Salivary Gland Tumor Flashcards

1
Q

Non epi sg tumor is even …

A
Neurofibroma
Hemangioma
Lymphangioma
50% of children 
5% of adults
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2
Q

Salivary tumors In adults and children

A

Adults

• Salivary gland tumors occur primarily in older adults

Females more commonly affected, except Warthin’s tumor and high-grade

carcinomas Epithelial (80%) tumors

predominate Benign neoplasms are more common (75%) among the

epithelial tumors

The smaller the salivary gland, the higher the proportion of malignant tumors:

parotid gland (15-32%); submandibular gland (41-45%);

sublingual gland (70-90%); minor salivary gland (>50%)

Children (under age of 18)

Rare in general; only 1.7-3% of all salivary tumors occur in children

In infants, mesenchymal tumors (hemangioma and lymphangioma) are the commonest tumors; in older children, epithelial tumors predominate

F Malignant neoplasms are common (60%) among the epithelial tumors

Most malignant tumors in children are low grade, hence tumor mortality and morbidity are low

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3
Q

Macroscopic picture of pleomorphic adenoma

A
  • oval or round nodular or smooth

- capsule is not continuous and tissues may be continuous with surrounding sg tissue

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4
Q

Pleomorphic adenoma size and site

A
  • smaller if minor sg
  • large if major
  • palate
  • tail of patotid
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5
Q

Wharthin tumor names

A

Papillary cyst adenoma lymphomatosum

Adenolymphoma

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6
Q

Prevalence and factors related to warthin tumors

A

2nd most common sg benign tumor

Related to smoking

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7
Q

Warthin tumors special signes

A

3 to 4cm
May be bilateral
Fluctuant

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8
Q

Macro pic of warthin

A
  • mucoid or gelatinous or chocolate
  • well capsulated
  • round oval nodular smooth
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9
Q

Histology of warthin

A
--Epi--
..2 layers
..Inner col palisades with round to oval nucleus vesicular  and granular eosinophil cytoplasm
Between them goblet cells
..outer flat or cuboidal cells

–lymphoid–
..Reticular lymphatic aggregates with germinal centers
..convoluted

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10
Q

Site of warthin vs oncocytoma

A

Both in parotid and minot sg
Onco is in buccal and palate
And make up 1% of parotid gland tumors

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11
Q

Oncocytoma factors

A

Age
Rarely before 60y
20% of patients associated with radiation exposure

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12
Q

Histology of oncocytoma

A
-well capsulated
Ct septa separating lobules
Large round or polygonal cells
Central nucleus
Esinophylic Granular cytoplasm of atypical mitocondria
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13
Q

Cellular origin of the 3 malig sg tumors

A

Acc—myoepi cells and intercalated ducts cells

Mec—totipotent cells of excretory duct that has potential for transformation into columnar squamous and mucous cells

Acinic– serous acini cells

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14
Q

Origin of intra-osseous tumors (central MEC

A

:

  1. Salivary tissue entrapped within the mandible. 2. Entrapped oral epithelium → mucous metaplasia.
  2. Odontogenic cysts (lining of dentigerous cyst).
  3. Lining of maxillary sinus
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15
Q

Central malignant s g tumors

A

Acinic

MEC

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16
Q

Most common malig. S g tumor in sub mand gland

A

Adenoid C.C.

17
Q

Site of acinic c c

A

Central–
..minor >major
Peripheral–
..mand >max

18
Q

Site of mec

A

Central
..mand pm and m more than max

Peri.
..minor than major
Lower lip

19
Q

Adenoids cystic site

A

Minor more than major

  • parotid >submandibular >sub lingual
  • most common malig tumor of sub m gland
20
Q

Clinical of both acinic cell and mec

A

Low grade tumor
Same as pleomorphic

High grade tumor
Painful,rapidly infiltrative leading
to fixation and ulceration

21
Q

Clinical of ACC

A
  1. Slow growth, painful mass.
  2. Ulceration of the oral mucosa may be seen. 3. Fixation to the deeper structures
  3. Neurological symptoms →→ as turnor spreads along nerve pathway then numbness.

sensation then cut of nerve leading to loss of sensation or facial palsy.

  1. Bone may be involved, as it grows through marrow spaces at 1” without destroying the trabeculae then in late stage cause destruction of bone trabecula.
22
Q

Clinical of acc

A
  1. Slow growth, painful mass.
  2. Ulceration of the oral mucosa may be seen. 3. Fixation to the deeper structures.

Low grade tumor

High grade tumor

  1. Similar

a 1 Painful,

rapidly infiltrative leading

growing and to fixation

  1. Neurological symptoms →→ as turnor spreads along nerve pathway then numbness

pleomorphic

adenoma.

ulceration.

sensation then cut of nerve leading to loss of sensation or facial palsy.

  1. Bone may be involved, as it grows through marrow spaces at 1” without destroying the trabeculae then in late stage cause destruction of bone trabecula.
23
Q

X ray of 3 malig sg tumor

A

All ill defined multi locular

Except acc has no xray in early lesion

24
Q

Capsule of 3 malig sg tumor

A

Acc —not
Mec—partual or un –also cystic or solid

Acinic cell – partially cap or not