6. Pathology of Connective and Submucosal Tissues Flashcards

(35 cards)

1
Q

Two types of connective tissue

• Connective tissue proper
– ____ connective tissue
– ____ connective tissue

 Specialized connective tissue
– \_\_\_\_ connective tissue supporting lymphoid organs
– Bone
– \_\_\_\_
– Ligaments
– \_\_\_\_
– Blood
	• Proper
		○ Oral mucosa
		○ Skin
	• Specialized
		○ Blood
		○ Bone
		○ Cartilage
		○ Fat
A
loose
dense
reticular
cartilage
adipose
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2
Q
Cellular components
• Fixed cells develop and remain in place
– \_\_\_\_
– Adipocytes
– \_\_\_\_
– Mast cells
– \_\_\_\_
	• Resident within the CT
	• Fibroblasts
		○ Give rise to collagen and reticular fibers
	• Adipocytes
		○ Give rise to fat
	• Pericytes
		○ Like smooth muscle cells > contractile
		○ Found wrapped around \_\_\_\_
	• Mast cells
		○ Immune
	• Macrophages
		○ Resident and transient cells
		○ Live in \_\_\_\_ worlds
	• Pathology from mast/macro's > pathology is \_\_\_\_ in nature
A

fibroblasts
pericytes
macrophages

capillaries
both
hematologic

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3
Q
• Reactive lesions
		○ \_\_\_\_
		○ Peripheral ossifying
		○ \_\_\_\_
		○ Most common occurring on the gingival tissues
			§ Of the 3, only one on gingiva or elsewhere > \_\_\_\_
				□ Reddish blue looking
				□ Not tumors
		○ Reacting to chronic irritation
A

pyogenic granuloma
peripheral giant cell
pyogenic granuloma

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4
Q
Choristoma
• Normal tissue found in an \_\_\_\_ location
• Most found in \_\_\_\_
– Posterior third near \_\_\_\_
• Usually \_\_\_\_ and/or osseous
• Other reactive lesions that may look like tumors but not \_\_\_\_
• Most commonly presenting lesion on posterior dorsum tongue close to the foramen cecum (embryonic structure through tongue arises during embryogenesis)
• Not a reactive lesion, it's not a tumor > \_\_\_\_ lesion
• Composed of bone and/or cartilage
	○ The bone/cartilage looks normal except it's not occurring in the \_\_\_\_ place
A
abnormal
tongue
foramen cecum
cartilaginous
developmental
normal
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5
Q

Mr. Potato Head sitting on a dining room table = ____

Scrambled Mr. Potato Head in a child’s bedroom = ____

• Hamartoma is also developmental, looks like tumor/mass except it's a lesion that’s composed of histologically normal tissue arranged \_\_\_\_ but where it's supposed to be actually located
	○ Mixed up, but sitting in kid's bedroom where it should be found
A

choristoma
hamartoma
abnormally

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6
Q

Inflammatory papillary hyperplasia of the palate

• Etiologic factors
– Ill–fitting \_\_\_\_
– Denture hygiene
– Dentures \_\_\_\_ hours / day – \_\_\_\_??
• Also known as palatal papillomatosis
• Choristoma is not reactive it's developmental
• These following lesions are all caused by dentures
	○ Poorly fitting dentures
	○ Or poorly maintained dentures
	○ Patients who keep the dentures in the oral cavity for long periods of time
• IPHP and PP are synonomyous
• They're not papillomas
	○ A papilloma is a true benign epithelial \_\_\_\_
	○ Which may be caused by \_\_\_\_
	○ Lesions look \_\_\_\_ and wart-like
	○ Only occur on the \_\_\_\_ underneath the denture base
• Associated with candida
	○ Question whether it's predisposing or it's an opportunistic infection
	○ Seen superinfecting the papillary growths
A
denture
24
candida albicans
tumor
HPV
papillomatous
hard palate
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7
Q

Inflammatory papillary hyperplasia of the palate

• Microscopically:
○ ____ appearance
§ They look like fingers, up-and-down lumpy-bumpy > reflects it clinically
• Therapy:
○ If robust (in the picture) > surgeon will reline the denture, apply an ____ to the denture base to reduce the candidiasis with the hope that these two steps will resolve the lesion
○ If it doesn’t > surgeon will take a diamond acrylic ____ and drill the palate and then will reline the denture and allow to resolve
○ Cannot ____ this surgically because the palate is so thin

A

papilloma
antifungal
bur
excise

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8
Q

Palatal papillomatosis
• Treatment
– Denture reline / ____
– Topical anti-____ medication – Surgical ____

A

refrabication
fungal
excision

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9
Q

Epulis fissuratum

  • Due to irritation from denture ____
  • Develops within ____(s)
  • Epithelial and fibrous ____• Reactive pathology
    • The vestibules are affected where the denture flange is sitting
    ○ The edge of the denture will chronically irriate the surrounding mucosa > overgrowth of tissue on ____ sides of the flange (lingual and facial) > a fissure is formed
    • The tissue is reactive > epitehlial and ____ hyperplasia
    ○ But looks like a tumor clinically
A
flange
vestibules
hyperplasia
both
fibrous
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10
Q

Epulis fissuratum
Squamous cell carcinoma mimicking epulis fissuratum

• Similar lesion
• \_\_\_\_ in the center and flap of tissue on both sides of the fissure
• Both patients had ill-fitting \_\_\_\_
	○ One has EF and one had SCC
A

fissure

denture

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11
Q

Denture-associated pathologies

  1. Inflammatory papillary ____ of the palate
  2. Epulis ____
  3. ____ fibroma
  4. Osseous and ____ (Cutright lesion)• All denture pathologies become more commonly in ____, older patients
    ○ Assume that estrogen and progest play a role in pathogenesis
    § Like in ____pathogenesis
    • Leaf fibroma
    ○ ____ mass
    ○ ____ lesion that flattened due to pressure of denture over time
    ○ Clip the fibroma off and one stitch to close up the wound
    ○ Microscopically: expression of epithelial and fibrous ____
    • Small mass on gum > thought one of the three P’s > was in fact a osseous and chondromatous metaplasia
    ○ Not hyperplastic > ____: one normal cell type replaced with another normal cell type
    § Seeing CT becoming metaplastic bone and ____
    § Specifically on the ____
    • Mass-forming in appearance but not tumors
A

hyperplasia
fissuratum
leaf
chondromatous metaplasia

female
pyogenic granuloma
pedunculated
reactive

hyperplasia
cartilage
alveolar ridge

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12
Q

Origin of soft tissue neoplasms

• Any \_\_\_\_ type can give rise to a tumor
– Epithelium
– Fibrous
– Vascular
– Nerve
– Smooth muscle
– Skeletal muscle
– Fat
– Salivary gland
– Bone
– Cartilage

Assess which tissue types are most ____ in the area in question – include those diagnoses in the differential diagnosis

A

tissue

abundant

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13
Q
Lipoma
• \_\_\_\_ decades
• Soft, \_\_\_\_ consistency
– Yellowish color
• Usually arise in areas of \_\_\_\_ – Buccal mucosa, vestibules
• Vascular pathologies
	○ May appear clinically pigmented, and may be confused with \_\_\_\_ or \_\_\_\_
• These tumors will not be red or blue, and will not have coloration
• May all look somewhat alike clinically but derived from different cell types

Lipoma
• Benign tumor of fat
○ ____, floor of mouth, vestibules, buccal mucosa
○ Won’t occur on the ____ (no fat here); not the dorsum tongue
○ Does not correlate with ____; if you gain weight > will increase in size, but once you lose the weight it won’t ____ in size
• Occurs in older age group
• Has a doughy feel when palpated
○ Yellowish color - fat is yellow
• Indication you’re dealing with lipoma > rising of fat tissue to surface in ____, all other tissues not fat based will drop to the bottom of the bottle
• ____ completely in order to treat

A

5th-7th
doughy
fat

nevi
melanoma
ventral tongue
hard palate
weight
reduce
formadelhyde
excise
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14
Q

Neural origin
• Neurofibroma
– ____

• Schwannoma
– ____

• Granular cell tumor
– ____

• Mucosal neuroma
– ____

Schwann cells
– Form ____ and unmyelinated axon sheaths
– Located only in ____ nervous system

• Nerve cells can give rise to various tumors
• Periphery: schwann cells
	○ Myelinating cells that myelinate axons in PNS and not the CNS (\_\_\_\_)
• NF, schwannoma and GCT are thought to be derived from \_\_\_\_ cells
A

neurofibromatosis type I
neurofibromatosis type II
congenital epulis
multiple endocrine neoplasia type 3

myelinated
peripheral
oligodendrocytes
schwann

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15
Q

Neurofibroma
Small, ____-surfaced
Usually ____
____ excision

• Most commonly occurring benign tumor of \_\_\_\_ tissue
• Nothing distinctive clinically
	○ Could be a \_\_\_\_ cyst, maybe a fibroma (reactive lesion)
• \_\_\_\_ excision is more than adequate for treatment
	○ Only upon biopsy you'll know what you're dealing with \_\_\_\_
A
smooth
asymptomatic
simple
nerve
lymphoepi
simple
microscopically
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16
Q

Schwannoma / Neurilemmoma

  • Derived from ____ cells
  • ____ gene mutation• Has a characteristically occurring gene mutation > sporadic
    ○ Merlin
    § Chromosome ____
    § When mutated > gives rise to a schwannoma
    § Mutated in germ line > multiple schwannomas occurring ____ the body and other complications as well
    § Non-germline > formation of ____ lesion
    • Not descriptive ____
    ○ Only upon microscopy will it be revealed
    • Slow growing, and will grow if left untreated
A
schwann
merlin
22
throughout
one
clinically
17
Q

Histopathology

• \_\_\_\_
• Antoni A
– Cellular areas composed of \_\_\_\_ cells
– \_\_\_\_ nuclei around central, acellular eosinophilic material (\_\_\_\_ body)
• Antoni B
– Less \_\_\_\_ areas
• Histology is \_\_\_\_ for this tumor
• Encapsulated
	○ Surrounded by fibrous capsule
	○ Well defined mass
• Microscopically:
	○ Well defined
	○ Antoni A tissue (pathognomonic for this tumor)
		§ Have tumor cells (schwann cells) where the nuclei are arranged in a \_\_\_\_ pattern > palisading
		§ Another packet of cells that are arranged in a parallel pattern
		§ In between the two packets > microscopically looks \_\_\_\_
			□ \_\_\_\_ processes of the cells intermingling with one another
		§ Collectively the whole structure is called a verocay body
	○ Antoni B tissue
		§ \_\_\_\_ arranged tissue
• Remove tumor in entirety: \_\_\_\_ and curative
A
encapsulated
schwann
palisading
verocay
cellular
pathognomonic
palisading
pink
cytoplasmic
randomly
diagnostic
18
Q

Granular cell tumor
• F : M -> ____ : 1
• >80% in ____ cavity
– Usually ____ tongue

• Benign nerve tumor > granular cell tumor
	○ Female predilection
• Can occur anywhere in the body
	○ Of all possible anatomic site, the most common is the \_\_\_\_ tongue > don't take on distinctive appearance
	○ Mass on the dorsum tongue > should think of \_\_\_\_
• Distinctive histology:
	○ Granular cell tumor > tumor cells have a very \_\_\_\_ cytoplasm
		§ Like salt and pepper
	○ How to know nerve in origin > cytokeratin are expressed in epithelial cells, but nerve cells express \_\_\_\_
		§ Stain the tumor with S100 > will light up with this ab > implying it's derived from a nerve cell origin
	○ Overlying epithelium over these tumors > peculiar pattern > almost looks like a SCC overlying the tumors macroscopically
		§ Not cancer!
		§ \_\_\_\_
			□ \_\_\_\_ change to overlying epithelium that makes think invading SCC
				® Patients are commonly \_\_\_\_ and tongues are removed
• Excise the tumor in its entirety
A

2
oral
dorsum

dorsum
GCT
grainy
S100
pseudoepitheliomatous hyperplasia
reactive
misdiagnosed
19
Q
Histopathology
• Cells with \_\_\_\_ cytoplasm
• Tumor cells express \_\_\_\_ protein
• May show pseudoepitheliomatous hyperplasia
– May be mistaken for \_\_\_\_
A

granular
S100
squamous cell carcinoma

20
Q
Congenital epulis
• Unknown \_\_\_\_
• F:M -> \_\_\_\_:1
• Appears at \_\_\_\_ or in utero (not after)
• Exclusively on \_\_\_\_
• S100 \_\_\_\_
• Similarly appearing tumor microscopically that only occurs in newborn infants
	○ Not \_\_\_\_ in origin, but it's a soft tissue tumor
• Not a nerve tumor, but looks identical to the GCT
	○ Context is in newborn
	○ Tumor that occurs only on alveolar
	○ Always occurs anteriorly
	○ And sometimes occurs on both the top and the bottom
• More striking female predilection
• These tumors do not stain with S100
• Unknown which \_\_\_\_ give rise to these tumors
• On high power has a \_\_\_\_ granular appearance
• Never evidence of \_\_\_\_
	○ Only difference bt GCT
• Not thinking \_\_\_\_ nodules, but they are both newborns
A
pathogenesis
9
birth
alveolar ridge
negative
neural
cells
grainy
psuedoepi hyperplasia
bohn's
21
Q

Muscle tissue

Striated muscle
Skeletal muscle
– ____
– Attached to bone and other tissues

Non-striated muscle
• Smooth muscle – \_\_\_\_
– Walls of hollow structures
• Blood vessels
• Gastrointestinal tract
• Urinary bladder
• Airways
A

voluntary

involuntary

22
Q

Leiomyoma
• ____ muscle tumor
• Vascular leiomyoma mimics ____

• Benign smooth muscle tumor
	○ Nomenclature is not intuitive
• Take one two appearances:
	○ (1) Not \_\_\_\_
	○ (2) Vascular leiomyoma > mimic \_\_\_\_ clinically (or a hematoma, or a pyogenic granuloma)
		§ Not a vascular tumor (the caps aren't becoming neoplastic and are proliferating), the smooth muscle around the BV is proliferating
		§ Within the center of the tumor is a \_\_\_\_ > gives rise to reddish color of tumor
			□ Surrounding is the \_\_\_\_ tissue
			□ Staining with a muscle protein ab > \_\_\_\_ (expressed by muscle cells)
				® Center isn't staining (the BV itself)

• Benign skeletal muscle pathology is very \_\_\_\_
• Of all tissue types that give rise to tumors of the body, the only tissue where the \_\_\_\_ is more common than benign tissue is the skeletal muscle
	○ Will find a malignant version more commonly than a benign neoplastic version; the only case
	○ Benign skeletal muscle > \_\_\_\_
A
smooth
hemangioma
descriptive
hemangioma
BV
muscle
desmin
rare
malignancy
rhabdomyoma
23
Q

Cowden syndrome

Autosomal ____
– High ____, variable expressivity

____ mutation

Cutaneous lesions
– ____
– Palmoplantar keratosis
– ____ fibromas

• Caused by mutation on chromosome \_\_\_\_ in germline of gene called PTEN
• Characterized by primarily a skin as well as tumors of skin and oral lesions
• In the \_\_\_\_ > the lesions are hamartomas and tumors
	○ True tumors of skin > \_\_\_\_ fibromas
		§ Very densely collagenized fibromas in a distinctive histologic pattern
• Palmoplantar keratosis
	○ \_\_\_\_ (not pathognomonic)
	○ Differentiates it from \_\_\_\_ (hands and feet are involved)
	○ Wouldn not differentiate cowden from pachnic because they're both characterized by this manifestation
• Prone to developing fibromas
	○ Not neoplastic; numerous fibromas
	○ This is \_\_\_\_ for cowden syndrome
		§ \_\_\_\_, multifocal fibromas in the oral cavity
• Biopsy more than \_\_\_\_ lesion to get the diagnosis
• Patients may have breast cancer in families, ovarian, thyroid and GI cancer
	○ Give rise to genetic \_\_\_\_
• Nothing you can do - will live like this unless it gets so bad they cannot live (rare)
	○ Thing to worry about is the development of significant \_\_\_\_ they may develop (either benign or malignant)
A

dominant
penetrance
PTEN

hamartomas
sclerotic
10

skin
sclerotic
pachynictic congenita
white sponge nevus
pathognomonic
diffuse
one
cancers
tumors
24
Q

Cowden syndrome

Oral lesions
– ____

Benign and malignant tumors
– \_\_\_\_
– Thyroid
– \_\_\_\_
– Female genitourinary tract
A

fibromas
breast
GI

25
Neurofibromatosis Type 1 von Recklinghausen’s disease Autosomal ____ – High penetrance, variable expressivity Mutation in ____ gene Increased risk for ____ • Charcaterized by a germline mutation in ____ called neurofibromin ○ Formation of multiple ____ § Each papule, nodule and mass represents a distinct neurofibroma § Lots of tumors - the risk is ____ > more likely tumors become malignant □ At risk for cancer derived from nerve tissue > ____ (not carcinoma - epithelail cancer); sarcoma implies cancer of ____ elements • ____ neurofibromas - pathognomonic for NFT1 ○ Plexiform NF > sack hanging off of skin
dominant neurofibromin neurofibrosarcoma ``` chr21 neurofibromas additive neurofibrosarcoma CT two ```
26
Neurofibromatosis Type 1 ``` Diagnostic criteria • ____ or more café-au-lait macules • ≥ ____ neurofibromas or ____ neurofibroma • Freckling in ____ region – Crowe’s sign • ≥ 2 ____ nodule ``` • Café-au-lait spots ○ Pigmented lesions on the skin ○ 6+ = pathognomonic ○ These are ____ • Tumors feels like a bag of marbles • Smaller freckling in armpits and in groin (axillary) > crowe's sign = pathognomonic • ____ spots in eyes > Lisch nodules = pathognomonic • Treatment: ○ Don't treat them ○ If ____ you treat them ○ Functional deficit you treat, or treat the cancer if they develop ○ Cannot excise all the tumors § Risk of treatment is ____ than leaving these untreated
``` 6 2 plexiform axillary lisch ``` macular brown symptomatic worse
27
Neurofibromatosis Type 2 • Autosomal ____ • ____ gene mutation • ____ NOT neurofibromas • Characterized by Merlin mutations in the germline ○ Same gene that gives rise to schwannoma • Prone to developing multiple schwannoma, not neurofibromas! • When occurs single lesion, when occur in brain in area of ____ nerve ○ Pathognomonic - a single acoustic neuroma, as long has another element on list of diagnosis ○ Acoustic neuroma (not a neurofibroma - it's a schwannoma)
dominant merlin schwannomas acoustic
28
Neurofibromatosis Type 2 • Diagnostic criteria – Bilateral ____ schwannomas OR – Family history AND either ____ vestibular schwannoma OR two of the following • ____, meningioma, ____, cataract – OR ____ vestibular schwannoma AND one of the above • Bilateral acoustic neuromas > pathogonomic on it's own • One single acoustic neruoma and one on the skin • Acoustic neuroma and father has known sydnrome • Prone to other tumors > meningioma and glioma ○ Other types of brain tumors • Will not treat patients unless producing ____ impingement and deafness ○ Cannot chase bc the whole body contains this mutation
``` vestibular unilateral schwannoma glioma unilateral ``` nerve
29
Multiple endocrine neoplasia Type 3 (= Type 2B) • Autosomal ____ • Mutation in proto-oncogene ____ ``` • Multiple findings – ____ carcinoma – Pheochromocytoma – ____ neuromas – Marfanoid habitus ``` • Not caused by mutation in TSG ○ Cowden - PTEN, and merlin for NF are ____ ○ This disorder > proto-oncogene RET > chr ____ • Includes an array of tumors ○ Tumor in adrenal gland > ____ ○ Tumors in thyroid (malignant) > medullary thyroid carcinoma ○ Nodular lesions involving oral tissues § Look like cowdens, but are not fibromas § These nodules are ____ (can be seen microscopically) □ Diagnosed as mucosal neuromas ® Pathognomic for this syndrome (MEN type 3) ◊ MICROSCOPICALLY
dominant RET medullary thyroid multiple mucosal TSGs 10 pheochromocytoma fibromas
30
Mucosal neuromas (MEN type 3) • ____, tongue, commissures • Neuromas of ____, GI tract, bronchi • ____ histology • Occur in mucosal sites including the oral cavity ○ GI tract, eyes ○ First sign of disease may be rectal ____ • In photo > nodules on the commisures ○ Pathognomic for this disorder (MEN type 3) • Don't need to know microscopically • Composed of aberrant ____ tissue ○ This is pathognomonic for this tissue
``` lips eyes pathognomonic bleeding nerve ```
31
``` Malignant neoplasms Most common cancers in oral cavity – ____ – ____d neoplasms – ____a / Leukemia Soft tissue ____ are rare ``` • Many tumors are characterized by distinctive molecular changes > usually ____ • Can get malignant soft tissue tumor occuring in oral cavity > rhabdomyosarcoma (malignant skeletal muscle cancer) ○ Very ____!
``` squamous cell carcinoma salivary gland lymphoma malignancies translocations rare ```
32
Malignant soft tissue tumors • Any ____ type can give rise to cancer • Don’t let appearance of lesion fool you • Distinct molecular changes or etiologic agents characterize certain cancers • Do not let appearance of lesion sway you to benign vs malignant consideration • When cancers occur in oral cavity > ____ in origin (smooth, skeletal, fat) > characterized by distinctive molecular changes > chromosomal ____ • Sequenced Rhabdomyosarcoma > identified unique translocation that has a treatment specifically designed for that translocation > the translocation resulted in new fusion protein which triggers growth of the tumors ○ Specific treatment via ____ therapies! • Don't recognize clinically • Treated with a massive resection ○ Liposarcoma is ____ ○ Lipoma is ____ • Still see the same hallmarks of malignancy (pleo, hyperchrom, inc N:C, anaplasia, etc.)
``` tissue soft tissue translocation targeted benign malignant ```
33
Metastatic cancer • ≈ ____% of all oral cancers • May develop within ____ or soft tissue • Tumor cells travel through ____ or lymph • May represent first sign of ____ disease • Most common soft tissue site is ____ • Metastasize thorugh BV or lymphatic channels > go ____ sites • Tumors from other sites can go oral cavity ○ Most common site to go to oral cavity > ____ bone; and when go to the soft tissue most commonly they go to the ____ § Which is why you biopsy things that you think are pyogenic granulomas, peripheral ossifying or peripheral giant cell
``` 1 bone blood malignant gingiva ``` distant jaw gingiva
34
Breast adenocarcinoma * Lesions that mimiced the ____ * Both patients have metastatic breast cancer
three P's
35
Colon carcinoma Hepatocellular carcinoma Renal cell carcinoma • Abscess on RCT > colon cancer metastasis • Patient spending a year in prosthodontic therapy > during the procedure developed lesion > the dentist kept excising > recurred > a month later > dentist sent for biopsy as ____ cancer (metastatic) ○ Must analyze the tissue • Was ____ cancer metastasis to the oral cavity
liver | kidney