Pathology identification FINAL

Hyperkeratosis of the palms of the hands and soles of the feet, affected individuals have tooth mobility
Papillon-Lefevre syndrome
Peutz-jeghers
Trisomy 21
Turner syndrome
The form of amelogenesis imperfecta is due to hypomaturation of enamel
Type 1
Type 2
Type 3
Type 4
Radiograph of the jaws reveals a characteristic "soap bubbles" or multilocular appearance.
Cherubism
Gardner syndrome
Peutz-jeghers
Dentinogemesis imperfecta
This condition exhibits multiple melanotic macular pigmentation on perioral skin oral mucosa
Dentiogenesis imperfecta
Peutcs-jeghers
Paget disease
Turner syndrome
Occurs most commonly in the anterior mandible of patients older than 30 years
Hyperparathyroidism
Periapical cemento-osseous dysplasia
Paget disease
Cleidocranial dysplasia
Enlargement of affected bone
Paget disease
Cleidocranial dysplasia
Gardner syndrome
Mandibulofacial dysostosis
Composed of well-vascularized connective tissue containig many multinucleated giant cells
Turner syndrome
Hyperparathyroidism
Central giant cell granuloma
Trisomy 13
Multiple quadrants are affected a type of fibro-osseous lesion
Acanthosis nigricans
Pernicious anemia
Squamuos cell carcinoma
Florid cemento-osseous dysplasia
Patients with this condition go through cycles of PMN depletion
Cleidocranial dysplasia
Cyclic neutropenia
Peutz-jeghers
Peg lateral
This condition includes absent or malformed clavicles and multiple supernumerary teeth
Gardner syndrome
Central giant cell granuloma
Cleidocranial dysplasia
Hyperparathyroidism
Radiographically, teeth short roots and an almost complete lack of pulp chambers may appear opalescent browniish-blue
Dentinogenisis imperfecta
Ciclyic neutropenia
Turner syndrome
Gardner syndome
People born with this condition may exhibit microphthalmia or even anophthalmia
Turner syndrome
Trisomy 21
Paget disease
Trisomy 13
Patients with this syndrome have only an X chromosome
Turner syndrome
Peg lateral
Pernicious anemia
Trisomy 13
Pt with inherited disorder have intestinal polyps become cancerous at 30 or after they acquire osteomas in various bones.
Amelogenesis imperfecta
Turner syndrome
Gardner syndrome
Hyperparathyroidism
This condition that results from enamel that does not develop to a normal tickness
Central giant cell granuloma
Hypoplastic type of amelogenesis imperfecta
Dentinogenesis imperfecta
Cleidocranial dysplasia
People with this inherited disorder have a vaulted palate or cleft palate and the mouth appears "fish-like"
Amelogenesis imperfecta
Acanthosis nigricans
Pernicious anemia
Mandibulofacial dysostosis
Teeth number 7-10 are smaller in this inherited condition
Osteonecrosis of the jaw
Peg lateral
Papilloma
Central giant granuloma
In a person with hyperparathyroidism this is known as a brown tumor
Hyperparathyroidism
Squamous cell carcinoma
Central giant cell granuloma
Verrucous carcinoma
Endocrine disorder glass appearance of bone lesions identical to central giant cell granuloma are called browns.
Cleomorphobe carcinoma
Hyperparathyroidism
Acanthosis nigricans
Ameloblastoma
An indicator of type II diabetes velvety hyperpigmented plaques
Osteonecrosis of the jaw
Verrucous carcinoma
Papilloma
Acanthosis nigricans
Loss of papillae on the dorsum of the tongue, this pt does not produce intrinsic factor
Osteonecrosis of the jaw
Squamous cell carcinoma
Pernicious anemia
Calcifies odontogenic cyst
Complications with bisphosphonate therapy
Osteonecrosis of the jaw
Compound odontoma
Sickle cell anemia
Pernicious anemia
A drug that suppresses the immune system and can lead to candidiasis and oral infections.
Prednisone
Inhaled corticosteroids
Antibiotic
All of the above
Microscopic appereance shows fingerlike projections surfaced by squamous epithelium
Lipoma
Papilloma
Acromegaly
Sickle cell anemia
Ulcerated mass on lateral border of tongue microscopic feature keratin pearl
Squamous cell carcinoma
Verrucous carcinoma
Cleomorphobe carcinoma
This malignant neoplasm is related to smokeless tobacco
Squamous cell carcinoma
Cleomorphobe carcinoma
Verrucous carcinoma
The most benign salivary gland tumor
Ameloblastoma
Pleomorphic adenoma
Papilloma
Verrucous carcinoma
This odontogenic tumor presents as multilocular radiolucencies
Neuroma/ neurofibroma
Cleomorphobe carcinoma
Acromegaly
Ameleoblastoma
Unlike odontogenic tumors pain is a frequent sympton
Cementoblastoma
Compound odontoma
Ameloblastoma
This neoplasm shows ghost cell keratinization
Cementoblastoma
Ameloblastoma
Compound odontoma
Calcifies odontogenic cyst
Small smooth-like radiopacities surrounded by a radiolucent halo
Compound odontoma
Calcifies odontogenic cyst
Sickle cell anemia
Derived from shawnn cells and perineural fibroblast
Neuroma/neurofibroma
Lipoma
Acromegaly
A tumor of adipose tissue
Lymphoma
Lipoma
Sickle cell
Carcinoma
Dietary deficiency of iron causes the loss of filiform papilla
True
False
Abnormal tabeculation is seen in this inherited form of anemia
Anemia
Pernicious anemia
Sickle cell anemia
This disorder of excessive growth hormone results in macroglossia occurs after epiphyseal closure
Acromegaly
Lipoma
Compound odontoma
Giant cell
This benign tumor of fat cell clinically appears as a yellowish mass surfaced by a thin layer of epithelium is referred
Lipoma
Acromegaly
Lymphoma
{"name":"Pathology identification FINAL", "url":"https://www.quiz-maker.com/QPREVIEW","txt":"Hyperkeratosis of the palms of the hands and soles of the feet, affected individuals have tooth mobility, The form of amelogenesis imperfecta is due to hypomaturation of enamel, radiograph of the jaws reveals a characteristic \"soap bubbles\" or multilocular appearance.","img":"https://www.quiz-maker.com/3012/CDN/93-4516048/1k.png?sz=1200-00000016710821905300"}
Powered by: Quiz Maker