OM- OFG and Systemic diseases Flashcards

1
Q

Compare Orofacial granulomatosis to an angio-oedema?

A

Increased fluid in the oral and facial soft tissues.

Orofacial granulomatosis is due to a blockage of the lymphatic drainage causing accumulation of fluid in the soft tissues.
There is no increase in exudate from the capillaries into the tissues.
Histologically-we see giant cells that are obstructing the lymphatics.

Angio-oedema is due to increased vascular permeability allowing fluid to leak out of the capillaries into the soft tissues. The lymphatic drainage is working but is overwelmed. Histologically we see fluid in the connective tissue region.

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2
Q

What causes Orofacial granulomatosis?

A

Granulomas present in the tissues. This can be due to:
* Sarcoidosis- unusual unless present in other sites e.g. lymph nodes or salivary glands.
* Tuberculosis- usually in mouth or face without pulmonary disease
* Chron’s disease-

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3
Q

Why do we get granulomas?

A

In type 4 hypersensitivity reactions macrophages are activated to phagocytose the allergen.
If there is a problem removing the allergen, the macrophages fuse together to produce a giant cell granuloma.

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4
Q

List symptoms of orofacial granulomatosis?

A
  • Erythema of the peri-oral tissues (Disease extending well out from the mouth)
  • Angular cheilitis
  • Swollen lips
  • Fissured lips
  • Full thickness gingivitis (not plaque related)
  • Enlarged submandibular duct (Stag horning)
  • Cobblestoning.
    Angular cheiltitis
    Orofacial eryethma
    Cobblestoning
    Fissured tongue
    Fissured lips.
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5
Q

If a child presents with OFG. How does this influence our treatment of the patient?

A

Chron’s screening.
Get parents to be aware of any changes in bowel habits/ abdominal pain.
Growth monitoring at each visit (nutritional problem= problem with bowel)

Refer for foecal calproctectin test (good marker for inflammatory bowel changes in patients >7 years old.

It can be related to dietary triggers so we could place the patient on an exclusion diet.

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6
Q

What is an exclusion diet?

A

When you avoid the following foods containing:
* Benzoic acid (Found in tomatoes & tomato sauce.
* Sorbic acid.
* Cinnamon products
* Chocolate
* E210-219
100% Compliance for 3 months and then you can reintroduce any favourite excluded foods unless they cause symptoms.

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7
Q

How do we treat Orofacial granulomatosis medically?

A

Topical treatment-
Angular cheilitis- topical miconazole gel 20 mg/g
Tacrolimus ointment- for areas of lip swelling and facial erythema to help disperse obstructed giant cells.

Intralesional steroid injection (Triamicinolone injected into the area of swelling)
Systemic treatment to help immune modulation:
Pulsed azithromycin
Prednisolone pulse
Aziathioprine/ mycophenolate .

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8
Q

What is the difference between orofacial granulomatosis and oral chrons?

A

If the patient has chron’s disease then we call it Oral chron’s. If the patient does not have chron’s disease it is known as orofacial granulomatosis.

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9
Q

How can systemic diseases manifest dentally?

A

It can affect the:
* tooth structure formation.
* Content of tooth. .

If it affects primary teeth (cause by something prenatally/ perinatally)
If it affects secondary teeth (caused by a perinatal/ childhood)

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10
Q

Your patient has attended with this clinical presentation.
What has caused this?

A

ectodermal dysplasia

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11
Q

Your patient has attended with this clinical presentation.
What has caused this?

A

Syphillis infection - changes to incisors- more triangular or peg like (Hutcheson’s incisors)

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12
Q

Your patient has attended with this clinical presentation.
What has caused this?

A

Any illness-
So the damage to development occurs at the same time but this affects different teeth at different stages of development.

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13
Q

Your patient has attended with this clinical presentation.
What has caused this?

A

This is pigmentation as a result of the buildup of bilirubin in the blood.

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14
Q

Your patient has attended with this clinical presentation.
What has caused this?

A

This is pigmentation due to tetracycline use during dental development.

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15
Q

Your patient has attended with this clinical presentation.
What has caused this?

A

This is due to porphyria.
(change in the haem levels in the blood)

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16
Q

What systemic diseases can cause excess parathyroid hormone and discuss the impact of these levels on the mouth?

A

Renal failure. Hypocalcaemia. Parathyroid tumour.

Increased PTH increases the calcium broken down from bone. This causes a loss of cortical bone around the teeth (once the caue is treated the cortical bone will return)

17
Q

What systemic disease can cause raised ACTH levels and discuss the impact of these levels on the mouth.

A

Cushings and addisons disease,
Raised ACTH a reactive melanosis of the oral mucosa (pigmentation)

18
Q

What causes haematinic deficiencies and what effect can this have on the mouth ?

A

Malabsorption (GI diseases- coeliac/ Crohn’s)
Blood loss (Crohn’s/ ulcerative colitis/ Peptic ulcer disease/ bowel cancer/ liver disease)
Increased demand

Effect- oral ulceration and a painful tongue.

19
Q

Patient presents with this clinically,
Give differential diagnoses and how would we final a final diagnosis ?

A

White striae on an erythematous background.
Systemic lupus erythematous
Lichen planus
Would use immunology to distinguish between these.

20
Q

How does systemic sclerosis affect the connective tissues?

A

There is a loss of elasticity around the mouth (peri-oral fibrosis)

21
Q

Discuss this clinical presentation?

A

Wegner’s granulomatosis- A vascularitic change on the gingivae causing ischaemia and necrosis of the tissues that can spread to the airway.

22
Q

How can immune deficiencies affect the mouth?

A

Warts
Accquired infections e.g. candida
HIV (purple change of the mucosa known as Kaposki’s sarcoma)
Reactivation of herpes simplex.

23
Q

Give the oral effects of medical therapy?

A

Dry mouth
Oral ulceration e.g. Nicoradnil
Lichenoid reaction- ACE inhibitors/ beta blocker
Angiooedema
Osteonecrosis (bisphosphonates)