Squamous Cell Carcinoma

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Squamous cell carcinoma

Incidence
 Squamous cell carcinoma accounts for 90 per cent or more of all oral malignant
neoplasms.

Etiology
 Tobacco smoking
o pipes
o cigars
o cigarettes
o bidis
o reverse smoking
 Smokeless tobacco
o snuff dipping
o tobacco sachets
o tobacco chewing
o Betel chewing, betel quid, areca nut
 Alcohol
o spirits
o wines and beers
o alcohol and tobacco synergism
 Diet and nutrition
o iron deficiency
o vitamins A, C and E
o nutritional deficiencies and alcoholism
 Dental factors
 Ultraviolet light
 Viruses
o herpes simplex viruses
o human papillomaviruses
o human immunodeficiency virus
o Epstein-Barr virus
 Immunosuppression
 Chronic infections
o candidosis
o syphilis
 Occupation
Clinical Features

 Commonly occurs in 4th decade.


 Male predilection.
 Early diagnosis is the most important factor influencing prognosis.

1. Early lesion
 Usually asymptomatic, having variable appearances such as white patch, a small
exophytic growth (with or without ulceration or erythema), a small indolent ulcer, or
an area of erythroplakia.
 Pain can be a feature.
 Ulceration, induration and fixation of affected tissue to underlying structures.
 Underlying bone destruction in case of carcinoma arising from alveolar mucosa.
 Lymph node may not be involved. If the are palpable, they are due to inflammatory
response.
2. Advanced lesion
 Presented as broad-based exophytic mass with a rough, nodular, warty,
hemorrhagic, or necrotic surface.
 Or as a deeply destructive and craterlike ulcer with raised, rolled evened edges.
 Infiltration of the oral musculature may result in functional disturbances.
 Difficulty in swallowing if tongue is involved.
 Pain may be feature.
 Bone invasion may be detected on radiographs.
 Mobility of teeth.
 Alteration of taste over the distribution of mental nerve.
 Pathological fracture.
Sites
SCC of alveolar ridge is most common, followed by retromolar region (Oropharynx)
gingiva, floor of the oral cavity, lower lip, and base of the tongue.

Investigations
 Photographs
 Incisional biopsy
 FNAC (Lymph node cytology)
 OPG
 CXR
 ECG
 CBC
 MRI and CT head and neck (for staging)
Histology

A. Epithelium

1. Well-differentiated tumours
 Neoplastic squamous epithelium with masses of prickle cells and limiting basal
cells around periphery.
 Intercellular bridges are recognizable.
 Keratin pearls (keratin surrounded by whorls of prickle cells) are found within
masses of infiltrating cells.
 Nuclear and cellular pleomorphism is not prominent.
 A few mitotic figures.

2. Moderately-differentiated tumours
 Epithelium is still recognized as squamous in type.
 Show less keratinization.
 More cellular and nuclear pleomorphism.
 More mitotic activity

3. Poorly-differentiated tumour
 Epithelial cells are hardly recognizable as epithelial cells in some poorly-
differentiated tumours.
 Keratinization is usually absent.
 Prominent cellular and nuclear pleomorphism.
 Abundant mitoses.

4. Undifferentiated tumours
 Show complete anaplasia.
B. Stroma
 Variable lymphocytic and plasma cell infiltration.
 2 patterns of infiltration:
i. Cohesive invasive front consists of broad groups of sheets of malignant
cells. It has better prognosis.
ii. Non-cohesive consists of small islands and narrow strands as individual
cell infiltration.

Variants of SCC
 Verrucous carcinoma
 Nasopharyngeal carcinoma
 Adenoid SCC
 Basaloid SCC
 Basal cell carcinoma
 Adenosquamous carcinoma
 Spindle cell carcinoma
Spread of carcinoma

1. Local invasion
 lymphatic permeation
 vascular invasion
 sarcolemmal spread
 perineural spread
 invasion of bone (edentulous/dentate)

2. Metastatic spread to regional lymph nodes in neck


 intracapsular spread (tumour confined within capsule of node)
 extracapsular spread (tumour infiltrates through the capsule into the adjacent
tissue of the neck)

3. Blood-borne metastases to distant sites occur relatively late during the disease.

TNM staging

Primary tumour staging (T)


 Tx - tumour cannot be assessed
 T0 - no evidence of primary tumour
 Tis - carcinoma in situ
 T1 - tumour 2 cm or less in greatest dimension
 T2 - tumour greater than 2 cm and less than 4 cm in greatest dimension
 T3 - tumour greater than 4 cm in greatest dimension
 T4 - tumour invades adjacent structures (mandible, maxilla, skin, extrinsic muscles of the
tongue)

Nodal status (N)


 Nodal staging is the same for SCCs of the oral cavity, oropharynx, hypopharynx and
larynx.
 Nx - nodes cannot be assessed
 N0 - no regional nodal metastases
 N1 - single ipsilateral node, ≤ 3cm
 N2
o N2a - single ipsilateral node, 3-6 cm
o N2b - multiple ipsilateral nodes, < 6 cm
o N2c bilateral nodal metastases OR contralateral nodal metastases < 6 cm
 N3 - any nodal metastasis > 6 cm

Metastases (M)
 M0 - no metastases
 M1 - distant metastases present
Clinical Staging
Stage 1 Tl NO MO
Stage 2 T2 NO MO
Stage 3 T3 NO MO or
Tl, T2, or T3 Nl MO
Stage 4 T4 NO or Nl MO or
any T N2 orN3 MO or
anyT any N Ml

Management
 Management regimens for cancer must focus on longevity and quality of life.
 Coordinated by a multidisciplinary team, including maxillofacial surgeons, oncologists,
radiotherapists, speech therapists, dedicated oncology nurses, and other personnel
involved in rehabilitation.
 The treatment of choice depends on several factors including patient preference,
biological age, general health, and site and staging of the tumour.
 Majority of cases involves surgery (with reconstruction), radiotherapy, or a combination
of both.
 Chemotherapy is not routinely used.

Differential Diagnosis
 Actinic keratosis
 Basal cell carcinoma
 Pyoderma gangrenosum
 Viral wart
 Keratocanthoma

References
Tyldesly’s Oral Medicine 5th Edition
Oral Pathology by J. V. Soames 4th Edition
Written by:
Izaz Ullah
3rd Year BDS
KMU-IDS, Kohat

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