Head and Neck Flashcards
Approximately x% of cancers of the head and neck are SCCs, with the remainder largely consisting of x of salivary gland origin.
95
Adenocacrinomas
Head and neck SCC
The pathogenesis is multifactorial:
* x now the primary cause of SCC of the oropharynx.
* Within North America and Europe, oral cavity SCC x
* In India and Asia, x is a major regional predisposing influence.
* x are known predisposing influences for cancer of the lower lip.
- Infection with high-risk human papillomavirus (HPV) is now the primary cause of SCC of the oropharynx.
- Within North America and Europe, oral cavity SCC has classically been a disease of middle-aged individuals who have been chronic users of smoked tobacco and alcohol.
- In India and Asia, the chewing of betel quid and paan is a major regional predisposing influence.
- Actinic radiation (sunlight) and pipe smoking are known predisposing influences for cancer of the lower lip.
- The incidence of oral cavity SCC (particularly involving the tongue) in individuals younger than 40 years of age, who have no known risk factors, has been on the rise. The pathogenesis in this group of patients, who are nonsmokers and are not infected with HPV, is unknown.
In the oropharynx, as many as x% of SCCs, particularly those involving the tonsils, the base of the tongue, and the pharynx, harbor oncogenic variants of x
In the oropharynx, as many as 80% of SCCs, particularly those involving the tonsils, the base of the tongue, and the pharynx, harbor oncogenic variants of HPV, particularly HPV-16.
SCC may arise anywhere in the head and neck region that is lined by x. For the “classic” HPVnegative keratinizing SCC, the favored locations are the x
SCC may arise anywhere in the head and neck region that is lined by stratified squamous epithelium. For the “classic” HPVnegative keratinizing SCC, the favored locations are the ventral surface of the tongue, floor of the mouth, lower lip, soft palate, and gingiva
Differences Between HPV-Associated and Non-Associated SCC
HPV-associated SCC is characterized by the proliferation of nests and lobules of x and basaloid cells growing within sheets of lymphocytes
nonkeratinizing
Immunohistochemical detection of x protein expression can serve as a marker for HPV-associated SCC
p16 protein
The dentigerous cyst originates …
The dentigerous cyst originates around the crown of an unerupted tooth as a result of fluid accumulation between the developing tooth and the dental follicle. Radiographically, these are unilocular lesions most often associated with impacted third molar (wisdom) teeth. Histologically, they are lined by a thin layer of stratified squamous epithelium, and there is frequently a dense chronic inflammatory cell infiltrate in surrounding connective tissue. Complete surgical excision is curative.
The keratocystic odontogenic tumor must be differentiated from other odontogenic cysts because of its aggressive behavior.
Can be seen at any age but are most common between x and x years of age, in x(gender), and within the x.
The keratocystic odontogenic tumor, which was previously referred to as odontogenic keratocyst, must be differentiated from other odontogenic cysts because of its aggressive behavior. Keratocystic odontogenic tumors can be seen at any age but are most common between 10 and 40 years of age, in males, and within the posterior mandible. The lesions are well-defined unilocular or multilocular radiolucencies with a lining consisting of a thin layer of keratinized stratified squamous epithelium with a prominent basal cell layer and a corrugated epithelial surface. Treatment requires complete excision because of locally aggressive behavior. Recurrence rates for inadequately removed lesions can be as high as 60%. About 80% of the lesions are solitary, but patients with multiple cysts should be evaluated for nevoid basal cell carcinoma syndrome (Gorlin syndrome), which is associated with mutations in the tumor suppressor gene PTCH (Patched) on chromosome 9q22
Nasopharyngeal angiofibroma is a x tumor that occurs almost exclusively in x who are often x and x.
Nasopharyngeal a fibroma is a benign, highly vascular tumor that occurs almost exclusively in adolescent males who are often fair-skinned and red headed.
Because nasopharyngeal angiofibroma is often locally aggressive, with intracranial extension, recurrence rates can approach 20%, and 9% of cases can be fatal
Fungi may cause severe chronic sinusitis (e.g., in x), especially in x patients.
Fungi may cause severe chronic sinusitis (e.g., in mucormycosis), especially in diabetic patients.
Sinonasal papilloma is a x neoplasm arising from the respiratory or Schneiderian mucosa lining the nasal cavity and paranasal sinuses.
These lesions occur in three forms: exophytic (most common), endophytic (or inverted), and oncocytic (formerly known as cylindrical cell).
Sinonasal papillomas are most common in males between x and x years of age.
benign
30 and 60 years of age
The endophytic form may invaginate into the underlying stroma. Although this is a benign neoplasm, it can display locally aggressive behavior within both the nose and the paranasal sinuses, including invasion into the orbit or cranial vault, and has a high rate of recurrence if not adequately excised. Malignant transformation occurs in approximately 10% of cases. Most endophytic sinonasal papillomas have EGFR gene mutations. The remaining cases generally harbor HPV DNA, often low-risk types 6 and 11.
Olfactory neuroblastomas arise from neuroectodermal olfactory cells within the mucosa, particularly in the x(sup/inf/post/ant) of the nasal cavity.
Olfactory neuroblastomas arise from neuroectodermal olfactory cells within the mucosa, particularly in the superior aspect of the nasal cavity.
The age distribution is bimodal, with peaks at 15 and 50 years.
Histologically, olfactory n blastomas are small, blue, round cell neoplasms, a category that includes lymphoma, small cell carcinoma, Ewing sarcoma/ peripheral neuroectodermal tumor, rhabdomyosarcoma, melanoma, and sinonasal undifferentiated carcinoma.
Nasopharyngeal carcinoma is characterized by a distinctive geographic distribution, a close anatomic relationship to x tissue, and an association with x infection.
The nomenclature for nasopharyngeal carcinomas continues to evolve, but, at present, is described as one of three patterns:
close anatomic relationship to lymphoid tissue, and an association with EBV infection.
(1) keratinizing SCCs
(2) nonkeratinizing SCCs
(3) basaloid SCCs
The three principal factors that influence development of nasopharyngeal carcinomas are heredity, age, and EBV infection.
Antrochoanal polyps (ACP) are x sinonasal polyps that arise within the x sinus.
Antrochoanal polyps (ACP) are solitary sinonasal polyps that arise within the maxillary sinus (antrum). They pass through and enlarge the sinus ostium and posterior nasal cavity at the level of the choana.
ntrochoanal polyps represent only ~5% of sinonasal polyps 3. They are most commonly seen in young adults in their 3rd to 5th decades.
Laryngitis may occur as the sole manifestation of allergic, viral, bacterial, or chemical insult, but it is more commonly associated with generalized upper respiratory tract infection, heavy environmental toxin exposure (e.g., x), or x
(e.g., tobacco smoke), or gastroesophageal reflux due to irritating effects of gastric contents.
The vast majority of branchial cysts are thought to arise from remnants of the x branchial arch and are most commonly observed in x between x and x years of age.
The vast majority of branchial cysts are thought to arise from remnants of the second branchial arch and are most commonly observed in young adults between 20 and 40 years of age.
Paragangliomas arise from neuroendocrine cells associated with the x and x x systems and occur at many sites
x are the most common paraganglioma
Paragangliomas arise from neuroendocrine cells associated with the sympathetic and parasympathetic nervous systems and occur at many sites.
Adrenal medullary phaeochromocytomas are the most common paraganglioma.
Approximately 70% of extra-adrenal paragangliomas occur in the head and neck.
The carotid body tumor is a typical parasympathetic x. It rarely exceeds 6 cm in diameter and arises close to or envelops the bifurcation of the common carotid artery.The tumor tissue is red-pink to brown, and the microscopic features are characteristic of paragangliomas at all sites.
Nests (zellballen) of round to oval chief cells with abundant, clear or granular, eosinophilic cytoplasm and uniform, round to ovoid, sometimes vesicular, nuclei are surrounded by delicate vascular septae
paraganglioma
Carotid body tumors, and paragangliomas in general, are rare, slow-growing, painless masses that usually arise in the x decades of life.
Tumors associated with multiple endocrine neoplasia type x most often occur within the adrenal pheochromocytomas.
Carotid body tumors frequently x after incomplete resection and, despite their benign appearance, may metastasize to regional lymph nodes and distant sites.
Carotid body tumors, and paragangliomas in general, are rare, slow-growing, painless masses that usually arise in the fifth and sixth decades of life. They commonly occur singly and sporadically but also may be familial.
Tumors associated with multiple endocrine neoplasia type 2 most often occur within the adrenal (pheochromocytomas)
Carotid body tumors frequently recur after incomplete resection and, despite their benign appearance, may metastasize to regional lymph nodes and distant sites.
About 50% ultimately prove fatal, largely because of infiltrative growth. Unfortunately, histologic features do not predict the clinical course of a carotid body tumor—mitoses, pleomorphism, and even vascular invasion are not reliable indicators.