Exam 3: Red Terms

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Last updated 5:26 PM on 7/30/26
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258 Terms

1
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What sex is Graves disease more common in? ***

women

<p>women</p>
2
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What happens to the thyroid in Graves disease? ***

diffuse thyroid enlargement

<p>diffuse thyroid enlargement</p>
3
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What happens to the eyes in Graves disease? ***

occular involvement - unique to graves disease:

-characteristic stare w/ eyelid retraction and lid lag

-exophthalmos (protrusion) due to accumulation of glycoasminoglycans in retro-orbital CT

<p>occular involvement - unique to graves disease:</p><p>-characteristic stare w/ eyelid retraction and lid lag</p><p>-exophthalmos (protrusion) due to accumulation of glycoasminoglycans in retro-orbital CT</p>
4
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What is a thyroid storm? ***

abrupt onset of severe hyperthyroidism w/ an inappropriate release of large amounts of thyroid hormone at one time

5
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What may a thyroid storm precipitated by? ***

stress (i.e. dental appt)

infection

psychologic trauma

<p>stress (i.e. dental appt)</p><p>infection</p><p>psychologic trauma</p>
6
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How does a thyroid storm present and how should it be treated? ***

-delirium, convulsions, elevated temp, tachycardia

-hospitalize immediately to prevent mortality

7
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What are laboratory findings of hyperthyroidism? ***

-elevated T4

-TSH depressed

<p>-elevated T4</p><p>-TSH depressed</p>
8
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What is parathyroid hormone secretion by the parathyroid glands stimulated vs suppressed by? ***

-stimulated by hypocalcemia & hyperphosphatemia

-suppressed by hypercalcemia & hypophosphatemia

<p>-stimulated by hypocalcemia &amp; hyperphosphatemia</p><p>-suppressed by hypercalcemia &amp; hypophosphatemia</p>
9
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What 2 compounds regulate calcium levels? ***

parathyroid hormone (PTH)

vitamin D

10
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What is a Chvostek Sign? ***

-oral manifestation of hypoparathyroidism

-twitching of upper lip when facial nerve is tapped just below zygomatic process

<p>-oral manifestation of hypoparathyroidism</p><p>-twitching of upper lip when facial nerve is tapped just below zygomatic process</p>
11
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What is a catchy saying for the clinical and radiographic features of hyperparathyroidism? ***

stones, bones, and abdominal groans

<p>stones, bones, and abdominal groans</p>
12
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What are "stones" as clinical and radiographic features of hyperparathyroidism? ***

-increased tendency to develop renal calculi due to elevated serum calcium

-metastatic calcifications of soft tissues including blood vessel walls, subcutaneous soft tissues, sclera, dura, and tissues around joints

<p>-increased tendency to develop renal calculi due to elevated serum calcium</p><p>-metastatic calcifications of soft tissues including blood vessel walls, subcutaneous soft tissues, sclera, dura, and tissues around joints</p>
13
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What are "bones" as clinical and radiographic features of hyperparathyroidism? ***

-variety of osseous changes

-early sign - subperiosteal resorption of phalanges of index and middle fingers

-osteoporosis

-chondrocalcinosis

-osteitis fibrosa cystica

<p>-variety of osseous changes</p><p>-early sign - subperiosteal resorption of phalanges of index and middle fingers</p><p>-osteoporosis</p><p>-chondrocalcinosis</p><p>-osteitis fibrosa cystica</p>
14
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What are oral manifestations of hyperparathyroidism? ***

-generalized loss of lamina dura

-brown tumor

-alteration in trabecular pattern

-decreased trabecular density + blurring of normal trabecular pattern -> ground glass appearance

<p>-generalized loss of lamina dura</p><p>-brown tumor</p><p>-alteration in trabecular pattern</p><p>-decreased trabecular density + blurring of normal trabecular pattern -&gt; ground glass appearance</p>
15
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What is a Brown Tumor? ***

-oral manifestation of hyperparathyroidism

-commonly affect mandible + clavicle, ribs, pelvis

-dark-red tissue color due to abundant hemorrhage and hemosiderin deposition

-well-demarcated uni or multi-locular radiolucencies

-usually multiple (may be solitary)

-long standing lesions may cause expansion

<p>-oral manifestation of hyperparathyroidism</p><p>-commonly affect mandible + clavicle, ribs, pelvis</p><p>-dark-red tissue color due to abundant hemorrhage and hemosiderin deposition</p><p>-well-demarcated uni or multi-locular radiolucencies</p><p>-usually multiple (may be solitary)</p><p>-long standing lesions may cause expansion</p>
16
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What is a brown tumor identical to histopathologically? ***

central giant cell granuloma

<p>central giant cell granuloma</p>
17
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What are "abdominal groans" as clinical and radiographic features of hyperparathyroidism? ***

pts develop duodenal ulcers

<p>pts develop duodenal ulcers</p>
18
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What bone disorder occurs in secondary hyperparathyroidism? ***

renal osteodystrophy

<p>renal osteodystrophy</p>
19
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How does renal osteodystrophy in secondary hyperparathyroidism present in the oral cavity? ***

-striking enlargement of the jaws

-ground glass appearance radiographically

<p>-striking enlargement of the jaws</p><p>-ground glass appearance radiographically</p>
20
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What is the most common cause of hypercortisolism? ***

prolonged corticosteroid therapy

<p>prolonged corticosteroid therapy</p>
21
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What are clinical features of hypercortisolism? ***

signs develop slowly:

-weight gain in central area of body; accumulation in dorsocervical spine region -> buffalo hump

-facial deposition -> moon facies

-red-purple abdominal striae

-hirsutism

-osteoporosis

-hypertension

-mood changes

-hyperglycemia w/ thirst and polyuria

-muscle wasting w/ weakness

<p>signs develop slowly:</p><p>-weight gain in central area of body; accumulation in dorsocervical spine region -&gt; buffalo hump</p><p>-facial deposition -&gt; moon facies</p><p>-red-purple abdominal striae</p><p>-hirsutism</p><p>-osteoporosis</p><p>-hypertension</p><p>-mood changes</p><p>-hyperglycemia w/ thirst and polyuria</p><p>-muscle wasting w/ weakness</p>
22
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What are 3 medical conditions that diabetes mellitus is the leading cause of for in the US? ***

-kidney failure

-lower limb amputations

-adult-onset blindness

23
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What are complications of diabetes mellitus? ***

microangiopathy:

-occlusion of small blood vessels -> peripheral vascular disease

-ischemia predisposes to infection (gangrene)

-amputation of lower limbs often required

-occlusion of coronary or carotid arteries and branches may lead to MI or stroke

-blindness

-kidney failure

<p>microangiopathy:</p><p>-occlusion of small blood vessels -&gt; peripheral vascular disease</p><p>-ischemia predisposes to infection (gangrene)</p><p>-amputation of lower limbs often required</p><p>-occlusion of coronary or carotid arteries and branches may lead to MI or stroke</p><p>-blindness</p><p>-kidney failure</p>
24
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What are oral manifestations in Diabetes Mellitus? ***

-usually Type 1

-progressive periodontal disease

-enlarged erythematous gingiva

-delayed healing

-diabetic sialadenosis (diffuse bilateral enlargement of parotid glands)

-increased risk for candidiasis

-mucormycosis

-xerostomia

<p>-usually Type 1</p><p>-progressive periodontal disease</p><p>-enlarged erythematous gingiva</p><p>-delayed healing</p><p>-diabetic sialadenosis (diffuse bilateral enlargement of parotid glands)</p><p>-increased risk for candidiasis</p><p>-mucormycosis</p><p>-xerostomia</p>
25
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What is insulin shock in Type 1 DM and how is it treated? ***

-carbohydrates not consumed after insulin injection -> blood glucose levels drop below 40 mg/dL -> insulin shock

-treated w/ sublingual dextrose paste, IV infusion of dextrose solution or injection of glucagon

26
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What may be the first presenting sign of hypophosphatasia? ***

premature loss of primary teeth

27
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What are 4 examples of systemic disorders with premature attachment loss? ***

-blood dyscrasias: agranulocytosis, cyclic neutropenia

-hypophosphatasia

-langerhans cell disease

28
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What are oral features of childhood hypophosphatasia? ***

-premature loss of primary teeth

-enlarged pulp chambers

<p>-premature loss of primary teeth</p><p>-enlarged pulp chambers</p>
29
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How is hypophosphatasia diagnosed? ***

-decreased levels of serum alkaline phosphatase

-increased amts of phosphoethanolamine in urine and blood (bc normally broken down by alp)

<p>-decreased levels of serum alkaline phosphatase</p><p>-increased amts of phosphoethanolamine in urine and blood (bc normally broken down by alp)</p>
30
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What are oral manifestations of Vitamin D-Resistant Rickets? ***

-large pulp chambers w/ pulp horns extending to DEJ

-cuspal enamel may be worn down by attrition causing pulpal exposure

<p>-large pulp chambers w/ pulp horns extending to DEJ</p><p>-cuspal enamel may be worn down by attrition causing pulpal exposure</p>
31
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What is ectodermal dysplasia? ***

-RARE inherited conditions in which 2 or more ectodermally derived anatomic structures fail to develop (skin, hair, nails, teeth, sweat glands)

-inherited in several genetic patterns

<p>-RARE inherited conditions in which 2 or more ectodermally derived anatomic structures fail to develop (skin, hair, nails, teeth, sweat glands)</p><p>-inherited in several genetic patterns</p>
32
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What are clinical features of hypohidrotic ectodermal dysplasia? ***

hypo triad: hypohidrosis (decreased sweat glands, heat intolerance), hypotrichosis (fine sparse hair), hypodontia w/ delayed eruption

-X-linked

-mid face hypoplasia

-dystrophic and brittle nails

-xerostomia

-fine periocular wrinkling

-sparse eyelashes and eyebrows

<p>hypo triad: hypohidrosis (decreased sweat glands, heat intolerance), hypotrichosis (fine sparse hair), hypodontia w/ delayed eruption</p><p>-X-linked</p><p>-mid face hypoplasia</p><p>-dystrophic and brittle nails</p><p>-xerostomia</p><p>-fine periocular wrinkling</p><p>-sparse eyelashes and eyebrows</p>
33
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How may teeth appear in ectodermal dysplasia? ***

-oligodontia

-conical crown forms

<p>-oligodontia</p><p>-conical crown forms</p>
34
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What is the significance of intraoral lesions in dyskeratosis congenita? ***

tongue and buccal mucosa bullae and erosions become leukoplakic lesions which are premalignant (1/3 become malignant)

<p>tongue and buccal mucosa bullae and erosions become leukoplakic lesions which are premalignant (1/3 become malignant)</p>
35
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What are hematologic problems in dyskeratosis congenita? ***

-aplastic anemia develops in 80% (bone marrow stops making blood cells)

-thrombocytopenia

<p>-aplastic anemia develops in 80% (bone marrow stops making blood cells)</p><p>-thrombocytopenia</p>
36
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What are 3 key cutaneous manifestations of tuberous sclerosis? ***

-facial angiofibromas

-shagreen patches

-ash-leaf spots

-also periungual fibromas

<p>-facial angiofibromas</p><p>-shagreen patches</p><p>-ash-leaf spots</p><p>-also periungual fibromas</p>
37
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How do facial angiofibromas appear in tuberous sclerosis? ***

multiple, smooth-surfaced papules primarily in nasolabial fold area

<p>multiple, smooth-surfaced papules primarily in nasolabial fold area</p>
38
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What are shagreen patches in tuberous sclerosis? ***

connective tissue hamartomas of the skin (benign, tumor-like malformation w/ abnormal mix of mature cells and tissues)

<p>connective tissue hamartomas of the skin (benign, tumor-like malformation w/ abnormal mix of mature cells and tissues)</p>
39
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What are Ash-leaf spots in tuberous sclerosis? ***

ovoid areas of hypopigmentation

<p>ovoid areas of hypopigmentation</p>
40
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What are oral manifestations of tuberous sclerosis? ***

-developmental enamel pitting on facial sapect of anterior dentition

-multiple fibrous papules predominately in anterior gingiva

-diffuse fibrous gingival hyperplasia (usually due to anti-seizure meds)

-+/- radiolucencies of jaws

<p>-developmental enamel pitting on facial sapect of anterior dentition</p><p>-multiple fibrous papules predominately in anterior gingiva</p><p>-diffuse fibrous gingival hyperplasia (usually due to anti-seizure meds)</p><p>-+/- radiolucencies of jaws</p>
41
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What is there an increased risk for in epidermolysis bulla? ***

cutaneous squamous cell carcinoma

42
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What is often the 1st sign of systemic sclerosis? ***

Raynaud phenomenon - vasoconstrictive event triggered by emotional stress or cold

<p>Raynaud phenomenon - vasoconstrictive event triggered by emotional stress or cold</p>
43
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What are oral manifestations of systemic sclerosis? ***

-microstomia due to collagen deposition on perioral tissues

-furrows radiating from mouth - "purse string"

-loss of attached gingiva

-dysphagia

-firm hypomobile tongue

-xerostomia

<p>-microstomia due to collagen deposition on perioral tissues</p><p>-furrows radiating from mouth - "purse string" </p><p>-loss of attached gingiva</p><p>-dysphagia</p><p>-firm hypomobile tongue</p><p>-xerostomia</p>
44
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What are radiographic features of systemic sclerosis? ***

-diffuse widening of periodontal ligament

-resorption of ramus, coronoid process, or condyle

<p>-diffuse widening of periodontal ligament</p><p>-resorption of ramus, coronoid process, or condyle</p>
45
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What do laboratory studies reveal for diagnosis of systemic sclerosis? ***

anticentromere antibodies or anti-topoisomerase I antibodies

<p>anticentromere antibodies or anti-topoisomerase I antibodies</p>
46
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What is mucopolysaccharidosis? ***

deficiency of lysosomal enzymes needed to degrade glycosaminoglycans, an intercellular substance, leading to accumulation of substances such as heparan, dermatan, keratan, and chondroitin sulfate in tissues

<p>deficiency of lysosomal enzymes needed to degrade glycosaminoglycans, an intercellular substance, leading to accumulation of substances such as heparan, dermatan, keratan, and chondroitin sulfate in tissues</p>
47
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What are clinical features of mucopolysaccaridosis? ***

-cloudy degeneration of the cornea may lead to blindness

-vary depending on specific syndrome

-some degree of intellectual disability

-coarse facial features w/ heavy brow ridges

-skeletal changes including stiff joints

<p>-cloudy degeneration of the cornea may lead to blindness</p><p>-vary depending on specific syndrome</p><p>-some degree of intellectual disability</p><p>-coarse facial features w/ heavy brow ridges</p><p>-skeletal changes including stiff joints</p>
48
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What are intraoral manifestations of mucopolysaccaridosis? ***

-macroglossia

-gingival hyperplasia, esp anterior regions

<p>-macroglossia</p><p>-gingival hyperplasia, esp anterior regions</p>
49
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What is lacking in those with lipid reticuloendotheliosies and what does this lead to? ***

lack enzymes neccessary for processing specific lipids -> accumulation of lipids within a variety of cells

50
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What is the most common reticuloendothelioses? ***

Gaucher disease

<p>Gaucher disease</p>
51
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How do long bones appear in Gaucher Disease? ***

erlenmeyer flask deformities of long bone

<p>erlenmeyer flask deformities of long bone</p>
52
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What are oral manifestations of Gaucher Disease? ***

-ill-defined radiolucencies of the jaws

-walls of mandibular canal may be obliterated

-decreased salivary flow

-increased bleeding tendency

-increased risk of post-op infection

<p>-ill-defined radiolucencies of the jaws</p><p>-walls of mandibular canal may be obliterated</p><p>-decreased salivary flow</p><p>-increased bleeding tendency</p><p>-increased risk of post-op infection</p>
53
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What are those with Gaucher disease at an increased risk for? ***

hematologic malignancies

<p>hematologic malignancies</p>
54
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What is a key feature found in Types A and C of Niemann-Pick Disease but not Type B? ***

Types A and C = neuronopathic features

Type B = visceral involvement only

<p>Types A and C = neuronopathic features</p><p>Type B = visceral involvement only</p>
55
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What are neuronopathic features of Types A and C of Niemann-Pick Disease? ***

-psychomotor impairment

-dementia

-spasticity

-hepatosplenomegaly

-death during 1st 2 decades

56
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What occurs in Lipoid Proteinosis? ***

-rare autosomal recessive; mutation of ECM1 gene which encodes glycoprotein ECM protein 1

-deposition of waxy material in the dermis and submucosal connctive tissue

<p>-rare autosomal recessive; mutation of ECM1 gene which encodes glycoprotein ECM protein 1</p><p>-deposition of waxy material in the dermis and submucosal connctive tissue</p>
57
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What are oral manifestations of lipoid proteinosis? ***

-tongue, labial mucosa, and buccal mucosa: nodular, diffusely enlarged and thickened due to infiltration

-dorsal papillae destroyed -> smooth appearance of tongue

-tongue may become bound to floor of mouth

<p>-tongue, labial mucosa, and buccal mucosa: nodular, diffusely enlarged and thickened due to infiltration</p><p>-dorsal papillae destroyed -&gt; smooth appearance of tongue</p><p>-tongue may become bound to floor of mouth</p>
58
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What is jaundice caused by? ***

-excess bilirubin in the bloodstream -> yellowish discoloration of skin and mucosa

-increased bilirubin production or impaired liver fx

<p>-excess bilirubin in the bloodstream -&gt; yellowish discoloration of skin and mucosa</p><p>-increased bilirubin production or impaired liver fx</p>
59
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What 2 factors are associated with increased serum levels of bilirubin? ***

1. increased production of bilirubin

2. impaired liver function

60
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How does jaundice appear? ***

-diffuse uniform yellowish discoloration of skin and mucosa

-sclera, lingual frenum, soft palate

<p>-diffuse uniform yellowish discoloration of skin and mucosa </p><p>-sclera, lingual frenum, soft palate</p>
61
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What is amyloidosis characterized by? ***

Deposition of misfolded extracellular proteins (amyloid) in β-pleated sheet configuration leading to tissue and organ dysfunction

<p>Deposition of misfolded extracellular proteins (amyloid) in β-pleated sheet configuration leading to tissue and organ dysfunction</p>
62
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How may organ-limited amyloidosis present as? ***

amyloid nodule - solitary, asymptomatic submucosal deposit

<p>amyloid nodule - solitary, asymptomatic submucosal deposit</p>
63
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What is the etiology of most cases of primary and myeloma-associated types of amyloidosis? ***

most cases idiopathic

<p>most cases idiopathic</p>
64
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What are 15% of primary and myeloma-associated types of amyloidosis associated with? ***

myeloma (cancer of plasma cells)

<p>myeloma (cancer of plasma cells)</p>
65
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What are oral manifestations of primary and myeloma-associated types of amyloidosis? ***

-macroglossia - diffuse or nodular enlargement

-may show ulceration or submucosal hemorrhage

-rare xerostomia

<p>-macroglossia - diffuse or nodular enlargement</p><p>-may show ulceration or submucosal hemorrhage</p><p>-rare xerostomia</p>
66
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What does secondary amyloidosis develop as a result of? ***

-result of chronic inflammatory process (AA - cleavage fragments of circulating acute-phase reactant protein)

-causes: sarcoidosis, tuberculosis, osteomyelitis

-liver, kidney spleen, adrenal involvement (heart spared)

-rare in developed countries

<p>-result of chronic inflammatory process (AA - cleavage fragments of circulating acute-phase reactant protein) </p><p>-causes: sarcoidosis, tuberculosis, osteomyelitis</p><p>-liver, kidney spleen, adrenal involvement (heart spared)</p><p>-rare in developed countries</p>
67
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What is the histopathology of amyloidosis? ***

-extracellular deposition in the submucosal CT of an amorphous, eosinophilic material

-stains positively for congo red and appears apple-green on birefringence

<p>-extracellular deposition in the submucosal CT of an amorphous, eosinophilic material</p><p>-stains positively for congo red and appears apple-green on birefringence</p>
68
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What are clinical features of Vitamin A Deficiency? ***

-adult: night blindness, dryness of skin and conjuctiva

-infancy: blindness

<p>-adult: night blindness, dryness of skin and conjuctiva</p><p>-infancy: blindness</p>
69
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What population is beri-beri rare vs common in? ***

rare in western world except in alcoholics

may be seen after gastric bypass

<p>rare in western world except in alcoholics</p><p>may be seen after gastric bypass</p>
70
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What are oral manifestations of Vitamin B2 deficiency? ***

-glossitis

-angular cheilitis

-sore throat

-swelling and erythema of oral mucosa

-seborrheic dermatitis - skin

-+/- anemia

<p>-glossitis</p><p>-angular cheilitis</p><p>-sore throat</p><p>-swelling and erythema of oral mucosa</p><p>-seborrheic dermatitis - skin</p><p>-+/- anemia</p>
71
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What are clinical features of Vitamin B3 deficiency? ***

3 D's for B3:

-dermatitis (symmetric on sun-exposed areas)

-dementia

-diarrhea

<p>3 D's for B3:</p><p>-dermatitis (symmetric on sun-exposed areas)</p><p>-dementia</p><p>-diarrhea</p>
72
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What are oral manifestations of Vitamin B3 deficiency? ***

-stomatitis

-glossitis

-red and smooth tongue

<p>-stomatitis</p><p>-glossitis</p><p>-red and smooth tongue</p>
73
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What are oral manifestations of Vitamin B6 deficiency? ***

cheilitis and glossitis

<p>cheilitis and glossitis</p>
74
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What disease is caused by Vitamin C deficiency? ***

scurvy

<p>scurvy</p>
75
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What sx occur in Scurvy from vitamin C deficiency? ***

inadequate collagen synthesis (fragile vessels and tissues):

-widespread petechial hemorrhage and ecchymosis

-delayed wound healing

76
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What are oral manifestations of Scurvy from vitamin C deficiency? ***

scorbutic gingivitis:

-generalized gingival swelling w/ spontaneous hemorrhage

-ulceration

-tooth mobility

-periodontal disease

<p>scorbutic gingivitis:</p><p>-generalized gingival swelling w/ spontaneous hemorrhage</p><p>-ulceration</p><p>-tooth mobility</p><p>-periodontal disease</p>
77
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What disease is caused by Vitamin D deficiency? ***

rickets = infancy

osteomalacia = adults

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When does rickets from a Vitamin D Deficiency develop? ***

infancy

<p>infancy</p>
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What are clinical features of rickets from Vitamin D Deficiency? ***

-irritability

-growth impairment

-prominence of costochondral jxs (rachitis rosary)

-bowing of long bones due to poor mineralization

<p>-irritability</p><p>-growth impairment</p><p>-prominence of costochondral jxs (rachitis rosary)</p><p>-bowing of long bones due to poor mineralization</p>
80
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What is an oral manifestation of rickets from Vitamin D Deficiency? ***

hypomineralization of teeth:

-large pulp chambers of primary teeth

-pulp horns extend to DEJ

-taurodont-type pulp chamber

<p>hypomineralization of teeth:</p><p>-large pulp chambers of primary teeth</p><p>-pulp horns extend to DEJ</p><p>-taurodont-type pulp chamber</p>
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When does osteomalacia from a Vitamin D Deficiency develop? ***

adults

<p>adults</p>
82
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How does a cyst appear radiographically? ***

-radiolucent lesion bc bone replaced by soft tissue or air (less dense than bone)

-usually well-defined, +/- cortication, spherical, unilocular

<p>-radiolucent lesion bc bone replaced by soft tissue or air (less dense than bone)</p><p>-usually well-defined, +/- cortication, spherical, unilocular</p>
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What 5 components should be included in a radiographic description of a lesion? ***

-size

-borders (well-defined, corticated, punched out, poorly-defined)

-location (below or tooth bearing area of jaw, apex of non-vital tooth, lateral root, pericoronal)

-effect on neighboring teeth (displacement/root resorption, destruction surrounding intact roots)

-effect on cortical bone (no effect, expansion but cortex intact, destruction of cortex but no expansion)

<p>-size</p><p>-borders (well-defined, corticated, punched out, poorly-defined)</p><p>-location (below or tooth bearing area of jaw, apex of non-vital tooth, lateral root, pericoronal)</p><p>-effect on neighboring teeth (displacement/root resorption, destruction surrounding intact roots)</p><p>-effect on cortical bone (no effect, expansion but cortex intact, destruction of cortex but no expansion)</p>
84
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What does a corticated border look like and what does this typically indicate? ***

radiopaque line around border = slow growing, benign

<p>radiopaque line around border = slow growing, benign</p>
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What are the radiographic borders typically like of a cyst? ***

-well-defined and corticated

<p>-well-defined and corticated</p>
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What does a punched out border look like and what does this typically indicate? ***

-no border

-rapidly growing -> langerhans cell disease, multiple myeloma

<p>-no border</p><p>-rapidly growing -&gt; langerhans cell disease, multiple myeloma</p>
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What does a poorly defined border look like and what does this typically indicate? ***

-cannot draw boundaries

-think malignancy or infection (i.e. osteomyelitis)

<p>-cannot draw boundaries</p><p>-think malignancy or infection (i.e. osteomyelitis)</p>
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What lesions can be ruled out if the lesion if located below tooth bearing areas of the jaw? ***

rule out lesions associated w/ tooth development

i.e. stafne defect

<p>rule out lesions associated w/ tooth development</p><p>i.e. stafne defect</p>
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What are common lesions found in the tooth bearing areas of the jaw at the apex of a non-vital tooth? ***

periapical cyst

periapical granuloma

<p>periapical cyst</p><p>periapical granuloma</p>
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What are common lesions found in the tooth bearing areas of the jaw at the lateral root? ***

-lateral periodontal cyst

-periapical granuloma or cyst along lateral canal

-anything else (esp odontogenic keratocyst)

<p>-lateral periodontal cyst</p><p>-periapical granuloma or cyst along lateral canal</p><p>-anything else (esp odontogenic keratocyst)</p>
91
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What are common lesions found in the tooth bearing areas of the jaw in the pericoronal area? ***

-dental follicle

-dentigerous cyst

-other odontogenic neoplasm/cyst (adenomatoid odontogenic tumor)

<p>-dental follicle</p><p>-dentigerous cyst</p><p>-other odontogenic neoplasm/cyst (adenomatoid odontogenic tumor)</p>
92
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What does destruction of surrounding intact roots often indicate regarding the etiology of a lesion? ***

-"teeth floating in air"

-aggressive, rapidly growing lesion

<p>-"teeth floating in air"</p><p>-aggressive, rapidly growing lesion</p>
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What is the etiology and location of a lateral radicular cyst? ***

inflammatory cyst appearing along the lateral aspect of the root

<p>inflammatory cyst appearing along the lateral aspect of the root</p>
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What is the etiology and cause of a residual cyst? ***

peripapical inflammatory tissue that is not curetted at time of tooth removal

<p>peripapical inflammatory tissue that is not curetted at time of tooth removal</p>
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What are 3 examples of non-odontogenic developmental cysts? ***

nasopalatine duct cyst (most common one)

nasolabial cyst

median palatal cyst

<p>nasopalatine duct cyst (most common one)</p><p>nasolabial cyst</p><p>median palatal cyst</p>
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What is the most common non-odontogenic cyst of the oral cavity? ***

nasopalatine duct cyst

<p>nasopalatine duct cyst</p>
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What is a nasopalatine duct cyst called if only soft tissue is involved? ***

cyst of incisive papilla

<p>cyst of incisive papilla</p>
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What are radiographic features of a nasopalatine duct cyst? (size, shape, density, border, effect on neighboring teeth) ***

- >6 mm

-well-circumscribed radiolucency near midline of anterior maxilla

-round-oval w/ sclerotic border

-inverted pear or heart shaped

-+/- root divergence

<p>- &gt;6 mm</p><p>-well-circumscribed radiolucency near midline of anterior maxilla</p><p>-round-oval w/ sclerotic border</p><p>-inverted pear or heart shaped</p><p>-+/- root divergence</p>
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What is the most common developmental odontogenic cyst? ***

dentigerous cyst

<p>dentigerous cyst</p>
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Where can a dentigerous cyst ONLY be found? ***

crown of an unerupted tooth

attached at the CEJ

<p>crown of an unerupted tooth</p><p>attached at the CEJ</p>