective tissue
5. First described by Schwartz “atrophica idiopathic mucosae
oris” in 1952 among 5 Indian females in Kenya.
1953- Joshi from Bombay redesignated the condition as
Submucous Fibrosis.
6. Most widely accepted definition by Pindborg JJ & Sirsat S.M (1966)
states-
“OSMF is an insidious chronic disease affecting any part of the oral
cavity and sometimes the pharynx. Although, occasionally
preceeded by and/or associated with vesicle formation, it is always
associated with juxta epithelial inflammatory reaction, followed by a
fibroelastic change of the lamina propria, with epithelial atrophy
leading to stiffness of the oral mucosa and causing trismus and
inability to eat”.
DEFINITION
7. EPIDEMIOLOGY
Oral submucous fibrosis (OSF), first described in the early 1950s, is
a potentially malignant disease predominantly seen in people of Asian
descent.
The disease is predominantly seen in India, Bangladesh, Sri Lanka,
Pakistan, Taiwan, Southern China, Polynesia and Micronesia. Several
case-series are reported among Asian immigrants to the UK and
South and East Africa. A significant variation in the prevalence of OSF
in different countries has been reported.
Pindborg (1980) quotes it as almost exclusively occurring among
Indians, Pakistanis and Burmese.
8. The condition was first described in ancient Indian Manuscripts
by Sushruta describing it as “VEDARI” where he describes
patients suffering from narrowing of mouth, burning sensation
and pain.
The prevalence of this condition in Indian subcontinent is a
reflection of their food, cultural or religious habits.
More prevalent among younger individual (15-35 years)
2.3:1- M:F
9. NOMENCLATURE
AUTHORS YEAR NOMENCLATURE GIVEN
Schwartz 1952 Atrophia Idiopathica mucosa oris
Joshi 1953 Submucosa fibrosis of palate and pillars
Lal 1953 Diffuse oral submucous fibrosis
Su 1954 Idiopathic scleroderma of mouth
De sa 1957 Submucous fibrosis of palate and check
George 1958 Submucous fibrosis of palate and mucosa
membrane
Pindborg& Sirsat 1964 Oral submucous fibrosis
Goleria 1970 Sub-epithelial fibrosis
11. Based on clinical findings
Pindborg JJ 1989
Stage I- Stomatitis; erythematous mucosa, vesicles,
ulcers, petechiae
Stage II- Fibrosis in healing vesicles and ulcers;
blanching, palpable bands, mottled marble like
appearance
Stage III- Sequelae of OSMF; Leukoplakia, speech and
hearing deficit
12. Lai DR 1995
Based on interincisal distance
Group 1- >35mm
Group 2- between 30 and 35mm
Group 3- between 20 and 30mm
Group 4- <20mm
13. 13
Haider SM (2000)
Clinical stage:
Stage I: faucial bands only
StageII: faucial and buccal bands
Stage III: Faucial, buccal and labial bands.
Functional stage:
I. Mouth opening ≥ 20 mm.
II. Mouth opening 11-19 mm.
III. Mouth opening ≤10 mm.
14. Prakash R. et al
Based on morphologic variants of soft palate
Type 1: Leaf shaped
Type 2: Rat tail shaped
Type 3: Butt shaped
Type 4: Straight line
Type 5: Deformed S
Type 6: Crook shaped
15. 15
• Grade I : Epithelium shows Hyperkeratosis, intra cellular
edema, little basal cell hyperplasia, rete ridges present.
Histological classification- Bailor D.N.
• Grade II : Epithelium undergoing atrophy, rete ridges less
prominent, connective tissue showing thickened collagen
bundles, less cellularity, fibrosed blood vessels with moderate
amount of hyalinization.
• Grade III : Marked atrophy of epithelium, absence of rete ridges,
connective tissue showing abundant hyalinization, cellularity
absent in connective tissue.
18. ETIOLOGY
Multifactorial
Local factors:
Chillies and
Arecanut
Systemic factors :
Nutritional deficiency,
Genetic predisposition and
Autoimmunity.
Epidemiological and in vitro experimental studies - chewing
areca nut is the major etiological factor.
19. Chillies-
Capsaicin, an active principle, mild irritant, which brings about
epithelial and connective tissue changes in OSMF patients.
Elastic degradation of collagen and ultrastructurally, partial or
complete degeneration of collagen into elastin-like filaments,
sheets or dense amorphous material. (Sirsat & Khanolkar 1960).
20. Mutogenic and enhance the tumorigenicity of tobacco in
experimental animals. (Bhide 1992)
Increases the risk of cancers in the upper aero digestive
tract in a dose- dependent manner. (Notani 1992)
21. Nutritional deficiencies
May be secondary
OSMF patients cannot tolerate spicy food & the opening of
the mouth in OSF patients becomes smaller which may affect
normal food intake and lead to nutritional deficiencies.
22. Arecanut:
Four alkaloids- Arecoline, Arecaidine, Guvacine, Guvacoline.
Arecoline – main agent. (Tilakaratne 2006).
Flavanoid components- tannins and catechins.
Fibroblastic proliferation and inceased collagen formation.
23. Chronic placement of betel quid (areca nut)
Arecoline
Fibrosis
Rigidity & limited mouth opening
24. ROLE OF ARECOLINE
Arecoline
( Slaked lime) (Hydrolysis )
Arecaidine
Fibroblast stimulation & proliferation
Increased collagen synthesis
25. Large quantity of tannin present in areca nut
Inhibits collagenases
Reduced collagen degradation
Stabilization of collagen by tannins (and catachins polyphenols)
Arecoline + tannin → ↓ degradation of collagen
↑ production of collagen
26. Arecoline
Increased generation of ROS
(oxidative stress)
Activates various transcription factors
( NF kappa B, JNK & p38 MAPK)
Stimulates CTGF (fibroblasts and
endothelial cells)
Fibroblastic proliferation and increased
collagen formation.
27. Arecoline
Increased production of Tissue inhibitors of
metalloproteinase (TIMP)
Inhibits activated collagenase
Increased production of collagen/decreased
degradation of collagen
30. Presence of Copper in nut:
Copper content in areca nut
( Increased activity of lysyl
oxidase enzyme )
Fibroblast stimulation &
proliferation
Increased collagen synthesis
31. MATRIX METALLOPROTEINASES AND TISSUE
INHIBITORS OF MATRIX METALLOPROTEINASES
Arecoline
Increased ROS and DNA double strand breaks produced
by damaged mitochondria
TIMP-1 & 2/ MMP-1
Collagen production / collagen degradation
fibrosis
32. Fibrogenic cytokines
External stimuli
Increased levels of cytokines in the lamina
propria
Induce development of disease
TGF-ß Platelet derived growth
factor (PDGF)
Basic fibroblast growth
factor (bFGF)
33. ACCUMULATION OF COLLAGEN AND
OTHER CHANGES IN ECM
Early stage – tenascin, fibronectin, perlecan and collagen type III
were enhanced in lamina propria and submucosa.
Intermediate stage – elastin extensively and irregularly deposited
around muscle fibres together with above mentioned molecules
Advanced stage – all the ECM molecules get decreased and
replaced by collagen type I
34. Heat shock protein (HSP 47) is a collagen specific molecular
chaperone involved in the processing and/or secretion of
procollagen. HSP 47 is significantly upregulated in OSF. Arecoline
was found to elevate HSP 47 expression in fibroblasts.
Cystatin C, a non glycosylated basic protein is increased in a
variety of fibrotic diseases, Cystatin C was found to be
upregulated both at m–RNA and protein levels in the disease.
Arecoline is responsible for this enhancement in a dose
dependent manner
35. EPITHELIAL MESENCHYMAL TRANSITION (EMT)
ANE caused cell injury
ROS
MAPK & NF kB pathways involved in EMT
Alteration of normal keratinocyte
morphology
38. ANGIOGENESIS RELATED MOLECULES
Overexpression of iNOS, b-FGF, TGF-β, PDGF, HIF-1α
(increased MVD)
Maintain vascularity of underlying CT
Adaptive response of mucosa to cope up with the
hypoxia caused by fibrosis
40. ALTERATIONS OF CELL CYCLE
PCNA index is higher in OSF epithelium than normal oral mucosa
– increased malignant transformation potential.
Important molecules in G2/M phase ( cyclin B1, p34 and p-
survivin) are over expressed malignant transformation by
inhibition of apoptosis and encouraging mitosis in carcinogenesis.
Survivin as both prognostic and predictive marker in malignant
transformation of OSF
43. CLINICAL FEATURES
EARLY OSMF ADVANCED OSMF
Burning sensation
Blisters
Ulcerations
Excessive salivation
Defective gustatory sensation
Dryness of mouth
Blanced
Slightly opaque
White fibrous bands (vertically)
Fixation, shortening or deviation of uvula
Impairment of tongue movement
Inability to blow or whistle
Difficulty in swelling
Nasal voice
44. Blanching seen over left
buccal mucosa
Blanching seen on
ventral surface of
tongue, floor of
mouth and restricted
movements of tongue
45. Decreased mouth
opening in oral
submucous fibrosis
patient
Soft palate and
faucial pillars
showing redness
47. Histopathology
Histological findings in OSMF cases were found to vary depending
on the clinical severity of the cases and the site of biopsy
The observed epithelial changes are secondary to changes in
connective tissue.
The findings range from normal to atrophic and hyperplastic
epithelium (Sirsat & Khanolkar, 1957).
Pindborg and Sirsat (1966) observed marked changes in the form of
atrophy of epithelium with loss of rete pegs in 90% of the cases as
compared to normal oral mucosa.
EPITHELIAL CHANGES
48. The atrophic epithelium also exhibits intracellular edema, signet
cells and epithelial atypia (focal dysplasia).
Epithelial keratinization, especially the tendency of atrophic and
hyperplastic epithelium to show keratinization was higher when
compared to normal.
Increased mitotic activities were evident in a small number of
cases
49. Classical oral submucous fibrosis (OSMF) showing thin atrophic
epithelium with chronic inflammation and dense fibrosis in the
submucosa (hematoxylin-eosin, original magnification 200).
50. CONNECTIVE TISSUE CHANGES
Pindborg et al (1966) have described four consecutive stages in
submucous fibrosis cases based on sections stained with
haemotoxylin and eosin:
The changes are based on following criteria
Presence or absence of edema
Nature of the collagen bundles
Overall fibroblastic response
State of the blood vessels
Predominant cell type in the inflammatory exudates
51. Very early stage
Fine fibrillar collagen dispersed with marked edema and
strong fibroblastic response showing plump young fibroblasts
containing abundant cytoplasm will be observed.
Blood vessels - occasionally normal, but more often they are
dilated and congested.
Inflammatory cells- polymorphonuclear leukocytes with
occasional eosinophils, are present.
52. Early stage
In this stage juxta-epithelial area shows early hyalinization.
The collagen is still seen as separate bundles which are
thickened.
Plump young fibroblasts are present in moderate numbers.
The blood vessels are often dilated and congested.
The inflammatory cells are mostly lymphocytes, eosinophils
and the occasional plasma cells.
54. Moderately advanced stage
In this stage, the collagen is moderately hyalinised.
The amorphous change starts from the juxta-epithelial basement
membrane.
Occasionally, thickened collagen bundles are still seen
separated by slight residual edema.
The adult fibroblastic cells have elongated spindle shaped nuclei
and scanty cytoplasm.
Blood vessels are either normal or constricted as a result of
increased surrounding tissue.
The inflammatory exudate consists of lymphocytes, plasma cells
and occasional eosinophils.
55. Advanced stage
The collagen is completely hyalinised and is seen as a
smooth sheet with no distinct bundles or edema
Hyalinised connective tissue becomes hypocellular with thin
elongated cells.
Blood vessels are completely obliterated or narrowed.
The inflammatory exudate consists of lymphocytes and
plasma cells and occasional eosinophils.
Interestingly the melanin containing cells in the lamina propria
are surrounded by dense collagen, which explains the
clinically observed loss of pigmentation.
56. Histopathological picture of advanced stage oral submucous
fibrosis showing atrophied epithelium, increased fibrosis and
hyalinization of submucosal tissues
57. Khanna and Andrade (1995); grouped OSMF features into 4
groups based on histopathological features:
Group I : Very early changes
Common symptom is burning sensation in the mouth.
Acute ulceration and recurrent stomatitis
Not associated with mouth opening limitation.
Histology:
Fine fibrillar collagen network interspersed with marked edema.
Blood vessels dilated and congested.
Large aggregate of plump, young fibroblasts present with
abundant cytoplasm.
Inflammatory cells mainly consist of polymorphonuclear
leukocytes with few eosinophils.
Epithelium normal.
58. Group II : Early cases
Buccal mucosa appears mottled and marble-like
Widespread sheets of fibrosis palpable
Patients with an interincisal distance of 26-35mm
Histology:
Juxtaepithelial hyalinization present
Collagen present as thickened but separate bundles.
Blood vessels dilated and congested
Young fibroblasts seen in moderate number
Inflammatory cells mainly consist of polymorphonuclear
leukocytes with few eosinophils and occasional plasma cells.
Flattening or shortening of epithelial rete pegs evident with
varying degree of keratinization.
59. Group III : Moderately advanced cases
Trismus evident with an interincisal distance of 15-25mm
Buccal mucosa appears pale and firmly attached to underlying
tissues
Atrophy of vermilion border
Vertical fibrous bands palpable at the soft palate,
pterygomandibular raphe and anterior faucial pillars.
Histology:
Juxtaepithelial hyalinization present
Thickened collagen bundles faintly discernible, separate by very
slight, residual edema.
Blood vessels, mostly constricted
Mature fibroblasts with scanty cytoplasm and spindleshaped nuclei
60. Inflammatory exudates consists mainly of lymphocytes
Epithelium markedly atrophic with loss of rete pegs
Muscle fibers seen interspersed with thickened and dense
collagen fibers.
61. Group IV A : Advanced cases:
Trismus is severe with interincisal distance of less than 15mm
The fauces are thickened, shortened and firm on palpation.
Uvula is shrunken and appears as a small, fibrous bud
Tongue movements are limited
On palpation of lips, circular band felt around entire mouth.
Group IV B:
Advanced cases with premalignant and malignant changes.
Hyperkeratosis, leukoplakia, or squamous cell carcinoma can
be seen.
62. Histology:
Collagen hyalinized as smooth sheet.
Extensive fibrosis obliterating the mucosal blood vessels and
eliminating the melanocytes.
Fibroblasts markedly absent within the hyalinized zones.
Total loss of epithelial rete pegs.
Mild to moderate atypia present.
Extensive degeneration of muscle fibers evident
63. (a) Loss of striation in muscle; (b) Floculant material
showing degeneration
64. OSMF showing extensive fibrosis in the submucosa
(hematoxylin-eosin, original magnification 200).
65. OSMF with lichenoid reaction, showing bandlike
inflammatory exudate with fibrosis (hematoxylin-
eosin).
66. SPECIAL INVESTIGATIONS
SPECIAL STAINS
Van Gieson's Stain
Masson's trichrome
stain
Picrosirius red
IHC MARKERS
Heat shock proteins 47
Cystatin c
Survivin
Endothelial markers- CD31,
CD34, CD105
Basic fibroblastic growth factor
P53
Bcl-2
Ki-67
68. MALIGNANT POTENTIAL
The precancerous nature of OSF was first discovered by
Paymaster (1956), when he observed slow growing
squamous cell carcinoma in one third of the patients with the
disease.
69. This was confirmed with various groups & Pindborg (1972)
put forward five criteria to prove that the disease is
precancerous. They included:
1. High occurrence of OSF in oral cancer patients
2. Higher incidence of squamous cell carcinoma in patients with
OSF
3. Histological diagnosis of cancer without any clinical suspicion
in OSF
4. High frequency of epithelial dysplasia &
5. Higher prevalence of leukoplakia among OSF.
70. Malignant transformation rate of OSF was found to be in the
range of 7–13% (Tilakaratne 2006).
According to long-term follow-up studies a transformation rate
of 7.6% over a period of 17 years was reported (Murti1985).
71. BIOLOGICAL STUDIES
Blood chemistry and haematological variations.
Iron, vitamin B12, folate levels
ESR, anemia and eosinophilia,
gammaglobulin
72. TREATMENT
1) Restriction of habits:
Reduction or elimination of habit of areca nut chewing is an
important preventive measure.
2) Corticosteroids:
suppresses inflammatory response by their anti-inflammatory
action.
It prevents fibrosis by decreasing fibroblastic proliferation and
deposition of collagen.
local injection (intralesional injection), topical applications or
in the form of mouth washes.
73. 3) Hyaluronidase:
Break down hyaluronic acid, lower the viscosity of the
intercellular cement substance and also decreases collagen
formation.
Intralesional injection of Hyalase used in the dose of 1500 IU,
Chymotrypsin 5000 IU, Fibrinolytic agents (Hyalase) dissolved in
2% lignocaine.
4) Placental Extracts:
The combination of dexamethasone, hyaluronidase and placental
extract were found to give better results than with a single drug
74. 5) Nutritional support: High proteins, calories, vitamin B complex,
other vitamins and minerals.
6) Physiotherapy: forceful mouth openings, heat therapy.
7) Surgical treatment: cutting the fibrotic bands resulted in more
fibrosis and disability.
Excision of fibrotic tissues and covering the defect with split
thickness skin, fresh human amnion or buccal fat pad (BFP) grafts
have been applied to treat OSMF
75. 8) Stem cell therapy
Recently scientists have proven that intralesional injection
of autologous bone marrow stem cells is a safe and effective
treatment modality in oral sub mucosal fibrosis.
Autologous bone marrow stem cell injections
induces angiogenesis in the area of lesion which in turn
decreases the extent of fibrosis thereby leading to significant
increase in mouth opening
77. CONCLUSION
In summary, the available literature indicates that the main
aetiological factors for OSF are the constituents of areca nut,
mainly arecoline, whilst tannin may have a synergistic role.
The use of Areca nut should be avoided in commercial
smokeless tobacco products. It is an urgent need to educate
people about the adverse effects regarding oral cavity.
Future research should also focus on targeting various
molecules and pathways which have been identified, in order
to search for effective treatment as morbidity and mortality is
significantly higher in OSF.
78. REFERENCES
Neville B W, Damm D D, Allen C M, Bouquot J E. Oral &
maxillofacial pathology; elsevier ,noida,2nd
ed.
Rajendran R & Shivapathasundaram B. Shafer’s textbook of oral
pathology; Elsevier, Noida, 6th
ed.
Oral Submucous Fibrosis - A review [Part 2], Dr. Savita JK* Dr.
Girish HC** Dr. Sanjay Murgod Dr. Harish Kumar, , Journal of
Health Sciences and Research, Volume 1, Number 2, August –
2010
Oral Submucous Fibrosis - A review [Part 2], Dr. Savita JK* Dr.
Girish HC** Dr. Sanjay Murgod Dr. Harish Kumar, Journal of
Health Sciences and Research, Volume 2, Number 1, April –
2011
CLASSIFICATION SYSTEMS FOR ORAL SUBMUCOUS
FIBROSIS- FROM PAST TO PRESENT: A REVIEW, Vikas
Berwal et al, International Journal of Dental and Health Sciences
Volume 01,Issue 06
79. Oral Submucous Fibrosis: Review on Mechanisms of
Pathogenesis and Malignant Transformation, Rasika
Priyadharshani Ekanayaka and Wanninayake Mudiyanselage
Tilakaratne, J Carcinogene Mutagene S5: 002.
doi:10.4172/2157-2518.S5-002.
Oral submucous fibrosis: etiology, pathogenesis, and future
research, R. Rajendran, Bulletin of the World Health
Organization, 1994, 72 (6): 985-996
A prospective transmission electron microscopic study of muscle
status in oral submucous fibrosis along with retrospective
analysis of 80 cases of oral submucous fibrosis, Sumathi MK,
Narayanan Balaji, Malathi Narasimhan, Journal of Oral and
Maxillofacial Pathology Vol. 16 Issue 3 Sep - Dec 2012
Histochemical analysis of polarizing colors of collagen using
Picrosirius Red staining in oral submucous fibrosis, Surekha
Velidandla ey al, Journal of International Oral Health 2014;
6(1):33-38