Oral patho Flashcards
What is the difference between oligodontia and hypodontia?
oligodontia is absence of more than 6 teeth.. hypodontia is absence of few teeth
What are the characteristic of Dentinogenesis imperfecta?
- color: opalescent
- short roots
- constricted CEJ (tulip/bell shaped crowns)
- obliterated pulps (type I & II) only
- large pulp (type 3 only, aka brandywine) with multiple exposures and apical lesions
Dens in dente is ……..
invagination of the enamel organ during formation
In hypercementosis, teeth are ……..
vital
- usually in premolars
- associated with Paget’s, toxic goiter, gigantism, chronic tooth inflammation
- PDL space is continuous
Odontodysplasia affects ……
epithelium (enamel) & mesenchyme (dentin, cementum)
- Max. anterior are more affected
- Teeth are short, large pulps (aka. ghost teeth)
- Tx: exo
Most commonly ankylosed tooth is …….
primary second molar and its successor
Amelogenesis imperfecta will show normal pulp except …..
in case of abrasion, there’s obliteration of pulp due to secondary dentin
- Tx is cosmetic for AI
- open bite is common in AI. Caries rate is normal
- pulp and cementum are normal
- hereditary (could be AD, AR, X-linked)
Porphyria in teeth appears ……..
red or brown
* defect in heme synthesis
Dentin dysplasia is two types?
- Radicular
- Coronal
* Review Deck 12 (very important)
Substitution of valine for glutamate causes ……
sickle anemia
- Characterized by enlarged marrow spaces
- RBC life is 20 days instead of 120
Werlhof disease is ……..
Thrombocytopenic purpura
Lymph nodes are usually ….. size in chronic leukemia
normal (enlarged in acute form)
Methimazole causes …….
agranulocytosis
- It’s an antithyroid drug (along with carbimazole)
- Causes severe oral ulceration
- Cyclic neutropenia is an unusual form of agranulocytosis, causes severe gingivitis
Oral manifestation of thalassemia is ….
flaring of anterior teeth
* there’s low level of RBC & hemeglobin
Rhogam is a tx for ……
Rh incompatibility (given to mother during and after birth)
Philadelphia chromosome is .
translocation from chromosome 22 to 9 in CML
Most oral manif. of leukemia is in ……. type
AML & CML
- hemorrhage, gingivitis, hyperplasia, ulcerations
- Note: EBV & HTLV-1 may be the cause for leukemia
Osler’s disease is ………
hypoxia due to high altitude. Causes secondary polycythemia
* Note: Erythromelalgia is paroxysmal vasodilation of B.V with congestion and pain. Usually in limbs
Epulis granulomatosum is ……..
caused by retained foreign body after exo.
- Soft non painful, bleeds easily
- Granulation tissue with bone/dentin/cementum or foreign body
- Tx is curettage
What are MEN types?
- MEN I: pituitary, parathyroid, pancreas, adrenal cortex
- MEN II (Sipple syndrome): parathyroid, pheochromocytoma, medullary thyroid
- Men III: any of the two, plus “mucocutaneous neuroma”
* Thyroid medullary carcinoma is a risk with MEN III
Von recklinghausen disease is characterized by ….
- Cafe au lait and arm pit freckles
- Lisch nodules (iris freckles)
- multiple mucocutaneous neurofibroma
* Note: 6 or more cafe au lait is indicative
* High risk of malignancy
Scleroderma is ……
autoimmune inflammation, followed by deposition of type I & III collagen.
* Oral signs: uniform widening of PDL (Note: similar osteosarcoma)
Epulis granuloma of newborn is similiar to …….. with one difference
granular cell myoblastoma (usually on the tongue)
* difference: granular cell myoblastoma is covered with pseudoepithelium hyperplasia)
Most common tumor of nerve fibers is …….
neurofibroma