Pictorial Essay
Head and Neck Imaging
May 2005

Sonographic Evaluation of Cervical Lymph Nodes

Abstract

OBJECTIVE. Sonography is a useful imaging tool in the evaluation of cervical lymph nodes. Gray-scale sonography and color and power Doppler sonography are commonly used in clinical practice. This article documents the common sonographic appearances of different causes of cervical lymphadenopathy.
CONCLUSION. The sonographic appearances of normal nodes differ from those of abnormal nodes. Sonographic features that help to identify abnormal nodes include shape (round), absent hilus, intranodal necrosis, reticulation, calcification, matting, soft-tissue edema, and peripheral vascularity.

Introduction

Metastatic cervical lymph nodes are common in patients with head and neck [1] and non–head and neck [2] cancers. In patients with squamous cell carcinoma in the head and neck, the presence of a metastatic node reduces the 5-year survival rate to 50%, and the presence of another metastatic node on the contralateral side further reduces the 5-year survival rate to 25% [3]. Therefore, evaluation of cervical lymph nodes is important in patients with cancers because it aids in the assessment of patient prognosis and helps in planning treatment. Cervical lymph nodes are also common sites of involvement of lymphoma; tuberculous lymphadenitis; and other benign lymphadenitis such as Kikuchi's disease, Kimura's disease, and Rosai-Dorfman disease [4, 5].
Sonography is a useful imaging tool in the assessment of cervical lymph nodes. Gray-scale sonography is widely used in the evaluation of the number, size, site, shape, borders, matting, adjacent soft-tissue edema, and internal architectures of cervical lymph nodes. Although both color and power Doppler sonography are routine, 3D sonography is not commonly used to assess the intranodal vascular distribution. With the use of spectral Doppler sonography, the vascular resistance of lymph nodes can also be measured. The purpose of this article is to briefly reiterate and illustrate the sonographic features of normal and abnormal cervical lymph nodes.

Normal and Reactive Lymph Nodes

In sonography examinations, cervical lymph nodes are usually classified into eight regions (Fig. 1). Normal and reactive lymph nodes are usually found in submandibular, parotid, upper cervical, and posterior triangle regions. On gray-scale sonography, normal and reactive nodes tend to be hypoechoic compared with adjacent muscles and oval (short axis–to–long axis ratio [S/L] < 0.5) except for submandibular and parotid nodes, which are usually round (S/L ≥ 0.5), and to have an echogenic hilus [6] (Fig. 2A, 2B). The upper limit in minimal axial diameter of normal and reactive nodes is 9 mm for subdigastric and submandibular nodes and 8 mm for other cervical nodes [7].
Fig. 1. Schematic diagram of neck shows classification of cervical lymph nodes in sonography examinations.
Fig. 2A. Gray-scale sonograms of lymph nodes in healthy subjects. Image of 45-year-old man shows normal intraparotid lymph node is hypoechoic and oval. Lymph node shows echogenic hilus (arrows), which is continuous with adjacent soft tissues (arrowheads).
Fig. 2B. Gray-scale sonograms of lymph nodes in healthy subjects. Image of 20-year-old man shows normal posterior triangle lymph node is hypoechoic, elliptic, and elongated (arrows). Arrowheads indicate echogenic hilus that is continuous with adjacent soft tissues.
On color Doppler, power Doppler, and 3D sonography, normal cervical nodes show hilar vascularity or appear avascular, and reactive nodes predominantly show hilar vascularity [6] (Fig. 3A, 3B, 3C). On spectral Doppler sonography, normal and reactive nodes usually show low vascular resistance (resistive index [RI] and pulsatility index [PI]) [6] (Fig. 4A, 4B). Inflammation causes vasodilatation, which increases blood flow velocity in reactive lymph nodes. It may explain the low vascular resistance in reactive lymph nodes given that high blood flow velocity is always associated with a lower vascular resistance.
Fig. 3A. 42-year-old man with palpable submandibular lymph nodes. Color Doppler sonogram shows extensive vascularity originating in hilus and branching radially toward periphery of lymph node (arrows). Subsequent fine-needle aspiration cytology confirmed reactive node.
Fig. 3B. 42-year-old man with palpable submandibular lymph nodes. Power Doppler sonogram of same lymph node as in A shows hilar vascularity of reactive lymph node (arrows).
Fig. 3C. 42-year-old man with palpable submandibular lymph nodes. Three-dimensional power Doppler sonogram of same lymph node as in A and B shows hilar vascularity of reactive lymph node (arrows). More extensive vascularity is shown on 3D power Doppler sonography than power Doppler sonography.
Fig. 4A. 53-year-old man with confirmed reactive lymph nodes in neck. Spectral Doppler sonogram shows low vascular resistance of lymph node with resistive index (RI) of 0.59 and pulsatility index (PI) of 0.94, which are lower than cutoff values commonly used to differentiate benign and malignant nodes (RI, 0.7; PI, 1.5).
Fig. 4B. 53-year-old man with confirmed reactive lymph nodes in neck. Longitudinal gray-scale sonogram of same lymph node as in A shows lymph node is hypoechoic and oval (arrows). Arrowheads indicate echogenic hilus where blood vessels enter and leave lymph node.

Malignant Lymph Nodes

Malignant lymph nodes include metastatic and lymphomatous nodes. On grayscale sonography, metastatic nodes are usually hypoechoic, round, and without echogenic hilus (Fig. 5A). Coagulation necrosis, which appears as a demarcated echogenic focus, may be found in metastatic nodes (Fig. 5A). Eccentric cortical hypertrophy is a useful sign to indicate focal tumor infiltration (Fig. 5B). Lymph nodes with cystic necrosis are suggestive of malignancy, and intranodal cystic necrosis is common in metastatic nodes from squamous cell carcinomas (Fig. 5C).
Fig. 5A. Gray-scale sonograms of patients with metastatic nodes. Image of 63-year-old man with lung carcinoma and proven metastatic lymph nodes in lower cervical and supraclavicular regions shows lower cervical node is hypoechoic, round, and without echogenic hilus (arrows). Note intranodal coagulation necrosis that appears as demarcated echogenic focus and is not continuous with adjacent soft tissues (arrowheads).
Fig. 5B. Gray-scale sonograms of patients with metastatic nodes. Image of 60-year-old woman with carcinoma of breast and proven metastatic nodes in supraclavicular region and internal jugular chain shows eccentric cortical hypertrophy of upper cervical lymph node due to focal tumor infiltration (arrowheads).
Fig. 5C. Gray-scale sonograms of patients with metastatic nodes. Image of 70-year-old man with carcinoma of tongue and with bilateral metastatic upper cervical lymph nodes shows one of metastatic upper cervical nodes is hypoechoic, round, and without echogenic hilus (arrows). Lymph node also shows multiple areas of intranodal cystic necrosis (arrowheads).
A proven metastatic lymph node with illdefined borders may suggest extracapsular spread and patients may have a poor prognosis (Fig. 5D). Metastatic nodes from papillary carcinoma of the thyroid may be hyperechoic compared with adjacent muscles and have punctate calcifications [8] (Fig. 5E). In Hodgkin's lymphoma and non-Hodgkin's lymphoma, lymph nodes tend to be round, hypoechoic, and without echogenic hilus and tend to show intranodal reticulation [9] (Fig. 6).
Fig. 5D. Gray-scale sonograms of patients with metastatic nodes. Image of 25-year-old man with nasopharyngeal carcinoma and proven metastatic nodes in posterior triangle shows metastatic node in posterior triangle with ill-defined nodal borders (arrows), which indicates extracapsular spread.
Fig. 5E. Gray-scale sonograms of patients with metastatic nodes. Image of 44-year-old woman with papillary carcinoma of thyroid and associated metastatic node in right upper cervical region shows metastatic node appears hyperechoic (arrowheads) when compared with adjacent muscle and has intranodal punctate calcification (arrow). These sonographic features are common in metastatic nodes from papillary carcinoma of thyroid.
Fig. 6. 68-year-old man with proven bilateral non-Hodgkin's lymphomatous nodes in submandibular region. High-resolution gray-scale sonogram shows lymphomatous node appears hypoechoic, round, and without echogenic hilus and shows intranodal reticulation—that is, micronodular appearance (arrows). (Reprinted with permission from [8])
On color Doppler, power Doppler, and 3D sonography, metastatic and lymphomatous nodes usually show peripheral (Fig. 7A, 7B, 7C) or mixed (Fig. 8A, 8B) vascularity. On spectral Doppler sonography, malignant lymph nodes tend to have high RI and PI values [8] (Fig. 9). In metastatic nodes, blood vessels within the nodes are compressed by tumor cells, which grow and spread and replace a large portion of the lymph node, resulting in an increase in vascular resistance.
Fig. 7A. 43-year-old woman with nasopharyngeal carcinoma and proven metastatic nodes in posterior triangle. Color Doppler sonogram shows metastatic node with peripheral vascularity (arrows) that runs along periphery of nodes, with perforating branches into lymph nodes.
Fig. 7B. 43-year-old woman with nasopharyngeal carcinoma and proven metastatic nodes in posterior triangle. Power Doppler sonogram of same lymph node as in A shows peripheral vascularity (arrows) similar to that seen in A.
Fig. 7C. 43-year-old woman with nasopharyngeal carcinoma and proven metastatic nodes in posterior triangle. Three-dimensional power Doppler sonogram of same lymph node as in A and B shows peripheral vascularity of lymph node (arrows) is better depicted on 3D power Doppler sonography.
Fig. 8A. —43-year-old man with proven non-Hodgkin's lymphomatous nodes in posterior triangle. Color Doppler sonogram shows lymphomatous node with both hilar (arrows) and peripheral (arrowhead) vascularity.
Fig. 8B. —43-year-old man with proven non-Hodgkin's lymphomatous nodes in posterior triangle. Power Doppler sonogram of same lymph node as in A shows hilar (arrows) and peripheral (arrowheads) vascularity similar to that seen in A.
Fig. 9. 41-year-old man with nasopharyngeal carcinoma and metastatic lymph nodes in posterior triangle. Spectral Doppler sonogram shows high vascular resistance of lymph node with resistive index (RI) of 0.85 and pulsatility index (PI) of 2.18, which are higher than cutoff values commonly used to differentiate benign and malignant nodes (RI, 0.7; PI, 1.5).
Gray-scale sonography has a sensitivity of 95% and a specificity of 83% in differentiating metastatic and reactive nodes [10]. Color or power Doppler sonography is essential and useful to patients when gray-scale sonography is equivocal. In one study, power Doppler sonography aided in the diagnosis of 5% of patients with metastatic nodes and 17% of patients with reactive nodes [10].

Tuberculous Lymph Nodes

On gray-scale sonography, tuberculous nodes tend to be hypoechoic, round, and without echogenic hilus and tend to show intranodal cystic necrosis, nodal matting, and adjacent soft-tissue edema [8] (Fig. 10A, 10B). On color Doppler, power Doppler, and 3D sonography, the vascular distribution of tuberculous nodes is varied and simulates benign and malignant nodes. However, displacement of hilar vascularity is common in tuberculous nodes and is due to the high incidence of intranodal cystic necrosis, which displaces the vessels, in tuberculous nodes [11] (Fig. 11A, 11B, 11C).
Fig. 10A. Gray-scale sonograms of two patients with proven tuberculous lymphadenitis. Image of 59-year-old woman shows two tuberculous nodes (arrows) matted together without normal intervening soft tissues. Note cystic necrosis within lymph nodes (arrowheads), which is common in tuberculous lymphadenitis.
Fig. 10B. Gray-scale sonograms of two patients with proven tuberculous lymphadenitis. Image of 31-year-old woman shows hypoechoic and round tuberculous node in posterior triangle (arrows) with adjacent soft-tissue edema (arrowheads), which is common in tuberculous lymphadenitis.
Fig. 11A. 20-year-old man with proven tuberculous lymphadenitis. Color Doppler sonogram shows tuberculous node in posterior triangle with hilar vascularity (arrows) is being displaced by intranodal cystic necrosis (arrowheads).
Fig. 11B. 20-year-old man with proven tuberculous lymphadenitis. Power Doppler sonogram of same lymph node as in A shows displaced hilar vascularity (arrows) and intranodal cystic necrosis (arrowheads).
Fig. 11C. 20-year-old man with proven tuberculous lymphadenitis. Three-dimensional power Doppler sonogram of same lymph node as in A and B shows displaced vascularity (arrows); however, intranodal cystic necrosis (arrowheads) is not shown because 3D power Doppler sonography did not provide superimposed gray-scale image.

Unusual Lymphadenopathy

Diseases such as Kikuchi's disease (histiocytic necrotizing lymphadenitis), Kimura's disease (eosinophilic hyperplastic lymphogranuloma), and Rosai-Dorfman disease (sinus histiocytosis with massive lymphadenopathy) may show benign and inflammatory lymphadenopathy in the neck. Kikuchi's disease is a self-limiting and benign lymphadenitis in which cervical nodes are usually affected. Kimura's disease is an autoimmune eosinophilic granulomatous disorder with generalized lymphadenopathy. Rosai-Dorfman disease is a rare idiopathic benign histiocytic proliferation, and massive lymphadenopathy is usually found in the neck region with predominant sinusoidal histiocyte infiltration.
On sonography, lymph nodes involved with Kikuchi's and Kimura's diseases have an appearance similar to that of reactive nodes, which tend to be hypoechoic, and have an echogenic hilus. In patients with Kikuchi's disease, lymph nodes are usually oval (Fig. 12A), whereas lymph nodes in patients with Kimura's disease are usually round (Fig. 13A). On power Doppler sonography [12, 13], lymph nodes in patients with Kikuchi's disease and Kimura's disease tend to show hilar vascularity [12, 13] (Figs. 12B and 13B). In patients with Rosai-Dorfman disease, involved lymph nodes appear similar to malignant nodes, which are hypoechoic, round, and without echogenic hilus (Fig. 14A). On power Doppler sonography, involved lymph nodes in Rosai-Dorfman disease also have an appearance similar to that of malignant nodes and show peripheral or mixed vascularity [12] (Fig. 14B). Because the sonographic appearance of these unusual lymphadenopathies is similar to that of reactive or malignant nodes, the diagnosis is still based on histology.
Fig. 12A. 30-year-old woman with palpable nodes in upper cervical region proven to be Kikuchi's disease. (Reprinted with permission from [12]) Gray-scale sonogram of upper cervical node (small arrows) shows node is hypoechoic and elliptic and has echogenic hilus (arrowheads). Large arrows indicate common carotid artery, and asterisk indicates internal jugular vein. Note gray-scale sonographic appearance of lymph nodes in Kikuchi's disease is similar to that of reactive nodes.
Fig. 13A. 42-year-old man with palpable nodes in submandibular area that were subsequently proven to be Kimura's disease. Gray-scale sonogram shows submandibular lymph node (arrows) is hypoechoic, is round, and has echogenic hilus (arrowheads). Gray-scale sonographic appearance is similar to that of reactive nodes except that lymph nodes in Kimura's disease tend to be round and are located in the vicinity of the salivary glands.
Fig. 12B. 30-year-old woman with palpable nodes in upper cervical region proven to be Kikuchi's disease. (Reprinted with permission from [12]) Power Doppler sonogram of same lymph node as in A (arrows) reveals that lymph node involved with Kikuchi's disease shows hilar vascularity (arrowheads) that is similar to vascular pattern of reactive lymph nodes.
Fig. 13B. 42-year-old man with palpable nodes in submandibular area that were subsequently proven to be Kimura's disease. Power Doppler sonogram of same lymph node as in A (arrows) shows extensive hilar vascularity (arrowheads), which is similar to vascular pattern of reactive lymph nodes.
Fig. 14A. 13-year-old boy with palpable nodes in submental and submandibular areas that were subsequently proven to be Rosai-Dorfman disease. Gray-scale sonogram shows two submental nodes that are hypoechoic, round, and without echogenic hilus (arrows). Sonographic appearance is similar to that of malignant nodes.
Fig. 14B. 13-year-old boy with palpable nodes in submental and submandibular areas that were subsequently proven to be Rosai-Dorfman disease. Power Doppler sonogram of same submental node as in A shows peripheral vascularity (arrows), which is similar to malignant lymph nodes.

Footnote

Address correspondence to M. Ying.

References

1.
Baatenburg de Jong RJ, Rongen RJ, Lameris JS, Harthoorn M, Verwoerd CD, Knegt P. Metastatic neck disease: palpation vs ultrasound examination. Arch Otolaryngol Head Neck Surg 1989; 115:689 –690
2.
Ying M, Ahuja AT, Evans R, King W, Metreweli C. Cervical lymphadenopathy: sonographic differentiation between tuberculous nodes and nodal metastases from non-head and neck carcinomas. J Clin Ultrasound 1998; 26:383 –389
3.
Som PM. Detection of metastasis in cervical lymph nodes: CT and MR criteria and differential diagnosis. AJR 1992; 158:961 –969
4.
Lee YY, Van Tassel P, Nauert C, North LB, Jing BS. Lymphomas of the head and neck: CT findings at initial presentation. AJR 1987; 149:575 –581
5.
Reede DL, Bergeron RT. Cervical tuberculous adenitis: CT manifestations. Radiology 1985; 154:701 –704
6.
Ying M, Ahuja A. Sonography of neck lymph nodes. I. Normal lymph nodes. Clin Radiol 2003; 58:351 –358
7.
van den Brekel MW, Castelijns JA, Stel HV, Golding RP, Meyer CJ, Snow GB. Modern imaging techniques and ultrasound-guided aspiration cytology for the assessment of neck node metastases: a prospective comparative study. Eur Arch Otorhinolaryngol 1993; 250:11 –17
8.
Ahuja A, Ying M. Sonography of neck lymph nodes. II. Abnormal lymph nodes. Clin Radiol 2003; 58:359 –366
9.
Ahuja AT, Ying M, Yuen HY, Metreweli C. `Pseudocystic' appearance of non-Hodgkin's lymphomatous nodes: an infrequent finding with high-resolution transducers. Clin Radiol 2001; 56:111 –115
10.
Ahuja A, Ying M. Sonographic evaluation of cervical lymphadenopathy: is power Doppler sonography routinely indicated? Ultrasound Med Biol 2003; 29:353 –359
11.
Ahuja A, Ying M, Yuen YH, Metreweli C. Power Doppler sonography to differentiate tuberculous cervical lymphadenopathy from nasopharyngeal carcinoma. AJNR 2001; 22:735 –740
12.
Ying M, Ahuja AT, Yuen HY. Grey-scale and power Doppler sonography of unusual cervical lymphadenopathy. Ultrasound Med Biol 2004; 30:449 –454
13.
Ahuja A, Ying M, Mok JS, Anil CM. Gray scale and power Doppler sonography in cases of Kimura disease. AJNR 2001; 22:513 –517

Information & Authors

Information

Published In

American Journal of Roentgenology
Pages: 1691 - 1699
PubMed: 15855141

History

Submitted: August 4, 2004
Accepted: September 30, 2004
First published: November 23, 2012

Authors

Affiliations

Anil T. Ahuja
Department of Diagnostic Radiology and Organ Imaging, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong SAR, China.
Michael Ying
Department of Optometry and Radiography, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR, China.

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