L4 Perio-Oral medicine interface Flashcards

1
Q

What does perio-oral med interface describe?

A

The effect of systemic disease on the periodontium.

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2
Q

How can we classify systemic conditions which affect the periodontium?

A
  • Conditions that influence the coures of periodontitis by influencing periodontal inflammation. Can be genetic, immunodeficiency disorders, inflammatory, and other systemic disease.
  • Conditions that affect the periodontal supporting tissue independent of biofilm induced inflammation. These conditions are not actually gingivitis or periodontitis. Can be primary neoplasms, secondary metastatic neoplasms and other disorders.
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3
Q

Categorise genetic disorders which influence the course of periodontitis (via. influecing perio inflammation).

A

Blue writing indicates the strength of association between the condition and periodontitis. No writing = strong association.

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4
Q

What is Trisomy 21 and how does it affect oral health?

A
  • Down’s syndrome
  • Delayed eruption
  • Malocclusion
  • Crowding
  • Hypodontia
  • Significant amounts of bone loss in perio
  • Periodontitis has been reported in 50% of pts with Down’s syndrome
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5
Q

What is epidermolysis bullosa and how does it affect the periodontium?

A
  • Rare blistering disorder of the skin and mucous membranes
  • Blisters can occur with very minor trauma (pathergy)
  • Struggle to carry out OHI due to blistering and pain
  • Periodontitis tends to be much more severe and rapidly progressing
  • Can see significant bone loss in these images for a 16 year old
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6
Q

What is plasminogen deficiency and how does it affect oral health?

A
  • Rare genetic condition causing plasminogen deficiency
  • Causes thick, inflammed growths of the mucosa
  • Thick lining on gingival tissues
  • Significant bone loss
  • Vertical bone defects surrounding membranes
  • Severe and rapid progression of periodontitis
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7
Q

What is Ehlers-Danlos syndrome and how does it affect oral health?

A
  • Connective tissue disorder
  • Hypermobility of joints
  • Results in more severe and rapidly progressing periodontitis
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8
Q

Do acquired immunodeficiency disorders influence periodontal inflammation?

A

Inconclusive.
- Acquired neutropenia = weak association
- HIV infection = weak association

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9
Q

Which inflammatory diseases are associated with influencing periodontitis?

A
  • Epidermolysis bullosa acquisita: moderate association
  • Inflammatory bowel disease: strong association
  • Arthritis: strong association

Influence the course of perio by influencing periodontal inflammation.

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10
Q

Name other systemic disorders linked to periodontitis and how strong their association is.

A
  • Emotional stress and depression: weak
  • Hypertension: inconclusive evidence
  • Smoking: strong association
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11
Q

Which medications increase the amount of destruction in periodontitis?

A
  • Chemotherapy
  • VEGF inhibitors
  • TKIs (sunitinib)
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12
Q

Which medications decrease the amount of destruction in periodontitis?

A
  • NSAIDs
  • Anti-TNF therapies
  • Bisphosphonates
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13
Q

Which neoplasms have been found to cause loss of periodontal tissue independent of periodontititis?

A

Moderate association:
- Primary cancer: SCC, malignant odontogenic tumours
- Secondary metastatic neoplasms

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14
Q

Name other systemic disorders that have been found to cause loss of periodontal tissue independent of periodontitis.

A
  • Langerhans cell histiocytosis
  • Granulomatosis with polyangiitis
  • Giant cell granuloma
  • Hyperparathyroidism
  • Systemic sclerosis
  • Vanishing bone disease (Gorham-Stout syndrome)
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15
Q

Name 10 conditions of non-biofilm related loss of periodontal tissue.

A
  • Lichen planus
  • Primary herpetic gingivostomatitis
  • Pregnancy epulis
  • Orofacial granulomatosis
  • Pemphigus vulgaris
  • Graft vs host disease
  • Bullous pemphigoid
  • Amalgam tattoo
  • Thrombocytopenia
  • Langerhans cell histiocytosis
  • Moderately differentiated SCC
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16
Q

Describe the presentation of lichen planus.

A
  • Red gums aka desquamative gingivitis
  • White lacey patches on cheeks
  • Purple skin lesions

It is an immune-mediated condition involving T-cell mediated destruction of basal keratinocytes and hyperparakeratinisaiton of the epithelium.

17
Q

How is lichen planus managed?

A
  • May need biopsy to exclude lupus, lichenoid reaction, pemphigus and pemphigoid (Dr Atkin would disagree)
  • Treated with topical or systemic corticosteroids
  • Regular monitoring is required since oral lichen planus is classified as a potentially malignant disorder
18
Q

How would you treat the gingival lesions that this patient with lichen planus has?

A

Soft splint with gingival coverage (like a night guard) to apply topical corticosteroid for 10 minutes daily for 6 weeks- Fluocinolone acetonide.

19
Q

Describe the presentation of primary herpetic gingivostomatitis.

A
  • Manifestation of HSV-1 in children
  • Acute onset of very painful mouth and swollen gingivae
  • Raised temp, generally feeling unwell
  • Gingival tissue affected regardless of plaque presence
  • Widespread ulcers
  • Crusting of lips
  • Lymphadenopathy
20
Q

How is primary herpetic gingivostomatitis managed?

A

Supportive management:
- 0.2% Chx mouthwash to prevent bacterial infection of ulcers
- 2% lidocaine mouthwash or Difflam to manage pain
- Paracetamol and high fluid intake
- Self limiting, resolves in 7-10 days

21
Q

When are antiviral drugs recommended for primary herpetic gingivostomatitis?

A

Only recommended in very severe cases or immunocompromised patients
- Aciclovir suspension, 200mg 5 times a day

22
Q

Describe pregancy epulis.

A
  • Excisional biopsy required to confirm diagnosis
  • Although it is likely to be an epulis biopsy is still required to eliminate other possible diagnoses
  • Will resolve post-birth
  • May recur whilst pregnancy continues if removed
23
Q

Describe orofacial granulomatosis.

A
  • Rare condition of the mouth that causes lip swelling, and sometimes swelling of the face, inner cheeks, and the gums
  • Irregular appearance of labial mucosa
  • Lip swelling, angular cheilitis/midline fissure, full width gingivitis (goes beyond the muco-gingival junction), mucosal tags, cobblestone buccal mucosa and aphthous ulceration
  • Differential diagnoses: Crohn’s or sarcoidosis
24
Q

How is orofacial granulomatosis managed?

A
  • Biopsy
  • Blood test for B12, folate and ferritin
  • Skin patch test for allergerns
25
Q

Describe pemphigus vulgaris.

A
  • Rare autoimmune condition characterised by blistering of skin and mucous membranes
  • Blistering extends beyond the mucogingival junction (tells you that inflammation is not plaque induced)
  • Pts develop antibodies to desmosomes in the epithelium of mucous membranes and skin, causes blistering
  • More common to see blisters in loose mucosa rather than gingival tissues
  • DO NOT attempt Nikolsky’s sign (applying pressure to blister to see if shearing occurs) as it will make the ulcer larger and cause pain
26
Q

What is the management for pemphigus vulgaris?

A

Systemic immunosuppression for life: prednisolone, azathioprine, cyclophosphamide

27
Q

Describe Graft vs Host disease.

A
  • A proces that can occur following a bone marrow or stem cell transplant
  • Diagnosis based on history taking
  • Patients present with generalised oral discomfort, swollen gums and widespread ulceration
  • Biopsy required, may mimic other conditions
28
Q

Describe Bullous Pemphigoid.

A
  • Rare autoimmune condition similair to pemphigus vulgaris
  • Blistering, inflammation progressing beyond mucogingival junction, split epithelium from underlying CT
29
Q

What is the management for bullous pemphigoid?

A
  • Bloods and biopsy to confirm diagnosis
  • Systemic and/or topical immunosuppression: prednisolone, azathioprine, cyclophosphamide.
  • Needs ophthalmology involvement as pemphigoid can affect the eyes and even cause blindness
30
Q

Describe thrombocytopenia.

A
  • Reduced platelet count
  • Below 150×10^9/L is considered a medical emergency
  • FBC and bone marrow examination
  • Many causes e.g. Leukaemia or a drug reaction
  • Platelet transfusion required
31
Q

Describe Langerhans’ cell histiocytosis.

A
  • Very rare condition
  • Excess histiocytes = multiple granulomas
  • Symptoms/signs range from: a rash, lumps on the skull, swollen tummy, breathing difficulties
32
Q

Describe moderately differentiated gingival SCC.

A
  • Pt underwent right sided marginal mandibulectomy of LR4/5 region with level 5 radical neck dissection
33
Q

What is the surgical sieve? HIIINTS

A

Mnemonic to help to remember conditions discuess in this lecture.