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Pathophysiology X (100 Flash cards)

ACAPUN INSTITUTE Flashcards: PATHOLOGY Praxis Spanish 100 cards

Pathophysiology X (100 Flash cards)

Cards in this deck (100)

  1. 1OsteoporosisWeak bones
    Decrease in serum estrogen and calcium
    older females
    Osteoporosis
  2. 2OsteosarcomaNew bone is formed
    Pain, swelling, paristhesia
    PDL invasion results in uniform widening
    Mean age is 35; most common primary malignancy of bone in persons less than 25 yo
    mandible >Max
    Early lucency then opacity; trabaculae changes
    Osteosarcoma
  3. 3Paget's DiseaseAdults, older than 50
    Jaw: symmetrical enlargerment, dentures become too tight, diastemas and hypercemtosis may appear
    Jaw fracture and osteomyelitis are late complications secondary to bone sclerosis
    Lots of osteoblast and multinuc osteoclasts
    Reversal line with mosaic pattern
    Radographically: cotton wool appearance
    Paget's Disease
  4. 4Parulis (gum boil)Oral lesion characterized by a soft erythematous papule (red-yellow spot) that develops on the alveolar process in association with a non-vital tooth and accompanying dental abscess.
    Clinical evidence of a draining fistula
    Made up of inflamed granulation tissue.
    Parulis (gum boil)
  5. 5Pemphigus VulcarisAutoimmune
    *AB are directed against desmosomal protein*
    Manifests as multple, painful ulcers preceded by bullae that form w/in the eptithlium
    Coomon sites: lips, palate gingiva
    Positive Nikolsky sign
    Tx: corticosteroids or immunosuppresants
    Pemphigus Vulcaris
  6. 6Periapical Cemento-ossesous DysplasiaAppices of one or more mand anterior
    No sym, teeth are vital
    Mid aged black women
    Starts as circumscribed lucency, which gradually becomes opaque
    No tx
    Periapical Cemento-ossesous Dysplasia
  7. 7Periapical/radicular Cystnonvital tooth, at apex
    Most common odontogenic
    Acute-abscess; chronic=granuloma
    Later becomes a cyst
    xray: periapical lucency w/ thin radiopque line
    Periapical/radicular Cyst
  8. 8Peripheral Fibromafibrous hyperplaisa of the gingiva
    Caused by trauma or chronic hyperplasia
    Peripheral Fibroma
  9. 9Peripheral giant Cell granulomaSimilar in apperance to pyogenic granuloma but more blue
    Found usually anterior to permanant molars (alveolar ridge)
    Treatment with excision
    Peripheral giant Cell granuloma
  10. 10Peutz-Jeghers SyndromeOral and paraoral: pigmented macules (brown) on lips, tongue buccal mucosa, vermilion and skin of lip
    Intestinal polyposis
    Peutz-Jeghers Syndrome
  11. 11Physiologic pigmentation (racial pigmentation)Darkens w/ time; present most of a person's lifetime
    Af. Amer: upper or lower lip vermillion, attached gingiva, tongue, buccal mucosa
    series of splotchy brown macules
    Physiologic pigmentation (racial pigmentation)
  12. 12Pleomorphic adenomaMost common benign salivary gland tumor
    Mix of more than one cell type ( epithelial and ct)
    Palate is most common site for minor gland lesions
    Pleomorphic adenoma
  13. 13Primary herpetic gingivostomatitisHSV type 1
    usually affects children younger than 6
    Inflamed, enlarged marginal gingiva; gingival bleeding
    pin point vesicles -> ulcers throughout the mouth and lips w/ sig pain
    Malise
    low grade fever
    sore throat, lymphadenopathy
    doesnt want to drink water
    Primary herpetic gingivostomatitis
  14. 14Proliferative Periostitis (Garre's)Form of chronic osteomyelitis that involves the periosteum
    Usually assoc w carious molar in children
    Visible swelling
    Common in inferior border of posterior mandible
    Lucent or mottled radiographic pattern plus concentric periosteal layering (onion skin pattern)- bands of radiopaque lines that parallel cortical surface
    Tx: w tooth removal and AB
    Proliferative Periostitis (Garre's)
  15. 15Pyogenic granulomaUsually on gingiva at the interdental papilla
    not paniful
    Grows very fast
    proliferative
    not a fibroma
    Pregnancy turmor
    P. Intermedia
    Pyogenic granuloma
  16. 16RanulaMucous rentention cyst
    Submucosal nodule resulting from blockage of salivary duct by salivary stone (sialolith)
    Looks like frogs belly
    Bluish
    FOM
    history of recurrence
    Mucin will yield viscous aspirate
    Ranula
  17. 17Recurrent Aphthous StomatitisSeen on moveable mucosa: uvula, labial, buccal
    Recurrent type (minor and major) is *not preceded by vesicles*, white/gray with red halo
    Minor heals 7-14 days without scarring, not on gingiva or hard palate, 8-10 mm
    Major has scarring, can last up to 6 weeks , exceeds 1 cm
    Ass. with certain HLA type
    Cant treat, but can manage it with corticosteroids
    Herpetiform: many small crops 2-3 mm vesicles clustered together
    Recurrent Aphthous Stomatitis
  18. 18Recurrent Herpes Simplex labalisFrom nerve cells of trigeminal
    ulcers on lips around skin/ vermillion
    Can be on eye
    avoid aspirin -> reyes syndrome and corticosterioids for eyes
    Recurrent Herpes Simplex labalis
  19. 19Recurrent Intraoral HerpesHSV I
    Intraoral: hard palate and gingiva, vesicles ->ulcers
    triggered: stress, trauma, UV exposure
    More likely in Immunocompromise
    Recurrent Intraoral Herpes
  20. 20SarcoidosisPredominately pulmonary disease, but other organs may be affected: salivary glands and mucosa
    Bilateral hilar lymphadenopathy (chest x-ray)
    Cutaneous lesions
    tx: corticosteriods and immunomod drugs
    Sarcoidosis
  21. 21Scarlet FeverWhite coating on top of strawberry tongue
    Swollen hyperplastic fungiform papillae
    + strep throat symptoms -treat w/pencillin
    Scarlet Fever
  22. 22Schwannoma (neurilemoma)Benign neoplasm of Schwann's cells
    Displaces the nerve but doesn't envelope it
    tongue favored
    solitary; not syndrome- related
    Related to neurofibromatosis type 2
    Schwannoma (neurilemoma)
  23. 23SclerodermaAutoimmune, multiorgan disease, affects mainly women
    *Fibrous of tissue* leads to organ dysfunction
    Leads to restriction of orifice (trismus), uniform widening of the of the periodontal membrane, bony resorption of posterior margin of the mandibular ramus
    Scleroderma
  24. 24Sjogren's SyndromeAutoimmune disease that affects exocrine
    Dry eyes (keratoconjunctivits sicca), xerostomia
    Partotid swelling
    Elderly women
    Secondary seen w/ other disease: lupus rhumatoid artrithis
    Sjogren's Syndrome
  25. 25Squamous Cell CarcinomaMay manifest as chronic, non painful, indurated firm, nonhealing ulcer, red or white patch, or mass
    More likely in males
    HIgh risk sites: FOM lateral of tongue
    Least likely site: hard palate
    Metastasis most likely to a lymph node
    Radiographic: poorly defined lucencies w/o reactive sclertotic border
    Squamous Cell Carcinoma
  26. 26Squamous PapillomaBenign
    White to white pink papule/ nodule
    rough surface (cauliflower)
    Found on facial/lingual gingiva, soft/hard palate and tongue
    HPV 6 & 11
    Squamous Papilloma
  27. 27Stafne bone defectDevelopmental
    More in males
    Asymtomatic
    Teeth vital
    Diagnostic well demarcated radiolucency of the mandible secondary to invagination of the lingual surface of the jaw
    located in the posterior mandible below the mandibular canal
    Stafne bone defect
  28. 28Stevens-Jonhson SyndromeErythema Multiform Major
    Triggered by drugs
    Affects eyes (conjunctiva), mouth (labial mucosa, tongue, etc.) genitalia
    Stevens-Jonhson Syndrome
  29. 29Systemic Lupus ErythmatosusAutoimmune
    young adult female
    butterfly rash
    leads to endocarditis and glomerulonephritis
    discoid/chronic (skin and oral mucosa) type v. systemic/acute (butterfly rash and organ involvement)
    Systemic Lupus Erythmatosus
  30. 30Temporomandibular disorderDeviation of jaw toward painful side upon opening
    TMJ disc moves anterior and medially due to contraction of the lateral pterygoid muscle
    Popping clicking indicate internal derangement with reduction
    reduce opening to approx 45 mm
    will get neuritis ov VII cranail nerve
    Temporomandibular disorder
  31. 31Traumatic Bone CystRAdiolucent *dead space* (no epithelial lining) in the mandible of teenages
    Some (not all)associated with jaw trauma
    Undogoes sponataneous healing without treatment following exploatory surgery
    Pseudocyst
    Radiography: scalloped margino
    Traumatic Bone Cyst
  32. 32Traumatic NeuromaTransected nerve due to trauma w/ scar tissue
    leading to a painful/tender, firm nodule
    Likely seen near mental foramen and tongue
    Traumatic Neuroma
  33. 33Treacher Collins SyndromeUnderdeveloped facial bones
    Ears malformed/ absent
    Big mouth and small jaw (micrognathia)
    Droopy eyes
    Treacher Collins Syndrome
  34. 34Trigeminal NeuralgiaAge of onset usually older than 35
    Trigger points
    Trigeminal Neuralgia
  35. 35TuberculosisCaused by Mycobacterium tuberculosis
    Oral nonhealing chronic ulcers (ulcers mimick cancer on tongue) follow lung infection
    Caseating granulomas w/ multinucleated giant cells on chest- chest xray
    Multidrug therapy: isoniazid, rifampin, ethambutol
    Tuberculosis
  36. 36Turner Toothhypoplasia of perm tooth
    Usually just affects one tooth
    due to local trauma/ infection of the developing tooth bud from the primary tooth
    Turner Tooth
  37. 37VaricesLingual and lip
    Dilated veins- blue
    Seen typically in the elderly
    Lip varices may thrombose and subsequently calcify (i.e. phlebolith)
    Varices
  38. 38Verrucous CarcinomaWell-differentiated, slow growing form of carcinoma that infreq metastasizes
    Tobacco and HPV 16 & 18 have etiologic role
    Exhibits broad base verruciform architecture; lg elevated, papillary
    Most common site is buccal vestibule
    Verrucous Carcinoma
  39. 39Verrucous leukoplakiaHigh risk leukoplakia. Lesions start flat but become wart-like. High risk of transformation to carcinoma.Verrucous leukoplakia
  40. 40Warthin's tumorOncocytic tumor that also contains lyphoid tissue
    Usually found in the partotid of older men
    Occasionally bilateral
    Not in the oral cavity
    Warthin's tumor
  41. 41White Sponge NevusMutation of Keratin 4 or 13
    Auto dominant; genodermatosis
    Aysm mod extensive white folds of tissue white spongy-appearing
    buccal mucosa bilaterally
    No tx necessary
    No eye involvement
    White Sponge Nevus
  42. 42XerostomiaDry mouth
    Can result in retrograde infection of the glands, baldish, inflamed tongue
    Saliva sub or sips of water may be needed
    Xerostomia
  43. 43acquired melanocytic nevus -type?-Junctional type: most likely to malignant transformation (melanoma)
    -Intramucosal type: most common oral type. calledintradermal type on skin
    -Compound type
    acquired melanocytic nevus -type?
  44. 44Actinic Cheilitis Tx:?Cause UV ilight (esp UVB 2900-3000nm)
    -Lower lip shows epithelial atrophy and focal keratosis
    Upper lip min affected
    May progress to SCC (premaglignant)
    Junction of lip and lip vermillion and skin become indistinct
    -loss of vermillion border
    - Tx: 5-fluoracil, imquimide
    Actinic Cheilitis Tx:?
  45. 45Adenoid cystic carcinomahigh-grade salivary malignancy
    palate most common site
    Cribriform/ swiss cheese microscopic pattern
    spreads through perineural spaces
    Adenoid cystic carcinoma
  46. 46Adenomatoid odontogenic tumorUncommon to rare odontogenic hamartoma that contains epithelial duct-like spaces and calcified enameloid material
    - Young person (child / teenager)
    - 2/3 female 2/3 anterior 2/3 maxilla 2/3 over impacted crown
    - Snow flake calcifications in the radiolucency surronding the crown and a portion of the impacted tooth's root
    - swiss cheese
    - Tx: simple enucleation
    Adenomatoid odontogenic tumor
  47. 47Allergic Gingivitis- due to flavoring agent in toothpaste, candies, and chewing gums (cinnamon)Allergic Gingivitis
  48. 48Ameloblastic fibroma- Children and teens
    - mand molar
    unilocular/ multilocular radiolucnecy
    - slight pain and swelling, not aggressive
    - ameloblastic fibro-odontoma: similar except for odontoma component
    Ameloblastic fibroma
  49. 49Ameloblastoma- 34
    - histology: reverse polarization of the nuclei of the tail, columnar calles of periphery
    Benign but aggressive tumor w sig recurrence
    Most common in post mand but can be in the ant
    Most common true odontogenic tumor
    multilocular radiolucency (soap bubble)
    often assoc w/ impacted tooth
    reverse polarization
    Ameloblastoma
  50. 50Amelogenesis Imperfecta- Affects enamel
    Effects all teeth
    - Enamel is usually yellow in color, reduced in vol and pitted
    - dentin and pulp and shapes of root and crown are nomral
    Teeth are soft, there is no increase in caries rate
    tx: Full crown coverage
    - X-ray: open contact
    -odontodysplasia: ghost teeth, non-hereditary
    - Bell stage
    Amelogenesis Imperfecta
  51. 51Ankyloglossia-Congenital abnormality
    -Short thick frenum
    tongue-tied
    Ankyloglossia
  52. 52Antral Pseudocyst (Mucous Retention Pseudocyst)-Asymptomatic
    -No treatment necessary
    -Radiographic: slight radiopaque, dome- shape, emanating from floor of maxillary sinus
    -Inverted Y
    Antral Pseudocyst (Mucous Retention Pseudocyst)
  53. 53Aspirin BurnWhite= coagulative necrosis of the surface, not hyperkeratosis
    White rubs off with difficulty, hyperkeratosis does not wipe off
    Aspirin Burn
  54. 54Auriculotemporal syndrome (Frey syndrome)-Often after parotid gland surgery
    -Sweating of unilateral facial skin just prior to eating (strong salivation)
    -Does not affect cranial nerve VI (rather than V)
    -Starch Iodine test
    - Auriculotemporal nerve
    Auriculotemporal syndrome (Frey syndrome)
  55. 55Basal Cell Carcinoma- Low grade skin cancer (lip), rarely metasize (benign)
    -Usually in sun damage skin, very rare in mucosa
    Manifests as nonhealing, indurated chronic ulcer, raised margins
    -Begins as pearly papule
    - telangiectasia
    - nose
    Basal Cell Carcinoma
  56. 56Bell's Palsy- hit Parotid gland during IA
    - idiopathic
    - 7th nerve paralysis-> unilateral lip droop at corner, inability to close or wink eye lid
    - lasts usually less than one month
    Bell's Palsy
  57. 57Calcifying Odontogenic cyst (Gorlin Cyst) - location? - age? - Micro?-Anterior areas of the jaws.
    -Second to third decades but can be seen at almost any age.
    -XRay: unilocular radiolucency .
    -1/3 of cases, an impacted tooth is involved.
    -Microscopically, there are many cells that are described as "GHOST CELLS", enlarged eosinophilic epithelial cells without nuclei.
    ←
    Calcifying Odontogenic cyst (Gorlin Cyst) - location? - age? - Micro?
  58. 58Candidiasis Pseudomembranous- opportunistic infection (affects immunocompromise, immature immune sys, use of AB)
    - hyphae, spores (cytology smear)
    - *white, wipeable patch* (cottage cheese) w/ *red underlying base*
    - palate and buccal mucosa
    - "thrush"
    Candidiasis Pseudomembranous
  59. 59Cavernous Sinus Thrombosis- can arise from an infection
    - subcutaneous abscess of the upper lip
    - intrabony abscess of an anterior maxillary tooth
    - valveless facial veins
    Cavernous Sinus Thrombosis
  60. 60Central Giant Cell Granuloma- intrabony
    - radiolucency, sometimes loculated
    - *teenagers, female*
    - anterior mandible favored
    - benign
    - histology: fibroblasts and mutinucleated giant cells
    - *brown tumor of hyperparathyroidism*: no effect on saliva production. bone destruction secondary to chronic renal disease
    - TX: excision or calcitonin
    Central Giant Cell Granuloma
  61. 61Cervical emphysema-Introduction of air into oral soft tiss w resulting sudden painless swelling and crepitance
    ex: air/water syringe
    Cervical emphysema
  62. 62Cheek Nibbling- Morsicatio Buccarum
    - buccal mucosa
    - White, rough, tissue tags above and below the occlusal plane
    - Linea alba
    - other sites: lip and tongue
    Cheek Nibbling
  63. 63Cheilitis Glandularis-Mucous minor salivary glands of lips are inflammed
    -Mucus secretion
    -Premag ->SCC
    Cheilitis Glandularis
  64. 64Cherubism- auto dom cond seen in jaws of children (cease after childhood)
    - symmetrical swelling of one or both jaws
    - Stabilizes after puberty
    - Multilocular radiolucences (soap bubble) apperance
    - perivascular collagen puffing
    - premature shedding of prim. teeth but delated eruption of permanent.
    - No tx
    Cherubism
  65. 65Chronic osteomyelitis-Chronic inflammation of bone and bone marrow of the jaws
    -Mild to moderate pain and possibly an exudate
    -lucent or mottled radiographic pattern
    tx: AB and sequesrectomy
    - caused by Staph Aureus
    - Pain, malaise, fever
    -when pain tissue die because of loss blood supply
    Chronic osteomyelitis
  66. 66Cicatricial (mucous membrane) Pemphigoid- autoimmune
    - antibody reaction at the epithelial-connective tissue (BMZ)
    - vesculoerosive, ulcer
    - subepithelial split at the basement membrane
    - seen greater in *middle aged women*
    - seen in skin and eyes
    - subepithelial
    Cicatricial (mucous membrane) Pemphigoid
  67. 67Cleft palate-lack of fusion between palatal shelves
    -Approx 1 in 2000 births
    -Between lat incisor and canine
    -Xray: lucent line in max occlusal film
    -Cleft lip more common in male
    - Cleft palate more common in female
    Cleft palate
  68. 68Cleidocranial dysplasia-Delayed tooth eruption
    -Retention of primary teeth
    -Supernumerary teeth
    hypoplastic/aplastic clavicles
    cranial bossing
    Large head
    hypertelorism
    -shoulder moves in, high palate
    Cleidocranial dysplasia
  69. 69Condensing osteitis (sclerosing osteitis)- pulpitis, non vital tooth
    - posterior mandibular tooth (1st molar)
    Bone sclerosis (opacity) resulting from low-grade inflammation, usually secondary to chronic pulpitis, nonvital
    opacity
    - does not connect with root
    Asymtomatic and found on routine examination
    Tx: determining and addressing the cause, and possibly endo
    - differ cementoblastoma: does not connect wth root (can see PDL)
    Condensing osteitis (sclerosing osteitis)
  70. 70Condylar hyperplasia-Irregular, elongated condyle
    -Chin deviates away from affected side upon closure
    Condylar hyperplasia
  71. 71Condyloma Acuminatum- veneral wart (STD)
    - HPV 6,11
    - Ventral tongue- floor of mouth
    - Papillary/Cauliflower like
    Condyloma Acuminatum
  72. 72Crest syndrome- mild form of Scleroderma
    - Tx: steroids
    - C: Calcinosis cutis
    - R: Raynaud's phenomenon
    - E: Esophageal dysfunction
    - S: Sclerodactyly (fingers)
    - T: Telangiectasias of face, vermillion border of lip and tongue
    Crest syndrome
  73. 73Crohn's Disease-Systemic disease
    -Granulomatous inflammation of GI tract
    -Rectal bleeding
    -Granulomatous gingivitis
    -Minor aphthae
    Crohn's Disease
  74. 74Dens-in-dente (dens invagnatus) location most common teeth?-Most often found in anterior jaw, esp max lateral
    -invagination of inner enamel epithelium
    -talon cusp: evaginatus, not inva..
    Dens-in-dente (dens invagnatus) location most common teeth?
  75. 75Dentigerous Cyst-lucency around the crown of an impacted tooth
    -Third molar and canines most often affected
    -Most common site: post mand
    -Pericoronal radioluncency attached at CEJ of unerrupted tooth
    -Epithelial lining from reduced enamel epithelium has potential to transform into ameloblastoma
    Dentigerous Cyst
  76. 76Dentin Dysplasia-All teeth affected
    roots are extremely short "rootless"
    -Roots are surrounded by radiolucent granulomas or cysts that may contribute to tooth loss
    -Obliterated pulps but may have residual spaces (chevrons)
    -not a good candidate for restoration
    -draining fistula
    -mishapen teeth
    Dentin Dysplasia
  77. 77Dentinogenesis imperfecta- All teeth are affected
    teeth have yellow or opalescent color-blue/grey
    extreme occ wear secondary to enamel fracture (poor dentin support)
    - BWXs and PAs: short roots, bell shaped crowns w constricted cervical region and obliterated pulps and root canals
    - Maybe be seen w osteogenesis imperfecta:blue sclera, multple bone fractures
    tx: full crown coverage
    - Type 1: osteogenesis imperfecta
    - Type 2: Most common, dentin abnormality with no bone involvement
    - Type 3: Brandywin type: dentin abnormalities, more variation, multiple pulp exposure
    Dentinogenesis imperfecta
  78. 78Denture sore mouth- chronic candidiasis
    - red palate
    - due to patient not removing denture
    - TX: rinse mouth and soak denture in antifungal (Nystatin)
    Denture sore mouth
  79. 79Denture-induced fibrous hyperplasiaFibrous hyperplasia assoc w ill fitting dentures
    Usually seen in anterior labial vestibles
    Papillary hyperplasia is an ex
    No malignant potential
    Denture-induced fibrous hyperplasia
  80. 80Dermoid cyst-Mass in midline floor of mouth if above mylohyoid muscle
    -Mass in upper neck if below mylohyoid muscle
    -Slightly compressible "doughy:
    Dermoid cyst
  81. 81Eagle Syndrome- Elongated and/or calcification of the stylohyoid ligament
    - Head and neck pain is elicited by chewing, yawning, opening mouth
    Eagle Syndrome
  82. 82Ectodermal (hypohydrotic) Dysplasia common type?-Hypodontia or anodontia-> alveolar bone deficiency
    -hypohidrotic- common type : lack of skin appendages and hair + heat intolerance
    - no sweat gland
    - X-linked
    - Retain primary teeth, conical shaped anterior teeth
    -sparse hair
    Ectodermal (hypohydrotic) Dysplasia common type?
  83. 83Eosinophilic GranulomaType of Langerhans Disease
    Chronic localized form
    solitary/ multiple bone lesions
    young adults
    - most benign form
    - cupped out RL resembling periodontal disease/PA lesion, gingle/multiple well-circumscribed radiolucencies
    Eosinophilic Granuloma
  84. 84Epulis Fissuratum -Tx? -similar to?-hyperplastic tissue reaction caused by an ill-fitting or overextended flange in a denture
    -Tx: adjust denture border and use tissue conditioner; surgery is indicated if inadequate response
    - most similar to Fibroma
    Epulis Fissuratum -Tx? -similar to?
  85. 85Erythema Multiforme- Self-limiting hypersensitivity rxn that affects skin or mucosa or both
    - Minor form assoc w secondary herpes simplex hypersensitivity
    - Major form (stevens-johnson syndrome) often triggered by drugs
    - Young adult males
    - Crusted, bleeding vesicles, ulcers of vermilion of lips; intraoral sites excluding gingiva
    "target, iris, or bulls-eye lesions" of the hands and feet
    - also positive Nikolsky
    Erythema Multiforme
  86. 86ErythroplakiaRed plaque that does not wipe off
    High risk, most represent dysplasia or malignancy to carcinoma
    Biopsy mandatory
    icisional biopsy
    90% chance of being dysplasia
    Erythroplakia
  87. 87Extravasated BloodClinical - spontaneous resolve
    Purpura: generalized term
    Petechia: pinpoint bleeding
    Ecchymosis: large area
    Hematoma: large: elevated
    Extravasated Blood
  88. 88Fibroma- *most common connective tissue tumor*
    - reactive, not true tumor
    - slow growing
    - hyperplasia, not neoplasia
    - firm, smooth, pink elevated papule/nodule
    - common site: tongue
    Fibroma
  89. 89Fibrous dysplasia- Involves entire half of jaw (bilateral)
    - CC: teeth do not fit
    Painless swelling (cease at 20)
    - affects children and typically stops growing after puberty
    -RAdiographic pattern: diffuse opacity (groud-glass apperance)
    McCune-Albright syndrome consists of polyostotic fibrous dysplasia; cutaneous cafe au lait macules and endocrine abnormalities, esp precocious puberty
    Tx: surgical recontouring for cosmetic apperance after age 20 when stabilized
    Fibrous dysplasia
  90. 90Florid Osseous DysplasiaExuberant form of peripical cemento ossesous dysplasia that may involve the jaw
    -Multiquadrant (4 quadrants)
    -Fibro-osseous intraboy lesion
    -Hard product produced is avascular
    - likely complication: secondary osteomyelitis
    Xray: radiolucent and radiopaque
    No tx
    Florid Osseous Dysplasia
  91. 91Focal fibrous hyperplasiaCaused by trauma or chronic irritiation
    A small, solid mass on the tongue, lower lip, or the oral mucosa.
    Focal fibrous hyperplasia
  92. 92Fordyce granules- ectopic sebaceous glands
    - enlarged papules
    - seen on buccal and labial mucosa
    Fordyce granules
  93. 93Gardner Syndrome- Auto dominant
    - consists of intestinal polyps, facial osteomas (epidermoid cysts), skin lesions, impacted permanent and sumpernumerary teeth and odontomas
    intestinal polyps high rate of malignancy conversion
    Gardner Syndrome
  94. 94Garre's -age? -common location? -Xray? (similar)-Proliferative Periostitis
    -Form of chronic osteomyelitis that involves the periosteum
    -Usually assoc w carious molar in children
    -Visible swelling
    -Common in inferior border of posterior mandible
    -Lucent or mottled radiographic pattern plus concentric periosteal layering (onion skin pattern)- bands of radiopaque lines that parallel cortical surface
    -Tx: w tooth removal and AB
    -onion skin: Garre's, Erwing sarcoma
    Garre's -age? -common location? -Xray? (similar)
  95. 95Generalized gingival hyperplasia- fibrous hyperplasia caused by local factors and modified by systemic conditions
    - certain drugs: Phenytoin/ Ca channel blockers may contribute to gingival hyperplasia
    Generalized gingival hyperplasia
  96. 96Gingival cyst of the Adult - common location?-Arises from the rest cells of the dental lamina.
    -Common in the mandible near the anteriors, canines and premolars.
    -Middle-aged adults are more likely to be affected.
    -Swelling, elevated, fluid containing vesicle on attached facial gingiva or interdental papilla.
    -soft tissue counterpart of the developmental lateral periodontal cyst.
    Gingival cyst of the Adult - common location?
  97. 97Gingival hyperplasia - drugs- Benign
    Neoplasm of Schwann cells
    - Pseudoepithlimatous hyperplasia (microscopically mimics squamous cell carcinoma)
    - Most commonly seen on dorsum of tongue
    occurs on gingiva only as pedunculted mass
    surgerical excision, no recurrence
    - granular cell: cytoplasm
    Gingival hyperplasia - drugs
  98. 98Hand-Schuller- Christian diseaseLangerhans cell disease
    Chronic dissminated form
    Triad: diabetes insipus, Exophalmos, Bone lesions
    Chronic
    Hand-Schuller- Christian disease
  99. 99Heavy Metal systemic IntoxicationLead line: blue line that parallels free marginal gingivaHeavy Metal systemic Intoxication
  100. 100Hemangioma-Hamartoma
    -Red to blue elevated lesions
    -Blanches, compressible
    -Collection of sm or lg vessels filled w red blood cells
    Hemangioma

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Praxis Flashcards: PATHOLOGY Flashcards on Pathophysiology X (100 Flash cards), created by ACAPUN INSTITUTE on 09/07/2021.
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ACAPUN INSTITUTE · Jul 2021
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Jul 10, 2021
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