Literature DB >> 17208674

Imaging of tongue carcinoma.

Cheng K Ong1, Vincent F H Chong.   

Abstract

The tongue enables taste and plays a critical role in formation of food bolus and deglutition. The tongue is also crucial for speech and the earliest sign of tongue paresis is a change in the quality of speech. Given the importance of the tongue, tongue carcinoma should be accurately staged in order to optimise treatment options and preserve organ function. The intent of this review is to familiarize radiologists with the pertinent anatomy of the tongue and the behaviour of tongue carcinoma so as to map malignant infiltration accurately. (c) International Cancer Imaging Society.

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Year:  2006        PMID: 17208674      PMCID: PMC1766559          DOI: 10.1102/1470-7330.2006.0029

Source DB:  PubMed          Journal:  Cancer Imaging        ISSN: 1470-7330            Impact factor:   3.909


Introduction

The tongue is the centrepiece of the oral cavity and the oropharynx. It enables taste of food and plays a critical role in formation of food bolus and deglutition. The tongue is also crucial for speech. Speech is impaired by glossectomy, the degree of which depends on the extent of the resection. In fact, the earliest sign of tongue paresis is a change in the quality of speech. Given the importance of the tongue, tongue carcinoma should be accurately staged in order to optimise treatment options and preserve organ function. The intent of this review is to familiarise radiologists with the pertinent anatomy of the tongue and the behaviour of tongue carcinoma so as to map malignant infiltration accurately. It should be noted that surgical resection of the tongue base often necessitates total laryngectomy to prevent food aspiration.

Applied anatomy

The tongue has a dorsum, apex, inferior surface and root. The root (base) is attached to the hyoid bone and mandible while the apex forms the tip of the tongue. The sulcus terminalis, a shallow groove with the circumvallate papillae just anterior to it, divides the tongue into the oral (anterior two-thirds) and pharyngeal (posterior third) parts. As a general guide on axial imaging, a line joining the anterior aspect of the mandibular rami may be used as the dividing line between these two parts, which differ in their developmental origins and hence their nerve supplies. The mucosa of the oral tongue derives from the ectodermal lining of the midline tuberculum impar and the pair of lateral lingual swellings of the first pharyngeal (mandibular) arch. The sensory supply of this mucous membrane, excluding the region of the circumvallate papillae is by the lingual branch of the mandibular nerve whose trigeminal component mediates common sensation, and whose chorda tympani component mediates taste. The mucosa of the pharyngeal tongue (base of the tongue) originates from the endodermal lining of the third pharyngeal arch, with a small contribution from the fourth arch. This mucosa, together with the pre-sulcal area of the circumvallate papillae is predominantly supplied by the glossopharyngeal nerve, which mediates both common sensation and taste. The small area of lingual mucosa in the anterior wall of the vallecula, which develops from the fourth pharyngeal arch, is mediated by the internal laryngeal nerve. The oral tongue has a free margin bounded anteriorly and laterally by the alveolar margins. The pharyngeal tongue, which is really the anterior wall of the oropharynx, extends from the sulcus terminalis to the epiglottis and is bounded laterally by the glossopharyngeal sulci. The valleculae (which are considered as part of the tongue), are 1-cm strips of smooth mucosa that form the transition between the tongue base and the epiglottis. The tongue has a supporting fibrous framework consisting of the lingual septum (Fig. 1) and the hyoglossus membrane. The midline fibrous lingual septum divides the tongue into two symmetrical muscular halves.
Figure 1

(a) Axial T1 weighted image shows the tongue muscles, genioglossus (long arrow) and hyoglossus (short arrow). (b) Coronal T1 weighted image shows lingual septum (short arrow) and mylohyoid (long arrow), which forms the floor of the mouth.

The tongue is essentially a mass of skeletal muscles covered by mucous membrane. Its muscles are divided into intrinsic and extrinsic groups. The intrinsic muscles are entirely within the tongue with no bony attachment, and are organised into superior and inferior longitudinal, vertical and transverse bands. Their principle function is altering the shape of the tongue. The extrinsic muscles consist of genioglossus, hyoglossus, styloglossus and palatoglossus. These extrinsic muscles stabilise the tongue and alter its position, as well as its shape. The anatomy of the tongue is well demonstrated on magnetic resonance imaging (MRI). On axial T1-weighted images, fat with high signal intensity can be seen interspersed between the muscles of intermediate signal intensity (Fig. 1). Genioglossus is the largest of all the tongue muscles and forms the bulk of the tongue. It arises from the genial tubercle and is easily seen on computed tomography (CT) and MRI (Fig. 1). It fans out widely and inserts inferiorly into the hyoid bone; posteriorly into the tongue base; and superiorly into the entire ventral surface of the tongue. Hyoglossus is a thin quadrilateral sheet of muscle arising from the hyoid bone. It ascends superiorly, interdigitating with the fibres of the styloglossus, and attaches to the side of the tongue. The hyoglossus muscles define the lateral margins of the tongue and are readily identified on CT and MRI (Fig. 1). Both the styloglossus (which arises from the styloid process and stylohyoid ligament) and the palatoglossus (which originates from the palatine aponeurosis) cannot be seen with certainty on imaging studies. Tongue muscles are derived from the myotomes of the occipital somites, which migrate anteriorly carrying their nerve supply. All the muscles of the tongue, intrinsic and extrinsic, are thus innervated by the hypoglossal nerve. The exception being palatoglossus, which being essentially a palate muscle, is supplied by the pharyngeal plexus. The lingual artery, a branch of the external carotid artery, supplies the bulk of each half of the tongue. There are small contributions from the tonsillar branch of the facial artery and from the ascending pharyngeal artery. The fibrofatty lingual septum restricts any significant vascular anastomosis across the midline except the tip of the tongue. One lingual artery may be sacrificed, but sacrificing both arteries leads to high risk of anterior tongue necrosis and almost certain loss of the tongue base [1]. The tongue has a rich lymphatic network. Unlike the vascular supply that remains largely unilateral, lymph from one side, particularly from the tongue base, drains into nodes on both sides of the neck. Lymph from the tip of the tongue may drain to the submental nodes. Marginal lymphatics from the outer third of the rest of the oral tongue are directed to ipsilateral submandibular and jugulodigastric nodes. Central lymphatics of the inner two-thirds of the oral tongue have pathways to nodes of both sides of the neck. As a clinical guide, tumour extending more than 5 mm from lateral tongue margin has an increased risk of bilateral metastatic lymphadenopathy [2] (Fig. 2).
Figure 2

(a) Axial T2 weighted fat-suppression image shows a right-sided tongue cancer extending more than 5 mm from the lateral margin of the tongue. (b) Coronal T2 weighted fat-suppression image shows bilateral submandibular lymphadenopathy (arrows), a result of the lymphatic drainage pathways of the inner two-thirds of the oral tongue.

Pathological anatomy

Staging

Accurate tumour staging is crucial in cancer management because it (i) aids treatment planning; (ii) gives some indication of prognosis; (iii) assists the evaluation of treatment outcomes; (iv) facilitates the exchange of information between treatment centres; and (v) contributes to the continuing research and study of human cancer. At present, the Tumour Node Metastasis (TNM) classification is the most commonly used system for describing malignant tumours, their regional involvement and distant metastases [3]. The TNM and stage grouping are presented in Tables 1 and 2. This TNM staging system should be the guide for every radiologist when reporting studies performed for assessment of tongue carcinomas.

Imaging

MRI is the preferred modality in the evaluation of tongue carcinomas (Fig. 3). The abnormal signals seen on MRI are well correlated with pathological findings [4]. Tumour invasion of the floor of the mouth is particularly well seen on coronal images (Fig. 4). Sagittal images provide information on tongue base involvement and the extent of pharyngeal infiltration that cannot be seen on CT (Fig. 5). However, cortical bone involvement, notably the mandible is diagnosed with a higher level of certainly on CT (Fig. 6).
Figure 3

(a) Axial T1 weighted, (b) post-contrast T1 weighted fat-suppression and (c) T2 weighted fat-suppression images show a left-sided oral tongue carcinoma. Note that the tumour is most conspicuous on T2 weighted fat-suppression sequence.

Figure 4

(a) Axial post-contrast T1 weighted fat-suppression image shows a right-sided oral tongue carcinoma (arrow). (b) Coronal T2 weighted fat-suppression image shows tumour infiltration of the floor of the mouth (long arrow). Note the normal contralateral mylohyoid muscle (short arrow). (c) Coronal T2 weighted fat-suppression image of another patient shows a right-sided oral tongue cancer (short arrow). Note the sublingual glands (long arrows), which should not be confused as tumour infiltration.

Figure 5

(a) Axial T2 weighted fat-suppression image shows a right-sided tongue base cancer (long arrows). An enlarged right jugulodigastric node is also seen (short arrow), the first echelon node of tongue base carcinoma. (b) Sagittal T2 weighted fat-suppression image of the same patient shows the extent of pharyngeal invasion of the tongue base tumour (arrow).

Figure 6

Axial T1 weighted image shows a tongue cancer with mandible invasion. However, early involvement of cortical bones is better seen on CT images.

Oral tongue carcinoma

Nearly all tumours of the oral tongue occur on the lateral and under surface. Dorsal tumours are uncommon but when they do occur, they are usually located near the midline and more posteriorly. Oral tongue tumours tend to remain in the tongue. Tumours in the anterior third of the oral tongue invade the floor of the mouth (Fig. 7). Middle-third lesions infiltrate the musculature of the tongue and later, the lateral floor of the mouth (Fig. 8). Carcinomas involving the posterior third of the oral tongue grow into the musculature of the tongue, the floor of the mouth, the anterior tonsillar pillar, the tongue base, the glossotonsillar sulcus and the mandible (Fig. 9).
Figure 7

(a) Sagittal T2 weighted fat-suppression image shows carcinoma in the anterior third of the oral tongue (arrow). (b) Sagittal T2 weighted fat-suppression image (same patient) shows tumour invading the floor of the mouth (arrow).

Figure 8

(a) Coronal T2 weighted fat-suppression image shows a carcinoma in the middle third of the oral tongue with early infiltration (long arrow) of the tongue musculature (genioglossus). Note the ipsilateral submandibular lymphadenopathy (short arrow). (b) Coronal post-contrast T1 weighted fat-suppression image of a more advanced case shows the tumour invading the lateral floor of the mouth (arrow).

Figure 9

(a) Axial post-contrast CT image shows a large left-side tongue base carcinoma. Note the extension across the midline (long arrow) and the ipsilateral enlarged jugulodigastric node (short arrow). (b) Axial post-contrast CT image shows tumour extension into the aryepiglottic (short arrow) and hypopharynx (long arrow).

MRI provides valuable information both within and without the tongue. The tongue carcinoma may extend far beyond the gross tumour margin seen on surgery, which is often deceiving. It is known that the most important factor governing local recurrence is the resection margin [5]. Whereas 1 cm is generally considered adequate for most squamous cell carcinomas, the margins for tongue cancer should be 1.5–2 cm. Tumours with deep margins are often difficult to assess during surgery. In addition, these tumours are technically more difficult to resect. Hence, deep margins are frequently the site of positive or inadequate resection margins. Up to 35% of patients have nodal metastasis on presentation (Fig. 8(a)). Five percent of these patients have bilateral lymph node involvement (Fig. 2(b)). The first echelon nodes are the submandibular and jugulodigastric nodes. Submental node involvement is uncommon except in patients with tumour at the tip of tongue. It should be noted that in patients with clinically N0 neck, the overall occult metastatic rate is approximately 30%. Various clinical studies have been performed to correlate the depth of tumour invasion with the likelihood of cervical nodal metastasis [6-8]. These studies reveal that the single most important factor in predicting lymph node metastasis is the depth of tumour invasion.

Tongue base carcinoma

This is a clinically silent region and tumours tend to spread with deep infiltration. As a general rule, the extent of these tumours is underestimated during clinical examination. Tongue base tumours tend to remain in the tongue except for laterally placed lesions or late cases [1]. Under such circumstances, tongue base tumours may extend into the tonsillar fossa (Fig. 10). Tonsillar carcinomas, on the other hand, have a tendency to invade the tongue base.
Figure 10

(a) Axial post-contrast T1 weighted fat-suppression image shows a large tongue base tumour (opposing arrows). (b) Axial post-contrast T1 weighted fat-suppression image shows inferior extension into the right pyriform fossa (arrow).

Vallecular lesions are relatively exophytic (Fig. 11) and spread along the mucosa to the lingual surface of the epiglottis, laterally along the pharyngoepiglottic fold and then to the lateral pharyngeal wall and anterior wall of the pyriform sinus [1]. Anterior infiltration involving the floor of the mouth and sublingual space, as well as invasion of the pre-epiglottic space is best evaluated with imaging [9]. The true extent of tumours in these regions is difficult to ascertain by clinical examination.
Figure 11

(a) Axial post-contrast CT image shows an exophytic a left-sided vallecular cancer (arrows). (b) Axial post-contrast CT image shows tumour involving the ipsilateral aryepiglottic fold (short white arrow) and the pyriform sinus (long white arrow). Note the enlarged necrotic left jugulodigastric node (black arrow).

For tongue base carcinoma, the first echelon nodes are the jugulodigastric nodes (Fig. 11), followed by mid and lower jugular nodes. Retropharyngeal nodes are occasionally involved. Submandibular nodes may be involved if there is anterior tumour extension. Submental nodes are rarely involved. Seventy-five percent of patients have positive nodes on presentation while 30% have bilateral nodal metastases (Fig. 12). Patients with clinically N0 neck have a 30%–50% rate of occult metastases.
Figure 12

Axial post-contrast CT image shows a tongue base carcinoma (black arrow) with bilateral malignant lymphadenopathy (white arrows), which occurs in up to 30% of patients on presentation.

Treatment

In general, radiation therapy and surgery have similar results for similar stages. Total glossectomy is associated with severe speech and deglutition dysfunction. It is poorly tolerated and the procedure is thus rarely performed [1, 2]. Hemiglossectomy preserves some speech and swallowing ability. The option between surgery and radiation therapy also depends on the practice and preference of a particular head and neck oncology service. Radiation therapy is often used as the first modality while surgery is reserved for recurrence. Surgical salvage is good for small lesions but the effectiveness drops with progressively larger lesions. Hence, partial glossectomy followed by radiation therapy is the method of choice in many centres. In view of the high incidence of occult metastases in clinically N0 neck, several studies have recommended elective neck dissection in this group of patients. Investigations have demonstrated the prognostic value of tumour volume measured on CT and tumour thickness (determined on ultrasound or MRI) in predicting occult metastases [10]. These studies suggest that tumours with thickness exceeding 4–6 mm or a tumour volume exceeding 13 ml have significant risk of occult metastases. Recently, segmentation techniques were introduced to measure carcinoma tumour volume on MR images [11]. In conclusion, MRI is the imaging modality of choice for evaluation of tongue carcinomas. Coupled with an in-depth understanding of the anatomy of the tongue and behaviour of the tongue carcinoma, this will allow accurate staging of the tumour, which in turn is crucial in optimising the treatment options.
Table 1

Tumour Node Metastasis (TNM) classification

T—Primary tumour
TXPrimary tumour cannot be assessed
T0No evidence of primary tumour
TisCarcinoma in situ
T1Tumour 2 cm or less in greatest dimension
T2Tumour more than 2 cm but not more than 4 cm in greatest dimension
T3Tumour more than 4 cm in greatest dimension
T4a (oral tongue)Tumour invades through cortical bone, into deep/extrinsic muscle of tongue (genioglossus, hyoglossus, palatoglossus, and styloglossus), maxillary sinus, or skin of face
T4b (oral tongue)Tumour invades masticator space, pterygoid plates, or skull base, or encases internal carotid artery
T4a (pharyngeal tongue)Tumour invades any of the following: larynx, deep/extrinsic muscle of tongue (genioglossus, hyoglossus, palatoglossus, and styloglossus), medial pterygoid, hard palate, and mandible
T4b (pharyngeal tongue)Tumour invades any of the following: lateral pterygoid muscle, pterygoid plates, lateral nasopharynx, skull base; or encases the carotid artery
N—Regional lymph nodes
NXRegional lymph nodes cannot be assessed
N0No regional lymph node metastasis
N1Metastasis in a single ipsilateral lymph node, 3 cm or less in greatest dimension
N2Metastasis in a single ipsilateral lymph node, more than 3 cm but not more than 6 cm in greatest dimension; or in multiple ipsilateral lymph nodes, none more than 6 cm in greatest dimension; or in bilateral or contralateral lymph nodes, none more than 6 cm in greatest dimension
N2aMetastasis in a single ipsilateral lymph node, more than 3 cm but not more than 6 cm in greatest dimension
N2bMetastasis in multiple ipsilateral lymph nodes, none more than 6 cm in greatest dimension
N2cMetastasis in bilateral or contralateral lymph nodes, none more than 6 cm in greatest dimension
N3Metastasis in a lymph node more than 6 cm in greatest dimension
M—Distant metastasis
MXDistant metastasis cannot be assessed
M0No distant metastasis
M1Distant metastasis

Note: Midline nodes are considered ipsilateral nodes.

Table 2

Stage grouping

Stage 0TisN0M0
Stage IT1N0M0
Stage IIT2N0M0
Stage IIIT1, T2NIM0
T3N0, N1M0
Stage IVAT1, T2, T3N2M0
T4aN0, N1, N2M0
Stage IVBAny TN3M0
T4bAny NM0
Stage IVCAny TAny NM1
  7 in total

1.  A comparison of the prognostic significance of tumor diameter, length, width, thickness, area, volume, and clinicopathological features of oral tongue carcinoma.

Authors:  A P Yuen; K Y Lam; W I Wei; K Y Lam; C M Ho; T L Chow; W F Yuen
Journal:  Am J Surg       Date:  2000-08       Impact factor: 2.565

2.  Tumor thickness predicts cervical metastasis in patients with stage I/II carcinoma of the tongue.

Authors:  T Asakage; T Yokose; K Mukai; S Tsugane; Y Tsubono; M Asai; S Ebihara
Journal:  Cancer       Date:  1998-04-15       Impact factor: 6.860

Review 3.  Depth of invasion as a predictive factor for cervical lymph node metastasis in tongue carcinoma.

Authors:  H Fukano; H Matsuura; Y Hasegawa; S Nakamura
Journal:  Head Neck       Date:  1997-05       Impact factor: 3.147

4.  Lingual carcinoma. Correlation of MR imaging with histopathological findings.

Authors:  A Arakawa; J Tsuruta; R Nishimura; Y Sakamoto; Y Korogi; Y Baba; M Furusawa; Y Ishimaru; Y Uji; A Taen; T Ishikawa; M Takahashi
Journal:  Acta Radiol       Date:  1996-09       Impact factor: 1.990

5.  Predictive value of tumor thickness in squamous carcinoma confined to the tongue and floor of the mouth.

Authors:  R H Spiro; A G Huvos; G Y Wong; J D Spiro; C A Gnecco; E W Strong
Journal:  Am J Surg       Date:  1986-10       Impact factor: 2.565

6.  Tongue carcinoma: tumor volume measurement.

Authors:  Vincent F H Chong; Jia-Yin Zhou; James B K Khoo; Jing Huang; Tuan-Kay Lim
Journal:  Int J Radiat Oncol Biol Phys       Date:  2004-05-01       Impact factor: 7.038

7.  Prognostic factors of clinically stage I and II oral tongue carcinoma-A comparative study of stage, thickness, shape, growth pattern, invasive front malignancy grading, Martinez-Gimeno score, and pathologic features.

Authors:  Anthony Po Wing Yuen; King Yin Lam; Lai Kun Lam; Chiu Ming Ho; Anna Wong; Tam Lin Chow; Wah Fun Yuen; William Ignace Wei
Journal:  Head Neck       Date:  2002-06       Impact factor: 3.147

  7 in total
  8 in total

1.  Differentiation of benign and malignant lesions of the tongue by using diffusion-weighted MRI at 3.0 T.

Authors:  S Li; J Cheng; Y Zhang; Z Zhang
Journal:  Dentomaxillofac Radiol       Date:  2015-03-31       Impact factor: 2.419

2.  Non-invasive intravital imaging of head and neck squamous cell carcinomas in live mice.

Authors:  Panomwat Amornphimoltham; Jamie Thompson; Nicolas Melis; Roberto Weigert
Journal:  Methods       Date:  2017-08-03       Impact factor: 3.608

3.  MR evaluation of tongue carcinoma in the assessment of depth of invasion with histopathological correlation: A single center experience.

Authors:  Reddy Ravikanth
Journal:  Indian J Radiol Imaging       Date:  2020-07-13

4.  PET/MRI in head and neck cancer: initial experience.

Authors:  Ivan Platzek; Bettina Beuthien-Baumann; Matthias Schneider; Volker Gudziol; Jens Langner; Georg Schramm; Michael Laniado; Jörg Kotzerke; Jörg van den Hoff
Journal:  Eur J Nucl Med Mol Imaging       Date:  2012-09-28       Impact factor: 9.236

Review 5.  Surgical errors and risks - the head and neck cancer patient.

Authors:  Ulrich Harréus
Journal:  GMS Curr Top Otorhinolaryngol Head Neck Surg       Date:  2013-12-13

6.  Foreign body granuloma in the tongue differentiated from tongue cancer: A case report.

Authors:  Zhen-Hua Jiang; Ran Xv; Li Xia
Journal:  World J Clin Cases       Date:  2022-06-26       Impact factor: 1.534

7.  Dental artifacts in the head and neck region: implications for Dixon-based attenuation correction in PET/MR.

Authors:  Claes N Ladefoged; Adam E Hansen; Sune H Keller; Barbara M Fischer; Jacob H Rasmussen; Ian Law; Andreas Kjær; Liselotte Højgaard; Francois Lauze; Thomas Beyer; Flemming L Andersen
Journal:  EJNMMI Phys       Date:  2015-03-11

8.  Large Vallecular Masses; Differential Diagnosis and Imaging Features.

Authors:  Ashim Kumar Lahiri; Krishna Kiran Somashekar; Bernd Wittkop; Christopher Ayshford
Journal:  J Clin Imaging Sci       Date:  2018-06-28
  8 in total

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