Salivary Gland Disease Flashcards

1
Q

Causes of permanent Xerostomia

A

Local radiation therapy 2 Sjogren’s syndrome.

3 Sarcoidosis DM & HIV infection.

S Salivary gland aplasia &

atresta 6) Aging

Deficiency of vit A vit 8

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2
Q

Temporary Xerostomia causes

A

1 Obstruction of salivary ducts.

  1. Inflammation of salivary glands bacterial & viral

sialadenitis 3. Medications antihypertensive, antidepressant,

antihistaminic. 4. Mouth breathing.
5. Smoking
5. Water & metabolites loss as in hemorrhage, persistent diarrhea, vomiting, dehydration, excessive sweating deficiency which lead to atrophy 7. Psychogenic emotional stress, anxiety, depression. 8. Decreased mastication

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3
Q

Clinical symptoms of xerostomia usually forgotten

A
  • oral candidiasis
  • atrophy of filliform papilla
  • residual saliva is thick foamy
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4
Q

Clinical of mumps

A
  • swelling I’m preauricular area
  • painful with moving jaw and salivary flow
  • tinder
  • bi or uni
  • 70%parotid rest in other 2
  • fever headache malaise anorexia and myalgia
  • swelling and redness of stenson Wharton duct opening
  • peak swelling at 2 to 3 days and decreases after 10d
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5
Q

Time of MMR vaccine

A
  • 12 to 15 month

Booster dose 4 to 6 y

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6
Q

Complications of mumps

A
- orchitis 
Tinder swollen painful 
Then atrophy and sterility
-oophoritis and mastitis with 25%  abortion in 1st trimester
-minengioenchephalitis
- permanent deafness
- pancreatitis nephritis and myocarditis
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7
Q

Mumps virus and its transmission

A

Paramyxovirus

Saliva
Urine
Respiratory droplets

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8
Q

Acute supportive sialadenitis surgical mumps or postoperative mumps systemic clinical symptoms

A

Low grade fever headache and malaise

Trismus

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9
Q

Histology of surgical mumps

A

-acute inflm. Cells in duct and acini

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10
Q

Why not use biopsy or sialography in surgical mumps

A

It helps spread the infection

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11
Q

Added notes to the histology of chronic sialadenitis

A
  • dilated duct near obstruction

- with fibrosis surrounding the area in this case called chronic sclerosing sialadenitis

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12
Q

Primary vs secondary sjogren

A

i. Primary Sjogren’s syndrome (Sicca syndrome):

➤Xerostomia and xerophthalmia only..

Cause more severe oral and ocular changes and has a higher risk of

malignancy than the secondary form (lymphoma).

il. Secondary Sjogren’s syndrome:

> Primary form + autoimmune connective tissue diseases (the most common →

rheumatoid arthritis then lupus erythematosus).

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13
Q

Sjogrens general symptoms

A

C/P:

  1. Age & sex→ 50 years, females: males (9:1).
    (2) From 1/3 to 1/2 of cases have diffuse firm unilateral or bilateral enlargement

of major salivary glands mainly.parotisl 3) May be slightly painful (intermittent or persistent).

4 Severe tiredness (patient rest or sleep 10-15 hours a day or more).

5 Various other body tissues are affected → dryness of skin, nasal and vaginal mucosa.
It has 2 forma 1ry and 2ry

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14
Q

Ocular symptoms of sjogren

A
  1. Keratoconjunctivitis

sicca →> tear

Xerostomia

production by the lacrimal glands or failure of tear secretion, lacrimal inflammation and mucoid discharge.,

  1. Patients complain of:

Scratchy, gritty sensation (feeling of a foreign body in the eyes).

Blurred vision and aching pain in eyes.

Less severe manifestation in the morning on wakening & ↑

symptoms as the day progress.

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15
Q

Etiology of sjogren

A

Lymphocyte-mediated destruction of exocrine glands & may include systemic CT disorders.

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16
Q

Sialography of sjogren

A

Fruit laden branchless tree

No branching of duct

17
Q

Lab finding of sjogren

A
  • Laboratory findings:
    i. Rheumatoid factor (RF) is positive in 75% of cases.
    ii. Elevated ESR.
    iii. Elevation of serum immunoglobulin levels. Ig
    iv. Antinuclear antibody (ANA)→ Anti-SS A (Ro) in Secondary SS, anti-SS B (La) in Primary SS.
18
Q

Histology of sjogren

A
  • dense infiltration of L. Around the intralobular ducts
  • destruction of acini
  • replacement of lobules by lymphocytes
  • proliferation of myoepithelial cells and duct epi
  • obliterating the duct
  • forming epimyoepithelial Islands surrounded by sheets of lymphocytes
19
Q

Treatment of xerophthalmia

A
  • sealing the lacrimal punctum to prevent drainage of the lacrimal secretion into the nose
  • sealed glasses to prevent evaporation
20
Q

Where does necrotizing sialometaplasia occur

A

In junction of soft and hard palate

Rarely other salivary gland sites

21
Q

necrotizing sialometaplasia etiology

A
  • cutting of blood supply/ischaemia due to trauma surgery or local anaesthesia causing discrete necrosis which lead to squamous metaplasia of remanants duct epi
22
Q

necrotizing sialometaplasia clinically

A
  • tinder erythematous welling
  • break down of mucosa
  • formation of deep ulcer with grayish yellow floor that last for 6to 8 w
23
Q

necrotizing sialometaplasia could be misdiagnosed as..

A

Sq.c.c

MEC

24
Q

necrotizing sialometaplasia H/P

A

Necrosis of salivary gland
Not a malignant tumor as
..Preserved lobular architecture
..No signes of dysplasia

There is squamous metaplasia of duct epi

inflammatory cells infiltration

25
Q

Post radiation sialadenitis

A

If any of the salivary glands is included in the field of therapeutic radiation; irreversible destruction of acini and replacement by fibrous tissue can result.

Serous acini are severely affected while mucous acini are more resistant; the ductal cells

tend to persist longer. As levels of radiation increase → decrease of salivary of salivary flow (xerostomia),