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Oral Pathology - NEETMDS- courses
NEET MDS Lessons
Oral Pathology

Chronic Osteomyelitis

  • As soon as pus drains intra or extraorally, condition ceases to spread and chronic phase commences.
  • Infection is localized but persistent as bacteria are able to grow in dead bone inaccessible to body’s defenses.

Clinical features

  • Primary – insidious in onset , slight pain , gradual increase in jaw size.
  • Secondary - Pain is deep pain and intermittent, temperature fluctuations , pyrexia , cellulitis eventually leading to abscess
  • New bone formation leads to thickening causing facial asymmetry.
  • Thickened or “wooden” character of bone in cr sec osteomyelitis.
  • Eventually cures itself as the last sequestra is discharged.

Radiographic Features

  • Trabeculae in the involved area become thin or appear fuzzy & then lose their continuity.
  • After some time “moth eaten” appearance is seen
  • Sequestra appear denser on radiographs.
  • Where the subperiosteal new bone formation , the new bone is superimposed upon that of jaw, “fingerprint” or “orange peel” appearance is seen
  • Cloacae seen as dark shadows passing through opacity.

Histologic features

  • Areas of acute and subacute inflammation in the cancellous spaces of the necrotic bone.
  • Foci of acute inflammation
  • Active osteoclastic resorption of bone noted in peripheral portions

Chronic Subperiosteal Osteomyelitis

  • Cortical plate deprived of its blood supply undergoes necrosis, underlying medullary bone  is slightly affected.
  • Multiple small sequestra form, eventually discharged through sinuses with pus.
  • Following extrusion of sequestra, healing occurs.
  • Spontaneous drainage poor in submassetric area.
  • Much of  body of mandible is lost due to poor central blood supply of the region.

D/D

  • Paget’s disease – particularly wen periosteal bone is involved
  • Fibrous dysplasia
  • Osteosarcoma

Chronic sclerosing osteomyelitis

– focal

- diffuse

Focal Sclerosing Osteomyelitis

Clinical features

  • Most commonly in children and young adults, rarely in older individuals.
  • Tooth most commonly involved is the mandibular third molar presenting with a large carious lesion.
  • No signs or symptoms other than mild pain associated with infected pulp.

Radiographic features

  • Entire root outline always visible with intact lamina dura.
  • Periodontal ligament space widened.
  • Border smooth & distinct appearing to blend into surrounding bone

D/D for focal sclerosing osteomyelitis

  • Local bone sclerosis
  • Sclerosing cementoma
  • Gigantiform cementoma

Treatment & prognosis

  • Affected tooth may be treated endodontically or extracted.
  • Sclerotic bone  not attached to tooth and remains behind after tooth is removed.
  • This dense area may not get remodeled.
  • Recognizable on bone years later and is referred as bone scar.

Diffuse Sclerosing Osteomyelitis

  • May occur at any age, most common in older persons, esp in edentulous mandibles
  • vague pain, unpleasant taste.
  • Many times spontaneous formation of fistula seen opening onto mucosal surface to establish drainage
  • Slowly progressive, not particularly dangerous since it is non destructive & seldom produces complications

Radiographic features

  • Diffuse patchy, sclerosis of bone – “cotton wool” appearance
  • Radiopacity may be extensive and bilateral.
  • Due to diffuse nature, border between sclerosis & normal bone is often indistinct

D/D for DIFFUSE sclerosing osteomyelitis

FLORID OSSEOUS DYSPLASIA

SCLEROTIC CEMENTAL MASSES

TRUE CHR DIFFUSE SCLEROSING OSTEOMYELITIS

FIBROUS DYSPLASIA

Treatment & Prognosis

  • Resolution of adjacent foci of chronic infection often leads to improvement.
  • Usually too extensive to be removed surgically,
  • Acute episodes treated with antibiotics.

  • Blood: Aneurysmal bone cyst, Vascular lesion, Vessel puncture.

  • Air: Traumatic bony cyst (Simple Bone Cyst/Hemorrhagic Bone Cyst), Maxillary sinus.

  • Chocolate Colored Fluid: Warthin's Tumor (salivary gland cyst).

  • Pioneer bacteria invade dentinal tubules before clinical signs
  • Tubules contain pure forms:
    • One tubule → cocci
    • Adjacent tubule → bacilli or threads
  • No mixed forms within a single tubule

  • Derived from Reduced Enamel Epithelium (REE):

    • Dentigerous Cyst

    • Eruption Cyst

    • Paradental Cyst

  • Derived from Rests of Serres (remnants of dental lamina):

    • Odontogenic Keratocyst (OKC)

    • Gingival Cyst of Newborn

    • Gingival Cyst of Adult

    • Lateral Periodontal Cyst

    • Glandular Odontogenic Cyst

  • 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)

 General Features

  • Caused by mutation in DSPP gene (dentin sialophosphoprotein).

  • Teeth appear translucent or opalescent.

  • Enamel fractures easily due to poor dentin support.

  • Pulp chambers are obliterated or enlarged depending on type.

  • Also called Hereditary Opalescent Dentin or Shell Teeth.

Type II DI

  • Pulp chambers are normal but rapidly obliterate.

  • Associated with progressive hearing loss.

Type III DI

  • Pulp chambers are large and shell-like.

  • Seen in Brandywine isolate population.

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

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