Soft Tissue Tumors Flashcards

1
Q

irritation / traumatic fibroma

A

most common “tumor” of the oral cavity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

common locations of irritation / traumatic fibroma

A

buccal mucosa > labial mucosa, tongue, gingiva

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

etiology of irritation / traumatic fibroma

A

happens along lines that teeth contact soft tissue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

clinical features of giant cell fibroma

A

-not associated with trauma or irritation
-asymptomatic, sessile, or pedunculate nodules
-younger age than fibroma (50% less than 30)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

location of giant cell fibroma

A

-mandibular gingiva, tongue, palate
-papillar surface common

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

microscopic appearance of giant cell fibroma

A

-thin, atrophic epithelium
-loose fibrous CT
-large multinuclear stellate fibroblasts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

retrocuspid papilla

A

anatomical structure, part of normal oral anatomy!

resembles giant cell fibroma histopathologically

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

location of retrocuspid papilla

A

-common (25-99%) in children and adolescents
-only 6-19% of adults

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

histology of retrocuspid papilla

A

resembles giant cell fibroma histopathologically

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

epulis fissuratum (other names)

A

inflammatory fibrous hyperplasia
denture injury tumor
denture epulis
denture granuloma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

etiology of epulis fissuratum

A

associated with the flange of an ill fitting denture

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

demographics of epulis fissuratum

A

-middle aged or older adults
-maxilla = mandible
-anterior&raquo_space; posterior
-F&raquo_space; M (2-3:1)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

clinical appearance of epulis fissuratum

A

-single or multiple folds in vestibular tissue (usually labial or buccal)
-denture flange fits in between the folds
-variable inflammation and ulceration
-variable size
-chronic inflammation and ulceration (due to chronic trauma)
-occasional osseous and chrondromatous metaplasia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

management of epulis fissuratum

A

surgical removal
denture reline / remake
good prongosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

another name ofr inflammatory papillary hyperplasia

A

denture papillomatosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

location of inflammatory papillary hyperplasia

A

-multiple papillary growths on hard palate
-usually asymptomatic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

etiology of inflammatory papillary hyperplasia

A

-ill fitting denture
-poor denture hygiene (contsant wear)
-mouth breathing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

treatment of inflammatory papillary hyperplasia

A
  1. surgical excision
  2. denture reline
  3. leave denture out at night
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

3 Ps of benign gingival mass

A

periperal ossifying fibroma
peripheral giant cell granuloma
pyogenic granuloma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

clinical features of peripheral ossifying fibroma

A

-thought to arise form the PDL
-gingival growth, young adults, anterior jaws, females, often ulcerated

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

histopathological features of peripheral ossifying fibroma

A

spindle cell proliferation with variable calcificaitons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

treatment of peripheral ossifying fibroma

A
  1. excision, removal of local irritants
  2. full thickness flap to remove
23
Q

rate of recurrence of peripheral ossifying fibroma

24
Q

clinical features of peripheral giant cell granuloma

A
  1. alveolar or gingival mass, adults (40-50)
  2. blush-red mass, may be ulcerated, may cause “cupping” of ulderlying bone
  3. soft consistencly
  4. arise from PDL space
25
histopathological features of perihperal giant cell granuloma
1. abundant multinucleate giant cells 2.marked hemorrhages -> hemosiderin 3. acute and chronic inflammation 4. occasional reactive bone or dystrophic calcification
26
treatment of peripheral giant cell granuloma
1. local surgical excision 2. aggressive SRP
27
rate of recurrence of peripheral giant cell granuloma
10-18%
28
clinical features of pyogenic granuloma
1. rapidly growing, painless, reddish mass 2. children and young adults 3. any body surface; bleeds easily 4. gingiva, lipds, tongue 5. frequently during prengancy
29
histopathological features of pyogenic granuloma
granulation tissue
30
treatment of pyogenic granuloma
excise remove irritants
31
rate of recurrence of pyogenic granuloma
15%
32
lipoma
benign tumor of adipose (fatty tissue)
33
features of lipoma
1. adult patients 2. slow growing, non-tender, soft, doughy, usually encapsulated 3. common in head and neck; occassionally found intraorally 4. yellow if clsoe to the surface 5. tend to float in formalin 6. demarcated or encapsulated collection of mature fat cells
34
treatment of lipoma
excisional biopsy no recurrence
35
traumatic neuroma
uncommon reaction to sectioning of a nerve (amputation neuroma)
36
clinical features of traumatic neuroma
1. smooth surfaced, dome shaped papules, usually less than 1cm 2. tongue, buccal vestibule (mental foramen region common affected) 3. may be tender on palpation
37
histology of traumatic neuroma
1. microscopically, a tangled mass of peripheral nerve fibers is seen 2. usually set in a collagenous background
38
management of traumatic neuroma
surgical excision -lack of sensation in supplied areas -revent resurrected ends from meeting
39
neurilemmoma / schwannoma
benign tumor of schwann cell origin (myelin)
40
clinical features of neurilemoma
1. most identified in adults 2. slow growing, solitary, encapsulated, fubbery-firm, nontender mass 3. 25-48% in head and neck including oral cavity 4. lips, tongue, buccal mucosa 5. may be seen within the mandible
41
histology of neurilemoma
1. well developed connective tissue capsule 2. benign proliferaiton of spindle shaped schwann cells 3. antoni a and antoni B patterns seen
42
management and prognosis of neurilemoma
conservative exision
43
neurofirboma
benign tumor of neural fibroblast origin -over 90% are solitary; remainder are multiple and associated with neurofibromatosis -soft dome shaped nontender superficial nodule affecting skin or mucosa -demarcated but encapsulated
44
neurofibromatosis
one of the most common autosomal genetic problems that affect humans -approximatley half are transmitted as autosomal dominant trait; other half appear to be new mutations
45
clinical features of neurofibromatosis
-highly variable gene expression -variety of manifestations, both cutaneous and oral -skin lesions -lisch nodules (benign pigmented nodule of iris) -oral lesions consist of neurofbiromas that may affect the tongue, gingiva, or bone -multiple comorbidities
46
skin lesiosn of neurofibromatosis
cafe aulait spots multiple neurofibromas axillary freckinling (crowe sign)
47
lisch nodules
benign pigmented nodules of iris
48
comorbidities of neurofibromatosis
hypertension CNS tumors macrocephaly mental defect seizures
49
malignant transformation of neurofibromatosis
-treatment consist of removing traumatized neurofibromas or disfiguring lesions -genetic counseling -decreased longevity -follow for potential malignant transofmraiotn -potential to beome malignant peripheral nerve sheath tumor
50
MEN
multiple endocrine neoplasia syndromes
51
MEN1
parathyroid, pancreatic tumors, phaeochromocytoma, pituitary tumors -ajority of tumors in people with MEN1 are benign -however, approximatley 1/3 pancreatic neuroendocrine tumors and mediastinal neuroendocrine tumors are malignant -all benign tumors
52
MEN2a
men1 and medullary carcinoma of thyroid
53
MEN2b
men 2a and neuromas
54
features of type 2b
autosomal dominant