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DIAGNOSIS OF ULCERATIVE,
VESICULAR AND BULLOUS
LESIONS
R.K.Haritha
CONTENTS
 HSV
 VZV
 CMV
 CV
 NUG, NUP
 Erythema multiforme
 Steven-Johnson syndrome and Toxic epidermal necrolysis
 Plasma cell stomatitis
 Recurrent aphthous stomatitis
 Behçet’s syndrome
 Pemphigus
 Pemphigoid
 Traumatic injuries causing solitary ulcerations
 Traumatic ulcerative granuloma
HSV
1. Prodrome – fever, loss of appetite, malaise
and myalgia + headache, nausea
2. Erythema and clusters of vesicles and/or
ulcers
3. Vesicles break down to ulcers (1-5mm)
4. Coalesce to form large ulcers with scalloped
borders and marked surrounding erythema
5. Gingiva – erythematous
6. Pharyngitis – swallowing difficulties
RECRUDESCENT HSV
 History of triggers – fever, ultraviolet radiation,
trauma, stress and menstruation
 Site – lips (20-40% of young adult population)
 Prodrome – Itching, tingling, or burning
 Appearance of papules, vesicles, ulcers,
crusting and resolution
PRIMARY VZV
Low grade fever
Development of intensely pruritic, maculopapular rash
Vesicle formation ‘dew-drop like’
Cloudy and pustular, burst and scab
Crusts fall off in 1-2 wks
 First 2 decades
 CNS – Cerebellar ataxia and encephalitis
 Other complications – Pneumonia, myocarditis and hepatitis
 Oral – Acute onset ulcerations in the mouth that often pale
 Immunocompromised – more blisters + often involvement of
lungs, CNS and liver – higher mortality rate
HERPES ZOSTER (SHINGLES)
Prodrome - deep, aching or burning pain
Vesicles in dermatomal or Zosteriform pattern – 2-
4days
Scarring and hypopigmentation – 2-4wks
 V1 – lesions on the upper eyelid, forehead, & scalp -
blindness
 V2 – lesions of the midface and upper lip – Prodrome of
pain, burning and tenderness, usually on the palate on
one side – painful, clustere ulcers (1-5mm) – coalesce
– heal 10-14days
 V3 – Blisters and ulcers on the mandibular gingiva &
tongue (uncommon)
CMV
 90% of AIDS have circulating Ab to CMV – single
large ulcers + usually painful +present for
weeks or months Marked lymphocytosis + Fever
+ 1/3rd coinfected with HSV/ VZV
 Occasional reports – mandibular osteomyelitis &
tooth exfoliation
 Serious complications – meningoencephalitis,
myocarditis, and thrombocytopenia
COXSACKIE VIRUS
INFECTION
 <10yrs
 Low grade fever + sore
mouth + erythematous
macules  vesicles 
ulcers
 Site – tongue, hard and
soft palate & buccal
mucosa
 Skin rash – hands & feet
75-100%; buttocks 30%
 <10yrs
 Epidemics in summer
 Fever, headache,
myalgia 1-3days
 Sore throat + pain on
swallowing + erythema
 Site - oropharynx, soft
palate & tonsillar pillars
HFM disease – Herpangina –
NUG & NUP
 Excessive salivation + metallic taste + sensitivity
of the gingiva  extremely painful & erythematous
gingiva + scattered punched out ulcer 
malodour + gingival bleeding + plaque buildup
 Immunocompromised and neutropenic –
osteonecrosis or necrosis of soft tissue
 Severe immunodeficiency – cone shaped orofacial
lesions – base of the cone within the oral cavity +
sloughing + sequestration of necrotic bone & teeth
 mortality 70-90% if not treated
ERYTHEMA MULTIFORME
 Prodrome Rapid skin lesions redmacules –
papular (several forms) {target or iris lesion} 
centripetal towards the trunk from hands  skin
feel itchy & burnt  Postinflammatory
hyperpigmentation
 Oral – mild erythema and erosion to large painful
ulceration  large & confluent ulceration –
difficulty in eating, drinking, & swallowing 
blood tinged saliva
 Extensive lip involvement – inflammation,
ulceration & crusting (common)
STEVENS-JOHNSON SYNDROME &
TOIC EPIDERMAL NECROLYSIS
 SJS less severe variant of TEN
 H/O medication use and M.pneumoniae 
sulfonamides, penicillins, anticonvulsants, NSAIDs
in children; allopurinol, oxicams, nevirapine in
adults
 Oral – extensive oral ulceration with hemorrhagic
crusts on the vermillion border. Localised in the
epidermis
PLASMA CELL STOMATITIS
 Brightly erythematous macular areas + ulcers
(sometimes) + swollen and edematous gingiva +
pain, sensitivity & bleeding + angular chelitis,
fissuring, dry atrophic lips (sometimes
 Site – marginal & attached gingiva, alveolar
mucosa, max and man sulcus or buccal mucosa
RECURRENT APHTHOUS
STOMATITIS
 RAS Minor – Prodromal brurning or sensation of a
small bump 2-48hrs before ulcers  small white
papule forms (round, symmetric, & shallow)
ulcerates , gradually enlarges (0.3-1 cm) 48-72hrs
 begin healing  healing without scarring 10-
14days
 RAS Major – >1cm + become confuent 
extremely painful, interfering with speech & eating
 heal after weeks or months with scars 
decreased mobility of tongue & uvula
 Herpetiform – More than 10 small punctate ulcer +
<5mm + scattered over large portions of the oral
mucosa
BEHÇET’S SYNDROME
 Diagnostic criteria
1. Oral, ocular, genital lesion – 2 points
2. Skin lesions, neurologic & vascular
manifestation – 1 point
3. Positive pathergy test (optional) – 1 point
4 or more points – strongly associated
PEMPHIGUS VULGARIS
 Classic bulla on a non inflamed base/ shallow
irregular erosions & ulcers  thin epithelium
peels away in irregular pattern – denuded base 
extend peripherally for weeks
 Site – buccal mucosa often in areas of trauma
along occlusal plane, palatal mucosa, gingiva
 Candidiasis may mask
PARANEOPLASTIC
PEMPHIGUS
 Rapid onset + Severe blistering & erosions +
severe oral & conjuctival lesions + lesions in
palms & soles (characteristic) + respiratory
epithelium (severe)  continue to progress over
weeks to months
 Oral – inflamed & necrotic with large erosions
covering the lips, tongue & soft palate +
hemorrhagic crusts on lips(characteristic)
PEMPHIGUS VEGETANS
Gingival lesions may be
1. Lace-like ulcers with a purulent surface on a red
base
2. Granular or cobblestone appearance
BULLOUS PEMPHIGOID
 Tense blister on an inflamed base + urticarial
plaques in scalp, abdomen, extremities, axilla &
groin + pruritis  self limiting last months to
years
 1 episode or recurrence
 Oral (10-20%) – smaller, form slowly & less
painful than P.vegetans + desquamative gingivitis
(sometimes)  early remission than mucous
membrane pemphigoid
MUCOUS MEMBRANE
PEMPHIGOID (CICATRICIAL)
 Older than 50 yrs
 F 2x> M
 Oral (80%) – Desquamative gingivitis (most common)
+ intact vesicles/ nonspecific appearing erythema &
erosions  scars rarely
 Eye – Conjuctiva (2nd common) – symblepharon;
corneal damage, progressive scarring  blindness
 Genital mucosa – pain & sexual dysfunction
 Laryngeal – pain hoarseness, difficulty in breathing 
death due to asphyxiation
 Esophageal – dysphagia  debilitation & death
 Skin lesions (20-30%) – head & neck region
LAD & BULLOUS DISEASE OF
CHILDHOOD
 Annular pruritic papules & blisters  ‘cluster of
jewel’
 Oral (70%) – blisters, erosions & ulcers of the
mucosa accompanied by desquamative gingivitis
TRAUMATIC INJURIES
CAUSING ULCERATIONS
 Acute ulceration & necrosis of the mucosa + h/o
trauma
 Electrical burns – charred & dry appearing 
sloughs  excessive bleeding when underlying
structures exposed
 Burns from hot foods & beverages – small &
localised to hard palatal mucosa or lips +
tenderness & erythema  ulcers within hours 
several days to heal
 Ulcers from vascular compromise – necrotising
sialometaplasia & vasculitic lesions – last for weeks
or months
TRAUMATIC ULCERATIVE
GRANULOMA
 Congenital incapacity to sense pain
 Children – anterior, ventral or dorsal tongue
associated with erupting max & man inciors
 Adults – posterior & lateral aspect of tongue
 Ulcers - Painless + clearly punched out +
surrounding erythema & keratosis (if present for
weeks or months), >0.5cm
REF: MICHAEL GLICK,BURKET’S ORAL
MEDICINE 12 TH EDITION

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Diagnosis of ulcerative, vesicular and bullous lesion

  • 1. DIAGNOSIS OF ULCERATIVE, VESICULAR AND BULLOUS LESIONS R.K.Haritha
  • 2. CONTENTS  HSV  VZV  CMV  CV  NUG, NUP  Erythema multiforme  Steven-Johnson syndrome and Toxic epidermal necrolysis  Plasma cell stomatitis  Recurrent aphthous stomatitis  Behçet’s syndrome  Pemphigus  Pemphigoid  Traumatic injuries causing solitary ulcerations  Traumatic ulcerative granuloma
  • 3. HSV 1. Prodrome – fever, loss of appetite, malaise and myalgia + headache, nausea 2. Erythema and clusters of vesicles and/or ulcers 3. Vesicles break down to ulcers (1-5mm) 4. Coalesce to form large ulcers with scalloped borders and marked surrounding erythema 5. Gingiva – erythematous 6. Pharyngitis – swallowing difficulties
  • 4. RECRUDESCENT HSV  History of triggers – fever, ultraviolet radiation, trauma, stress and menstruation  Site – lips (20-40% of young adult population)  Prodrome – Itching, tingling, or burning  Appearance of papules, vesicles, ulcers, crusting and resolution
  • 5. PRIMARY VZV Low grade fever Development of intensely pruritic, maculopapular rash Vesicle formation ‘dew-drop like’ Cloudy and pustular, burst and scab Crusts fall off in 1-2 wks  First 2 decades  CNS – Cerebellar ataxia and encephalitis  Other complications – Pneumonia, myocarditis and hepatitis  Oral – Acute onset ulcerations in the mouth that often pale  Immunocompromised – more blisters + often involvement of lungs, CNS and liver – higher mortality rate
  • 6. HERPES ZOSTER (SHINGLES) Prodrome - deep, aching or burning pain Vesicles in dermatomal or Zosteriform pattern – 2- 4days Scarring and hypopigmentation – 2-4wks  V1 – lesions on the upper eyelid, forehead, & scalp - blindness  V2 – lesions of the midface and upper lip – Prodrome of pain, burning and tenderness, usually on the palate on one side – painful, clustere ulcers (1-5mm) – coalesce – heal 10-14days  V3 – Blisters and ulcers on the mandibular gingiva & tongue (uncommon)
  • 7. CMV  90% of AIDS have circulating Ab to CMV – single large ulcers + usually painful +present for weeks or months Marked lymphocytosis + Fever + 1/3rd coinfected with HSV/ VZV  Occasional reports – mandibular osteomyelitis & tooth exfoliation  Serious complications – meningoencephalitis, myocarditis, and thrombocytopenia
  • 8. COXSACKIE VIRUS INFECTION  <10yrs  Low grade fever + sore mouth + erythematous macules  vesicles  ulcers  Site – tongue, hard and soft palate & buccal mucosa  Skin rash – hands & feet 75-100%; buttocks 30%  <10yrs  Epidemics in summer  Fever, headache, myalgia 1-3days  Sore throat + pain on swallowing + erythema  Site - oropharynx, soft palate & tonsillar pillars HFM disease – Herpangina –
  • 9. NUG & NUP  Excessive salivation + metallic taste + sensitivity of the gingiva  extremely painful & erythematous gingiva + scattered punched out ulcer  malodour + gingival bleeding + plaque buildup  Immunocompromised and neutropenic – osteonecrosis or necrosis of soft tissue  Severe immunodeficiency – cone shaped orofacial lesions – base of the cone within the oral cavity + sloughing + sequestration of necrotic bone & teeth  mortality 70-90% if not treated
  • 10. ERYTHEMA MULTIFORME  Prodrome Rapid skin lesions redmacules – papular (several forms) {target or iris lesion}  centripetal towards the trunk from hands  skin feel itchy & burnt  Postinflammatory hyperpigmentation  Oral – mild erythema and erosion to large painful ulceration  large & confluent ulceration – difficulty in eating, drinking, & swallowing  blood tinged saliva  Extensive lip involvement – inflammation, ulceration & crusting (common)
  • 11. STEVENS-JOHNSON SYNDROME & TOIC EPIDERMAL NECROLYSIS  SJS less severe variant of TEN  H/O medication use and M.pneumoniae  sulfonamides, penicillins, anticonvulsants, NSAIDs in children; allopurinol, oxicams, nevirapine in adults  Oral – extensive oral ulceration with hemorrhagic crusts on the vermillion border. Localised in the epidermis
  • 12. PLASMA CELL STOMATITIS  Brightly erythematous macular areas + ulcers (sometimes) + swollen and edematous gingiva + pain, sensitivity & bleeding + angular chelitis, fissuring, dry atrophic lips (sometimes  Site – marginal & attached gingiva, alveolar mucosa, max and man sulcus or buccal mucosa
  • 13. RECURRENT APHTHOUS STOMATITIS  RAS Minor – Prodromal brurning or sensation of a small bump 2-48hrs before ulcers  small white papule forms (round, symmetric, & shallow) ulcerates , gradually enlarges (0.3-1 cm) 48-72hrs  begin healing  healing without scarring 10- 14days  RAS Major – >1cm + become confuent  extremely painful, interfering with speech & eating  heal after weeks or months with scars  decreased mobility of tongue & uvula  Herpetiform – More than 10 small punctate ulcer + <5mm + scattered over large portions of the oral mucosa
  • 14. BEHÇET’S SYNDROME  Diagnostic criteria 1. Oral, ocular, genital lesion – 2 points 2. Skin lesions, neurologic & vascular manifestation – 1 point 3. Positive pathergy test (optional) – 1 point 4 or more points – strongly associated
  • 15. PEMPHIGUS VULGARIS  Classic bulla on a non inflamed base/ shallow irregular erosions & ulcers  thin epithelium peels away in irregular pattern – denuded base  extend peripherally for weeks  Site – buccal mucosa often in areas of trauma along occlusal plane, palatal mucosa, gingiva  Candidiasis may mask
  • 16. PARANEOPLASTIC PEMPHIGUS  Rapid onset + Severe blistering & erosions + severe oral & conjuctival lesions + lesions in palms & soles (characteristic) + respiratory epithelium (severe)  continue to progress over weeks to months  Oral – inflamed & necrotic with large erosions covering the lips, tongue & soft palate + hemorrhagic crusts on lips(characteristic)
  • 17. PEMPHIGUS VEGETANS Gingival lesions may be 1. Lace-like ulcers with a purulent surface on a red base 2. Granular or cobblestone appearance
  • 18. BULLOUS PEMPHIGOID  Tense blister on an inflamed base + urticarial plaques in scalp, abdomen, extremities, axilla & groin + pruritis  self limiting last months to years  1 episode or recurrence  Oral (10-20%) – smaller, form slowly & less painful than P.vegetans + desquamative gingivitis (sometimes)  early remission than mucous membrane pemphigoid
  • 19. MUCOUS MEMBRANE PEMPHIGOID (CICATRICIAL)  Older than 50 yrs  F 2x> M  Oral (80%) – Desquamative gingivitis (most common) + intact vesicles/ nonspecific appearing erythema & erosions  scars rarely  Eye – Conjuctiva (2nd common) – symblepharon; corneal damage, progressive scarring  blindness  Genital mucosa – pain & sexual dysfunction  Laryngeal – pain hoarseness, difficulty in breathing  death due to asphyxiation  Esophageal – dysphagia  debilitation & death  Skin lesions (20-30%) – head & neck region
  • 20. LAD & BULLOUS DISEASE OF CHILDHOOD  Annular pruritic papules & blisters  ‘cluster of jewel’  Oral (70%) – blisters, erosions & ulcers of the mucosa accompanied by desquamative gingivitis
  • 21. TRAUMATIC INJURIES CAUSING ULCERATIONS  Acute ulceration & necrosis of the mucosa + h/o trauma  Electrical burns – charred & dry appearing  sloughs  excessive bleeding when underlying structures exposed  Burns from hot foods & beverages – small & localised to hard palatal mucosa or lips + tenderness & erythema  ulcers within hours  several days to heal  Ulcers from vascular compromise – necrotising sialometaplasia & vasculitic lesions – last for weeks or months
  • 22. TRAUMATIC ULCERATIVE GRANULOMA  Congenital incapacity to sense pain  Children – anterior, ventral or dorsal tongue associated with erupting max & man inciors  Adults – posterior & lateral aspect of tongue  Ulcers - Painless + clearly punched out + surrounding erythema & keratosis (if present for weeks or months), >0.5cm
  • 23. REF: MICHAEL GLICK,BURKET’S ORAL MEDICINE 12 TH EDITION