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123 Cards in this Set
- Front
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|
what is:
a strictly clinical term, more descriptive actually clinical dx of exclusion clinically a white patch/plaque premalignant prognosis varies on location |
Leukoplakia
|
|
what is:
something occurs > 40 yr, ave 60 70% males recognized more now than past 4% transform to malignant biopsy mandatory, unless obviously benign cause |
Leukoplakia
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|
name 3 things that are considered possible causes of Leukoplaki
|
Tobacco
alcohol UV radiation microorganisms trauma |
|
what is:
similar to actinic kearatosis, but on mucosa (lower lip) fair skinned >45 yr, 10X male blotchy pale area, blurr vermillion border epi atrophy, solar elastosis, hyperkeratosis permalignant, ulcerations. tx w sunscreen, biopsy suspicious |
actinic cheilosis
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|
3 clinical features of Leukoplakia are: 1. homogenous or thick leukoplaka
2. thin leukoplakia 3 granular or nodular leukoplakia what are other 3? |
4. verrucous or verruciform leukoplakia
5. proliferative verrucous leukoplakia 6. speckled leukoplaia or erythroleukoplakia |
|
you see leukoplakia on floor of mouth, you're thinking
1 2 3 |
1. epithelial dysplasia or worse
2. hyperkeratosis 3. lichen planus |
|
you see leukoplakia on tongue, ventral or lateral, you're thinking
1 2 3 |
1. epi dysplasia or worse
2. lichen planus 3. oral hairy leukoplakia |
|
you see leukoplakias on tongue (dorsal), you're thinking
1 2 3 |
1 candidiasis
2 lichen planus 3 hyperkeratosis |
|
what is:
associated w/ toothpaste/rinse containing something (what something? 80%) Pt develops a true leukoplakia located in mx vestibule or mx alveolar mucosa epi may show dysplasia but cancer risk unk |
sanguinaria - associated keratosis
leukoplakia may persist for years even after cessation |
|
what is PVL?
|
proliferative verrucous leukoplakia
|
|
what is:
concept: simple leukoplakia --> verrucal hyperplasia --> cancer go thru verrucous carcinoma stage then to invasive SSE w/in 8 yrs 1:4 male female (tobacco no association) lesions tend to slowly spread, rarely progress, dificult to eradicate despite therapy |
PVL
proliferative verrucous leukoplakia |
|
what is:
5% to 25% oral leukoplakias microscopic changes (premalignant) graded mild to ... |
epithelial dysplasia
epi dysplaisa grades 1. mild, 2. moderate, 3. severe, 4. carcinoma in situ |
|
what is:
enlarged nuclei & cells large/prominant nucleoli increased nuclear/cytoplasmic ratio hyperchromatic nuclei nuclear & cellular pleomorpism dyskeratosis, increased mitosis, abnormal mitosis |
dysplasia
|
|
what else is seen with dysplasia microscopically?
|
dysplasia
bulbous rete pegs, loss of polarity keratin or epi pearls loss of typical cellular cohesiveness |
|
leukoplakia is 77X more common
up to 90% of all erythroplakias represent severe epi dysplasia or worse clinically red patch, clearly this |
erythroplakia
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|
what is:
well demarcated erythematous macule/plaque w/ soft/velvety texture. old men floor of mouth, tongue,soft tissue often symptomatic may be adjacent or associated with leukoplakia |
erythroplakia
|
|
why might a lesion be of concern clinically?
name 3 |
1. ulcers unrelated to trauma/infection
2. leukoplakia in floor of mouth 3. erythroplakias 4. mucocele-like lesions in locations other than lower lip, floor of mouth or ant. ventral tongue 5. palatal soft tissue masses |
|
how is population doing on SCC?
|
over last 20 yrs % (HNSCC) decreasing, less tobacco
increase of tongue palatal tonsil, base of tongue in white 20-44 yr olds. All other sites declined |
|
what causes SCC?
name 5 |
1. tobacco (smoke/chew) 2. alcohol 3. radiation
4. iron or vit A deficiency 5. syphilis, candidal infection, oncogenic virus 6. immunosupression 7 oncogenes & tumor supressor genes |
|
what is:
young - less alcohol/tobacco sexually transmitted, late dx in oropharynx often, low differentiation = better prognosis |
HPV
subtypes HPV 16,18,31,33,45 unknown if HPV vaccines protect |
|
oral cancer in oregon a problem
|
yes
369 cases in 2005 110 dead compare: 39 female deaths from oral cancer vs. 42 from cervical cancer |
|
clinical features of SCC
name 3 |
exophytic mass (mass forming)
endophytic (ulcerating) leukoplakic (white patch) erythroplakic (red) or erythroleukoplakic |
|
grading of SCC
grade 1 - grade 2 - grade 3 - grade 4 - |
grade 1 - well differentiated (85%)
grade 2 - moderately " grade 3 - poorly " grade 4 - anaplastic (9%) |
|
what is:
low grade SCC 1-10% oral carcinomas spit related, other sites too may be HPV associated 65-70 ave age, men mostly metastasis rare, 90% 5 yr disease free |
Veerrucous Carcinoma
|
|
what is:
rare SCC, dysplastic surface epi & invasive spindle element sarcoma looking often after radiotherapy polypoid, rapidly growing, ave 57 yr 30% 5 yr disease free (high grade) |
Spindle cell carcinoma
|
|
what is:
rare SCC (variant) combo of adenocarcinoma & SCC posterior tongue, floor of mouth prognosis? |
adenosquamous carcinoma
poor prognosis |
|
what is:
symptomatic for long time until fills sinus elderly, few more males. palatal pain, "toothache" protrusion of eye, nasal drainage surgery & radiation tx, survival? |
Carcinoma of max sinus
10-30% 5 yr survival rate |
|
25X more common in south China. age 50-55 ave,
cervical lymph node involvement 1st sign 60% of time tx? prognosis? |
Nasopharyngeal Carcinoma
Tx: radiotherapy/chemotherapy prognosis: good to poor, depending on stage |
|
what is:
new lesion of upper aerodigestive tract, in hypopharynx/tongue base. in older smoking/drinking men ave survival? Tx? |
Basaloid Squamous Carcinoma
23 mo survival tx: surgery then radiation (80% have carvical mets @ time of dx) |
|
what is:
locally invasive, spreads slow 80% of all skin cancers (85 H&N) b/c sun exposure rarely metastasizes, tx? prognosis? |
Basal Cell Carcinoma
surgical excision, electrodesiccation, curettage, excellent prognosis unless neglected (30% chance of 2nd lesion) |
|
what is:
age spots, liver spots (Senile Lentigo), benign frecle, macular lesion, brown/tan, sun damage, 90% whites over 70, dorsa hands, face/arms Tx? |
Actinic Lentigo
no Tx required increased # of melanocytes & increased pigmentation of basal cells |
|
what is:
macular pigmentations of unk cause, sun exposed skin usually in children, but any age increased # of melanocytes increased pigmentation of basal cells, Tx? |
Lentigo Simplex
no Tx needed |
|
what is:
oral pigmentation, focal increase of basal melanin pigmentation, b/c increased # of melanocytes ave age 43, 2:1 female lowe lip then buccal mucosa, solitary Tx? |
Oral Melanotic Macule
no tx needed except to rule out melanoma a case of melanoma developing in a previously benign oral melanotic macule has been reported |
|
what is:
benign & uncommon pigmented lesion of oral mucosa, brown/black melanocytes scattered throughout thickness of epi aquired & appears reactive in blacks, females common, buccal mucosa 30-40's. growth? |
oral melanoacanthosis
may demonstrate rapid growth & resolve after removal of irritation |
|
what is:
very common, 10-4- nevi/person childhood develops to max before age 35, white women mostly. above waist w/ head & neck common site. w what are 3 basic clinical types? |
Malanocytic nevi
1. junctional 2. compound 3. intradermal |
|
what is:
uncommon, palate & gingiva are most common sites 2/3 in females, 35 ave age intradermal type most common |
intraoral melanocytic nevi
most common type is intradermal type (intramucosal) |
|
what are the variants of melanocytic vevus?
there's 4. 1. congenital melanocytic nevus. 2.3.4. |
1. congenital melanocytic nevus
2. halo nevus 3. spitz nevus 4. blue nevus |
|
congenital melanocytic nevus, present at age? _% population, 2 types: LG & SM b/c __cm, % in head and neck?
malignant? |
present at birth, 1% population. >20cm lg. (otherwise sm) 15% head and neck area
- 5-10% of lg congenital melanoctic nevi ungergo malignant change |
|
what is:
melanocytic nevus, pale hypopigmented border, immune attack of adjacent melanocytes nevus often regresses, 2nd decade of life, location? |
halo nevus
usually seen on trunk 2nd decade of life |
|
what is:
uncommon, benign, most in childhood, extremities & face (not mouth) architecture of compound nevus w/ spindle/ epithelioid cells TX? |
Spitz nevus
tx: surgical excision |
|
what is:
b/c proliferation of dermal melanocytes, blue/black appearance 2nd common orally, usually where? elongated, dendritic, dermal mealocytes in subepithelial location |
blue nevus
seen on palate, may occur at any skin or mucosal site, common sites are dorsa of hands/feet/face/scalp, sacral or butt |
|
what is:
malignant neoplasm of melanocytes |
melanoma.
pre exisiting melanocytic lesion or arise de novo sun damage. acute damage worse, 2-8X change if relative has it fair complexion = predispose |
|
what is:
3rd most common skin cancer? annual incidence increasing dramatically. 1 in 100 lifetime risk. ___% head and neck, __% extermities. prognosis bad if how thick? |
Melanoma
5% of cutaneous malignancies 25% head/neck 40% extremities bad prognosis if thicker than 1.7mm |
|
what are 4 melanoma types?
1. lentigo maligna melanoma 2. ssm 3. nm 4. alm |
1. lentigo maligna melanoma 5%
2. superficial spreading melanoma 70% 3. nodular melanoma 15% 4. acral lentiginous melanoma |
|
ABCD's of melanoma
|
A - asymmetry
b - border irregularity c - color variation d - diameter greater than 6mm |
|
BANS have worse prognosis
BANS? |
B - Back - interscapular area
A - posterior Arm N - Neck - posterial/lateral S - Scalp |
|
What is?
commoner in Japan/Uganda <1% melanomas, 50's+. 4of 5 max mucosa. starts brown/black and spreads - nodular then ulcerates prognosis/Tx? |
Oral Melanoma
poor prognosis 4-20% 5 yr survival Tx: radical surgical excision |
|
3 types of salivary glands?
|
serous glands
mucous glands mixed mucous & serous glands |
|
what is:
largest gland? almost completely what type? it's encapsulated, escapes from ___duct. nerve passes thru? contains lymph nodes |
parotid glands
- largest gland, almost all serous - encapsulated, Stenson's duct - facial nerve passes thru - contains lymph nodes |
|
what is:
2nd largest gland. encapsulated. in submandibular triangle. type of gland? duct name? |
Submandibular Glands
- mixed - serious predominant - in submandibular triangle - Whartons Duct |
|
what is:
smallest of glands (composite of 1 larger & several sm). No Capsule location? duct? |
Sublingual Glands
- mixed-mucous predominant - floor of mouht, above myohyoid muslce Bartholins duct & rivinus ducts |
|
what is:
mostly mucous, throughout submucosa Type? 3 glands (bn,ve,lg) |
Minor Oral Salivary Glands
- Blandin & Nuhn: ant ventral tongue Von Ebner - vallate papilla (serous) Labial glands - mixed, perdominately mucous |
|
what is:
severance of salivary duct, spills mucin into CT kids/young adults common where? |
Mucous Escape Rxn
(mucocele) seen in ant. ventral tongue, "superficial mucoceles" in palate & retromolar area |
|
what is:
lined by ductal epi, partial obstruction of duct. age 42.8 yr old Tx? rule out? |
Mucous Duct Cyst (salivary duct cyst)
conservative surgical excision, rule out mucoepidermoid carcinoma |
|
what is:
calcified mass, in duct rare under age 20, 3:2 female where? symptoms? |
Sialolithasis
calcified mass in duct. common in submandibular gland. see swelling and pain |
|
what is:
benign, inflammatory, self healing. arises spontaneously, afe age 48, male slightly more, asymptomatic palatal ulcer, confused w/ malignancy |
Necrotizing Sialometaplasia
|
|
what is:
most mucous, located throughout submucosa. lingual glands mostly mucous, some all mucous glands: B&N, goVE |
Minor Oral Salivary Glands
Glandin & Nuhn: ant. ventral tongue Glands of Vallate papilla (glands of Von Ebner) = pure serous |
|
s
Salivary Gland neoplasms PEARLS for every 100 parotid tubors X minor gland tumors X submandibular gland tubors X sublingual gland tumor |
Salivary Gland neoplasms
PEARLS for every 100 parotid tubors 40 minor gland tumors 15 submandibular gland tubors <1 sublingual gland tumor |
|
s of 200+ cases of oral minor salivary gland tumors
X = benign neoplasms X= pleomorphic adenoma X= canalicular ademoma X= Oncocytoma |
of 200+ cases of oral minor salivary gland tumors
56% = benign neoplasms 78%= pleomorphic adenoma 21% = canalicular ademoma .8% = oncocytoma |
|
s 5 most common minor salivary gland tumors
X - mixed tumor X- Mucoepidermoid carcinoma X- polymorphous low grade Ca X - Canalicular adenoma X - Adenoid Cystic Carcinoma |
41% - mixed tumor
15- Mucoepidermoid carcinoma 11 - polymorphous low grade Ca 11 - Canalicular adenoma 9 - Adenoid Cystic Carcinoma |
|
s what is: most common neoplasm of salivary gland origin, mixed tumors in mn glands rarely have capsules (well developed at least) mixed tumors of minor glands have litle propensity for reoccurance
locations? |
PEARLS (pleomorphic ademoma)
Palate > upper lip > buccal mucosa > retromolar region ave age 46 female 65 to 34 male |
|
s what is:
occur in young, hard palate especially. salivary galnd tumors rare in lwoer lip, rare in upper lip yet most commin salivary gland tumor in lower (mimics mucocele). can occur central w/in jaw. |
pearls - MEC
(mucoepidermoid carcinoma) ave age 55, female 70:30 |
|
s what is:
favors upper lip (75%), misdx b/c non-encapsulated, multifocal, features of tubular pattern (adenoid cystic carcinoma) |
Pearls - CA
Canalicular Adenoma ave age 64, female 80:20 |
|
s what is:
called "Wolf in sheeps clothing" & "always gets a man" tumors of minor glands may have worse prognosis microscopic pattern makes a difference in survival rates |
Pearls - ACC
Adenoid cystic carcinoma |
|
s what is:
commonly misDx as adenoid cystic carcinoma, but better prognosis, occur in minor glands and never metastasize. |
Pearls - PLGA
Polymorphous Low grade Adenocarcinoma Palate 44% buccal 22% retromolar 11% ave age 64 female 55:44% |
|
s what is:
"not otherwise specified" Pearl |
Adenocarcinoma
Age 61, 3:1 female, palate, lip |
|
s Other Pearls
Ca ex mixed tumor Acinic cell carcinoma Cystadenocarcinoma Papillary cystadenocarcinoma ages & locations? |
Ca ex mixed tumor - male 37&75 yr old. buccal mucosa & retromolar
Acinic cell carcinoma - male age 57, lower lip Cystadenocarcinoma - female, age 47 hard palate Papillary cystadenocarcinoma - male age 35 buccal mucosa |
|
s SUMMARY - ratio of benign to malignant is consistent w/ other reports. Pleomorphic adenoma is most common minor salivary gland neoplasm - excision of overlying mucosa might be indicated during excisional biopsy more (flip)
|
SUMMARY - palate is most common site for minor gland neoplasms (44%), benign neoplasms tend to be much more commin in lower lip. malignant neoplasms mrore common in lower lip
|
|
s what is:
benign growth of blood vessels, common non-epi salivary gland tumor most common salivary gland tumor <1yr, 85% parotid, 2X females, involute by school age |
Hemangioma
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|
s Reactive/inflammatory lymph nodes, metastases to lymph nodes
tumor associated lymphoid response lymphoma infiltrating gland/node benign lymphoepithelial lesion BLEL - rare |
Lymphoid lesions
|
|
s
what are the 5 epithelial neoplams Major glands - Benign ? |
Pleomorphic adenoma
Basal Cell adenoma warthins tumor Adenoma, NOS Oncocytoma |
|
s what is:
most common salivary gland neoplasm 60-70% where? 40-70% where? ave age 41 yrs, female 2:1, Tx? recur? |
Pleomorphic Adenoma (mixed tumor)
60-70% parotic gland tumor 40-70% minor gland tumor afe age 41 yrs may recur |
|
s
what is: 2nd most common benign tumor, 73% where? ave age 58, 2:1 female, tx? recur? |
Basal Cell adenoma
73% parotid surgical tx similar to pleomorphic adenoma (complete surgical excision) recurrance rate less than pleomorphic adenoma |
|
s what is:
95% where? ave age 57, 1.2:1 male 96% white, 5-10% bilateral, Pathognomonic microscopic pattern superficial parotidectomy |
Papillary Cystadenoma Lymphomatosum
(Warthins tumor) |
|
s
what is: 78% parotids, 1 cell type, 64 yr old ave, may be multifocal, usually superficial parotidectomy |
Oncocytoma
(oxyphilic adenoma) |
|
s
what is: not one of other recognized tumors, 66% mj glands, ave age 56 yrs, mor common in 5th-8th decades intermediate to high grades prognosis variable |
Adenocarcinoma, NOS
|
|
s What is:
usually low grade, 81% parotid, 59% female, ave age 44, seen on superficail parotidectomy best prognosis of all tumors |
ACA
Actinic Cell Adenocarcinoma |
|
s what is:
carcinoma ex mixed tumor carcinosarcoma malignant mixed tumor |
Bad Pleomorphic Adenomas
|
|
s what is:
develops in previous benign pleomorphic adenoma age 56 64% paraotid histologic patterns Agressive Tumor, Tx? |
Carcinoma ex Mixed Tumor
Tx: wide surgical excision, lymph node dissection, radiation |
|
s What is:
reactive hyperplasia of fibrous tissue, commonmost along bite line usually smooth surfaced & normal color or pale, usually <1.5cm in diameter 4th to 6th decades, Tx? |
Fibroma
Tx with excision |
|
s 5% of oral fibrous proliferations
sessile or pedunculated, usually <1cm surface papillary, may look papilloma-y. most common first 3 decades. 1/2 on gingiva. microscope sees? Tx? |
Giant Cell Fibroma
mic: Lg, multinucleated "stellate" fibroblasts & elongated rete pegs Tx: surgical excision |
|
s What is:
reactive fibrous & epithelial hyperplasia due to flange of ill fitting denture, older women more 1-2 rolls of redundant tissue facial to alveolar ridge. firm, fibrous, may be focally ulcerated & erythematous Tx? |
Epulis Fissuratum
(inflammatory hyperplasia or denture injury tumor) Tx: excision & constructino of better fitting denture |
|
s what is:
reactive fibrous & epi hyperplasia, related to ill fitting denture, bad hygiene, in hard palate red, papillary surface. see pseudoepitheliomatous hyperplasia excie reactive tissue, new denture & leave denture out at night |
inflammatory papillary hyperplasia
|
|
s what is:
reactive tumor like growth on gingiva exuberant tissue response to trauma, red/purple tissue, freq. ulcerated, females, often prego, complete excision & removal of irritation |
Pyogenic granuloma
|
|
s what is:
reactive tumor-like growth, on gingiva, ant. to molars, dark red/ulcerated, females. cellular vascular stroma with osteoclast-like multinucleated giant cells, tx? recur? |
Peripheral giant cell granuloma
tx: excision & removal of irritation recur 10% |
|
s what is:
reactive lesion seen only on gingiva, teens, young adults 2/3 female, ulcerated. fibrous proliferation w/ reactive bone or other calcified tissue Tx? Recurrance? |
Peripheral Ossifying Fibroma
tx: excise down to periosteum & remove irritation 16% recurrance |
|
s what is:
benign umor of adipose tissue, ver common - but less in oral cavity most common lcoations are buccal mucosa and vestibule, tongue, floor of mouth then lips most pts age 40+ Tx? |
Lipoma
Tx: conservative local incision |
|
s what is:
exuberant attempt at repair of injured nerve painful, common oral location is mental foramen, tx? |
Traumatic neuroma
tx: excision |
|
s what is: benign neural neoplasm composed of schwann cells. painless, well circumscribed, 25-5-% head/neck, in tongue or bone, usually solitary but may be neurofibromatosis associated.
encapsulated with Antoni A tissue & verocay bodies Tx? |
Neurilemma
Tx: surgical excision |
|
s what is:
peripheral never neoplasm composed of mix of nerve lements: antoni A tissue not seen slow growing painless, not enapsulated solitary, associated w/ neurofibromatosis skin is most freq location, but oral cavity too, tongue, buccal mucosa or bone, Tx? |
Neurofibroma
Tx: local surgical excision |
|
s made of granular cells of disputed histogenesis, favor schwann cell origin
any age, most tongue, 10% show pseudoepitheliomatous hyperplasia. tx? recur? |
Granular cell tumor
40% tongue, 50% incompletely excised, 10% recur , 10% multifocal |
|
s what is:
present at birth, 90%female, 2X max gingiva/ant, 10% multiple Does not have pseudoepitheliomatous hyperplasia Tx? |
Congenital Epulis
does not recur after simple surgical excision |
|
s what is:
benign proliferation of blood vessels, many are hamartomatous in nature. 12% kids have 1+, most common head/neck, Tx? |
Hemangioma
surgery, laser, cryotherapy emobilization, sclerosing agents, pressure many undergo involution |
|
s what is:
congenital hemangiomas, involves 1 side of face & meninges. may have neruologic disorders convolutional calcifications on skill may involve oral mucosa and jaws (vascular gingiva proliferations can resemble pyogenic granulomas |
Sturge Weber Angiomatosis
(encephalotrigeminal Angiomatosis) |
|
s what is:
benign hamartomatous tumors of lymph vessels. Arbitrary classification: lymphaginoma simplex, cavernous lymphangioma, cystic lymphangioma 75% head/neck, post triangle, 90% by age 2. oral lesions on ant 2/3 tongue, Tx? |
Lymphangioma
Tx: surgery is tx of choice |
|
s what is:
markedly dilated lymph vessels most common in neck/axilla may become massive mortality 2-6% |
cystic hygroma
|
|
s benign muscle neoplams vs malignant muscle neoplasms. name striated muscle vs smooth muscle.
|
benign
striated - rhabdomyoma smooth - leiomyoma malignant striated - rhabdomyosarcoma smooth - leiomyosarcoma |
|
s what is:
benign neoplasm of smooth m. rare in oral cavity, often uterus & GI. most oral cases from blood vessels (vascular leiomyomas) other locations? pain? Tx? |
Leiomyoma
also in lips, palate, tongue cheek, most are painless, but hurt occasionally Tx = surgical excision |
|
s what is:
benign neoplasm of skeletal m. head/neck main sites, oral, FOM, tongue soft palate, buccal, multinodular or multifocal, Tx? |
Rhabdomyoma
Tx: excision |
|
s what is:
unusual vascular neoplasm, seen w/ HHV8, multicentric, 4 clinical presentations? |
Kaposi's sarcoma
1. classic 2. endemic 3. latrogenic immunosuppression-associated 4. Aids Related |
|
s Kaposi's 3 stages?
microscopic features range from granulation tissue type appearance to fibrosarcoma type spindle cell proliferation Prognosis? |
Kaposi's Sarcoma
1. patch (macular) 2. plaque 3. Nodular prognosis and therapy varies w/ clinical subtype and stage of disease |
|
s what is:
effects 90% men, late adult life, "chronic" form of disease, italian, jwish, slvic descent, lsow growing red plaques & nodules on skin & lower extermities, often get lymphoreticular malignancy 10-20% mortality in 8-13 years |
Kaposi's Sarcoma
Classic Type |
|
s there are four types of African Endemic type of Kaposi's sarcoma:
1. BN - similar to classic but in young adults 2. A or I - progressive development and invasive 3. F - rapidly progressive & widely disseminated, often visceral involvement 4. L - primarily young black kids, generalized rapidly growing tumors of lymph nodes & viscera |
1. Benign Nodular - similar to classic but in young adults
2. Aggressive or Infective - progressive development and invasive 3. Florid - rapidly progressive & widely disseminated, often visceral involvement 4. Lymphadenopathic - primarily young black kids, generalized rapidly growing tumors of lymph nodes & viscera |
|
s Kaposis sarcoma type ?
it is most often in organ transplant pt's, .4% of kidney transplant pt's , probably due to loss of cellular immunity similar racial predilection as classic form may run more aggressive course than classic |
Iatrogenic Type
|
|
s What is:
most common in usa, begins a single lesion on skin/mucosa trunk,arms,head & neck common oral lesions seen in 50% of AIDS Kaposi's pt's Progressive w/ wide dissemination to lymph nodes & organ systems, Tx how? |
AIDS related type
tx: HAART & sometimes local chemotherapy |
|
s what is:
malignant neoplasm of striated muscle, common soft tissue sarcoma of children. 1st decade, 40% head & neck, painless, rapidly growing mass, may be botryoid, before 60's, 90% fatal now 63% microscopic pattern? |
Rhabdomyosarcoma
microscopic patterns 1. embryonal (1st decade) 2. alveolar (age 16) pleomorphic (age 50) |
|
s what is:
malignant peripheral nerve tissue, 50% of neurofibromatosis, most commin in proximal portions of extremitites & trunk mandible, lips, buccal muclosa Tx? 5 yr? common w/ who? |
Neurogenic Sarcoma
commonmost w/ young adults -neurofibromatosis, age 29 de novo - age 40 5 yr: 16% (neurofibromatosis) 53% (others) |
|
s What is:
malignant tumor of fibroblasts, most common in extremities, 10% head/neck - most in nose/paranasal sinuses, more in young adults/kids slow growing mass. Tx? 5 yr? Spindle cells often in herringbone pattern |
Fibrosarcoma
|
|
s what is:
has both fibroblastic & histocytic differentiation - used to be most common soft tissue sarcoma in adults (older) extermitites & retroperitoneum most common, rare head/neck Tx? recurrance? |
MFH
Malignant Fibrous Histiocytoma (pleomorphic sarcoma) tx w radical surgical resection 40% recurrance, 40% metastasis |
|
s what is:
malignant tumor of muscle (smooth), most common in GI tract (rare orally), middle age/older, appears nonspecific mass, microscopic spindle shaped cells w/ pink cytoplasm Tx? prognosis? |
Leiomyosarcoma
Tx: excision, sometimes with chemo/radiation prognosis (oral) - poor |
|
s What is: malignant neoplasm of fatty origin, 2nd most common soft tissue malignancy in adults. most common thughs, retroperitoneum, & inguinal region, rare head/neck. peaks 40-60. soft/slow growing, ill defined mass
pain/tenderness uncommon Tx? recurrance? 5 yr? |
Liposarcoma
Tx: radical excision, 505 recurrance, 57-70% 5 yr survival |
|
melanocytic lesion shave pigment in 2 says - endogenous & exogenous. 2 examples of each?
|
endo
1.melanin 2. blood/hemosiderin exo 1. heavy metals pigmentation 2. foreign materials |
|
melanin pigmentation comes from melaocytes, tell 3 facts about melanocytes
|
Neural crest origin
clear cell in epithelium possess dendritic processes ability to form melanin may give rise to melanoma |
|
what is:
occurs in mucosa/any race (dark's more affected) symmetrical involment & flat (macular) normal # melanocytes, increased amnt of melain in basal cell layer |
melanoplakia
(physiologic pigmentation) |
|
what is:
common pigment of skin, <3mm, fair skin, dark b/c sun, increase in melanin w/ normal to slightly less # melanocytes sunscreen/avoid sun will decrease / lighten lesions |
ephelis (freckle)
|
|
what is sun induced/symmetrical hyperpigmentation of face/neck
midface/forehead, upper lip, chin. pregnant, or contraceptives, protect from sun helps |
Melasma (mask of pregnancy)
|
|
what is:
rare 1/100K, TB old #1 cause, now leukemic infiltrate/ amyloidosis decreases adrenal cortical hormones, pit to increase ACTH which has MSH type effect on melaocytes pigmentation is eary sign, dark elbows, knees, knuckles, |
addison's disease
(chronic adrenal cortical deficiency) |
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what is:
autosomal dominant, dark freckling around orifaces - oral mucosa/fingers, intestinal polyps common - hamartomatous, can be seen throught GI tract, esp Sm Intestine. |
Peutz Jegher Syndrome
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what is:
light brown macular pigmentation that may be associated w/ syndromes. coast of cali / maine |
Cafe-au-lait pigmentation
cali - neurofibromatosis maine - polyostotic fibrous dysplasia |
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match
mcCune Albright synd., Jaffe's type of fibrous dysplasia w/ - less severe w/o endocrine distrbances - more severe w/ endocrine distrubances |
mcCune Albright synd
Jaffe's type of fibrous dysplasia = more severe w/ endocrine distrubances Jaffe's type of fibrous dysplasia = less severe w/o endocrine distrbances |
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what is:
common 10-40/person. max # by 35, white women, above waist, H&N, form these: |
Acquired Melanocytic Nevi
form Jxnal, compound & intradermal |
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slip slap slop?
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slip on a shirt
slap on a hat slop on the sunscreen |
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melanoma - changes that may hearld transformation of the bnign lesion to malignant one:
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- rapid change size/color
- inflammation - bleeding - ulceration - appearance of pigment around lesion |