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- NEETMDS- courses
NEET MDS Lessons
Oral Pathology

  • Class III (Underdeveloped Maxilla) → Cleidocranial dysplasia, Craniofacial dysostosis, Achondroplasia, Down syndrome, Osteogenesis imperfecta
  • Class II (Underdeveloped Mandible) → Treacher Collins syndrome, Pierre Robin syndrome
  • Both Jaw Underdevelopment → Hypopituitarism
  • Maxillary Enlargement → Metastatic fibrous dysplasia
  • Mandibular Enlargement → Acromegaly
  • Bimaxillary Enlargement → Paget’s Disease
  • Mandibular Asymmetry → Caffey’s Disease
  • Prominent Premaxilla → Thalassemia
  • Underdeveloped Premaxilla → Congenital Syphilis

  • Pemphigus → Granular IgG intercellular
  • Lichen Planus → Linear anti-fibrinogen at BM, with lamina propria extensions
  • Cicatricial Pemphigoid → Patchy linear IgG/C3 at BM
  • Bullous Pemphigoid → Patchy linear IgG at BMZ
  • Erythema Multiforme → Patchy linear fluorescence
  • Discoid Lupus (Lesional mucosa) → Speckled pattern (IgG, IgM, IgA, C3, fibrinogen)

  • Café au Lait Spots:

    • "Coast of California": Associated with Neurofibromatosis (Type 1).

    • "Coast of Maine": Associated with Fibrous Dysplasia.

  • Carpet Tack Lesions: Characteristic of Discoid Lupus Erythematosus.

  • Cerebriform Tongue: Seen in Pemphigus Vegetans.

  • Charcot's Triad: Seen in Multiple Sclerosis, characterized by:

    • Intention tremor

    • Nystagmus

    • Dysarthria

  • Chipmunk Facies: Seen in Thalassemia.

  • Chvostek's Sign: Indicative of Hypoparathyroidism (facial muscle twitching upon tapping the facial nerve).

  • Buffalo Hump: A characteristic clinical sign of Cushing's Syndrome (fat pad on the upper back).

  • 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.

  • 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

Paget's Disease

  • Chief Complaint: Denture tightening (due to arch expansion)
  • Fractures: Chalk-stick fractures
  • Facial Feature: Leontiasis ossea (lion-like facies)
  • Radiology: Cotton wool appearance
  • Histology: Jigsaw puzzle pattern
  • Clinical: Bone warm to touch (↑ vascularity)
  • Laboratory: ↑ Alkaline phosphatase (>250 Bodansky units)
  • Other Signs: Osteoporosis circumscripta, platybasia
  • Memory Aid: "Paget's Patients Prefer Tight Dentures"

Osteopetrosis

  • Radiographic Sign: Rugger Jersey Spine (classic)
  • Fractures: Chalk-stick fractures

Fibrous Dysplasia

  • Facial Feature: Leontiasis ossea
  • Histology: Chinese script pattern
  • Radiology:
    • Ground glass appearance
    • Rind sign, orange peel appearance
  • Bone Deformity: Hockey stick/Shepherd's crook deformity (femur)
  • Key Feature: Lesional bone fused with normal bone (vs COF)
  • Memory Aid: "Fibrous Faces Feel Funny"

Cemento-Ossifying Fibroma (COF)

  • Histology: Chinese script pattern
  • Facial Feature: Leontiasis ossea
  • Difference: NOT fused with normal bone (vs Fibrous Dysplasia)

Hyperparathyroidism

  • Radiology: Ground glass appearance (brown tumor)
  • Histology: Numerous giant cells, vascular stroma, hemosiderin deposits

Cherubism & Central Giant Cell Granuloma

  • Histology: Same as hyperparathyroidism (giant cells + vascular stroma + hemosiderin)
  • Note: Cherubism previously called "Familial fibrous dysplasia"
  • Memory Aid: "Giant Cells Have Three Homes" (Hyperparathyroidism, Cherubism, CGCG)

Juvenile Ossifying Fibroma

  • Aggressiveness: More aggressive than Cemento-ossifying fibroma
  • Types:
    • Trabecular type: Common in jaws
    • Psammomatoid type: Involves base of skull

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