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Oral Pathology

Disease Serum Marker Changes
Paget’s Disease ↑ Alkaline phosphatase
Caffey’s Disease Fibrous dysplasia; may show ↑ alkaline phosphatase
Hyperparathyroidism ↑ Alkaline phosphatase
Osteopetrosis (Marble Bone Disease) ↑ Acid phosphatase
Osteogenesis Imperfecta Normal calcium & phosphate; ↑ bone fragility due to collagen defect
Chondrodysplasia Normal alkaline phosphatase
Odontogenic Myxoma ↑ Acid phosphatase
Thalassemia Prominent premaxilla; marrow expansion may affect jaw bones

Exception Alert: Serum alkaline phosphatase is raised in all of the following except: ➡️ Osteogenesis Imperfecta

  • Pioneer Bacteria: S. mutans are considered pioneer bacteria as they multiply and synthesize extracellular matrix polymers, initiating biofilm formation.

  • Caries Progression - Key Bacteria:

    • Initiation of caries: S. mutans.

    • Progression of caries / Dentinal caries: Lactobacillus.

    • Root surface caries: Actinomycetes.

  • Body of the Lesion (Enamel Caries): Shows increased prominence of the striae of Retzius.

  • Sugar Intake: Frequency of sugar intake is of more importance than the total amount consumed in caries development.

  • Actinomycosis (Sulfur Granules):

    • Yellow sulfur granules: Are actually bacterial colonies.

    • Histopathology: Colonies appear "cotton wool" shaped. (Note: "Cotton wool appearance" is seen radiographically in Paget's disease).

  • Tuberculosis (TB):

    • Diagnosis (Gold Standard): Presence of acid-fast bacilli in sputum.

    • Staining Method: Ziehl-Neelsen staining method is used to identify acid-fast bacilli.

    • Scrofula: TB of cervical lymph nodes.

    • Lupus Vulgaris: TB of skin.

  • Tongue & Gingival Appearance in Systemic Conditions:

    • Strawberry tongue and Raspberry tongue: Seen in stomatitis of Scarlet Fever.

    • Strawberry Gingivitis: Seen in Wegener's Granulomatosis.

Bacterial & Fungal Infections

Syphilis - Congenital

Hutchinson's Triad:

  1. Mulberry molars & peg-shaped incisors
  2. VIII nerve deafness
  3. Interstitial keratitis

Higoumenaki Sign: Thickened sternoclavicular joint

Rhinoscleroma

  • Also Called: Hebra nose

Sarcoidosis

  • Diagnostic Test: Kveim–Siltzbach
  • Histology: Schaumann bodies

Candidiasis

  • Id Reaction: Hypersensitivity to Candida antigen
  • Chairside Diagnosis: Wet smear in 10% KOH

  • SLE → IgG, IgM, IgA deposits at BMZ + superficial lamina propria
  • Lichen Planus (Erosive/Atrophic) → Autoimmune T-cell; BMZ involvement
  • Cicatricial Pemphigoid → Subepidermal blistering from anti-BMZ antibodies

  • Inverted Pear-shaped Radiolucency: Globulomaxillary cyst.

    • Associated teeth need not be non-vital.

    • Klestadts’s cyst: Soft tissue variant of Globulomaxillary cyst.

  • Tear Drop-shaped Radiolucency: Lateral Periodontal Cyst.

    • Associated teeth are vital.

  • Cluster of Similar Cysts / Cluster of Grapes: Botryoid Odontogenic Cyst.

Leukoplakia

  • Type: Clinical term
  • Histology: Hyperkeratosis ± Dysplasia

Verrucous Carcinoma

  • Type: Variant of SCC
  • Features:
    • Intact basement membrane
    • Parakeratin plugging
    • Broad "elephant-foot" rete ridges

Adenosquamous Carcinoma

  • Features: Mixed adenocarcinoma + SCC

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