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Original Article
2009
:6;
9
doi:
10.4103/1742-6413.52831

Inadequate fine needle aspiration biopsy samples: Pathologists versus other specialists

Department of Pathology and Cytopathology, Monterrey, Nuevo Leon, Mexico. Madero y Gonzalitos S/N Col. Mitras centro, Monterrey, N.L.,México. 64460
Department of Investigation of the Autonomous University of Nuevo Leon, Monterrey, Nuevo Leon, Mexico. Madero y Gonzalitos S/N Col. Mitras centro, Monterrey, N.L.,México. 64460
Licence

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Disclaimer:
This article was originally published by Medknow Publications and was migrated to Scientific Scholar after the change of Publisher.

Abstract

Background:

Fine needle aspiration biopsy (FNAB) is a simple, sensitive, quick and inexpensive method in which operator experience is essential for obtaining the best results.

Methods:

A descriptive study in which the aspiration biopsy cases of the Pathology and Cytopathology Service of the University Hospital of the UANL (2003–2005) were analyzed. These were divided into three study groups: Group 1, FNAB performed by a pathologist; Group 2, FNAB performed by specialists who are not pathologists, Group 3, FNAB guided by an imaging study with immediate evaluation by a pathologist. The samples were classified as adequate and inadequate for diagnosis, the organ, the size and characteristics of the lesions were taken into consideration.

Results:

A total of 1905 FNAB were included. In Group 1: 1347 were performed of which 1242 (92.2%) were adequate and 105 (7.7%) were inadequate. Of the 237 from Group 2, 178 were adequate (75.1%) and 59 inadequate (24.8%); in Group 3 there were 321 of which 283 (88.1%) were adequate and 38 (11.8%) inadequate. A statistically significant difference was found between FNAB performed by Group 1 (p< 0.001) and the other groups. A multivariate analysis was done where the organ punctured, the study groups, the size and characteristics of the lesion by study group were compared, finding that the most important variable was the person who performed the procedure.

Conclusion:

The experience and training of the person performing the aspiration biopsy, as well as immediate evaluation of the material when it is guided, substantially reduces the number of inadequate samples, improving the sensitivity of the method as well as reducing the need for open biopsies to reach a diagnosis.

Keywords

Fine needle aspiration biopsy
adequate specimens
influence of training
pathologist
other specialists

INTRODUCTION

Fine needle aspiration biopsy (FNAB) is a quick, sensitive and inexpensive technique for diagnosing benign and malignant palpable lesions[1] and non-palpable lesions from which material can be obtained with image-guidance.[2] The greatest advantage of this minimally invasive technique is its high sensitivity and specificity.[3] As a result, it is often utilized in the initial diagnostic evaluation of lesions identified in the breast,[4] thyroid[5] lymph nodes[6] and other organs.

The lower cost-benefit ratio of FNAB over other traditional biopsy types has been well documented. In addition, FNAB can be accurately performed as an outpatient procedure with fewer complications than an open biopsy.[7] The experience and training of the physician performing the FNAB has been shown to be a key factor in the quality and adequacy of the FNAB specimen. Yusef et al. showed that, when a physician lacked training, the rate of inadequate specimens for diagnosis was up to 29.5% in contrast to 4.6% when the sample is obtained by an appropriately trained pathologist.[8]

On the other hand, immediate cytologic evaluation of aspiration specimens obtained by an interventional radiologist has been shown to be crucial for the success of this procedure.[9] Immediate cytologic evaluation is also important when FNAB are performed by other specialists using imaging methods, such as endoscopic ultrasound-guided FNAB.[10]

This study evaluated the rates of inadequate material for diagnosis based on the physician performing the procedure, the importance of immediate cytologic assessment of samples obtained by image-guided aspiration, the influence of organ site and the size and characteristics of the lesions aspirated.

MATERIALS AND METHODS

This descriptive retrospective study was performed in the Universidad Autónoma de Nuevo León Pathology and Cytopathology Laboratories of the University Hospital. The data were obtained by reviewing the laboratory database and cytology reports of the FNABs performed between January 2003 and December 2005. The FNABs were divided into three study groups: Group 1: FNABs performed by pathologists and/or residents under their supervision; Group 2: FNABs performed by non-pathology specialists, and Group 3: Image-Guided FNABs with immediate cytologic evaluation by a pathologist at the time of aspiration.

The FNABs in the three study groups were performed using a 10 ml plastic syringe with a 22-gauge needle; Group 1 also used a Cameco syringe pistol. The Group 1 FNABs consisted of four smears from each aspiration and a maximum of three punctures per procedure; two smears were fixed in alcohol and stained with diff quick stain for immediate pathologist evaluation. The other two smears were fixed in alcohol and stained using the Papanicolaou technique. The Group 1 FNABs were performed by pathologists, pathology residents and occasionally by residents from other specialties (surgery and gynecology) under a pathologist's supervision. In Group 2, the FNAB procedure, smear preparation, and alcohol fixation were carried out by other specialists who are not pathologists and subsequently sent to the pathology service. No immediate cytologic evaluation was performed during these procedures. These FNABs had an average of 2 to 4 slides prepared from an unknown number of punctures. All the slides in this group were stained with the Papanicolaou technique and interpreted by a pathologist. In Group 3, the FNAB was performed by a radiologist with smear preparation and fixation done by a pathology resident, who was present during the procedure for immediate evaluation. The smears were stained with the Papanicolaou technique. An average of three punctures with 4 to 6 slides were prepared per procedure.

The same adequacy criteria were used for all three study groups. Samples were considered adequate for interpretation when they contained a minimum of three well-preserved cell groups per slide and no fixation artifacts in the thin smears. All slides that were classified as inadequate for interpretation and 50% of the adequate slides were reevaluated in a blinded fashion by two cytopathologists using the aforementioned criteria.

The results were analyzed by study groups, organ sites punctured, and grouped by frequency.

The FNAB specimens were classified as adequate [Figure 1] or inadequate [Figure 2] for diagnosis. A comparative analysis of the three study groups was done using the X2 statistical test. Also, multivariate analysis was performed using the primary study groupings, organ sites punctured, the lesion sizes (less than 1cm, 1 to 3 cm and more than 3 cm), and the characteristics of the lesion, using the Kruskal-Wallis test. When less than five specimens were present in a subgroup, the Jonckheere-Terpstra test was used. A p value of <0.05 was considered to be statistically significant.

Figure 1
Adequate specimen
Figure 2
Inadequate specimen

RESULTS

1905 FNABs were identified for study and divided into the three primary study groups as follows: Group 1 n=1347 (70.7%), Group 2 n=237 (12.4%), and Group 3 n=321 (16.9%). The original diagnosis was confirmed in all of the reevaluated cases. In Group 1, 1242 (92.3%) of the FNABs were adequate for interpretation and 105 (7.7%) were inadequate. In Group 2, 178 (75.2%) were adequate and 59 (24.8%) were inadequate. In Group 3, 283 (88.2%) were adequate and 38 (11.8%) were inadequate. Group 1 contained a statistically higher percentage of adequate FNABs that the other two groups (p<0.001) [Table 1].

Table 1 Results according to study group
Adequate % Inadequate % Total
Group 1 (Pathologists) 1242 92.2 105 7.7 1347
Group 2 (Other physicians) 178 75.1 59 24.8 237
Group 3 (Image-guided) 283 88.1 38 11.8 321

P = 0.001 in favor of group 1

The frequency of adequate and inadequate FNAB samples from each organ site is presented in Table 2. When subdivided by organ site, the Group 1 FNABs generally showed higher rates of adequacy.

Table 2 Comparsion of punctured organs
Carried out by pathologists Image-guided External Total P
A % I % A % I % A % I %
Breast 425 94.4 25 5.5 22 91.6 2 8.3 49 72 19 27.9 542 < 0.05
Thyroid 166 89.2 20 10.7 26 81.2 6 18.7 38 67.8 18 32.1 274 < 0.01
Lymph node 288 90.2 31 9.7 18 85.7 3 14.2 17 85 3 15 360 NS
Soft tissue 266 92.6 21 7.3 6 100 0 0 45 83.3 9 16.6 347 NS
Others 97 92.3 8 7.6 4 100 0 0 29 74.3 10 25.6 148 NA
Total 1242 92.2 105 7.7 76 87.3 11 12.6 178 75.1 59 24.8 1671 NA

A= Adequate, I = Inadequate, NS= Not significant, NA = Not analyzed

The organ site with the greatest number of FNABs was the breast with a total of 542 procedures. Group 1 performed 450 of the breast FNABs with 94.5% adequacy and 5.5% inadequacy rates. In comparison, Group 2 performed 68 FNABs with 72.0% being adequate and 28.0% inadequate for interpretation. Group 3 performed 24 FNABs with 91.6% being adequate and 8.4% inadequate for interpretation. Group 1 contained a statistically higher percentage of adequate FNABs than the other two groups (p<0.05).

The second most frequent organ site was from the lymph nodes with 360 cases. Group 1 performed 319 of these FNABs with 90.3% being adequate and 9.7% inadequate for interpretation. Group 2 carried out 20 of these FNABs with 85.0% being adequate and 15.0% inadequate. Group 3 performed 21 of these FNABs with 85.7% being adequate and 14.3% inadequate. In this subgroup, no significant difference was identified.

Soft tissue FNABs were the third most common procedure with a total of 347 specimens. Group 1 performed 287 of these FNABs with 92.6% being adequate and 7.4% inadequate samples. Group 2 performed 54 FNABS with 83.4% being adequate and 16.6% inadequate. In Group 3, six FNABs were performed with all being adequate. In this subgroup, no significant differences were identified.

The fourth organ in frequency was the thyroid gland with 274 punctures. Group 1 performed 186 of the FNABs with 89.2% being adequate and 10.8% inadequate. Group 2 carried out 56 FNABs with 67.8% being adequate samples and 32.2% inadequate samples. Group 1 contained a statistically higher percentage of adequate FNABs that the other two groups (p<0.01).

Deep organs such as the pancreas, liver, lung and others were biopsied using imaging techniques with pathology processing the specimen and providing immediate adequacy assessment of the material obtained; a total of 207 cases were performed of which 88.5% were adequate and 11.5% inadequate for interpretation [Table 3].

Table 3 Deep organ puncture/image-guided
Organ Adequate % Inadequate % Total
Pancreas
Biliary tree 51 89.4 6 10.5 57
Liver 75 91.4 7 8.5 82
Mediastinum 23 82.1 5 17.8 28
Lung 32 86.4 5 13.5 37
Kidney 26 86.6 4 13.3 30
Total 207 88.4 27 11.5 234

When comparing the lesion's size with specimen adequacy for each organ group, Group 1 generally showed statistically higher rates of adequacy, regardless of the lesion's size (less than 1 cm, 1 to 3 cm and more than 3 cm) (p<0.001) [Table 4]. With regard to the smaller number of inadequate samples, a statistical Group 1 advantage was not documented for soft tissue lesions less than 1 cm or with lesions greater than 3 cm in the breast and lymph nodes. In these latter groups, the number of cases was small [Table 5].

Table 4 Comparison of size of adequate lesions by organ punctured and study group
Organ Study group Less than 1 cm (Adequate) 1 to 3 cm (Adequate) More than 3 cm (Adequate) Total
A % P A % P A % P
Group 1 55 82 350 97.2 20 86.9 425
Breast Group 2 3 50 *0.000 43 75.4 *0.000 3 60 *0.000 49
Group 3 8 88.8 14 93.3 0 0 22
Thyroid Group 1 29 87.8 130 89.6 7 87.5 166
Group 2 3 75 *0.000 34 68 *0.000 1 50 *0.000 38
Group 3 8 80 18 81.8 0 0 26
Group 1 62 84.9 218 92.3 8 80 288
Lymph node Group 2 1 50 *0.000 15 93.7 *0.000 1 50 *0.000 17
Group 3 5 71.4 12 92.3 1 100 18
Group 1 19 86.3 65 87.3 182 95.2 266
Soft tissues Group 2 3 75 *0.000 10 83.3 *0.000 32 84.2 *0.000 45
Group 3 3 100 2 100 1 100 6
Group 1 15 88.2 68 94.4 14 87.5 97
Others Group 2 1 25 *0.000 20 90.9 *0.000 8 61.5 *0.000 29
Group 3 1 100 3 100 0 0 4
Total 216 82.4 1002 91.1 278 89.9 1496
P in favor of group 1. A=Adequate
Table 5 Comparison of size of inadequate lesions by organ punctured and study group
Organ Study group Less than 1 cm (Inadequate) 1 to 3 cm (Inadequate) More than 3 cm (Inadequate) Total
I % P I % P I % P
Group 1 12 17.9 10 2.7 3 13 25
Breast Group 2 3 50 *0.000 14 24.5 *0.000 2 40 0.083 NS 19
Group 3 1 11.1 1 6.6 0 0 2
Thyroid Group 1 4 12.1 15 10.3 1 12.5 20
Group 2 1 25 *0.046 16 32 *0.000 1 50 NA 18
Group 3 2 20 4 18.1 0 0 6
Group 1 11 15 18 7.6 2 20 31
Lymph node Group 2 1 50 *0.000 1 6.25 *0.000 1 50 0.157 NS 3
Group 3 2 28.5 1 7.6 0 0 3
Group 1 3 13.6 9 12.1 9 4.7 21
Soft tissues Group 2 1 25 0.083 NS 2 16.6 *0.005 6 15.7 *0.001 9
Group 3 0 0 0 0 0 0 0
Group 1 2 11.7 4 5.5 2 12.5 8
Others Group 2 3 75 *0.046 2 9 *0.025 5 38.4 *0.014 10
Group 3 0 0 0 0 0 0 0
Total 46 17.5 97 8.8 32 10 175
P in favor of group 1. I = Inadequate. NS = Not significant, NA = Not analyzed

The deep organs punctured by radiologists were also classified according to lesion size with most of the lesions biopsied in this group measuring 1 to 3 cm [Table 6].

Table 6 Size of lesions according to deep organ punctured/image-guided
Organ Less than 1 cm % E 1 to 3 cm % More than 3 cm % Total
Pancreas and biliary tree 14 24.5 38 66.6 5 8.7 57
Liver 8 9.7 26 31.7 48 58.5 82
Mediastinum 0 0 7 25 21 75 28
Lung 9 24.3 20 54 8 21.6 37
Kidney 1 3.3 12 40 17 56.6 30
Total 32 13.6 103 44 99 42.3 234

With regards to the lesion's characteristics such as consistency (soft or firm), fibrosis, necrosis and cystic degeneration, the FNABs were compared by study group and organ site biopsied. Group 1 showed a statistical advantage (p< 0.001) in terms of adequate sample acquisition and lower numbers of inadequate samples [Tables 7 and 8].

Table 7 Comparison of adequate lesion characteristics by group
Characteristics of the lesions Group 1 adequate (N=1347) Group 2 adequate (N=237) Group 3 adequate (N=321) Total P
A % A % A %
Consistency
Soft 257 19.0 52 21.9 103 32.0 412 (SC) *0.000
Firm 985 73.1 126 53.1 174 54.2 1285 (FC) *0.000
Presence of fibrosis 226 16.7 32 13.5 25 7.7 283 *0.000
Presence of necrosis 195 14.4 27 11.3 61 19.0 283 *0.000
Cystic degeneration 168 12.4 28 11.8 33 10.2 229 *0.000
P in favor of group 1; (SC) = Soft consistency; (FC) = Firm consistency; A = Adequate
Table 8 Comparison of inadequate lesion characteristics by group
Characteristics of the lesions Group 1 Inadequate (n=1347) Group 2 Inadequate (n=237) Group 3 Inadequate (n=321) Total P
i % i % i %
Consistency
  Soft 40 2.9 11 4.6 18 5.6
  Firm 65 4.8 48 20.2 26 8.0
Presence of fibrosis 95 7.0 14 5.9 11 3.4 120 *p= 0.000
Presence of necrosis 65 4.8 11 4.6 9 2.8 85 *p=0.000
Cystic degeneration 30 2.2 6 2.5 10 3.1 46 *p=0.000
p in favor of group 1. SC = Soft consistency, FC = Firm consistency, I = Inadequate

With regard to the FNABs done by pathologists or pathology residents (pathology personnel) and residents from other specialties that rotate on the service, 1012 FNABs were performed by pathology personnel 94.0% being adequate and 6.0% being inadequate. A total of 335 FNABs were performed by other specialty residents that rotated on the pathology service with 87.0% being adequate and 13.0% being inadequate. The FNABs performed by pathology personnel contained a statistically significant higher percentage of adequate FNABs than the other group (p<0.01), which supports the premise that experience and adequate operator training in the procedure are directly proportional to the rate of obtaining adequate samples [Table 9].

Table 9 Physicians who carried out FNAB in the aspiration room
Adequate % Inadequate % Total
Pathology personnel 952 94 60 5.9 1012
*Medico rotatorio 290 87.1 45 13.4 335

P < 0.01 in favor of t pathology personnel

Other specialty residents that rotated on the pathology service

DISCUSSION

FNAB is a currently accepted procedure for the initial diagnosis of patients with lesions when combined with clinical data and imaging. FNAB can be used to evaluate a number of diverse organ pathologies in the thyroid,[1116] breast,[1723] lymph node[2427] and other organs. Its usefulness has increased in the diagnosis of deep organ lesions when combined with image guidance techniques such as conventional ultrasound, computerized tomography[2829] or transendoscopic ultrasound.[3032]

In addition to its high specificity and sensitivity [Table 10], FNAB has numerous advantages[33] such as lower cost, outpatient technique, minimally invasive approach and the possibility of obtaining material for special histochemical or immunohistochemical staining, electronic microscopy, flow cytometry and/or culture.[34] To use these adjuvant tests, it is essential that the cytologic material be adequate in both quality and quantity to make an accurate diagnosis. In the literature, reports of unsatisfactory or inadequate quantities of material varies from 3.0% to 14.0%.[835] These studies have linked the results to the knowledge and experience of the aspiration biopsy technique by the physician.

Table 10 Sensitivity and specificity of FNAB according to other studies
Organ % Sensitivity % Specificity
Breast 4 98 97
Lymph node 25 90 82.3
Thyroid 11 77.5 90.1
Diverse organs 3 93 100

Carson et al.[35] reviewed 2199 FNABs and found a significant difference in the percentage of inadequate material for interpretation cases between clinicians (14.0%) and pathologists (3.0%). Similarly, Yusef et al.[8] studied 692 FNABs and found that 29.5% were unsatisfactory samples when performed by surgeons in comparison with 4.6% when performed by pathologists. Other studies have described similar percentages.[33536] In this study, other specialists, such as endocrinologists and gynecologists were included in addition to surgeons.

Ljung et al.[36] showed a notable difference in the results when FNAB is performed by physicians with training in the technique (2.0% inadequate material) versus physicians without training (25.0% inadequate material). The results of this study are similar with 7.7% inadequate specimens obtained in the aspiration clinic by trained pathology personnel versus 24.8% of specimens obtained by other specialists. The factors that contributed to this difference appeared to be mainly skill in the technique and the availability of immediate cytologic evaluation of the aspirate for adequacy. The latter assisted in determining if another organ aspiration was necessary and what specimens should be put aside for special studies. In addition, the pathologist performing the procedure has the advantages of being able to directly interact with the patient to obtain relevant clinical data and establish the characteristics of the lesion such as its exact location, size and consistency.[833]

Variables such as the lesion's size and characteristics did not appear to affect the rate of obtaining adequate samples when the FNAB was performed by pathology personnel in comparison with the other groups. Multivariate analysis indicated that adequate training, skill in the technique, and immediate cytologic evaluation carried more weight in predicting the success of obtaining an adequate sample.

The relationship between inadequate samples and the organ site showed that the breast had the lowest percentage of unsatisfactory samples by pathology personnel (5.5%), in contrast to 10.7% for the thyroid and 9.7% for lymph nodes [Table 2]. Yusef et al. in their study showed a greater percentage of non-diagnostic aspirates in breast tissue, followed by lymph node and thyroid.[8]

Multidisciplinary collaboration between a radiologist and a pathologist when performing image guided FNAB in deep organs is also fundamental, since recent studies have indicated that immediate cytologic evaluation of the sample by a pathologist influences specimen adequacy and improves the cost-benefit ratio.[3738] In this study, ultrasound or computerized tomography guided FNABs that were initially evaluated by a pathologist had better results (11.8% inadequate samples) than those without an immediate cytologic evaluation by a pathologist (24.8% inadequate samples).

In contrast to other studies, a difference was identified between FNABs performed by pathology personnel (5.9% inadequate material) and residents from other specialties who were in training on the pathology service (13.4% inadequate material, p<0.01). These results support that more training time and supervision produces better results.

CONCLUSION

Based on the results of this study, it is recommend that fine needle aspiration biopsy be performed preferably by a pathologist who has received specific training in this technique, who can carry out an immediate evaluation of the material, decide if it is necessary to re-aspirate and can distribute the aspirated material for ancillary studies. The aforementioned contrasts with the results obtained by other specialists where it is unknown if they have received specific FNAB training and knowledge of the aspiration smear technique. The results of this study support that it is essential to include aspiration biopsy techniques in pathology residency training under the direct supervision of an experienced cytopathologist.

On the other hand, it is important to emphasize that deep organ aspirations and lesions under 1 cm may be performed by interventional radiologists in concert with a pathologist to ensure optimal smearing, fixation, and immediate evaluation with the goal of lowering the rate of unsatisfactory results and increasing the cost-benefit of the procedure.

COMPETING INTEREST STATEMENT BY ALL AUTHORS

No competing interest to declare by any of the authors

AUTHORSHIP STATEMENT BY ALL AUTHORS

All authors of this article declare that we qualify for authorship as defined by ICMJE.

Authorship credit: GM substantial contributions to conception and design, acquisition of data, or analysis and interpretation of data; GG and BQ drafting the article or revising it critically for important intellectual content; SL performed the statistical analysis. GM, GG, BQ, and SL final approval of the version to be published.

Each author has participated sufficiently in the work and take public responsibility for appropriate portions of the content of this article.

ETHICS STATEMENT BY ALL AUTHORS

This study was conducted with approval from Institutional Review Board (IRB) of all the institutions associated with this study. Authors take responsibility to maintain relevant documentation in this respect.

EDITORIAL/PEER-REVIEW STATEMENT

To ensure integrity and highest quality of CytoJournal publications, the review process of this manuscript was conducted under a double blind model (authors are blinded for reviewers and reviewers are blinded for authors) through automatic online system.

Available FREE in open access from: http://www.cytojournal.com/text.asp?2009/6/1/9/52831

REFERENCES

  1. . Needle aspiration biopsy: Past, present, and future. Hum Pathol. 1989;20:504-17.
    [Google Scholar]
  2. , , , , , . Computed tomography guided needle biopsy: Experience from 1,300 procedures. Sao Paulo Med J. 2006;5(124):10-4. Epub 2006 Apr 3
    [Google Scholar]
  3. , , , , . Cancer Committee of the Henry Mayo Newhall Memorial Hospital. The reliability of fine-needle aspiration biopsy as the initial diagnostic procedure for palpable masses: A 4-year experience of 730 patients from a community hospital-based outpatient aspiration biopsy clinic. Cancer. 2006;107:406-16.
    [Google Scholar]
  4. , , , , , , . Fine-needle aspiration of clinically suspicious palpable breast masses with histopathologic correlation. Am J Surg. 2002;184:410-3.
    [Google Scholar]
  5. , , , . Fine-needle aspiration of thyroid nodules: A study of 4703 patients with histologic and clinical correlations. Cancer. 2007;111:306-15.
    [Google Scholar]
  6. , , , . The diagnostic value of fine needle aspiration cytology (FNAC) in the assessment of palpable supraclavicular lymph nodes: A study of 218 cases. Cytopathology. 2003;14:201-7.
    [Google Scholar]
  7. , , . Comparison of fine needle aspiration cytology and needle core biopsy in the diagnosis of radiologically detected abdominal lesions. J Clin Pathol. 2002;55:93-7.
    [Google Scholar]
  8. , , , , , . Comparison of specimen adequacy in fine-needle aspiration biopsies performed by surgeons and pathologists. Ann Saudi Med. 2004;24:124-6.
    [Google Scholar]
  9. , , . Diagnostic value and cost-effectiveness of on-site evaluation of fine-needle aspiration specimens: Review of 5,688 cases. Diagn Cytopathol. 2002;27:1-4.
    [Google Scholar]
  10. , , , , , , . Diagnosis of gastrointestinal tract lesions by endoscopic ultrasound-guided fine-needle aspiration biopsy. Cancer. 2004;102:157-63.
    [Google Scholar]
  11. , , , , . Fine needle cytology of the thyroid gland. Tidsskr Nor Laegeforen. 2004;124:2359-61.
    [Google Scholar]
  12. , , , . The impact of assessing specimen adecuacy and number of needle passes for fine- needle aspiration biopsy of thyroid nodules. Thyroid. 2006;16:55-60.
    [Google Scholar]
  13. , , , . Implications of follicular neoplasms, atypia, and lesions suspicious for malignancy diagnosed by fine-needle aspiration of thyroid nodules. Ann Surg. 2002;235:656-64.
    [Google Scholar]
  14. . Current evaluation of thyroid nodules. Trends Endocrinol Metab. 1994;5:365-9.
    [Google Scholar]
  15. , , , , , , . Fine-needle aspiration of the thyroid and correlation with histopathology in a contemporary series of 240 patients. Am J Surg. 2003;186:702-10.
    [Google Scholar]
  16. , , , , , . Us-guided fine-needle aspiration biopsy of thyroid nodules: Adequacy of cytologic material and without immediate cytologic analysis. Radiology. 2001;10:12-23.
    [Google Scholar]
  17. , , , . Role of sample adequacy in fine needle aspiration biopsy of palpable breast lesions. Am J Surg. 2001;182:369-71.
    [Google Scholar]
  18. , , , , , . Adequacy evaluation of fine-needle aspiration biopsy in the breast health clinic setting. Cancer. 2004;102:295-301.
    [Google Scholar]
  19. , , , . Fine-needle aspiration cytology for diagnosis and management of palpable breast mass. Aust N Z J Surg. 2000;70:791-4.
    [Google Scholar]
  20. . Uniform approach to breast fine needle aspiration biopsy. Acta Cytol. 1998;42:440.
    [Google Scholar]
  21. , , , . Breast fine needle aspiration cytology: Utility as a screening tool for clinically palpable lesions. Acta Cytol. 1993;37:461-71.
    [Google Scholar]
  22. , , , , , , . Influence of training and experience in fine-needle aspiration biopsy of breast: Receiver operating characteristics curve analysis. Arch Pathol Lab Med. 1987;111:518-20.
    [Google Scholar]
  23. , , , , , , . Florence-Sydney Breast Biopsy Study: Sensitivity of ultrasound-guided versus freehand fine needle biopsy of palpable breast cancer. Breast Cancer Res Treat. 2005;89:55-9.
    [Google Scholar]
  24. . Uses and limitations of fine needles aspiration cytology in the diagnostic work-up of patients with superficial lymphadenopathy. Nig Q J Hosp Med. 2007;17:144-7.
    [Google Scholar]
  25. , , . Fine needle aspiration biopsy in the diagnosis of lymphadenopathy in 1,103 patients: Role, limitations and analysis of diagnostic pitfalls. Acta Cytol. 1995;39:76-81.
    [Google Scholar]
  26. , , , . Accuracy of fine needle aspiration cytology in the evaluation of peripheral lymphadenopathy. J Med Assoc Thai. 1997;80:S155-61.
    [Google Scholar]
  27. , . Fine-needle aspiration cytology in the diagnosis of superficial lymphadenopathy: A 5-year Brazilian experience. Diagn Cytopathol. 2006;34:130-4.
    [Google Scholar]
  28. , , , , . US guidance for thoracic biopsy: A valuable alternative to CT. Radiology. 1999;210:721-6.
    [Google Scholar]
  29. , , , , . Application of a single needle type for all image-guided biopsies: Results of 100 consecutive core biopsies in various organs using a novel tri-axial, end-cut needle. Cancer Imaging. 2006;6:43-50.
    [Google Scholar]
  30. , , , , , , . Endoscopic ultrasound-guided fine-needle aspiration biopsy: A study of 103 cases. Cancer. 2002;96:232-9.
    [Google Scholar]
  31. , , , , . Biopsia por aspiració;n con aguja fina guiada por ultrasonido endoscópico. Experiencia del Hospital Universitario, UANL. Rev Hosp Gral. 2005;68:193-7.
    [Google Scholar]
  32. , , , , , , . Diagnosis of gastrointestinal tract lesions by endoscopic ultrasound-guided fine-needle aspiration biopsy. Cancer. 2004;102:157-63.
    [Google Scholar]
  33. . The surgical pathologist's approach to fine needle aspiration. Clin Lab Med. 1998;18:367-72. v
    [Google Scholar]
  34. , , . Clinical significance of cultures collected from fine-needle aspiration biopsy. Diagn Cytopathol. 2008;36:85-8.
    [Google Scholar]
  35. , , , . Unsatisfactory aspirates from fine- needle aspiration biopsies: A review. Diagn Cytopathol. 1995;12:280-4.
    [Google Scholar]
  36. , , , , , , . Diagnostic accuracy of fine-needle aspiration biopsy is determined by physician training in sampling technique. Cancer. 2001;93:263-8.
    [Google Scholar]
  37. , . Positive economic and diagnostic accuracy impacts of on-site evaluation of fine-needle aspiration biopsies by pathologists. Acta Cytol. 1996;40:1227-30.
    [Google Scholar]
  38. , , . The value of onsite adecuacy assessment of thyroid fine-needle aspirations is a function of operator experience. Cancer Cytopat. 2006;108:110-3.
    [Google Scholar]
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