Head Michiel Wietse

W.M. van den Brekel, MD #{149} Jonas Luth, MD #{149} Jaap Valk, MD, PhD

Occult Metastatic and US-guided

Neck Fine-Needle

The

authors performed a prospective of the value of ultrasonography (US) and US-guided fine-needle aspiration cytology (FNAC) for assessment of NO lesions in the neck. Preoperative US was performed in 107 patients with squamous cell carcinoma of the head and neck, who underwent 132 elective neck disseclions. During the US examination of the last 54 patients, who underwent 70 elective neck dissections, USguided FNAC was performed. US alone was found to be an unreliable method for detecting occult lymph node metastasis; the accuracy never exceeded 70% (93 of 132), with a sensitivity of 60% (32 of 53) and a specificity of 77% (61 of 79). In contrast, US-guided FNAC had an accuracy of 89% (62 of 70), a sensitivity of 76% (25 of 33), and a specificity of 100% (37 of 37). Because of the high sensitivity and specificity of US-guided FNAC for the assessment of the NO neck, this modality may play an important role in directing treatment of these patients in the future. study

Index

terms: Head and neck neoplasms, 262.37, 271.37, 276.37, 28.314 #{149}Lymphatic systern, neoplasms, 20.37, 99.33, 99.82 #{149}Lymphatic system, US studies, 99.1298, 99.12985, 99.12986 Radiology

A. Castelijns, #{149} Isaac van

J.

1991;

180:457-461

I

(CT)

From the Departments of Otorhinolaryngoland Head and Neck Surgery (M.W.M.v.d.B., G.B.S.), Diagnostic Radiology (J.A.C., W.J.L., J.V.), Pathology and Cytology (H.V.S.), and Oral Pathology (I.v.d.W.), Free University Hospital, P0 Box 7057, 1007 MB Amsterdam, The Netherlands.

Received quested March

accepted from

the

January 30, 1991; revision re12; revision received March 28; April 8. Supported by grant IKA 88-19 Queen Wilhelmina Fund for Cancer Address reprint requests to

Research. M.W.M.v.d.B. 0

RSNA,

1991

and

magnetic

V. Stel, MD, PhD Gordon B. Snow,

remains.

nodes

(9-13).

This

can

be

explained by the fact that US does not reliably depict tumor cells in either lymphatic tissue or necrotic tumor tissue; neither does it reliably depict tumor keralinization. Therefore, the only criteria left for accurate differentialion between reactive and metastatic lymph nodes are size (minimal axial diameter) and grouping of three or more borderline lymph nodes (21). US-guided fine-needle aspiration (FNAC)

may

give

cytologic

evidence of tumor in a large percentage of metastatic nodes. Although some authors studied US-guided FNAC in patients with head and neck cancer (11,18,20), to our knowledge none of them has studied this technique in a homogeneous group of previously untreated patients who underwent elective neck dissection because results of palpation were negative. In this study, the value of US and US-guided FNAC for the detection of occult cervical lymph node metastasis

One hundred and

neck

is assessed.

seven

squamous

was previously examined with years.

PhD

US

These

METHODS

patients

with

head

cell carcinoma

that

untreated (Table US over a period

107 patients

1) were of 1’/

underwent

a to-

tal of 132 elective neck dissections that were either comprehensive or selective. contain

these

132 necks

were

no lymph

node

involvement

the decision to perform was made on the basis

At

found

to

(NO);

elective dissection of the site and

stage of the primary tumor. In principle, negative findings

at US and

FNAC had no influence on the of treatment of the neck. In four however, the finding of positive

US-guided

Most studies of ultrasonography (US) of the neck claim that US is superior to palpation for enabling deteclion and classification of cervical lymph node metastasis (9-20). Although some authors defined criteria for diagnosis of malignant or benign nodes at US (14-17), US alone does not enable differentiation between enlarged reactive nodes and enlarged metastatic

MD,

AND

MATERIALS

palpation,

resonance

(MR) imaging have enabled detection of 38%-67% of these occult lymph node metastases (6-8). Consequently, the need for a more sensitive technique

Radiology

Disease: Detection with Aspiration Cytology’

with primary squamous cell carcinoma of the head and neck, staging of neck lesions with palpation is reported to yield false-negalive results in O%-77% of cases (1,2), depending on the site (3), size (4), and other parameters (5) of the primary tumor. To date, computed tomography

Neck

#{149}

N patients

cytology

ogy

MD, PhD #{149} Herbert der Waal, DDS, PhD

and

direction lesions,

aspirate necessitated unanticipated neck specimens

performance of an dissection. Of the 132

obtained,

53 (40%)

contained

metastatic lymph nodes, whereas 79 (60%) were negative at histopathologic examinalion. Consequently, accuracy of palpation was 60%. In the second

part

the 107 patients neck dissections. 33 of the

ination,

found

to contain

whereas tumor.

37 (53%) US-guided

lesions All

of this

study,

54 of

underwent 70 elective At histopathologic exam70 specimens

metastatic

(47%)

lymph

were

nodes,

were found to be free of FNAC of 57 of these 70

was performed. specimens

obtained

at neck

dissec-

lion were thoroughly examined histopathologically; all nodes that were visible

on the radiograph of the specimen or were palpable in the specimen itself were documented by one physician (M.W.M. v.d.B.). Depending on the type of neck dissection, an average of 43 lymph nodes (range,

24-.87)

were

found

in comprehen-

sive specimens, whereas an average of 16 lymph nodes (range, 6-48) were found in specimens. The number of posilive lymph nodes varied from zero to five (mean, 1.8 in the specimens that were positive for tumor). Depending on the size of selective

the lymph ery

ined

node,

sections

were

made

ev-

and all sections were examhistopathologically, as described in

2-4

mm,

our previous

Abbreviation:

studies

FNAC

(6,21). Exact docu-

=

fine-needle

aspiration

cytology.

457

Table

1

of Patients

Number

Lesions

with

at Various

Sites

and T Stages

Stage

t..1. Primary

Tumor

Ti

T2

T3

T4

Total

2 1 1 0 0 0 0 0 0 0

7 12 5 0 5 2 3 4 2 4

8 7 0 3

0 4 1 1

17 24 7 4

4

2

11

3 4 4 7 0

1 0 4 6 0

6 7 12 15 4

4

44

40

19

107

-

Mobile tongue Floor of mouth I

Alveolar

process

Base of tongue Tonsil, soft palate

!‘-

Pharyngealwall Piriformsinus Supraglottic larynx (Trans)glottic larynx Figure

1.

US image

obtained

with

Lip,nose

a 7.5-

MHz,

linear array transducer during aspiration of a subdigastric node. Note the hyperechogenic spot inside the node (arrow), representing the needle tip.

Total

Table

2

Sensitivity,

mentation nodes that

of the size and were examined

site of all lymph in the speci-

Size

(mm)*

at US-guided FNAC with the lymph node that was resected in the great majority of specimens. Correlation among findings at histopathologic examination, US, or USFNAC

was

determined

for

each

was

were

(H.V.S.,

reviewed

650;

B-scan

Aloka,

US examinations

Tokyo)

were

by

89

33

55

85 81 60

44 59 77

61 68 70

8 9 10

42 26 15

85 95 97

67 67 64

transducer. sides of the

neck were

for the presence

lymph

mandibular

and

nodes

(level

submental,

I

lymph

nodes,

2, 3, 4

indicating

of the node

and the region

neck

imaged.

being

The

diameter

our

the

one =

size

previous

that the minimal

is the most

accurate

axial

criterion

for

size, we again used this criterion for evaluation of lesions depicted at US. For subdigastric

was that

minimal axial diameter to be 1 mm larger than nodes. In addition, a group-

nodes,

ing of three

or more

borderline

drainage

regions

malignant.

was

In this

also

study,

considered several

size

last 8 months

of the

all US-guided

the

FNACs

performed

one

physician

(M.W.M.v.d.B.).

458

#{149}

Radiology

were

nodes

(1 mm

larger Nodes

for subdigastric were

nodes)

and

not considered

for groups

to be grouped

punctured

lymph

per

Most

side.

punctured

twice

cient material After sterile was

was nodes

lymph

to ensure

was obtained. preparation,

performed

in

of three

if the diam-

was introduced

and

inside

was

gently

the

lymph

up

and

ethanol

and

of a

1)

obtain

additional

smears.

and

Papanico-

and stained solution.

to be

examined

(Fig

the needle

fixed by using with

revised

All

by one

with The nee-

(Ta-

guided

smears

FNAC,

sensitivity

necks

were

malignancy Necks

were

chance

a cytologic

of demonstrating

diag-

positive

findings with US or US-guided FNAC in a side of the neck that contained metastasis, whereas the specificity was the chance of demonstrating negative findings when no metastatic lymph nodes were present. Accuracy

was

positive by the

and true-negative results, total number of examinations.

were

estimated

as the

sum

of true-

divided

RESULTS US

a high

the

for

observer at US-

considered

be positive if one or more aspirates to be positive for tumor or suspicious

by

was

material

with CarboConn) to

(H.V.S.).

To obtain

at cyto-

that contained

nosis were considered to be negative. Sensitivity, specificity, and accuracy of US and US-guided FNAC were estimated by using the histopathologic findings in the neck dissection specimens as a standard of reference. Findings at US and histopathologic examination were compared for each side of the neck and not for each node or for each patient. The sensitivity

node

either stained

to be negative

Smears

(and, or if all

insufficient

down.

were

found

tumor

obtained)

nodes

use

by moving

were

was

suspi-

in the drain-

that suffi-

into the skin 0.5-

continued

of the primary

logic examination.

if no

visualized

aspirate

smears

1.0 cm from the transducer, at the middle of the long axis of the transducer. Aspiralion was started after the needle point was visualized

no

punc-

biopsy guide attached to the transducer, by using a syringe holder (Cameco, Taeby, Sweden) and a 0.6 x 25-mm needle. The

needle

thus,

examination

were

were

US-guided

without

FNAC

nodes

age regions

regions

of the neck

US-guided

cious

lymph

drainage

to three

axial

punctured.

(largest)

tumor

sides

One

in minimal

were

dle and syringe were washed wax (Union Carbide, Danbury,

study,

Lymph

or both

FNAC

mm

suspicious in the

were

3-12

than

na

ble2). During

of single

laou stain or air-dried May-GrUnwald-Giemsa

crite-

for lesions seen at US were compared to assess which was most accurate for evaluation of clinically negative necks

most

tured.

70%

nodes

(each of which was I or 2 mm smaller the size criterion chosen) in the tumor

were

The smears

the

considered of other

diameter

from 57 necks

node(s)

and side of the

Since

(21) showed

study

that

diameter

sub-

=

levels level 5

nodes

high-, mid-, low jugular, = supraclavicular). All nodes that were visible at US were measured on screen. The jugular chain nodes in levels 2-5 were examined craniocaudally in the axial plane. Only the nodes in level 1 were examined in the coronal and sagittal planes. Radiographic prints were made of all enlarged

axial

nodes that were each 1 or 2 mm smaller. eter of each was not at least 7 mm.

us-

ing a 7.5-MHz, linear array Levels I through 5 of both of enlarged

(%)

Accuracy

(SSD

performed

fully examined

at US

(%)

Specificity

or more

slides

by two physicians

I.v.d.W.). Real-time,

cm-

(%)

Sensitivity

Size Criteria

5 6 7

Minimal

*

specimen, as only this correlation ically relevant. All histopathologic

of Different

4

men enabled us to retrospectively correlate the lymph node that was punctured

guided

and Accuracy

Specificity,

at cytologic

examination.

considered

to be negative

to

proved for

at

Findings US

findings

were

compared

the histopathologic findings neck dissection specimens patients. All US examinations diagnostic.

Because

metastalic

with

in the of all 107 were lymph

August

1991

Table

-#{149}

3 at US-guided

Findings

Histopathologic

Positive

I

.J

25 8

0 37

45

Total

33

37

70

sis.

=

76%,

25

specificity

=

100%.

These

necks

were

considered

neg-

alive; however, three proved to be positive at histopathologic examina-

-

Total

at US examination, US-guided FNAC was not performed. Consequently, aspiration was not performed in 13 patients. The necks of these 13 palients were considered to be negative at US-guided FNAC and proved to be negative at histopathologic examinalion of the neck dissection specimen. In six necks, insufficient material was aspirated for a cytologic diagno-

‘.:

s;:d

,.:

Negative

Positive Negative

Note-Sensitivity

-

ye rsus

Pathologic Finding

Finding at US-guided FNAC

-,

FNAC

Examination

S-

lion. L

.#{149}

#{149}‘‘:

There

was

tween

d.

C.

Figure

2.

(a) US scan

of 57-year-old

man

with

a T4N1

mobile

tongue

carcinoma.

The

image

shows

a submandibular node (arrow), with a hyperechogenic area inside. M = mandible, H = hyoid muscle. (b) Histopathologic section of the same submandibular node shows that the hyperechogenic area was caused by fat tissue (F) in the hilar structure. L = preexisting lymphatic tissue. (c) Axial US image of a midjugular node (arrow) in a patient with a T2NO carcinoma of the floor of the mouth. Note the very similar hyperechogenic area inside the node. I = internaljugular vein, C = carotid artery, L = preexisting lymphatic tissue, S = sternocleidomastoid muscle. (d) Histopathologic section of the same midjugular node shows that this hyperechogenic area was caused by a metastatic keratinizing squamous cell carcinoma (K). L = preexisting lymphatic tissue, T = tumor tissue.

the

malignancy. neity were

US pattern and compared between

homogemeta-

static and reactively enlarged nodes. Although large metastatic nodes often exhibited an inhomogeneous pattern

crolic tumor,

at US-reflecting

tumor, fat,

cystic

lymphatic

tissue,

or keralinizing

these

inhomogeneous

were

less

or ne-

solid

tumor-

US patterns

frequently

encountered

hypoechogenic.

Furthermore,

areas of hyperechogenicity could represent fatty tissue or keratinizing tumor (Fig 2). Thus, we used only the criterion

of lesion

size

at US to predict

malignancy. Volume

180

#{149} Number

2

were tivity, these

minimal

axial

optimal

sion mm and

had

(70%)

(8 mm when

when

a minimal

in the each

axial

a single

subdigastric lesion

in a group

of 7

area) of at

least three borderline lesions was not more than 2 mm smaller in minimal axial diameter. The corresponding optimal sensitivity and specificity are 60% and 77%, respectively. Findings

at US-guided

benode

and

in 96%.

3 shows

that

25 aspirates

were considered to be positive at USguided FNAC; 19 were malignant and six were suspicious for malignancy.

Results

le-

diameter

lymph

chance to obtain a diagnostic smear for lymph nodes this size was 67%. Smears from larger nodes were diagTable

compared. In Table 2 the sensispecificity, and accuracy of criteria are shown. Accuracy

was

relationship

of the

than 5 mm in axial diameter. A total of 12 aspirates were obtained from lymph nodes that were not more than 5 mm in axial diameter; therefore, the

diameters

in

small nonpalpable lymph nodes. With use of a 7.5-MHz transducer, reaclively enlarged nodes, as well as small metastalic nodes, were often found to be well circumscribed and homogeneously

Several

size

the ability to obtain sufficient material for a diagnostic smear. Four of the six insufficient aspirates were obtained from lymph nodes that measured less

noslic

nodes often contain necrotic or keratinizing tissue, as well as preexisting lymphatic tissue, we looked for specific US features to serve as criteria for

a clear

#{149}

FNAC

Results of US-guided FNAC were available for 54 patients who underwent 70 elective neck dissections. A total of 57 lesions were aspirated. Lymph nodes were aspirated only if the minimal axial diameter was at least 3-4 mm, depending on the level of the node in the neck. If no lymph nodes exceeding this size were found

at US-guided

negative

in 32 cases

necks total

were

not

of 45 sides

FNAC and

were

13 sides

aspirated,

making

of necks

considered

of

a to

be negative. Eight of these 45 sides of necks were found to have false-negalive results. In five of the eight sides of necks with false-negative results, no malignant cells were aspirated, even though correlation between the US

and

histopathologic

reports

re-

garding the size and site of the punctured node indicated that the correct node had been punctured (Fig 3). In two of these five punctures, insufficient

material

was

obtained

for

a diag-

nosis, whereas in the other three punctures the aspirates were obtained from the wrong part of the node and only lymphatic the other three

cells were aspirations

found. with

Radiology

In false-

459

#{149}

negative

results,

the

wrong

nodes

were aspirated; at histopathologic examination it was found that

a reac-

tively enlarged node had been aspirated that was not in the same region as the smaller metastatic node. The sensitivity, specificity, and accuracy US-guided FNAC were 76%, 100%,

_.;-

-

-

-

of

-;

-r,

and

89%, respectively. If the six nondiagnostic smears (those with insufficient material) were left out of the study, the sensitivity, specificity, and accuracy of US-guided FNAC

would

be 83%,

100%,

and

92%,

respectively.

b. DISCUSSION Palpation

rate

is known

technique

neck

Figure

to be an

with

tastasis

in the

In selected phylactic

neck

and

neck

if an

exceeds

accurate

available

of occult

that

if

those

method

the

However,

the

risk

need for elective dissection can only be ruled out for patients in whom the neck does not have to be entered for excision of the primary tumor, such as patients

with

geal,

nasal,

glottic

and small (T1-T2) oral Elective dissection can out in the contralateral

mas.

ruled patients

with

extend these for

lip,

tumors

over patients

regular

approach

to re-stage

have

a lesion

of these

tastases

have

thermore,

both

disadvantages

CT and of being

70%, as any accompanied

rise

sary

to enable

between proved

nodes

lymph more 460

and

and

is in

of necks the opneces-

nodes. study

(21),

lymph Radiology

#{149}

As shown groupings

nodes

that

for

all other

in our are each

or

a

carcinoma

of the

from

size

ranging that are

small

of the

nodes

from more

96% than

all sides of necks in this NO, whereas patients in

previous

study

were

not

to any one stage; size of the metastatic

selected therefore, nodes

study was smaller. Second, as necrosis cannot be a criterion at

loss

of sensitivity

studied

has

and

to be com-

on

the

radio-

logic modality employed. Cytologic examination of lymph nodes detected with US enables a more accurate diagnosis of malig-

only

moderate

the accuracy In this study,

discomfort

to the

of the

aspiration needles carotid artery was in our

for lymph nodes 5 mm in minimal

of

pa-

rare and use of thin

matoma nor bleeding shown in the Results the chance of obtaining

neither

he-

occurred. As section herein, a diagnostic

to 67%

less

negative was

than

results;

present

in lymph

5 mm

nodes

in diameter.

In two aspithat were less the cytologic but gave false-

a micrometastasis

in these

nodes.

Selection of the correct pirate is very important.

node to asA thorough

knowledge of the lymph drainage pathways in the neck is necessary. As a simple guide, enlarged nodes in areas 3 (midjugular), 4 (low jugular),

5 (mid-,

clavicular) metastases. occur more

(23). Although the punctured in one

study,

are

as

decreases,

However, use of US-guided FNAC enabled detection of metastatic tumor cells in two nodes that measured 5

and

tient. Although seeding of tumor cells along the needle tract has been reported after use of Tm-Cut needles (Baxter Healthcare, Pharmaseal, Valencia, Calif) (22), to our knowledge such seeding is extremely has never occurred with

that

diameter

node

mm or less in diameter. rated metastatic nodes than 5 mm in diameter, report was diagnostic

the

floor

decreases

lymph

at palpation, study were

patient

previ-

of three

a T2NO

axial

US-guided FNAC proved to be a quick (10-20 minutes) and safe (no complications) technique that caused

distinction

7 mm

from in a

the

positive and negative lesions to be 8 mm for subdigastric

lymph ous

accurate

markedly

previously

nancy and increases the US examination.

in sensitivity by a decrease

(Table 2). For sides that are negative at palpation, timal minimal axial diameter

the

meFur-

expensive

with

smear

pensated for by a decrease in the size criterion. This illustrates that size criteria depend very much on the group

of sides results at 33%-

specificity

should

all

not readily accessible for repeated use in follow-up of patients. The results of this study show that the accuracy of US alone never exceeds always

differ

reported

of patients

MR have

smaller malignant.

US,

in a

occult lymph node not been detected.

man,

or

been

upward

of a 63-year-old

random study of a group of patients with various head and neck cancers with use of CT and MR (ie, 11 mm and 10 mm, respectively) (21). This difference has two major causes. First,

in this tumor

visits.

MR imaging

criteria we

according the mean

carcinoalso be neck of

large percentage (38%.-67%) of necks with false-negative palpation (6-8). Consequently, 62%

laryn-

midline. However, must agree to return

follow-up

CT and used

the

that

US scan

Image of a subdigastric node 6 x 9 mm area (arrow) that demonstrates appearance of lymph node. S = sternocleidomastoid muscle. (b) Detail of a histopathologic section the same subdigastric node shows a micrometastasis (arrow) that was not detected US-guided FNAC. L = preexisting lymphatic tissue.

These

of probe

minimized

(a) Axial

maximum of 2 mm also be considered

15%-20%.

staging

metastasis.

with

most advocate dissection node me-

cases, performance neck dissection could

avoided

were

of the

head

cancer (1-6). Consequently, head and neck surgeons performance of elective the risk of occult lymph

mouth. normal through

maccu-

for assessment

of patients

3.

low

mental and (subdigastric thermore,

midline

and

tumors

that

or extend

for nodes 1 (sub-

over (or

study,

approach

it may

2 Furthe

give

contralateral)

me-

false-negative

at US-guided FNAC were aspirating the wrong node cases), obtaining insufficient

(two cases), wrong part In six cases,

supra-

suspicious enlarged in areas

submandibular) and and high posterior).

rise to bilateral tastasis.

In this

posterior,

are always Reactively frequently

the

results result of

(three aspirate

or aspirating from the of the node (three cases). obtaining these false-neg-

alive results appeared to be inevitable because either the metastases inside

the lymph themselves

nodes were

or the lymph nodes too small to allow

sufficient aspiration of tumor cells 3). Thus, the sensitivity of US-guided FNAC could be only slightly in-

August

(Fig

1991

creased by aspirating more often. However, tastases

cannot

lion is indicated. Careful follow-up with US-guided FNAC should be performed in all such patients. #{149}

more nodes as microme-

be reliably

detected

with either US-guided FNAC or any other currently available technique, the sensitivity of US-guided FNAC will probably not rise much over 82% (27 of 33). The specificity of US-guided FNAC does not fall much under the 100% reported herein, as false-positive results at cytologic examination of squamous

cell

carcinoma

or suspicious

FNAC, as can study previously irradiated

results

and Dr.J.S. Lameris for giving us the opportunity to learn the US-guided FNAC technique

To our

knowledge,

and specificity FNAC in this

the

sensitivity of USare higher

than those reported for CT or MR in the literature (6-8); therefore, the technique described herein deserves an important role in enabling deteclion of occult metastatic neck disease. However, as one-fourth of the occult metastases are not detected at USguided FNAC, it is questionable whether this technique fully solves the problem of when to recommend elective neck treatment. We believe, however, that the need for elective (sometimes contralateral) neck treatment can be diminished by performance of US-guided FNAC. This is especially the case for the patient groups involved in this study, for whom elective neck treatment would mean the risk of increased morbidity. Such patients include the elderly or those in whom the neck does not have to be entered for primary tumor excision or in whom the need for a contralateral therapeutic neck dissec-

Volume

180

#{149} Number

2

W, HaelsJ,

13.

HospitaL

G.

14.

1.

2.

McGavran

MH, Bauer

The incidence

of

WC, Ogura

cervicallymph

me-

tastasis from epidermoid carcinoma of the larynx and their relationship to certain characteristics of the primary tumor. Can-

3.

4.

5.

6.

cer 1%1; 14:55-66. All 5, Tiwari RM, Snow GB. False positive and false negative neck nodes. Head Neck Surg 1985; 8:78-82. Byers RM, Wolf PF, Baliantyne AJ. Rationale for elective modified neck dissection. Head Neck Surg 1988; 10:160-167. Okamoto M, Ozeki 5, Watanabe T, lida Y, Tashiro H. Cervical lymph node metastasis in carcinoma of the tongue: correlation between dlinicaland histopathologic findings and metastasis. J Craniomaxillofac Surg 1988; 16:31-34. van den BrekelMWM, CastelijnsJA, Cmli GA, et al. Magnetic resonance versus pal-

pation of cervical

7.

8.

9.

lymph

node

MS. Helier KS. Computed tomography of the clinically negative neck. Head Neck 1990; 12:109-113. Close LG, Merkel M, Vuittch MF, ReischJ, Schaefer SD. Computed tomographic evaluation of regional lymph node involvement in cancer of the oral cavity and oropharynx. Head Neck 1989; 11:309-317. Koch T, Volirath M, Reimer P, Milbrath H. Die relevanz der sonographischen halslymphknotendiagnostik bei tumoren des kopf-und halsbereiches. HNO 1989; 37:144-147.

10.

11.

16.

17.

Leicher-Duber A, Thelen M, Bleier R. Palpation und sonographie von halslymphknotenmetastasen. Rontgenblatter 1989; 42:195-198. Baatenburg dejong RJ, Rongen RJ, Lam#{233}ris JS, Harthoorn M, Verwoerd CDA, Knegt P. Metastatic neck disease: palpation vs ultrasound examination. Arch Otolaryngol Head Neck Surg 1989; 115:689-690.

U, Ga-

beurteilung bei kopf-

JN, Roux

HNO 1988; 36:16-21. P, Caramella E, Demard

Chauvel P. Ear, nose, and ultrasound diagnosis of menodes.

Radiology

Grasl MC, Neuwirth RK, Gritzmann N, Schurawitzki H, Braun 0. Wertigkeit sonomorphologischer kriterien bei der identifikation regionarer metastasen von plattenepithelkarzinomen des iches. HNO 1989; 37:333-337.

HNO-bere-

Penn B, Gardellin G, Nisi E, Perini L, Lunghi F, Frasson P. Identificazione ecotomografica di area iperecogena centrale nei linfonodi: segno di linfoadenopatia benigna. Radiol Med 1987; 74:535-538. Bruneton JN, Normand F. Cervical lymph nodes. In Bruneton JN, ed. Ultrasonography of the neck Berlin: Springer-Verlag, 1987; 81-91.

18.

Siegert R, Schrader ultraschallgefuhrte

pathologigischer 19.

metastasis. Surg 1991;

Arch Otolaryngol Head Neck 117:667-673. Stern WBR, Silver CE, Zeifer BA, Persky

Bruneton

tastasis to cervicallymph 1984; 152:771-773.

15.

JH. node

T, Mende und

von halslymphknotenmetastasen hals-tumoren: ein methodenvergleich. Laryngol Rhinol Otol (Stuttg) 1989; 68:327332. Eichhorn T, Schroeder HG, Schwerk WB. Erfahrungen mit der B-scan sonographie ala bildgebendem diagnoseferfahren im

F, VallicioniJ, throat cancer:

Spiro RH, Strong EW. Epidermoid cardnoma of the mobile tongue: treatment by partial glossectomy alone. AmJ Surg 1971;

Lenartz

Nachweis

HNO-fachgebiet.

at

of aspirates from lymph nodes

(100%) study

University

References

(24). (76%) guided

in the Rotterdam

Heppt demann

Dr. R.J. Bonten-

burg-DeJong

122:707-710.

in cervical

lymph nodes are rare. However, study of aspirates obtained from salivary glands might result in inaccurate false-positive

We thank

Acknowledgments:

12.

B, Baretton G. feinnadelpunction

raumforderungen

kopf-hals-bereich. HNO Hajec PC, Salomonowitz Tscholakoff D, Kumpan

1990;

E, Turk R, W, Czembirek

22. 23.

24.

H. with

US. Radiology 1986; 158:739-742. Baatenburg dejong RJ, Rongen RJ, dejong PC, Lam#{233}risJS,Knegt P. Screening for lymph nodes in the neck with ultrasound. Clin

21.

im

38:287-291.

Lymph nodes of the neck: evaluation 20.

Die

Otolaryngol

1988;

13:5-9.

van den Brekel MWM, Stel HV, Castelijns JA, et a!. Cervical lymph node metastasis: assessment of radiologic criteria. Radiology 1990; 177:379-384. Frable WJ. Thin needle aspiration biopsy. AmJ Clin Pathol 1976; 65:168-181. Engzell V,Jakobsson PA, Sigurdson A, ZajicekJ. Aspiration biopsy of metastatic carcinoma in lymph nodes of the neck Acta Otolaryngol 1971; 72:138-147. Baatenburg dejong RJ, Rongen RJ. Ultrasound examination of the head and neck Thesis. Rotterdam University Hospital, Rotterdam, The Netherlands, 1990; 59-75.

Radiology

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#{149}

Occult metastatic neck disease: detection with US and US-guided fine-needle aspiration cytology.

The authors performed a prospective study of the value of ultrasonography (US) and US-guided fine-needle aspiration cytology (FNAC) for assessment of ...
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