Onco in Greek means swelling or mass.
For neoplasia to occur, an irreversible change must take place in the cells, and this change must be passed on to the new cells.
Unlike hyperplasia, neoplasia is an uncontrolled abnormal process.
Cells are abnormal; proliferation of these cells is uncontrolled and unlimited.
Radiation from sunlight (ultraviolet rays), x-rays, nuclear fission, or other sources is well established as a cancer-producing agent in humans.
Tumors are divided into two categories: benign and malignant.
Cancer is synonymous with malignancy.
Refer to Table 7.1: Comparison of Benign and Malignant Tumors.
Figure 7.1: Photomicrographs of malignant tumors show pleomorphic (P) and hyperchromatic (H) nuclei and mitotic figures (MI). A, Squamous cell carcinoma. B, Osteosarcoma.
Normal and abnormal mitotic figures are seen in the nucleus of the neoplastic cells.
Table 7.2 lists names of tumors.
The prefix of the name of a tumor is determined by the cell or tissue of origin.
The suffix -oma is used to indicate tumor.
The names of some malignant tumors sound like benign tumors. Lymphoma, melanoma, and myeloma sound benign, but are always malignant.
For malignant tumors, often a combination of two or three modalities is used.
Three different types of epithelial tumors occur in the oral cavity.
These are the types of squamous epithelium tumors that are discussed in this section.
Figure 7.2, A shows the clinical appearance of a papilloma of the oral mucosa that shows a cauliflower-like appearance and rough surface resulting from fingerlike projections.
Figure 7.2, B shows the microscopic appearance of a papilloma that shows fingerlike projections surfaced by squamous epithelium and supported by thin cores of fibrous connective tissue.
Three types of premalignant lesions are discussed in this section.
Figure 7.3 shows the clinical appearance of leukoplakia. A, Floor of the mouth. B, Maxillary alveolar mucosa and palate. The cause of these lesions could not be identified.
Leukoplakia is a clinical term that does not refer to a specific microscopic appearance.
Sometimes called idiopathic leukoplakia to indicate that the specific cause of the lesion is not known.
Figure 7.4 shows the clinical appearance of a white lesion that was associated with smokeless tobacco (smokeless tobacco–associated keratosis). This lesion developed on the lower labial mucosa at the site where the tobacco was held.
Depending on the study, approximately 5% to 25% of leukoplakias examined microscopically demonstrate epithelial dysplasia.
A specific form of leukoplakia called proliferative verrucous leukoplakia is characterized by the development of persistent, slowly spreading, rough-surfaced, keratotic plaques.
In one study, 60 cases of leukoplakia were seen for every 1 case of erythroplakia.
When examined microscopically, more than 90% of cases of erythroplakia demonstrate epithelial dysplasia or squamous cell carcinoma.
Malignant transformation of oral submucous fibrosis to squamous cell carcinoma has been reported to be between 2% and 8%.
Figure 7.5 shows the microscopic appearance of epithelial dysplasia. Loss of the normal stratification of the epithelium, hyperplasia of the basal cells, and enlarged, hyperchromatic nuclei are seen.
Unlike squamous cell carcinoma, the cellular changes in epithelial dysplasia may revert to normal if the stimulus, such as tobacco smoking, is removed.
These lesions are developmental and characterized by disordered growth. They are not considered premalignant lesions.
All dysplastic lesions should be excised surgically.
Close long-term follow-up examinations are indicated because of the potential for recurrence.
It is also called epidermoid carcinoma.
Squamous cell carcinoma can infiltrate and destroy bone.
Figure 7.6: A, Clinical appearance of a squamous cell carcinoma of the posterolateral tongue shows an exophytic, ulcerated mass. B, Clinical appearance of a squamous cell carcinoma on the left side of the soft palate and facies. C, Clinical appearance of a squamous cell carcinoma on the floor of the mouth. D, Left side of a panoramic radiograph shows destruction of the mandible by a squamous cell carcinoma.
The essential microscopic feature of a squamous cell carcinoma is the invasion of tumor cells through the epithelial basement membrane into the underlying connective tissue.
Figure 7.7: A, Microscopic appearance (low power) of a squamous cell carcinoma shows infiltration of the tumor into the connective tissue. B, High-power photomicrograph shows abnormal keratinization and keratin pearls (K).
In addition to normal surface keratin, the keratin may be see in individual cells within the tumor and as structures called keratin pearls.
Figure 7.8: A and B, Clinical appearance of squamous cell carcinoma of the lower lip. Squamous cell carcinoma (arrow) is seen with actinic (solar) cheilitis in (A).
The majority of squamous cell carcinomas occur in patients over 40 years of age.
Avoidance of sun exposure and the use of a sun-blocking agent are important in preventing the damaging effects of sunlight.
The proportion of smokers is much higher among patients with oral squamous cell carcinoma than among the general population.
There is no evidence that chronic irritation is an initiating factor in the development of oral cancer.
TNM staging is shown on the next slide.
Table 7.3 shows the TNM staging system.
The higher the stage, the worse the prognosis.
It is important to clinically identify asymptomatic areas of leukoplakia and erythroplakia while they are small and to remove all potentially premalignant lesions.
Figure 7.9, A shows the clinical appearance of a verrucous carcinoma occurring on the commissure and anterior buccal mucosa.
Most cases occur in men over 55 years of age.
Figure 7.9, B shows the clinical appearance of a verrucous carcinoma occurring on the maxillary alveolar ridge.
Treated by surgical excision. Although it is a carcinoma, it usually does not metastasize; therefore prognosis is better for verrucous carcinoma than for squamous cell carcinoma.
Figure 7.10 shows the clinical appearance of a basal cell carcinoma (arrow), illustrating the characteristic “rolled” borders.
Locally invasive tumor that can become quite large and disfiguring if not removed
As a general rule, a patient should be referred to an oral and maxillofacial surgeon or dermatologist to have a biopsy performed on any nonhealing ulcer of the skin or lips that has been present for more than 2 weeks.
Tumors of minor salivary gland origin are much more common in the upper lip than in the lower lip.
Figure 7.11, A shows a benign salivary gland tumor of the palate (pleomorphic adenoma).
All salivary gland tumors are diagnosed on the basis of their microscopic appearance.
Figure 7.11: B, Malignant salivary gland tumor of the palate (adenoid cystic carcinoma). Biopsy site should be noted. C, Benign salivary gland tumor of the upper lip (pleomorphic adenoma). D, Malignant salivary gland tumor of the buccal mucosa (mucoepidermoid carcinoma). E, Malignant salivary gland tumor of the tongue (adenoid cystic carcinoma).
A biopsy and microscopic examination of the tissue are required to establish a specific diagnosis.
Tumors of minor salivary gland are much more common in the upper lip than in the lower lip.
The most common extraoral location for the pleomorphic adenoma is the parotid gland; the most common intraoral location is the palate. However, these tumors may occur wherever salivary gland tissue is present.
Figure 7.12 shows the microscopic appearance of a pleomorphic adenoma. A, Low-power photomicrograph shows a capsule (C). B, High-power photomicrograph shows a mixture of epithelium (E) and connective tissue (CT).
Most pleomorphic adenomas occur in individuals over 40 years of age, and a female predilection has been noted.
A small percentage (2% to 4%) of long-standing pleomorphic adenomas have been reported to undergo malignant transformation.
Figure 7.13 shows the microscopic appearance of a portion of a monomorphic adenoma.
Recently, more specific names rather than monomorphic adenoma have been used for this group of tumors. Canalicular and basal cell adenomas are monomorphic-type adenomas that are named for the microscopic pattern of the tumor.
Figure 7.14 shows the microscopic appearance of a portion of a papillary cystadenoma lymphomatosum (Warthin tumor), with spaces lined by epithelium and surrounded by sheets of lymphocytes.
Often develops bilaterally and occurs predominantly in adult men.
A higher incidence is noted in individuals who smoke.
Most studies shows that the mucoepidermoid carcinoma represents the most common malignant salivary gland neoplasm.
Figure 7.15: A, Microscopic appearance (low power) of a mucoepidermoid carcinoma shows cystic structures, mucous cells, and epidermoid cells. B, Radiograph of a central mucoepidermoid carcinoma shows a multilocular radiolucency.
On occasion, a mucoepidermoid carcinoma may arise centrally within bone.
May occur over a wide age range.
Usually occurs in adults after middle age; this tumor is the most common malignant salivary gland neoplasm in children.
Low-grade tumors have a 92% 5-year survival rate after initial treatment.
For high-grade tumors, only 49% of patients survive 5 years after the initial treatment.
Unencapsulated and infiltrates surrounding tissue.
The adenoid cystic carcinoma is a slow-growing malignant tumor.
Figure 7.16 shows the microscopic appearance of an adenoid cystic carcinoma, with perforated islands of uniform cells. The tumor (T) is seen infiltrating the adjacent adipose tissue.
Radiation treatment has been attempted and has been shown to be of benefit in some cases.
Metastasis occurs late in the course of the disease.
About 30% of patients experience cervical lymph node involvement.
In addition to the adenoid cystic and mucoepidermoid carcinomas, several other malignant salivary gland tumors exist.
Odontogenic tumors are derived from tooth-forming tissues.
Some odontogenic tumors are composed of epithelium only; some are composed of mesenchymal tissue only, and others are composed of a mixture of both elements.
Table 7.4 shows the classification of central odontogenic tumors.
Malignant odontogenic tumors occur but are rare.
Most odontogenic tumors are benign.
These are the types of epithelial odontogenic tumors.
Figure 7.18, B is a radiograph of an ameloblastoma showing multilocular radiolucency in the molar area of the mandible.
When it occurs in the maxilla, death can result from direct extension into the brain and adjacent vital structures.
Figure 7.17: Microscopic appearance (low power) of a follicular ameloblastoma shows dental follicle–like islands composed of epithelial cells consisting of peripheral ameloblast-like cells (A) and stellate reticulum–like areas (S).
80% of ameloblastomas arise in the mandible.
Figure 7.19 (top) shows a radiograph of an ameloblastoma that formed in association with an impacted tooth and dentigerous cyst.
Figure 7.18, A (bottom) is a radiograph of an ameloblastoma showing multilocular radiolucencies in the molar area of the mandible.
Recurrence is common.
When these occur in the gingiva and do not involve bone, they’re known as peripheral ameloblastomas.
Figure 7.20, A shows the microscopic appearance (low power) of a calcifying epithelial odontogenic tumor, with sheets of epithelial cells (E), amorphous material (A), and calcifications (C).
It is also known as a Pindberg tumor.
Figure 7.20, B is a radiograph of a calcifying epithelial odontogenic tumor showing a multilocular radiolucency.
Majority of affected patients are adults.
Recurrence is rare; lower than that for an ameloblastoma.
Figure 7.21, B is a radiograph of an adenomatoid odontogenic tumor showing a unilocular radiolucency surrounding the crown of an unerupted maxillary cuspid. (Note that the radiolucency extends beyond the cemento-enamel junction.)
Many are associated with the crown of an unerupted tooth.
Figure 7.21, B shows the microscopic appearance of a portion of an adenomatoid odontogenic tumor, with the capsule (C), epithelial cells, and ductlike structures (D).
Microscopic examination reveals a dense, fibrous connective tissue capsule surrounding ductlike structures.
Clinician should treat an AOT conservatively by enucleation.
Recurrence is rare.
Figure 7.22, B is a radiograph of a calcifying odontogenic cyst showing a unilocular radiolucency of the mandible.
No significant sex predilection is noted; lesions occur equally in maxilla and mandible.
Figure 7.22, A shows the microscopic appearance of a calcifying odontogenic cyst, with a cystic structure lined by odontogenic epithelium (E) with associated ghost cells (G).
The solid variant may exhibit more aggressive behavior and should be treated by a more extensive surgical procedure.
These are the three types of mesenchymal odontogenic tumors that are discussed in this section.
Figure 7.23, B is a radiograph of an odontogenic myxoma showing a multilocular, honeycombed radiolucency.
The tumor may be quite large and cause tooth displacement.
Figure 7.23, A is a photomicrograph of an odontogenic myxoma showing background substance containing widely dispersed cells with long cytoplasmic processes.
The extent of the surgery depends on the size of the tumor.
The recurrence rate is approximately 25%, and most recurrences take place within 2 years of treatment.
Figure 7.24, C is a radiograph of a central cementifying fibroma showing a well-circumscribed radiolucent lesion.
Figure 7.24, A is a photomicrograph of a central cementifying fibroma showing rounded, globular calcifications (GC) and cellular fibrous connective tissue (FCT). B is a radiograph of a central cementifying fibroma showing a radiolucent and radiopaque lesion.
Because these lesions are well delineated, they separate easily from the surrounding bone.
Figure 7.25 is a radiograph of a benign cementoblastoma showing a well-circumscribed radiopaque mass surrounded by a radiolucent halo and attached to the roots of a mandibular first molar.
The radiolucent halo represents the periodontal ligament.
These are three types of mixed odontogenic tumors that are discussed in this section.
Most cases occur in individuals younger than 20 years of age.
Figure 7.26, A shows the microscopic appearance of an ameloblastic fibroma, with a combination of odontogenic epithelium (E) and mesenchymal tissue (M).
Most patients are asymptomatic.
Figure 7.26, B is a radiograph of an ameloblastic fibroma showing a poorly defined unilocular radiolucency.
Radiographically, the ameloblastic fibroma appears as either a well-defined or poorly defined unilocular or multilocular radiolucency.
Some patients may experience swelling of the affected area.
This is a well-circumscribed lesion that usually separates from the surrounding bone.
Figure 7.27 is a radiograph of a compound odontoma showing a collection of numerous, small, toothlike radiopacities surrounded by a radiolucent halo.
An odontoma is an odontogenic tumor composed of mature enamel, dentin, cementum, and pulp tissue.
Figure 7.28 is a radiograph of a complex odontoma showing a radiopaque mass surrounded by a radiolucent halo.
There is no sex predilection.
These tumors generally do not recur.
Several of the odontogenic tumors have been reported to occur on the gingiva without underlying bone involvement.
Figure 7.29 shows the clinical appearance of a peripheral ameloblastoma.
The peripheral ossifying fibroma is composed of a combination of fibrous tissue and islands or strands of odontogenic epithelium.
Surgical excision is the preferred treatment for peripheral ossifying fibroma.
Tumors of soft tissue include benign and malignant tumors of adipose (fat) tissue, nerve, muscle, blood vessels, and lymphatic vessels.
Figure 7.30, A shows the clinical appearance of a lipoma.
No sex predilection is noted.
Figure 7.30, B is a photomicrograph of a lipoma showing mature fat cells.
A lipoma generally does not recur.
These are the types of tumors of nerve tissue that are discussed in this section.
Figure 7.31, A shows the clinical appearance of a neurofibroma, with a nonulcerated mass on the lateral border of the tongue.
A schwannoma is derived from Schwann cells and perineural fibroblasts.
Figure 7.31, B shows a photomicrograph of a neurofibroma.
Schwannomas have been reported to occasionally cause a complaint of pain.
Figure 7.32, A shows the clinical appearance of a granular cell tumor of the tongue with a nonulcerated mass.
This tumor most likely arises from a neural or primitive mesenchymal cell.
Figure 7.32, B is a photomicrograph of a granular cell tumor showing granular cell(s) (G) between striated muscle fiber(s) (M). C is a photomicrograph of a granular cell tumor showing overlying pseudoepitheliomatous hyperplasia.
This tumor is treated by surgical excision and does not recur.
This neoplasm most likely arises from a primitive mesenchymal cell.
Occasional examples have regressed without treatment.
Rhabdomyomas and leiomyomas are called vascular leiomyomas and occasionally occur in the oral cavity.
Despite treatment, the prognosis is poor.
These are the types of vascular tumors discussed in this section.
Figure 7.33, B shows the clinical appearance of a vascular malformation of the lower lip.
This common vascular lesion is considered by many to represent a developmental lesion rather than a tumor.
Figure 7.33, C is the clinical appearance of a vascular malformation of the buccal mucosa.
More than half of the hemangiomas that occur in the body occur in the head and neck area.
When a hemangioma occurs in an adult, it should be referred to as a vascular malformation.
Figure 7.33, D shows the microscopic appearance of a cavernous hemangioma, with large dilated blood vessels (B) filled with red blood cells (RBC).
Injection of a sclerosing solution into the lesion will cause it to shrink or resolve.
Unlike a hemangioma, a lymphangioma will not shrink after injection with a sclerosing solution.
Malignant vascular tumors arising from endothelial cells include an angiosarcoma and Kaposi sarcoma.
In the 1980s, with the advent of HIV, Kaposi sarcoma appeared in a much more aggressive form.
In HIV-positive patients, recurrence is common, and the disease may progress rapidly.
These are two types of tumors of melanin-producing cells that will be discussed in this section.
Figure 7.34 is the clinical appearance of a melanocytic nevus showing a well-defined pigmented lesion on the labial mucosa.
What is the plural form of nevus? (Nevi)
Intraoral tumors consist of tan-to-brown macules or papules that occur most often on the hard palate.
Pigmented lesions that exhibit ulceration, an increase in size, or a change in shape or color may be malignant.
What does ABCDE stand for in terms of assessing pigmented skin? (Asymmetry, Border, Color, Diameter, and Evolving)
Figure 7.35 is the clinical appearance of malignant melanoma showing a darkly pigmented lesion in the area of the facies.
All melanomas are malignant.
Melanoma usually presents as a rapidly enlarging, blue-to-black mass.
The prognosis for oral melanoma is poor.
These are the types of tumors of bone and cartilage discussed in this section.
Multiple osteomas are a component of Gardner syndrome, which is transmitted genetically and is discussed in Chapter 6.
Figure 7.36 is a radiograph of an osteoma that shows a radiopacity of the posterior mandible.
Figure 7.37, A is the clinical appearance of an osteogenic sarcoma showing swelling.
Tumors that involve the long bones occur at an average age of 27 years.
Some patients initially present with a toothache or tooth mobility.
Figure 7.37, B is a radiograph of an osteogenic sarcoma in the left molar area showing a poorly defined radiopaque lesion.
In some cases, asymmetric widening of the periodontal ligament space and a sunburst pattern may be seen radiographically.
Only about 20% of patients with an osteosarcoma of the jaws survive 5 years.
Only about 30% of patients with chondrosarcoma involving the jaws survive 5 years after the diagnosis.
Figure 7.38 is the clinical appearance of a chondrosarcoma showing an exophytic mass in the anterior mandible.
These tumors of blood-forming tissues are discussed in this section.
Figure 7.39 shows the clinical appearance of a patient with leukemic infiltration of the gingiva, resulting in diffuse enlargement.
Several types of leukemia are classified according to the kind of cells that are proliferating: myelocytes, lymphocytes, or monocytes.
Leukemias are divided into two forms—acute and chronic.
Rarely, a lymphoma may present as a primary lesion in the oral soft tissues or bone.
The prognosis depends on the type of lymphoma and the extent of involvement.
Figure 7.40, A is the microscopic appearance of multiple myeloma showing a proliferation of plasma cells.
Pathologic fracture of an involved bone is common and typically occurs in bones weakened as a result of their destruction by the proliferation of neoplastic plasma cells.
Oral complications related to this treatment are discussed in Chapter 9.
On occasion, the oral metastatic tumor is the first manifestation of a primary tumor elsewhere.
Radiographically, the appearance of metastatic tumors varies.
Systemic bisphosphonate medication is used to prevent bone destruction in patients with tumors such as breast and prostate cancer that metastasize to bone.
Figure 7.41 is a radiograph showing diffuse radiolucent and radiopaque changes resulting from metastatic carcinoma of the prostate gland.