NEET MDS Lessons
Oral Pathology
Intraepithelial Bulla
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Location: Within the epithelium
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Associated Conditions:
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Herpes simplex
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Herpes zoster
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Chicken pox
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Pemphigus
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Hailey-Hailey disease (Familial benign pemphigus)
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Epidermolysis bullosa (dystrophic recessive form)
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Oral lesions of erythema multiforme
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Subepithelial Bulla
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Location: Below the epithelium
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Associated Conditions:
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Pemphigoid
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Bullous pemphigoid (most common subepithelial blistering disease)
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Bullous lichen planus
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Dermatitis herpetiformis
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Epidermolysis bullosa
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Skin lesions of erythema multiforme
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Calcifying Odontogenic Cyst (COC) / Gorlin Cyst: Characterized by Ghost Cells.
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Aneurysmal Bone Cyst (ABC): Associated with a "blood-soaked" appearance on gross examination.
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Radicular Cyst - Common Site: Maxillary anterior teeth (due to higher incidence of trauma).
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Odontogenic Keratocyst (OKC) / Keratocystic Odontogenic Tumor (KCOT):
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Most common site: Posterior mandible (similar to ameloblastoma).
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Expansion: Tends to expand antero-posteriorly; buccal and lingual expansion seen in late stages.
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Basal layer histology: Tall columnar cells with palisaded nuclei – "row of tombstones" or "picket fence appearance."
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Classification: Now considered a benign odontogenic neoplasm (KCOT) in recent WHO classifications.
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Leukoedema
- Diagnostic Feature: Lesions do not rub off; disappear when cheek is stretched
Heck's Disease (Focal Epithelial Hyperplasia)
- Appearance: Cobblestone mucosa
- Also Seen In: Pyostomatitis vegetans, Keratosis follicularis
Infectious Mononucleosis
- Nickname: Kissing disease
- Etiology: Epstein–Barr Virus (EBV)
Trotter’s Syndrome
- Key Features: Pharyngeal pain due to nasopharyngeal carcinoma
- Associated Structures: CN V, CN IX, CN X
Post-Herpetic Neuralgia
- Key Features: Persistent pain after Herpes Zoster, often affecting the ophthalmic division
- Associated Structures: CN V1
Ramsay Hunt Syndrome (Herpes Zoster Oticus)
- Key Features: Facial paralysis, ear pain, vesicles, hoarseness, vertigo
- Associated Structures: Geniculate ganglion, CN VII
Reader’s Syndrome (Para-Trigeminal Syndrome)
- Key Features: Trigeminal pain with ocular sympathetic paralysis
- Associated Structures: CN V + sympathetic fibers
Sphenopalatine Neuralgia (Sluder’s / Horton’s / Lower Half Headache)
- Key Features: Unilateral pain in eye, maxilla, ear, mastoid, zygoma; no trigger zone; may occur at same time daily
- Associated Structures: Vidian nerve, cavernous sinus
Horner’s Syndrome
- Key Features: Triad of miosis, ptosis, anhidrosis; facial vasodilation
- Associated Structures: Sympathetic chain lesion
Frey’s Syndrome (Auriculotemporal Syndrome)
- Key Features: Gustatory sweating during eating; flushing in temporal region
- Associated Structures: Auriculotemporal nerve (CN V3)
Glossopharyngeal Neuralgia
- Key Features: Sharp pain in ear, pharynx, tonsil, posterior tongue; trigger zone in tonsillar fossa
- Associated Structures: CN IX
Occipital Neuralgia
- Key Features: Unilateral pain in neck and occipital region; tender spot below superior nuchal line
- Associated Structures: Cervical plexus sensory branches
Eagle’s Syndrome (Stylohyoid Syndrome)
- Key Features: Deep dull pain in oropharynx, posterior auricular region, dysphagia, limited neck motion
- Associated Structures: Elongated styloid process or calcified stylohyoid ligament
Acute suppurative osteomyelitis
- Serious sequela of periapical infection.
- Leads to spread of pus through the medullary cavities of bone.
- Depending upon the main site of involvement of bone, can be of two types-
- Acute intramedullary
- Acute subperiosteal
Acute Intramedullary Osteomyelitis
CLINICAL FEATURES:
- Patient experiences dull , continuous pain , indurated swelling forms over the affected region of jaw involving the cheek , febrile.
- When mandible involved, loss of sensation occurs on lower lip on affected side due to involvement of inferior alveolar nerve.
- Teeth become loose later along with tender on percussion
- Pus discharge , trismus , foul smell , regional lymphadenopathy , weakness
RADIOGRAPHIC FEATURES
- Earliest radiographic change is that trabeculae in involved area are thin, of poor density & slightly blurred.
- Subsequently multiple radiolucencies appear which become apparent on radiograph.
- In some cases there is saucer shaped area of destruction with irregular margins.
- Loss of continuity of lamina dura, seen in more than one tooth.
HISTOLOGIC FEATURES:
- Dense infiltration of marrow by polymorphonuclear leukocytes.
- Bone trabeculae in involved site (sequestrum) are devoid of cells in the lacunae.
- separation of considerable portions of devitalized bone.
Acute Subperiosteal Osteomyelitis
CLINICAL FEATURES
- Pain , febrile condition , i/o and e/o swelling , parasthesia
- Bone involvement limited to localized areas of cortex.
- Pus ruptures rapidly through the overlying cortex, tracks along the surface of mandible under the periosteal sheath.
- Elevation of periosteum from cortex is followed eventually by minute cortical sequestration.
Epithelial cysts
Developmental odontogenic cysts
Odontogenic keratocyst
Dentigerous cyst (follicular cyst)
Eruption cyst
Lateral periodontal cyst
Gingival cyst of adults
Glandular odontogenic cyst (sialo-odontogenic)
Inflammatory odontogenic cysts
Radicular cyst (apical and lateral)
Residual cyst
Paradental cyst
Non-odontogenic cysts
Nasopalatine cyst
Nasolabial cyst
Non-epithelial cysts (not true cysts)
Solitary bone cyst
Aneurysmal bone cyst
General Features
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Caused by mutation in DSPP gene (dentin sialophosphoprotein).
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Teeth appear translucent or opalescent.
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Enamel fractures easily due to poor dentin support.
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Pulp chambers are obliterated or enlarged depending on type.
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Also called Hereditary Opalescent Dentin or Shell Teeth.
Type II DI
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Pulp chambers are normal but rapidly obliterate.
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Associated with progressive hearing loss.
Type III DI
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Pulp chambers are large and shell-like.
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Seen in Brandywine isolate population.