César Vivian Lopes1, Antônio Atalíbio Hartmann2, Everson Luiz de Almeida Artifon3. 1. Department of Gastroenterology and Digestive Endoscopy. 2. Department of Pathology, Santa Casa Hospital, Porto Alegre, RS. 3. Department of Surgery, University of São Paulo School of Medicine, São Paulo, SP, Brazil.
Abstract
BACKGROUND: Tissue diagnosis is required for gastric subepithelial lesions for differential diagnosis of GISTs. However, there has not been consensus about the best needle for EUS-guided sampling of these lesions. AIM: To evaluate the diagnostic yield of EUS-FNA for gastric subepithelial lesions of the proper muscle layer with large-bore 19 gauge needles. METHODS: A prospectively maintained database was retrospectively reviewed to identify consecutive patients who underwent EUS-FNA with 19 and 22 gauge needles for gastric subepithelial lesions of the fourth endosonographic layer in a tertiary care referral center. EUS-FNA was performed by the same endosonographer, using the fanning technique, without on-site cytopathologist. Specimens were analysed through cell blocks by the same pathologist. Procedure results were categorized into diagnostic, defined as enough material for histopathology and immunohistochemistry, or nondiagnostic. RESULTS: Eighty-nine patients (mean age: 59 years, 77% women) underwent 92 EUS-FNA with 19 (75) or 22 (17) gauge needles. Mean lesion size was 22.6 mm. Overall diagnostic yield was 88%. The diagnostic yield of 19 gauge was higher than that of 22 gauge needle (92%x70.6%; p=0.0410), and similar for lesions >2 cm and <2 cm (93.7%x90.7%; p=0.9563). The best performance for 19 gauge needles was obtained performing <3 needle passes. Complication rate was 2.8%. CONCLUSIONS: Diagnostic yield of EUS-FNA with 19 gauge needles is 92% for gastric subepithelial lesions of the proper muscle layer. It is safe and highly valuable for differentiation between GIST and leiomyoma, no matter the size of the lesion.
BACKGROUND: Tissue diagnosis is required for gastric subepithelial lesions for differential diagnosis of GISTs. However, there has not been consensus about the best needle for EUS-guided sampling of these lesions. AIM: To evaluate the diagnostic yield of EUS-FNA for gastric subepithelial lesions of the proper muscle layer with large-bore 19 gauge needles. METHODS: A prospectively maintained database was retrospectively reviewed to identify consecutive patients who underwent EUS-FNA with 19 and 22 gauge needles for gastric subepithelial lesions of the fourth endosonographic layer in a tertiary care referral center. EUS-FNA was performed by the same endosonographer, using the fanning technique, without on-site cytopathologist. Specimens were analysed through cell blocks by the same pathologist. Procedure results were categorized into diagnostic, defined as enough material for histopathology and immunohistochemistry, or nondiagnostic. RESULTS: Eighty-nine patients (mean age: 59 years, 77% women) underwent 92 EUS-FNA with 19 (75) or 22 (17) gauge needles. Mean lesion size was 22.6 mm. Overall diagnostic yield was 88%. The diagnostic yield of 19 gauge was higher than that of 22 gauge needle (92%x70.6%; p=0.0410), and similar for lesions >2 cm and <2 cm (93.7%x90.7%; p=0.9563). The best performance for 19 gauge needles was obtained performing <3 needle passes. Complication rate was 2.8%. CONCLUSIONS: Diagnostic yield of EUS-FNA with 19 gauge needles is 92% for gastric subepithelial lesions of the proper muscle layer. It is safe and highly valuable for differentiation between GIST and leiomyoma, no matter the size of the lesion.
Endoscopic ultrasonography-guided fine-needle aspiration (EUS-FNA) is a minimally
invasive technique for sampling gastric subepithelial lesions (SELs), which are a
challenge for the differential diagnosis of gastrointestinal stromal tumors (GISTs).
The yield of EUS-FNA for diagnosis of these lesions ranges from 49-73% with 22 gauge
needles
,
,
, but often the specimens are insufficient for immunostaining. Regarding the
needle size, the literature about large-bore needles is too limited.The objective of this study was to review the results of EUS-FNA with 19 gauge
needles for gastric SELs of the proper muscle layer performed under the same routine
technique, and with specimens evaluated through cell blocks.
METHODS
Study design
Eligible patients included those referred for EUS-FNA at a single
tertiary-referral center. Inclusion criteria were patients with hypoechogenic
gastric SELs of the proper muscle layer (Figures
1A e 1B). Exclusion criteria were an INR>1.5 or platelet count
<50,000, lesions from the submucosa (ectopic pancreas) and cysts. The first
25 EUS-FNA of SELs were also excluded, of which 18 gastric and seven esophageal
SELs, in order to reach the minimum number of EUS-FNA procedures before
competency can be assessed according to the guidelines from American and
European Societies of Gastrointestinal Endoscopy
,
. All patients signed informed consent before enrollment.
FIGURE 1
A) Gastric subepithelial lesion from the greater curvature of the
body; B) linear EUS array demonstrating a lesion from the proper
muscle layer; C) EUS-FNA specimens after a total of three needle
passes with a 19 gauge needle; D) histopathology confirming a
spindle cell tumor (H&E); E) immunohistochemistry stain positive
for actin; F) negative for c-kit; G) DOG-1, confirming a gastric
leyomioma.
EUS-FNA technique
All procedures were performed by the same endosonographer with a curvilinear
array echoendoscope (Olympus GF-UCT140-AL5, Olympus America Inc., New York,
USA), coupled to an ultrasound unit Aloka Prosound alfa-5 SX. Needles for
EUS-FNA were 19 or 22 gauge (EchoTip Ultra Echo-19 or 22, Cook Medical,
Winston-Salem,USA) until July 2015, and only 19 gauge needles after that time.
EUS-FNA was performed under deep sedation with the assistance of an
anesthesiologist. The needle was advanced under EUS guidance into the target
lesion, the stylet was removed, 10 ml of suction was applied, and the needle was
moved back and forth 10 to 20 times in a fan-like motion within the lesion
during each needle pass. After removal of the needle, the specimens were placed
in 20% buffered formalin. The specimens were regarded as adequate in the
presence of whitish cores (tumor tissue) and reddish cores (coagula with tumor
tissue, Figure 1C). On-site cytopathologist
was not available. No smears were prepared. Patients were monitored for 1 h
after the procedure.
Pathology
The histological analysis of the specimens were made through cell blocks by the
same experienced gastrointestinal pathologist. The material was stained with
H&E (Figure 1D), and
immunohistochemistry stain for actin antibodies, c-kit, and DOG-1 was performed
in the presence of spindle cells lesions (Figures
1E, 1F and 1G). A specimen was defined as diagnostic when sufficient
for histopathologic evaluation and immunohistochemistry analysis. If the
biopsies were insufficient for complete evaluation, the specimens were
considered non-diagnostic.
Statistical analysis
Categorical variables were compared by chi-square test or Fisher’s exact test.
Continuous variables were compared by Student’s t-test. Statistical analyses
were performed using SPSS software (version 15.0, SPSS, Chicago, IL).
RESULTS
Patients demographics
From September 2009 to January 2017, a total of 129 patients who underwent 132
EUS-FNA procedures were studied. Twenty-two lesions were excluded from the
analysis, of which 13 submucosal lesions and nine duplication cysts. After
excluding the first 18 EUS-FNA of gastric SELs, the final study group was
composed of 89 patients with hypoechogenic gastric SELs of the proper muscle
layer, which were submitted to 92 EUS-FNA with 19 (n=75) or 22 gauge (n=17)
needles. Repeated EUS-FNA procedures were performed in two patients. The
baseline characteristics of the patients and lesions are summarized in Table 1.
TABLE 1
Demographics and characteristics of the patients/lesions
TOTAL
19 gauge needles
22 gauge needles
p
n
89
72
17
Sex (F/M)
69 / 20
57 / 15
12 / 5
Age, mean + SD (range), yr
58.7 + 14.5 (17-94)
59.2 + 13.5 (25-94)
56.3 + 18.4 (17-86)
0.4611
EUS-FNA
92
75
17
Size, mean + SD (range), mm
22.6 + 18.6 (5-140)
23.8 + 19.7 (6.5-140)
17.4 + 12.0 (5-50)
0.2027
Size > 2 cm
34
32
2
Size < 2 cm
58
43
15
Needle passes, mean + SD (range)
2.9 + 1.13 (1-6)
2.8 + 1.0 (1-5)
3.4 + 1.41 (1-6)
0.0341
< 3 needle passes
69
59
10
> 3 needle passes
23
16
7
Diagnosis
81 (88%)
69 (92%)
12 (70.6%)
0.0410
GIST
38
36
2
Leiomyoma
41
32
9
Schwannoma
1
1
0
Adenocarcinoma/linitis
1
0
1
Complications
2 (2.2%)
2 (2.8%)
0
Diagnostic yield of EUS-FNA: 19 x 22 gauge needles
Needle punctures were successful in all cases irrespective of lesion location.
The overall diagnostic yield of EUS-FNA was 88% (81/92). The diagnostic yield of
EUS-FNA with 19 gauge needles was higher than that of 22 gauge needles [92%
(69/75)x70.6% (12/17); p=0.0410].
Diagnostic yield of EUS-FNA with 19 gauge needles according to the lesion
size and number of needle passes
EUS-FNA with 19 gauge needles revealed the same diagnostic yield for lesions
>2 cm and <2 cm [93.7% (30/32)x90.7% (39/43); p=0.9563].The mean number of needle passes for gastric SELs of the proper muscle layer with
19 gauge needles was 2.8+1. For lesions >2 cm and <2 cm, the mean number
of needle passes were, respectively, 2.84+0.95 and 2.72+1.09, with median of
three needle passes. The diagnostic yields for EUS-FNA with 19 gauge needles
were, respectively, 98.3% (58/59) and 68.7% (11/16) when performing <3 or
>3 needle passes (p=0.00082).The diagnostic yields of EUS-FNA for lesions >2 cm with 19 gauge needles were
similar when performing <3 or >3 needle passes [96.1% (25/26)x83.3% (5/6);
p=0.8145]. On the other hand, for lesions <2 cm, EUS-FNA with 19 gauge
needles and <3 needle passes offered the best diagnostic yield [100%
(33/33)x60% (6/10); p=0.0014].
Complications
The complication rate was very low. Two (2.8%) cases developed epigastric pain
due to hematoma of the gastric wall after EUS-FNA with 19 gauge needles, one of
them with a 5 cm exofitic GIST requiring surgical intervention. The other case
was managed conservatively, with no need of blood transfusion.
DISCUSSION
In our experience, EUS-FNA was performed with 19 gauge needles for 75 gastric SELs of
the proper muscle layer, which represents the largest study published to date with
this needle for this kind of lesions. Its diagnostic yield was higher than that of
22 gauge needles (92%x70.6%; p=0.0410), and revealed results higher than 90% despite
the size of the lesions. Its diagnostic yields were, respectively, 98% and 68.7%
when performing <3 or >3 needle passes (p=0.00082).Concerning the different types of needles for EUS-guided sampling of SELs, Zhang
et al.
did not demonstrate difference in diagnostic rate for any kind of needle.
However, among 17 studies included in this meta-analysis, 14 used EUS-FNA needles,
but only three with 19 gauge needles
,
,
, corresponding to less than 9% of the evaluated cases. Other seven studies
evaluated EUS-FNB needles, five with trucut needles
,
,
,
,
, and two with a core trap needle (ProCore®))
,
. There was only five comparative studies
,
,
,
,
, and only one of them evaluating EUS-FNA with 19 gauge needles
. The number of evaluated cases for different types of needles was very small
in six studies, each one with less than 20 cases for every type of needle
,
,
-
. In regard to the type of SELs, six of 14 studies were not restricted to
gastric SELs
,
,
,
,1822, and three other studies were not restricted to SELs, but also
included lesions from other organs, especially pancreatic ones
,
,
. In reference to the wall layer evaluated, 10 of 17 studies were not
restricted to the proper muscle layer
,
,
,
,
,
,
,
,
,
, this information was unclear in four studies
,
,
,
, and only three analyzed specifically the proper muscle layer
,
,
, but two of them were not restricted to gastric SELs
,
, and none of them evaluated EUS-FNA with 19 gauge needles. At last, relating
to histopathology, cell blocks were used in only nine (53%) studies
,
,
,
,
,
,
,
,
, eight of them evaluating EUS-FNA
,
,
,
,
,
,
,
, but only a single study with 19 gauge needles
. This way, with significant heterogeneity among the selected studies, the
best needle for EUS-guided sampling of gastric SELs of the proper muscle layer has
not been already defined.The experience already published for the EUS-FNA with 19 gauge needles for gastric
SELs is constituted of four studies. In the experience by Larghi et
al.
, using a forward-viewing linear echoendoscope, adequate specimens for
histological examination and immunohistochemistry were obtained in 93% of the cases.
Our results were very similar to that study, but we used a curvilinear array
echoendoscope. Watson et al.
provided adequate specimens for diagnosis in 79% of the cases. This group
counted on on-site cytopathologist in 65% of the procedures, and cell block was
used. The diagnostic yields for SELs >20 and <20 mm were, respectively, 80%
and 45%, but this difference was not significant in multivariate analysis. Besides,
EUS-FNA with 19 gauge needles and a higher number of needle passes were not
associated with improved yield. In our experience, we demonstrated better results
with the large-bore needle, and the best yield was obtained with up to three needle
passes. Eckardt et al.
, without on-site cytopathologist, using a combined evaluation with cyto and
histopathology, with median lesion size of 24 mm, and an average number of two
needle passes, obtained diagnostic material in 52% of the cases. Nonetheless, this
material allowed immunohistochemistry stain in 91% of the cases. Unlike our study,
these authors evaluated gastric SELs of the proper muscle layer in only 61% of the
cases, which could explain the high rate of non-diagnostic cases, in spite of the
needle caliber, lesion size, and number of needle passes have been similar to ours.
At last, a study evaluating the specimens by means of cytopathology, without on-site
cytopathologist, obtained adequate material in only 58% of the cases
. The 19 gauge needle may obtain a hemorrhagic specimen, which can difficult
or even make unfeasible the cytopathologic evaluation. This needle must be used if
the intention is to obtain tissue cores, and not only a group of cells.Our diagnostic yield with a large-bore needle, with no restriction regarding the
lesion size, with three or less needle passes, without on-site cytopathologist, with
specimens evaluated through cell blocks is higher than that obtained with trucut
needles, and as good as that obtained with Procore®) needles. Beshir
et al.
comparing the trucut needle (EUS-TCB) to the EUS-FNA, demonstrated a
diagnostic yield of EUS-TCB and EUS-FNA for SELs of the proper muscle layer of 64.5%
and 66%, respectively. The literature is scarce on comparative studies between
EUS-TCB and EUS-FNA with 19 gauge needles. Nevertheless, it is unlikely a study like
this to be undertaken, as it is well know the higher incidence of technical failures
which not allow the puncture in up to 15% of the cases
,
,
,
, and the absence of higher diagnostic yield even when compared to EUS-FNA
with smaller caliber needles
. Concernig the Procore® needles, Kim et al.
conducted a study comparing EUS-FNB to EUS-FNA, both with 22 gauge needles,
for SELs >2 cm, neither restricted to the stomach nor to the proper muscle layer.
The Procore®) needle established the diagnosis with fewer number of
passes, with median of two passes, and revealed an important difference in the
diagnostic yield (92%x30%). However, the literature has not any comparative study
between EUS-FNB with Procore®) needles and EUS-FNA with 19 gauge needles
for gastric SELs of the proper muscle layer.Our complication rate was very low (2.8%) for EUS-FNA with 19 gauge needles. This
rate is a little higher than the bleeding of 2.2% described by Eckardt et
al.
, but lower than 8% described by Na et al.
with 22 gauge needles. With a better diagnostic yield, our complication rate
is lower than the rates of 3-4% for trucut needles
,
,
, and there has not been complication report with Procore®)
needles for SELs.This study is subject to the limitations inherent to its retrospective design, and
the experience of a single endosonographer in solely a referral center. Furthermore,
the diagnoses obtained by means of EUS-FNA were not compared to surgery
. However, as most patients were asymptomatic and their median lesion size
was 16 mm, it would not be possible to submit all GISTs to resection.On the other hand, this study has many strengths as well. After an initial experience
with 22 gauge needles, all EUS-FNA procedures were performed with 19 gauge needles
for all gastric SELs of the proper muscle layer despite their presumptive EUS
diagnosis, location and size. EUS-FNA with 19 gauge needles obtained a definitive
diagnosis in most cases. The routine histopathology processing for the specimens was
the same, and a single experienced gastrointestinal pathologist evaluated the
material. The small sample sizes of previous studies, inclusion of suspected
diagnoses, SELs from various sites of the gastrointestinal tract, and only lesions
>2 cm might have led to an overestimation of the diagnostic yield of different
needles in those studies. With a scarcity of studies comparing the yield of EUS-FNA
for gastric SELs of the proper muscle layer using different needle calibers, our
experience with 19 gauge needles is the largest when compared to other studies. We
found a significant higher diagnostic yield with the 19 gauge needle even in the
absence of on-site cytopathologists.The question about the best needle for EUS-guided biopsy for these lesions is still
unclear. Further comparative, randomized and multicentric studies are necessary to
define whether this approach is the best and most cost-effective diagnostic strategy
for gastric SELs of the proper muscle layer.
CONCLUSION
Endoscopic ultrasonography-guided fine-needle aspiration of subepithelial gastric
lesions of the own muscular layer in the absence of cytopathologist in the room,
with up to three punctures with 19 gauge needles and evaluation of the material
through cell blocks, allows a diagnostic gain of more than 90%. It is safe and
highly valuable for differentiation between GIST and leiomyoma, no matter the size
of the lesion.
Authors: G M Eisen; J A Dominitz; D O Faigel; J A Goldstein; B T Petersen; H M Raddawi; M E Ryan; J J Vargo; H S Young; J Wheeler-Harbaugh; R H Hawes; W R Brugge; J G Carrougher; A Chak; D O Faigel; M L Kochman; T J Savides; M B Wallace; M J Wiersema; R A Erickson Journal: Gastrointest Endosc Date: 2001-12 Impact factor: 9.427
Authors: L Camellini; G Carlinfante; F Azzolini; V Iori; M Cavina; G Sereni; F Decembrino; C Gallo; I Tamagnini; R Valli; S Piana; C Campari; G Gardini; R Sassatelli Journal: Endoscopy Date: 2011-05-24 Impact factor: 10.093
Authors: Rabindra R Watson; Kenneth F Binmoeller; Chris M Hamerski; Amandeep K Shergill; Richard E Shaw; Ian M Jaffee; Lygia Stewart; Janak N Shah Journal: Dig Dis Sci Date: 2011-03-01 Impact factor: 3.199
Authors: M Philipper; S Hollerbach; H E Gabbert; S Heikaus; A Böcking; N Pomjanski; H Neuhaus; T Frieling; B Schumacher Journal: Endoscopy Date: 2010-03-19 Impact factor: 10.093