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Oral Manifestations of Systemic Diseases
1. Oral Manifestations ofOral Manifestations of
Systemic DiseasesSystemic Diseases
Dr.Ramesh Parajuli MS(Otorhinolaryngology,Head and Neck surgery)Dr.Ramesh Parajuli MS(Otorhinolaryngology,Head and Neck surgery)
Chitwan Medical College Teaching Hospital, Bharatpur-10, Chitwan, NepalChitwan Medical College Teaching Hospital, Bharatpur-10, Chitwan, Nepal
2. Oral cavity- window to the bodyOral cavity- window to the body
Lesions of oral mucosa, tongue,Lesions of oral mucosa, tongue,
gingiva, dentition, periodontium,gingiva, dentition, periodontium,
salivary gland, facial skeleton, &salivary gland, facial skeleton, &
extraoral skinextraoral skin
Appropriate diagnosis &Appropriate diagnosis &
treatmenttreatment
6. Herpes Simplex StomatitisHerpes Simplex Stomatitis
HSV-1HSV-1:: Primary herpetic GingivostomatitisPrimary herpetic Gingivostomatitis
Recurrent herpes labialisRecurrent herpes labialis
HSV-2HSV-2::
Primary herpetic Gingivostomatitis:Primary herpetic Gingivostomatitis:
-most frequent cause of acute stomatitis in-most frequent cause of acute stomatitis in
childrenchildren
-varies in severity, many infections-varies in severity, many infections
-subclinical-subclinical
-misdiagnosed as “teething”-misdiagnosed as “teething”
-malaise, anorexia, irritability, fever,-malaise, anorexia, irritability, fever,
anterior cervical lymphadenopathy, diffuse,anterior cervical lymphadenopathy, diffuse,
purple, boggy gingivitispurple, boggy gingivitis
-multiple vesicles-multiple vesicles scarred ulcers(1-3mm)scarred ulcers(1-3mm)
-occasionally in adults-occasionally in adults
7. Diagnosis:Diagnosis:
-clinically-clinically
-scrapping or smears from the lesion-scrapping or smears from the lesion
-immunofluorescent staining-immunofluorescent staining
-exfoliative cytology- typical-exfoliative cytology- typical
multinucleated giant cellsmultinucleated giant cells
Treatment:Treatment:
-symptomatic-symptomatic
-acyclovir (systemic)-severe cases-acyclovir (systemic)-severe cases
8. Recurrent Intraoral Herpes Simplex InfectionRecurrent Intraoral Herpes Simplex Infection::
-may affect healthy individual-may affect healthy individual
-persistent lesions in immunocompromised-persistent lesions in immunocompromised
--chronic ulcer, raised, white borderchronic ulcer, raised, white border
-esp. at sites of trauma-esp. at sites of trauma
-acyclovir-acyclovir
9. Herpes zoster (Shingles)Herpes zoster (Shingles)
Reactivation of Varicella –Zoster virusReactivation of Varicella –Zoster virus
Predisposing factor:Predisposing factor:
Immunocompromised statusImmunocompromised status
One dermatome affected (trigeminalOne dermatome affected (trigeminal
nerve)nerve)
UnilateralUnilateral
Ulcers in the distribution of dermatomeUlcers in the distribution of dermatome
Mandibular nerve: ulceration of one sideMandibular nerve: ulceration of one side
of tongue, floor of the mouth, lower labialof tongue, floor of the mouth, lower labial
& buccal mucosa& buccal mucosa
Maxillary nerve: one side of palate, theMaxillary nerve: one side of palate, the
upper gingiva, buccal sulcusupper gingiva, buccal sulcus
Lesions persists for 2-3 wksLesions persists for 2-3 wks
Lesions on lips and chin
11. HerpanginaHerpangina
Common in childrenCommon in children
Coxsackie virus group A,Coxsackie virus group A,
Enteroviruses(30 & 71)Enteroviruses(30 & 71)
Self limiting vesicular eruptions inSelf limiting vesicular eruptions in
the oropharynx eg. soft palate,the oropharynx eg. soft palate,
uvula, tonsillar pillars, posterioruvula, tonsillar pillars, posterior
pharyngeal wallpharyngeal wall
Similar to herpes simplex exceptSimilar to herpes simplex except
the lesions more commonly inthe lesions more commonly in
oropharynx rather than oral cavityoropharynx rather than oral cavity
Diagnosis:Diagnosis: ClinicallyClinically
Treatment:Treatment: SupportiveSupportive
12. Hand, Foot and Mouth DiseaseHand, Foot and Mouth Disease
Enterovirus 71,Coxsackie viruses,Enterovirus 71,Coxsackie viruses,
some untypeable enterovirusessome untypeable enteroviruses
Young childrenYoung children
Vesicular eruption in the oral cavity &Vesicular eruption in the oral cavity &
oropharynxoropharynx dysphagia, dehydrationdysphagia, dehydration
Vesicles on the hands & feetVesicles on the hands & feet
Pyrexia, malaise, vomitingPyrexia, malaise, vomiting
Short lived(5-8 days)Short lived(5-8 days)
Diagnosis:Diagnosis: clinicallyclinically
Treatment:Treatment: supportivesupportive
24. Hyperemia and inflammation ofHyperemia and inflammation of
pharynx & soft palatepharynx & soft palate
Snail Track ulcer :-Snail Track ulcer :-
-Oral cavity & oropharnyx-Oral cavity & oropharnyx
-Ulcerated lesion covered with-Ulcerated lesion covered with
grayish white membranegrayish white membrane
which when scraped has pink basewhich when scraped has pink base
with no bleedingwith no bleeding
25. Syphilitic PharyngitisSyphilitic Pharyngitis
May be congenital or acquired byMay be congenital or acquired by
sexual intercoursesexual intercourse
Secondary stage most likelySecondary stage most likely
HIV positive patientsHIV positive patients
26. Tertiary SyphilisTertiary Syphilis
Tertiary syphilis - after a period of 4–7 yearsTertiary syphilis - after a period of 4–7 years
Typically painlessTypically painless
No lymphadenopathy unless secondaryNo lymphadenopathy unless secondary
infectioninfection
Gumma:Gumma:
-Characteristic lesion-Characteristic lesion
-Hard palate, Nasal septum, Tonsil, PPW, or-Hard palate, Nasal septum, Tonsil, PPW, or
LarynxLarynx
VDRL may be negativeVDRL may be negative
27. Congenital SyphilisCongenital Syphilis
Early:Early:
first 3 months of life, manifest asfirst 3 months of life, manifest as
snufflessnuffles nasal discharge purulentnasal discharge purulent
Late:Late:
Manifest at pubertyManifest at puberty
Gummatous lesionGummatous lesion
Oral lesions:Oral lesions: high-arched palate,high-arched palate,
short mandible, Hutchinson’s teeth,short mandible, Hutchinson’s teeth,
and Moon’s or mulberry molarsand Moon’s or mulberry molars
28. Diagnosis:Diagnosis:
1.Immunoflurorescence or dark field microscopy1.Immunoflurorescence or dark field microscopy
2. Biopsy2. Biopsy
3.Serology3.Serology
Non-treponemal antibody testsNon-treponemal antibody tests::
-VDRL, RPR-VDRL, RPR
-For screening and treatment follow up-For screening and treatment follow up
Treponema specific antibody tests:Treponema specific antibody tests:
-FTA-ABS test, TPHA-FTA-ABS test, TPHA
-For confirmation-For confirmation
-Usually remains positive for life-Usually remains positive for life
Treatment:Treatment: Penicillin( DOC)Penicillin( DOC)
Ceftriaxone, Erythromycin, or DoxycyclineCeftriaxone, Erythromycin, or Doxycycline
29. LeprosyLeprosy
Mycobacterium LepraeMycobacterium Leprae
Optimum temperature growth-less thanOptimum temperature growth-less than
body tempbody temp preference for skin, mucosa &preference for skin, mucosa &
superficial nervesuperficial nerve
Transmission- nasal dischargeTransmission- nasal discharge
Both Humoral & cellular immune responseBoth Humoral & cellular immune response
Clinically- Chronic granulomatousClinically- Chronic granulomatous
diseasedisease skin, peripheral nerve & nasalskin, peripheral nerve & nasal
mucosamucosa
40. Sjogren’s SyndromeSjogren’s Syndrome
AutoimmuneAutoimmune
FemaleFemale
Primary Sjogren’s Syndrome:Primary Sjogren’s Syndrome:
Secondary Sjogren’s SyndromeSecondary Sjogren’s Syndrome::
associated with RA, SLE, Scleroderma,associated with RA, SLE, Scleroderma,
Polymyositis, Polyarteritis NodusaPolymyositis, Polyarteritis Nodusa
Presents with xerostomia & parotidPresents with xerostomia & parotid
enlargementenlargement
Oral findings:Oral findings:
-Due to decreased saliva-Due to decreased salivadysphagia,dysphagia,
disturbances in taste & speech, burningdisturbances in taste & speech, burning
pain of mouth & tongue, increasedpain of mouth & tongue, increased
dental caries, increased predispositiondental caries, increased predisposition
to infection (candidiasis)to infection (candidiasis)
41. Mucosal changes: dry, red & wrinkledMucosal changes: dry, red & wrinkled
mucosamucosa
Fissured tongue, atrophy of tongueFissured tongue, atrophy of tongue
papillae and redness of tongue, crackedpapillae and redness of tongue, cracked
& ulcerated lips& ulcerated lips
Diagnosis:Diagnosis:
-Minor salivary gland biopsy (mucosa of-Minor salivary gland biopsy (mucosa of
lower lip)lower lip)
-Periductal lymphocytic infiltrate-Periductal lymphocytic infiltrate
-Serum: Autoantibodies (ANA, antilacrimal-Serum: Autoantibodies (ANA, antilacrimal
& antithyroid antibodies, RA factor)& antithyroid antibodies, RA factor)
Treatment :Treatment :
-Steroid & immunossuppresive drugs-Steroid & immunossuppresive drugs
-Artificial saliva-Artificial saliva
-Constant dental evaluation-Constant dental evaluation
42. Systemic Lupus Erythematosus(SLE)Systemic Lupus Erythematosus(SLE)
Approx. one quarter of SLEApprox. one quarter of SLEoraloral
lesionslesions
Oral lesions: superficial ulcersOral lesions: superficial ulcers
with surrounding erythemawith surrounding erythema
Lips & all oral mucosal surfacesLips & all oral mucosal surfaces
Periodontal diseases, xerostomiaPeriodontal diseases, xerostomia
43. SclerodermaScleroderma
Deposition of collagen in the tissuesDeposition of collagen in the tissues
or around nerves & vesselsor around nerves & vessels
Difficulty in opening mouth(due toDifficulty in opening mouth(due to
fibrosis of masticatory muscles),fibrosis of masticatory muscles),
immobility of tongue, dysphagia,immobility of tongue, dysphagia,
xerostomiaxerostomia
Telangiectasia: lips, oral mucosaTelangiectasia: lips, oral mucosa
Association with Sjogren’s SyndromeAssociation with Sjogren’s Syndrome
& CREST Syndrome(Calcinosis,& CREST Syndrome(Calcinosis,
Raynaud’s phenomena, EsophagealRaynaud’s phenomena, Esophageal
hypomotility, & Sclerodactly)hypomotility, & Sclerodactly)
44. Kawasaki diseaseKawasaki disease
Mucocutaneous lymph node syndromeMucocutaneous lymph node syndrome
Vasculitis- medium & large arteriesVasculitis- medium & large arteries
Children <5 yrs of ageChildren <5 yrs of age
High grade feverHigh grade fever
Cardiovascular complicationsCardiovascular complications
Oral findings:Oral findings: swelling of papillae on theswelling of papillae on the
surface of tongue(strawberry tongue),surface of tongue(strawberry tongue),
erythema of the buccal mucosa & lipserythema of the buccal mucosa & lips
Lips are cracked, cherry red, swollen &Lips are cracked, cherry red, swollen &
hemorrhagichemorrhagic
45. Laboratory tests:Laboratory tests: polymorphonuclear leukocytosis,polymorphonuclear leukocytosis,
thrombocytosis, raised ESR & CRPthrombocytosis, raised ESR & CRP
Diagnosis:Diagnosis: 4 out of 6 clinical features with evidence of4 out of 6 clinical features with evidence of
coronary dilatationcoronary dilatation
1.Fever persisting>5 days1.Fever persisting>5 days
2.Bilateral conjunctival congestion2.Bilateral conjunctival congestion
3.Erythema of lips, buccal mucosa & tongue3.Erythema of lips, buccal mucosa & tongue
4.Acute non-purulent cervical lymphadenopathy4.Acute non-purulent cervical lymphadenopathy
5.Polymorphous exanthema5.Polymorphous exanthema
6.Erythema of palms & soles (edema6.Erythema of palms & soles (edemadesquamation)desquamation)
Treatment:Treatment: Aspirin, IVIgAspirin, IVIg
Steroid avoided- risk of worsening coronary arterySteroid avoided- risk of worsening coronary artery
dilatationdilatation
46. Dermatomyositis-PolymyositisDermatomyositis-Polymyositis
Immunologic disease muscleImmunologic disease muscle
Tongue & the upper portion of theTongue & the upper portion of the
esophagusesophagus
Clinical features:Clinical features:
-Difficulty in phonation, chewing &-Difficulty in phonation, chewing &
deglutitiondeglutition
-Stomatitis-Stomatitis
Difficulty in swallowingDifficulty in swallowingaspirationaspiration
pneumoniapneumonia
Xerostomia & salivary hypofunctionXerostomia & salivary hypofunction
(2* sjogren’s syndrome)(2* sjogren’s syndrome)
47. Wegener’s GranulomatosisWegener’s Granulomatosis
Rare chronic granulomatous diseaseRare chronic granulomatous disease
ImmunologicalImmunological
Clinical features:Clinical features: necrotizingnecrotizing
granulomatousgranulomatous lesions of thelesions of the
respiratory tract, generalized focalrespiratory tract, generalized focal
necrotizing vasculitis, and necrotizingnecrotizing vasculitis, and necrotizing
glomerulitisglomerulitis
Oral lesions:Oral lesions: solitary or multiplesolitary or multiple
irregular ulcers, surrounded by anirregular ulcers, surrounded by an
inflammatory zoneinflammatory zone
Tongue, palate, buccal mucosa &Tongue, palate, buccal mucosa &
gingivagingiva
Laboratory tests:Laboratory tests: HPE, c-ANCAHPE, c-ANCA
Treatment:Treatment: Steroids, Azathioprine,Steroids, Azathioprine, &&
CyclophosphamideCyclophosphamide
48. SarcoidosisSarcoidosis
Systemic granulomatous diseaseSystemic granulomatous disease
Any organAny organ
Noncaseating granuloma:Noncaseating granuloma:
-characteristic lesion-characteristic lesion
Oral manifestations:Oral manifestations: multiple, nodular,multiple, nodular,
painless ulceration of the gingiva,painless ulceration of the gingiva,
buccal mucosa, tongue, lips, & palatebuccal mucosa, tongue, lips, & palate
Salivary gland swellingSalivary gland swelling
Diagnosis:Diagnosis: BiopsyBiopsy
Treatment:Treatment: Systemic steroidsSystemic steroids
49. Heerfordt SyndromeHeerfordt Syndrome
Uveoparotid FeverUveoparotid Fever
Rare form of SarcoidosisRare form of Sarcoidosis
Clinical features:Clinical features: B/L painless, firm,B/L painless, firm,
parotid swelling, ocularparotid swelling, ocular
involvement(uveitis, conjunctivitis,involvement(uveitis, conjunctivitis,
keratitis), facial paralysis, low gradekeratitis), facial paralysis, low grade
fever, sublingual & submandibularfever, sublingual & submandibular
gland may also enlargegland may also enlarge
50. Behcet’s SyndromeBehcet’s Syndrome
Chronic, multisystemic inflammatoryChronic, multisystemic inflammatory
disorderdisorder
Triad of symptomsTriad of symptoms: Aphthous ulcers,: Aphthous ulcers,
Genital ulcers & Ocular lesionsGenital ulcers & Ocular lesions
(uveitis, conjunctivits, keratitis)(uveitis, conjunctivits, keratitis)
EtiologyEtiology – unclear– unclear
Immunogenetic basisImmunogenetic basis
Clinical featuresClinical features -- common in malescommon in males
Onset -20–30 years ageOnset -20–30 years age
51. Diagnostic criteria :Diagnostic criteria :
1.1. Recurrent oral ulcers (aphthaeRecurrent oral ulcers (aphthae))
2.2. Recurrent genital ulcersRecurrent genital ulcers
3.3. Ocular lesions (conjunctivitis, iritisOcular lesions (conjunctivitis, iritis
with hypopyon, uveitis, retinalwith hypopyon, uveitis, retinal
vasculitis, reduced visual acuityvasculitis, reduced visual acuity
4.4. Skin lesions (papules, pustules,Skin lesions (papules, pustules,
folliculitisfolliculitis,, erythema nodosum,erythema nodosum,
ulcers, & rarely necrotic lesions)ulcers, & rarely necrotic lesions)
5.5. Positive Pathergy test:Positive Pathergy test:
The test is called positive, when theThe test is called positive, when the
needle puncture causes a sterileneedle puncture causes a sterile
red nodule or pustule that is greaterred nodule or pustule that is greater
than 2mm in diameter at 24 to 48than 2mm in diameter at 24 to 48
hourshours
52. Diagnosis:Diagnosis:
For accurate diagnosis, recurrent oralFor accurate diagnosis, recurrent oral
ulcers plus two of the four criteria mustulcers plus two of the four criteria must
be presentbe present
Treatment:Treatment:
Mild cases- Topical steroidMild cases- Topical steroid
Severe cases- Systemic steroid, & otherSevere cases- Systemic steroid, & other
immunosuppressive drugs (Ciclosporin,immunosuppressive drugs (Ciclosporin,
Thalidomide, Colchicine, Dapsone)Thalidomide, Colchicine, Dapsone)
53. Rheumatoid ArthritisRheumatoid Arthritis
Progressive destruction of articular &Progressive destruction of articular &
periarticular structure eg. TMJperiarticular structure eg. TMJ
TMJ pathology: clicking, locking, crepitus,TMJ pathology: clicking, locking, crepitus,
tenderness in the preauricular area, paintenderness in the preauricular area, pain
during mandibular movementduring mandibular movement
Oral cavity involvement-not commonOral cavity involvement-not common
Association with secondary Sjogren’sAssociation with secondary Sjogren’s
SyndromeSyndrome
Immunosuppressive drugsImmunosuppressive drugsacute stomatitis,acute stomatitis,
candidiasis, recurrent HSV infectioncandidiasis, recurrent HSV infection
54. Reiter’s SyndromeReiter’s Syndrome
Triggered by infectious agent inTriggered by infectious agent in
genetically susceptiblegenetically susceptible
Young male (20-30 yrs)Young male (20-30 yrs)
Characterized by conjunctivitis,Characterized by conjunctivitis,
asymmetric lower extremity arthritis,asymmetric lower extremity arthritis,
non-gonococcal urethritis, circinatenon-gonococcal urethritis, circinate
balanitis, keratoderma blennorrhagiabalanitis, keratoderma blennorrhagia
Mnemonic : “can’t see, can’t pee, can’tMnemonic : “can’t see, can’t pee, can’t
climb a tree”climb a tree”
Oral lesions:Oral lesions: papules & ulcerations onpapules & ulcerations on
the buccal mucosa, gingiva, palate, &the buccal mucosa, gingiva, palate, &
lipslips
Lesions on the tongue mimicLesions on the tongue mimic
geographical tonguegeographical tongue
Diagnosis:Diagnosis: HPEHPE
Treatment:Treatment: Systemic steroid, NSAIDSystemic steroid, NSAID
61. Osler-Weber-Rendu DiseaseOsler-Weber-Rendu Disease
(Hereditary Hemorrhagic Telangiectasia)(Hereditary Hemorrhagic Telangiectasia)
Autosomal dominantAutosomal dominant
Telangiectasia of dorsum of tongue,Telangiectasia of dorsum of tongue,
oral cavity, buccal mucosa, lips,oral cavity, buccal mucosa, lips,
palate & nasal mucosapalate & nasal mucosa
Apparent at pubertyApparent at puberty
Lung, liver, & GI tract arterio-venousLung, liver, & GI tract arterio-venous
malformationsmalformations
Treatment:Treatment: regular iron therapy,regular iron therapy,
laser therapylaser therapy
62. Plummer Vinson SyndromePlummer Vinson Syndrome
(Patterson-Brown-Kelly Syndrome)(Patterson-Brown-Kelly Syndrome)
Oral manifestations:Oral manifestations: Dysphagia, ironDysphagia, iron
def. anaemia, atrophic glossitis, angulardef. anaemia, atrophic glossitis, angular
stomatitis, & koilonychiastomatitis, & koilonychia
Female, in fourth decadeFemale, in fourth decade
Barium swallow: web in post-cricoidBarium swallow: web in post-cricoid
regionregion
Pre-malignantPre-malignant Post-cricoid carcinomaPost-cricoid carcinoma
Treatment:Treatment:
-Esophageal dilatation-Esophageal dilatation
(if symptoms from web)(if symptoms from web)
-Follow up-developing carcinoma-Follow up-developing carcinoma
63. Idiopathic Thrombocytopenic Purpura (ITP)Idiopathic Thrombocytopenic Purpura (ITP)
Oral lesionsOral lesions may be the firstmay be the first
manifestation of this conditionmanifestation of this condition
Petechiae, ecchymoses,Petechiae, ecchymoses,
& haematoma anywhere on the& haematoma anywhere on the
oral mucosaoral mucosa
Spontaneous bleeding from theSpontaneous bleeding from the
gingivagingiva
Treatment:Treatment:
-Systemic steroids, Splenectomy-Systemic steroids, Splenectomy
64. AgranulocytosisAgranulocytosis
EtiologyEtiology:: Drug or infectionDrug or infection
Clinical features:Clinical features:
Oral lesions -multiple necrotic ulcersOral lesions -multiple necrotic ulcers
covered with dirty pseudomembranecovered with dirty pseudomembrane
Buccal mucosa, tongue, palate,Buccal mucosa, tongue, palate, & tonsillar& tonsillar
areaarea
Severe necrotizing gingivitisSevere necrotizing gingivitis
Laboratory tests:Laboratory tests: White blood countWhite blood count &&
bone-marrow aspirationbone-marrow aspiration
Treatment:Treatment: Antibiotics, white blood cellAntibiotics, white blood cell
transfusions, granulocyte colony-transfusions, granulocyte colony-
stimulating factor (G-CSF) or granulocyte-stimulating factor (G-CSF) or granulocyte-
macrophage colony-stimulating factormacrophage colony-stimulating factor
(GM-CSF)(GM-CSF)
67. Crohn’s DiseaseCrohn’s Disease
Diffuse nodular swelling in lipsDiffuse nodular swelling in lips
(painless), angular cheilitis,(painless), angular cheilitis,
cobblestone appearance ofcobblestone appearance of
buccal mucosabuccal mucosa or mucosal tag,or mucosal tag,
Aphthous ulcerAphthous ulcer
May precede intestinal symptomsMay precede intestinal symptoms
or may be the onlyor may be the only
manifestations in some casesmanifestations in some cases
Systemic steroidsSystemic steroids
68. Ulcerative ColitisUlcerative Colitis
Destructive oral ulceration due toDestructive oral ulceration due to
immune mediated vasculitisimmune mediated vasculitis
Polystomatitis Vegetans:Polystomatitis Vegetans:
microabscess on lips, palate,microabscess on lips, palate,
ventral tongueventral tongue
May manifests as aphthous ulcersMay manifests as aphthous ulcers
Exacerbation & remissionExacerbation & remission
69. Gastroesophageal Reflux DiseaseGastroesophageal Reflux Disease
Mucosal & gingival erosionMucosal & gingival erosion
caused by acidcaused by acid
Erosion of tooth enamelErosion of tooth enamel
70. Peutz-Jegher’s SyndromePeutz-Jegher’s Syndrome
Autosomal dominantAutosomal dominant
Mucocutaneous pigmentation &Mucocutaneous pigmentation &
intestinal polyposis (hamartomas)intestinal polyposis (hamartomas)
Black spots (macule): perioral skin,Black spots (macule): perioral skin,
lips, buccal mucosa, tonguelips, buccal mucosa, tongue
Treatment:Treatment:
-Conservative or local excision-Conservative or local excision
73. Thyroid DiseasesThyroid Diseases
Hypothyroidism:Hypothyroidism: MacroglossiaMacroglossia
Congenital Hypothyroidism:Congenital Hypothyroidism: Macroglossia,Macroglossia,
pronounced lips, & delayed tooth eruptionpronounced lips, & delayed tooth eruption
with malocclusionwith malocclusion
Hyperthyroidism:Hyperthyroidism:
Facial & skin manifestations:Facial & skin manifestations: upper eyelidupper eyelid
retraction, exophthalmous,retraction, exophthalmous,
hyperpigmentation, & skin erythemahyperpigmentation, & skin erythema
Oral manifestations:Oral manifestations: early loss of primaryearly loss of primary
teeth with subsequent rapid eruption ofteeth with subsequent rapid eruption of
permanent teeth(young children)permanent teeth(young children)
lymphoid tissue hyperplasia- tonsillar &lymphoid tissue hyperplasia- tonsillar &
oropharynx (Grave’s disease)oropharynx (Grave’s disease)
74. Cushing’s SyndromeCushing’s Syndrome
Long term, high dose corticosteroidLong term, high dose corticosteroid
administrationadministration
Moon or round face, buffalo humps,Moon or round face, buffalo humps,
central obesity, osteoporosis, DM,central obesity, osteoporosis, DM,
HTNHTN
Oral symptoms:Oral symptoms:
-Increased susceptibility to oral-Increased susceptibility to oral
infections (candidiasis)infections (candidiasis)
-Muscle weakness-Muscle weakness difficulty withdifficulty with
speaking, & swallowingspeaking, & swallowing
Dx:Dx: Dexamethasone suppression testDexamethasone suppression test
RxRx: Depends on the cause: Depends on the cause
75. Addison’s DiseaseAddison’s Disease
Primary adrenal insufficiencyPrimary adrenal insufficiency
Destruction of adrenal cortex eg.Destruction of adrenal cortex eg.
autoimmune, metastasis, infection,autoimmune, metastasis, infection,
haemorrhagehaemorrhage
Oral manifestations:Oral manifestations: diffuse or patchydiffuse or patchy
pigmentation of the skin & mucouspigmentation of the skin & mucous
membranesmembranes (due to increased ACTH-(due to increased ACTH-
cross reacts with melanin receptors)cross reacts with melanin receptors)
Buccal mucosa, palate, lips, & gingivaBuccal mucosa, palate, lips, & gingiva
Diagnosis:Diagnosis: ACTH testACTH test
Treatment:Treatment: Replace steroidReplace steroid
(glucocorticoid/mineralocorticoid)(glucocorticoid/mineralocorticoid)
76. Renal DiseaseRenal Disease
(Uraemic Stomatitis)(Uraemic Stomatitis)
Painful plaques and crust on buccalPainful plaques and crust on buccal
mucosa, dorsum of tongue, & floor ofmucosa, dorsum of tongue, & floor of
mouth covered with graymouth covered with gray
pseudomembrane exudate, & painfulpseudomembrane exudate, & painful
ulcersulcers
Bleeding diathesis:Bleeding diathesis: inhibited plateletinhibited platelet
aggregation eg. petechiae, ecchymosesaggregation eg. petechiae, ecchymoses
Irritation & chemical injury of mucosa-Irritation & chemical injury of mucosa-
ammonium compoundsammonium compounds
Xerostomia, unpleasant taste, burningXerostomia, unpleasant taste, burning
mouth, uriniferous breath odourmouth, uriniferous breath odour
A/W with acute rise in blood urea nitrogenA/W with acute rise in blood urea nitrogen
Heal spontaneously after resolution ofHeal spontaneously after resolution of
uraemic state eg. after hemodialysisuraemic state eg. after hemodialysis
83. Erythema MultiformeErythema Multiforme
Skin and mucous membranesSkin and mucous membranes
Immunologically mediatedImmunologically mediated
Triggered by: infective agents (eg. HSV),Triggered by: infective agents (eg. HSV),
drugs (sulphonamides, barbiturates), fooddrugs (sulphonamides, barbiturates), food
additives or chemical, immunizationadditives or chemical, immunization
( BCG,HBV)( BCG,HBV)
Oral lesions:Oral lesions: begins as erythematousbegins as erythematous
areaareablisterblisterrupturesrupturesirregular painfulirregular painful
ulcersulcers
Lips, buccal mucosa, tongue, soft palate, &Lips, buccal mucosa, tongue, soft palate, &
floor of mouthfloor of mouth
Skin manifestations:Skin manifestations: erythematous, flat,erythematous, flat,
round macules, papules, or plaques,round macules, papules, or plaques,
usually in a symmetrical pattern-usually in a symmetrical pattern- target ortarget or
iris like lesionsiris like lesions
HPE & ImmunostainingHPE & Immunostaining
TreatmentTreatment:: supportive, systemic steroidssupportive, systemic steroids
84. Stevens–Johnson SyndromeStevens–Johnson Syndrome
Severe form of erythema multiforme, involving oralSevere form of erythema multiforme, involving oral
mucous membrane, eyes, & genital areamucous membrane, eyes, & genital area
EtiologyEtiology:: Drugs (salicylates, sulfonamides,Drugs (salicylates, sulfonamides,
penicillin, barbiturates,carbamazepine, phenytoinpenicillin, barbiturates,carbamazepine, phenytoin
etc.)etc.)
oral lesions -oral lesions - vesicle formation, followed by painfulvesicle formation, followed by painful
erosions - grayish-white or hemorrhagicerosions - grayish-white or hemorrhagic
pseudomembranes - extend to the pharynx, larynx,pseudomembranes - extend to the pharynx, larynx,
and esophagusand esophagus
Ulceration of skin & mucosal surfaces(eg. mouth,Ulceration of skin & mucosal surfaces(eg. mouth,
urethra, conjunctiva, & lungs)urethra, conjunctiva, & lungs)
Typical target lesions on palms & soles withTypical target lesions on palms & soles with
blistering in the centreblistering in the centre
DiagnosisDiagnosis:: Clinical presentationClinical presentation
TreatmentTreatment::
--self limitingself limiting
-Supportive, & Systemic steroids-Supportive, & Systemic steroids
87. Parkinson’s DiseaseParkinson’s Disease
Extrapyramidal symptomsExtrapyramidal symptoms
Loss of facial expressionLoss of facial expression
Difficulty with mastication, slowDifficulty with mastication, slow
speech, & tremors of head, lips, &speech, & tremors of head, lips, &
tonguetongue
Esophageal dysmotility &Esophageal dysmotility &
dysphagiadysphagia
Impaired lip sealImpaired lip seal droolingdrooling
fungal infection of lip commissurefungal infection of lip commissure
(angular cheilitis)(angular cheilitis)
88. Alzheimer’s DiseaseAlzheimer’s Disease
DementiaDementia
Inability to perform self care (oral hygiene)-Inability to perform self care (oral hygiene)-
self neglect & loss of cognitive and motor skillsself neglect & loss of cognitive and motor skills
Poor oral hygiene- increased prevalence ofPoor oral hygiene- increased prevalence of
dental plaque, dental caries, & gingivaldental plaque, dental caries, & gingival
bleedingbleeding
89. Multiple SclerosisMultiple Sclerosis
Demyelination of central nervousDemyelination of central nervous
systemsystem
Remitting & exacerbating courseRemitting & exacerbating course
Loss of muscle coordination,Loss of muscle coordination,
weakness of the tongue, & loss ofweakness of the tongue, & loss of
upper extremityupper extremity severely impairsseverely impairs
orodental hygieneorodental hygiene
Trigeminal neuralgia- also commonTrigeminal neuralgia- also common
characterized by excruciating,characterized by excruciating,
unilateral pain of the lips, gingiva,unilateral pain of the lips, gingiva,
or chin triggered by contact withor chin triggered by contact with
certain areas of the face, lips, orcertain areas of the face, lips, or
tonguetongue
90. Bell’s PalsyBell’s Palsy
Idiopathic unilateral lower motorIdiopathic unilateral lower motor
neuron palsy (7neuron palsy (7thth
cranial nerve)cranial nerve)
Lack of control of the muscles ofLack of control of the muscles of
facial expressionfacial expressiondistortion of facialdistortion of facial
appearanceappearance
Loss of functional ability of cheek &Loss of functional ability of cheek &
lips (affected side)lips (affected side)poor oro-dentalpoor oro-dental
hygienehygiene
91. Melkersson-Rosenthal SyndromeMelkersson-Rosenthal Syndrome
Characterized by -unilateral facial palsy, recurrent facialCharacterized by -unilateral facial palsy, recurrent facial
swelling, & lingua plicata (fissured tongue)swelling, & lingua plicata (fissured tongue)
93. Vitamin A deficiency:Vitamin A deficiency:
-Dyskeratotic changes of the skin & mucous-Dyskeratotic changes of the skin & mucous
membranesmembranes
-Angular cheilitis-Angular cheilitis
-Defects in the dentin & enamel of-Defects in the dentin & enamel of
developing teethdeveloping teeth
Vitamin B2 (Riboflavin) deficiency:Vitamin B2 (Riboflavin) deficiency:
-Angular cheilitis-Angular cheilitis
-Burning pain in the lips, mouth, & tongue-Burning pain in the lips, mouth, & tongue
Vitamin B3 (Niacin) deficiency (Pellagra):Vitamin B3 (Niacin) deficiency (Pellagra):
-Dermatitis, dementia,& diarrhoea-Dermatitis, dementia,& diarrhoea
-Oral manifestations: glossitis (red, swollen) &-Oral manifestations: glossitis (red, swollen) &
stomatitis, burning tonguestomatitis, burning tongue
94. Vitamin B6 deficiency:Vitamin B6 deficiency:
-Peripheral neuropathy-Peripheral neuropathy
-Oral lesions-similar to pellagra-Oral lesions-similar to pellagra
(i.e. glossitis & stomatitis)(i.e. glossitis & stomatitis)
Vitamin C deficiency (Scurvy):Vitamin C deficiency (Scurvy):
-Cofactor for collagen synthesis-Cofactor for collagen synthesis
-Weakened vessels are responsible for-Weakened vessels are responsible for
petechiae, ecchymoses, delayed woundpetechiae, ecchymoses, delayed wound
healinghealing
Deficiency of Vitamin B12 & Folic acid:Deficiency of Vitamin B12 & Folic acid:
-Megaloblastic anemia-Megaloblastic anemia
-Oral findings: angular cheilitis, recurrent-Oral findings: angular cheilitis, recurrent
aphthous ulcers, & glossitisaphthous ulcers, & glossitis
95. Vitamin D deficiency & Calcium deficiency:Vitamin D deficiency & Calcium deficiency:
-Calcium metabolism-Calcium metabolism
-Mandibular osteopenia/osteoporosis, enamel-Mandibular osteopenia/osteoporosis, enamel
hypoplasiahypoplasia
Vitamin k deficiency:Vitamin k deficiency:
-Haemorrhagic diathesis-Haemorrhagic diathesis
-Oral haemorrhagic bullae-Oral haemorrhagic bullae
Zinc deficiency:Zinc deficiency:
-Taste changes-Taste changes
-Acrodermatitis Enteropathica: angular cheilitis,-Acrodermatitis Enteropathica: angular cheilitis,
ulcers, glossitis, crusting, scaling of the lips as wellulcers, glossitis, crusting, scaling of the lips as well
as ulcers, erosions & fissuresas ulcers, erosions & fissures
96. Oral lesions associated with HIVOral lesions associated with HIV
Early recognition, diagnosis, & treatment ofEarly recognition, diagnosis, & treatment of
HIV associated oral lesions - reduce morbidityHIV associated oral lesions - reduce morbidity
Oral lesions-Oral lesions-
-Early diagnostic indicator of HIV infection-Early diagnostic indicator of HIV infection
-Stage of HIV infection-Stage of HIV infection
-Predictor of the progression of HIV disease-Predictor of the progression of HIV disease
99. Hairy LeukoplakiaHairy Leukoplakia
Epstein Barr virusEpstein Barr virus
Common, characteristic lesion-HIV infectionCommon, characteristic lesion-HIV infection
White, asymptomatic, raised, corrugated,White, asymptomatic, raised, corrugated,
unremovable patch on lateral marigns ofunremovable patch on lateral marigns of
tonguetongue
The surface is irregular and may haveThe surface is irregular and may have
prominent folds or projections, sometimesprominent folds or projections, sometimes
markedly resembling hairsmarkedly resembling hairs
Lateral marginsLateral margins may spread to dorsum ofmay spread to dorsum of
tonguetongue
Diagnosis:Diagnosis: BiopsyBiopsy
Treatment:Treatment:
--Usually asymptomatic-Rx not requiredUsually asymptomatic-Rx not required
-Antiviral(Aciclovir/valaciclovir)-Antiviral(Aciclovir/valaciclovir)
100. Kaposi’s SarcomaKaposi’s Sarcoma
Most common malignancy in HIV (+Ve)Most common malignancy in HIV (+Ve)
Human Herpes Virus-8(KSHV)Human Herpes Virus-8(KSHV)
Derived from capillary endothelial cellsDerived from capillary endothelial cells
Occur intraorally, either alone or in a/wOccur intraorally, either alone or in a/w
skin & disseminated lesions (lymphskin & disseminated lesions (lymph
nodes, salivary gland)nodes, salivary gland)
Intraorally-Intraorally- hard palate, buccal mucosa, &hard palate, buccal mucosa, &
gingivagingiva
-bluish, purple or red patches or-bluish, purple or red patches or
papulespapulesnodular, ulcerate & bleednodular, ulcerate & bleed
Diagnosis:Diagnosis: BiopsyBiopsy
Treatment:Treatment:
-Low dose radiation & chemotherapy-Low dose radiation & chemotherapy
(eg.Vinblastine)(eg.Vinblastine)
-Surgical excision (eg.CO2 laser)-Surgical excision (eg.CO2 laser)
-Immunotherapy (Interferon)-Immunotherapy (Interferon)
101. Non-Hodgkin’s LymphomaNon-Hodgkin’s Lymphoma
EtiologyEtiology:: Unknown, genetic &Unknown, genetic &
environmental factors (viruses,environmental factors (viruses,
radiation)radiation)
Clinical features:Clinical features:
Both sexes - any ageBoth sexes - any age
Lymph nodes involvedLymph nodes involved
Oral lesions - part of a disseminatedOral lesions - part of a disseminated
disease, or the only signdisease, or the only sign
Oral Lymphoma:Oral Lymphoma: diffuse, painlessdiffuse, painless
swelling, which may or may not beswelling, which may or may not be
ulcerated -soft palate, the posterior partulcerated -soft palate, the posterior part
of the tongue, the gingiva, & theof the tongue, the gingiva, & the
tonsillar areatonsillar area
HPE & Immunohistochemical examnHPE & Immunohistochemical examn
TreatmentTreatment:: Radiotherapy &Radiotherapy &
chemotherapychemotherapy