• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/79

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

79 Cards in this Set

  • Front
  • Back

Osler-weber-rendu syndrome

Also called as hereditary hemorrhagic telangiectasia.


Autosomal dominant disorder.


Characterized by triad of telangiectasia (dilation of blood vessels), recurrent epistaxis, positive family history.


Most commonly affected areas are lips, gingiva, buccal mucosa and palate, floor of the mouth and tongue.

Reed-sternbeg cells

Multinucleated


Malignant cells.


In Hodgkin's disease.


Derived from B lymphocytes or monocyte macrophage.

Basal cell carcinoma

Second most common cancer of skin.


Mostly involving the middle third of face.


Rarely seen in oral cavity.


No tendency of metastasis


Benign carcinoma


Etiology sunlight UV radiation


Historical feature shows nuclear palisading.

Junctional nevurs

Epithelium is thin and irregular.


Shows cell crossing the junction and growing down into connective tissue.


Called as abtropfung or dropping off.


May transfer in to malignant Melanoma.


Benign tumor of smooth muscle.

Leiomyoma.


Angiomyoma.

Malignant tumor of smooth muscle.

Leiomyosarcoma

Benign tumor of striated muscle

Rhabdomyoma.

Malignant tumor of striated muscles

Rhabdomyosarcoma.

Benign tumor of nervous tissue

Traumatic neuroma.


Neuro fribroma.


Neurilemmoma.

Malignant tumor of nervous tissue

Malignant schwannoma.


Olfactory neuroblastoma.

Criteria for diagnosis of epithelial dysplasia in carcinoma include

Increased abnormal Mitosis


Individual cell keratinization.


Epithelial pearls in the spinous layer.


Alterations in nuclear cytoplasmic ratio.


Loss of polarity and disorientation of cells.


Hyperchromatism.


Large nucleoli.


Dyskaryosis or nuclear atypism including giant nuclei.


Poikilokarynosis or division of nuclei without division of cytoplasm.


Basilar hyperplasia.


Note- individual cell keraterisation and epithelial Pearl formation is absent in carcinoma in situ or intraepithelial carcinoma.

Pseudocyst are


Stafne's cyst


Aneurysmal bone cyst


Hemorrhagic bone cyst/traumatic bone cyst


Mucocele extravasation type.

Bence jones

Is a unusual protein


Coagulase when urine is heated to 40 to 60 degree Celsius.


Disappears when urine is boiled.


Reappears when urine is cooled


Seen in patients with leukaemia polycythemia and multiple myeloma.

Precancerous lesions

Leukoplakia


Erythroplakia


Palatal keratosis associated with reverse smoking.


Squamous epithelial dysplasia


Squamous cell carcinoma in situ


Solar keratosis


Precancerous conditions

Sideropenic dysphagia


Lichen planus


Oral Submucous Fibrosis


Syphilis


Discoid lupus erythematosus


Xeroderma pigmentosa


Epidermolysis bullosa.

Burkitt lymphoma

Also called as African jaw lymphoma


B cell neoplasm


Children between 2 and 14 years


Macrophages are seen throughout


Starry Sky effect


Virus implicated-herpes simplex virus 4 or Epstein Barr virus.

Bowen's disease

Intraepithelial carcinoma


In patients who have had arsenical chemotherapy.


Open associated with internal or external cutaneous cancer.

Leukokeratosis nicotina palati

Also called as stomatitis nicotina or pipe smokers palate.


In heavy smokers


Keratotic patch In palate with red spot in centre of each nodule representing dilated or partially occluded orifice of accessory palatal salivary gland duct.

Herpes simplex 2 or genital herpes


Carcinoma of uterine cervix.

Herpes simplex 4 or Epstein Barr virus

African jaw lymphomas or burkitt's lymphoma and nasopharyngeal carcinoma.

Herpes simplex 8

Kaposi's sarcoma

Papovaviridae( human papillomavirus)

Cervical, penile,vulvar Cancers,


Squamous cell carcinoma.

Hepadna viridae(hepatitis B virus)

Hepatocellular carcinoma.

Retroviridae(HTL virus)

Adult t cell leukaemia.

Neurofibroma

Arises from schwann cell and perineural cells.


Non encapsulation


Potential for malignant transformation.


Cafe -au-lait,spots are seen In neurofibroma and polyostotic type of fibrous dysplasia.


Greenspan lesion

Hairy leukoplakia


Is not premalignant


Seen in HIV AIDS.

Most common malignancy in females

Breast cancer followed by lung cancer


Breast cancer commonly metastasis into jaw bones and is


Commonly primary cancers that metastasis to the oral region in females.

Most common malignancy in females in India

Breast cancer followed by carcinoma of uterine cervix


(Chennai)

Most common malignancy in males

Lung cancer


Commonly metastasis to the oral soft tissues.


Common primary cancers that metastasis to oral lesion in male.

Most common malignancy in males in India

Oral cancer

Most common skin cancer

Basal cell carcinoma followed by squamous cell carcinoma followed by malignant Melanoma.

Most common oral cancer

Squamous cell carcinoma

Most deadly of all human neoplasm

Malignant Melanoma


Twice as common in men than women occurring in between 40 to 70 years.


Most common in palate and maxillary gingiva or alveolar Ridge in oral cavity.


Is very painful


Rare in children


Depth of inversion is measured by breslow thickness.


Most common benign tumor of bone

Osteochondroma

Most common bone tumor of long bones

Osteosarcoma

Most common primary malignant bone tumor

Multiple myeloma

Third most common cancer in adolescence

Osteosarcoma

Most common malignant bone tumor in India

Osteosarcoma


Sunburst appearance in radiography


Codman's Triangle


Occurs in young person 10 to 25 years old.


Chiefly involve the femur and Tibia.

Most common malignant bone tumor in children

Osteosarcoma followed by ewings sarcoma

Most common leukaemia in children

Acute lymphocytic leukaemia or a l l

Most common leukaemia in elders

Chronic lymphocytic leukaemia

Most common malignant salivary gland tumor in children and adults


Most common salivary gland tumor in bone

mucoepidermoid carcinoma

Most common salivary gland tumor or most common tumor of parotid

Pleomorphic adenoma


benign tumor

Second most common salivary gland tumor

Warthins tumor

Most common benign soft tissue neoplasm in oral cavity

Fibroma

Multiple myeloma

Fatal malignant neoplasm


Of plasma cells


Poor prognosis


Survival time 2 to 3 years


Infection anaemia and kidney failure are common cause of death

All carcinoma metastasis by lymph nodes except renal cell carcinoma(occurs by blood)

All sarcomas metastasis by bloodstream except rhabdomyosarcoma(occurs by lymph)

Brachytherapy

Irradiation of tissue by implants within the tissue

Human papillomavirus type 6 and 11

Commonly associated with squamous papillomas.


Multiple papillomas lesion are seen in cowdens syndrome.


It is considered as cutaneous marker of breast cancer

Staghorn pattern

Important historical feature of hemangiopericytoma which resembles glomous tumour.

Classification of oral leukoplakia


L1 size of leukoplakia less than two centimetre


L2 size of leukoplakia 2 to 4 cm


L3 size of leukoplakia more than 4 cm


LX no size specified


PO no epithelial dysplasia


P1 distant epithelial dysplasia


PX dysplasia not specified.

Stage 1-L1 PO


Stage 2 L2 PO


Stage 3 L3 PO or L1 L2 P1


Stage 4 L3 P1.

Widening of pdl is seen in

Osteosarcoma,


Chondrosarcoma


Scleroderma


Trauma from occlusion

Obliteration of pdl is seen in

Hypercementosis


Ankylosis


Hypofunction of teeth


Paget disease.

storiform pattern of fibrous tissue

Seen in malignant fibrous histiocytoma

Proliferative verrucous leukoplakia

Described by Hansen and is associated with risk of squamous cell carcinoma.


May associated with human papillomavirus.


,


Seen where quid is kept.


Cauliflower white growth


Differential diagnosis verrucous carcinoma.



Nodular or speckled leukoplakia

Raised from surface red and white areas


Seen in angle of mouth in chronic smokers


Fissuring ulcer formation is seen


Epithelial dysplasia is common and tendency of malignancy is more.

granular cell myoblastoma

Benign tumor of muscle tissue


Common in tongue


Epithelium shows pseudo epitheliomatous hyperplasia.


Differential diagnosis epidermoid carcinoma.


Pseudoepitheliomatous hyperplasia is also seen in


Granular cell myoblastoma


Blastomycosis


Papillary hyperplasia


Discoid lupus erythematosus .

Most common bone cancer

Metastatic bone cancer.

Verocay bodies with predilection for occurrence in tongue.

Neurilemmoma


Histopathology picture shows Antoni type a and Antonitype b.


Type a tissue is made of cells with elevated spindle shaped nucleus.


Type b shows disorderly arrangement of cells and fibres.

Cancer which most commonly metastasis to jaw bones

Breast cancer commonly metastasis to jaw bone followed by lung,bone or colorectum and Kidneys.

Onion skin appearance, periosteal new bone formation or Neoperiostotis.

Infantile cortical hyperostosis or caffeys disease


Hypervitaminosis a


Syphilis


Ewing's sarcoma


Metastatic neuroblastoma


Garres osteomyelitis.

Teratoma

Hamartous developmental manifestation consisting of three different layers of tissue.


Made up of number of different types of tissue which are not native to that area.


teratoma may occur in various parts of body and is made up of various epithelial appendages such as hair, sweat glands, sebaceous glands and salivary glands. Teeth are usually normal and resembles premolars. inflammatory gingivitis may be seen.

Papules

Solid lesion raised above the skin surface that are smaller than 1 cm in diameter.

Plaque

Solid raised sections that are over 1 cm in diameter are called plaque.

Macules

Well circumscribed flat lesions that are noticeable because of change of colour.

Vesicles

Elevated blisters containing clear fluid that are under 1 cm in diameter

Hemangioma are associated with

Rendu osler Weber syndrome


Sturge Weber syndrome(port wine stain).


Kasabach Merritt syndrome

Cancer inversion into perineural areas

Adenoid cystic carcinoma


Keratoacanthoma.

Multiple endocrine neoplasia (m e n)

Type 1


hyperplasia of pituitary gland with acromegaly


Hyperplasia of parathyroid and adrenal cortex


Hyperplasia of pancreatic islets with increased production of insulin gastrin and glucagon with peptic ulcer and gastric hypersecretion.


Type 2 (sipples syndrome) hyperplasia of parathyroid


No tumors of pancreas, no peptic ulcer.


Patient may have pheochromo- cytomas of the adrenal medulla and medullary carcinoma of thyroid gland.


Type 3


pheochromo- cytomas and medullary carcinoma of thyroid gland.


Oral neuromas that are common on lips tongue and buccal mucosa


Lips are described as bumpy lips.

Human papillomavirus HPV conditions lesion are

Hecks disease


Proliferative verrucous leukoplakia


Squamous papilloma


Carcinoma of cervix


Condyloma acuminatum


Verrucous vulgaris (common wart of skin)


Molluscum contagious (caused by pox group virus with characteristic Henderson-peterson or molluscum bodies)


Oral squamous cell carcinoma.

Central ossifying fibroma of bone

Mandible is commonly involved


Displacement of teeth is an area clinical feature.


In early stages appears as radiolucent area which becomes clasified later.


Ultimately the lesion appears as a relatively uniform radiopaque mass.

Central Giant Cell granuloma and Giant cell tumor of bone.

Common in young below 30 years of age.


Usually shows no signs and symptoms but sometimes may cause expansion of cortex and perforation. mobility, displacement and root resorption of associated teeth.


M N G self and hemosiderin pigment are seen.

Peripheral ossifying fibroma

Involves gingiva


No radiological features


Shows different forms of calcification historically​

Peripheral Giant Cell granuloma

Involves alveolar process


Frequently anterior to molars


Originate from either periodontal ligament or mucoperiosteum.


Historical shows mng cells which resemble osteoclast


Numerous capillaries, foci of haemorrhage , hemosiderin pigment are characteristic feature.


Radiographically it exhibits superficial erosion of born with pathognomonic "peripheral cuffing" of bone.

Keratoacanthoma


Self healing carcinoma,


Mulluscum pseudo carcinomatosum.


Molluscum sebaceum.


Low grade malignancy


Originate from pilosebaceous glands.


Etiology is trauma, HPV virus ,genetic.


Twice common in men than woman.


Usually on sun exposed area


Lips and vermilion border affected.


Spontaneous healing by its own over 6 to 8 weeks.

Ewing sarcoma

Also called as round cell sarcoma, seen in children and young adults.


Painful swelling of bone


Facial Neuralgia and lip paraesthesia


Diffuse radiolucency, onion skin and sun Ray appearance of bone.


Intracytoplasmic glycogen of these cells helps in differenciation from reticulum cell sarcoma.

Sturge Weber syndrome

Congenital hemartomatous malformation.


Effects Eye Skin and CNS


Characterized by venous angioma of leptomeninges with ipsilateral angiomatous lesion of the face ,skull jaw and oral soft tissue.


The port wine nevi(cutaneous capillary venous angioma) are observed first at birth.

Pel ebstein fever in

Hodgkin's lymphoma

Elephantiasis neuromatosa.


Von recklinghausens disease.