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1 Introduction and Historical Perspective

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First reports of fine-needle aspiration cytology (FNAC) as a technique for obtaining diagnostic material date back to the 19th century when, at St Bartholomew’s Hospital, London, aspiration was undertaken on a large mass in the liver by the surgeons Stanley and Earle [1]. Sir James Paget advocated the use of aspiration as an investiga- tive technique in his lectures [2]. Menetrier was probably the first to use aspiration to investigate lung cancer [3]. Some years later, at the begin- ning of the 20th century, Griegg and Gray pu- blished the results of a lymph node aspirate for tripanosomiasis [4]. In 1921, Guthrie described using a 21-guage needle and a technique similar to that used today, but the first large-scale study was carried out at the Memorial Hospital, New York, by the pioneering team of Martin, Ellis and Stewart [5,6]. Stewart published the results of 2,500 tumours biopsied by an aspiration method using an 18-gauge needle [7]. Stewart emphasi- sed the importance of the technique of aspira- tion, sample preparation and close cooperation between clinician and pathologist to assure the degree of diagnostic accuracy achievable with needle aspiration. Despite the pioneering work of American pathologists, the technique initially did not have a following amongst all American pathologists, most of who viewed it with scep- ticism. The historical background of FNAC has been researched by Webb [8] and Grunze and Spriggs [9].

True fine needles for aspiration (22- to 27-gau- ge vs. 18-gauge) were first introduced in Europe in the 1950s by Lopez-Cardozo in The Nether- lands [10] (Fig. 1.1) and Soderström in Sweden [11]. It was, however, publications by Zajicek, from the Karolinska Hospital in Stockholm, that brought aspiration cytology to international at- tention [12, 13] (Fig. 1.2). Linsk described the

Introduction and Historical

Perspective 1

work of the aspiration cytology pioneers Zajicek, Esposti and Lowhagen [14]. At that time, the European clinicians, mainly from the ranks of haematologists (Fig. 1.3) developed the Roma- nowsky and May-Grünwald Giemsa stains for use on air-dried smears to allow for rapid inter- pretation (Fig. 1.4). Despite their success, it was not until the 1980s that FNAC became widely used. The reasons included lack of confidence in the sensitivity and specificity of the procedure, fear of tumour implantation in the needle track, apprehension of lawsuits and the reluctance of surgeons to relinquish the use of the formal hi- stological biopsy technique [15].

Fig. 1.1

True fine needles used for aspiration (22- to 27-gauge vs. 18-gauge) were first introduced in Europe by Paul Lopez-Cardozo in The Netherlands

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1

Fig. 1.2

The publications by Zajicek, from the Karolinska Hos- pital in Stockholm, have brought aspiration cytology to international attention

Fig. 1.3

Despite their success, it was not until the 1980s that fine-needle aspiration cytology (FNAC) became widely used, particularly in Europe. The pioneers of European cytology: Dr J. Jenny, Dr N. Husain, Dr E. Wachtel

FNAC is best understood as a method where a fine needle is used to remove a sample of cells from a suspicious mass for diagnostic purposes.

The material obtained is made into a cytologi- cal sample suitable for microscopic examination.

This is an aspiration cytology rather than a tissue biopsy technique. The architectural arrangement of the cells in the smear may also provide infor- mation about the histology of the tissue from which the sample was removed.

Cytopathologists have the skill to translate cyto- logical features into the tissue patterns needed for diagnosis. William Frable, a renowned Ame- rican cytologist, said „good surgical pathologists who have expressed a negative reaction to FNAC simply do not realise how closely allied recogni- tion patterns are between aspiration biopsy cell spread and its tissue section counterpart“ [16].

However, FNAC biopsy is not a substitute for conventional surgical histopathology. Instead, it should be regarded as being complementary to it, part of the diagnostic processes in combina- tion with clinical, radiological and other labora- tory data.

FNAC biopsy is regarded as a minimally inva- sive, cost-effective technique with diagnostic ac- curacy in the range of 90–99%. The scepticism of some histopathologists about the technique has largely abated along with fears that it may replace tissue diagnosis. Moreover, the task of convincing clinicians of the value of the technique has been extremely successful, since their expectations of a high level of accuracy have been met. While the use of the FNAC biopsy technique has widened, there are pressures for specialisation in this area, and a good balance between expertise and the availability of the test has to be achieved.

The advantages of FNAC are that it is safe, gi- ves a rapid report, is sensitive and specific for the diagnosis of malignancy, requires little equip- ment, cause minimal discomfort to the patient, is an outpatient procedure, reduces bed occupancy, allows preoperative diagnosis, avoids the use of frozen sections, reduces the incidence of explo- ratory procedures, allows a definitive diagnosis on inoperable patients, does not result in fibrosis (which may interfere with future investigations), does not require wound healing and is readily re- peatable and cost effective [15].

The disadvantages of FNAC are that the as- piration technique requires practice and skill, a certain percentage of the aspirates are unsatisf- actory, interpretation requires experience and diagnostic material is limited [15].

The diagnostic accuracy of FNAC depends on several factors, including the site and type of le- sion, the experience of the aspirator, the quality of the specimen preparation and the diagnostic skills of the cytopathologist [17–53]. Various

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studies have reported a greater accuracy in di- agnosis when the same person performs the aspiration procedure, prepares the smears and provides the interpretation. Regardless of the general uniformity of the procedure (a clinically suspicious mass, fine needle, palpation, aspirati- on, smearing, staining and adequate reading of the stained specimen) there are important site- specific considerations that should not be over- looked. The important gross distinction is bet- ween superficial and deep-seated lesions.

Superficial masses (breasts, lymph nodes, head and neck, thyroid and salivary gland) are palpable and usually do not pose a risk of a sam- pling error. In the case of a suspicious mass in the thyroid, for example, the most cost-effective diagnostic test for its evaluation is FNAC. It is the test of choice for the triage of patients requi- ring surgery, thus avoiding approximately 80% of all thyroid surgery. FNAC of deep-seated lesions is usually performed using radiographic image guidance. There is a general agreement that the diagnostic yield of the FNAC of deep-seated le- sions increases when a radiologist and a cytopa- thologist work together.

FNAC of palpable lesions is performed by pathologists with special expertise in both the aspiration technique and specimen preparati- on. This increases the diagnostic yield, because pathologists are able to make an on-site assess- ment of specimen cellularity. It also enhances the clinicopathological correlation, since the pathologist interpreting the specimen has also seen and examined the patient. The pathologists may obtain additional tissue at the time of the initial biopsy for special diagnostic studies that may help to further refine the diagnosis. Pati- ents are typically seen in the FNAC clinic on the same day that they are seen in other clinics. The pathologist performs the aspiration and contacts the referring physician with a preliminary dia- gnosis, typically within 1 hour of patient‘s arrival at the clinic. Performed on an outpatient basis or at patient‘s bedside, FNAC has the best safety record of any method of obtaining material for a morphological diagnosis.

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