Guidelines for cytopathologic diagnosis of epithelioid and mixed type malignant mesothelioma. Complementary statement from the International Mesothelioma Interest Group, also endorsed by the International Academy of Cytology and the Papanicolaou Society of Cytopathology

Anders Hjerpe; Valeria Ascoli; Carlos Bedrossian; Mathilde Boon; Jenette Creaney; Ben Davidson; Annika Dejmek; Katalin Dobra; Ambrogio Fassina; Andrew Field; Pinar Firat; Toshiaki Kamei; Tadao Kobayashi; Claire W. Michael; Sevgen Önder; Amanda Segal; Philippe Vielh

doi:10.4103/1742-6413.170726

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Review Article

2015

:12;

doi:

10.4103/1742-6413.170726

Guidelines for cytopathologic diagnosis of epithelioid and mixed type malignant mesothelioma. Complementary statement from the International Mesothelioma Interest Group, also endorsed by the International Academy of Cytology and the Papanicolaou Society of Cytopathology

Anders Hjerpe_{MD, PhD}, Valeria Ascoli¹_{MD, PhD}, Carlos Bedrossian²_{MD, PhD}, Mathilde Boon³_{MD, PhD}, Jenette Creaney⁴_PhD, Ben Davidson⁵_{MD, PhD}, Annika Dejmek⁶_{MD, PhD}, Katalin Dobra_{MD, PhD}, Ambrogio Fassina⁷_{MD, PhD}, Andrew Field⁸_{MD, PhD}, Pinar Firat⁹_{MD, PhD}, Toshiaki Kamei¹⁰_{MD, PhD}, Tadao Kobayashi¹¹_{MD, PhD}, Claire W. Michael¹²_{MD, PhD}, Sevgen Önder¹³_{MD, PhD}, Amanda Segal¹⁴_{MD, PhD}, Philippe Vielh¹⁵_{MD, PhD}

Address: Department of Laboratory Medicine, Division of Clinical Pathology/Cytology, Karolinska Institutet, Karolinska University Hospital Huddinge, SE-14186 Huddinge, Sweden

1Department of Radiological, Oncological and Pathological Sciences, Sapienza University, Rome, Italy

2Department of Pathology, Rush University Medical College, Chicago, Illinois, USA

3Leiden Cytology and Pathology Laboratory, Leiden, Netherlands

4National Centre for Asbestos Related Disease, School of Medicine and Pharmacology, University of Western Australia, QEII Medical Centre, WA 6009, Sydney

5Department of Pathology, The Norwegian Radium Hospital, Oslo University Hospital, N-0310 Oslo, Norway

6Department of Laboratory Medicine, Lund University, Malmö University Hospital, SE-205 02 Malmö, Sweden

7Department of Medicine, University of Padova, 35121 Padova, Italy

8Department of Anatomical Pathology, St. Vincents Hospital, Sydney

9Department of Pathology, İstanbul University, İstanbul Faculty of Medicine, Capa, Fatih 34093, Istanbul, Turkey

10Department of Pathology, Yamaguchi Grand Medical Center, Hofu City, Yamaguchi Pref, 747-8511, Osaka, Japan

11Cancer Education and Research Center, Osaka University Graduate School of Medicine, Osaka, Japan

12Department of Pathology, Case Western Reserve University, University Hospitals Case Medical Center, MSPTH 5077, Cleveland, OH 44106, USA

13Department of Pathology, Faculty of Medicine, Hacettepe University, Ankara, Turkey

14Department of Tissue Pathology, Pathwest Laboratory Medicine WA, QE2 Medical Centre, Western Australia 6009, Australia

15Department of Biopathology, Gustave Roussy Comprehensive Cancer Center, 94805 Vilejuif Cedex, France

*Corresponding author

Received: 2015-04-22, Accepted: 2015-04-22, Published: 2015-11

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Abstract

To provide practical guidelines for the cytopathologic diagnosis of malignant mesothelioma (MM). Cytopathologists involved in the International Mesothelioma Interest Group (IMIG) and the International Academy of Cytology (IAC), who have an interest in the field contributed to this update. Reference material includes peer-reviewed publications and textbooks. This article is the result of discussions during and after the IMIG 2012 conference in Boston, followed by thorough discussions during the 2013 IAC meeting in Paris. Additional contributions have been obtained from cytopathologists and scientists, who could not attend these meetings, with final discussions and input during the IMIG 2014 conference in cape town. During the previous IMIG biennial meetings, thorough discussions have resulted in published guidelines for the pathologic diagnosis of MM. However, previous recommendations have stated that the diagnosis of MM should be based on histological material only.[1 2] Accumulating evidence now indicates that the cytological diagnosis of MM supported by ancillary techniques is as reliable as that based on histopathology, although the sensitivity with cytology may be somewhat lower.[3 4 5] Recognizing that noninvasive diagnostic modalities benefit both the patient and the health system, future recommendations should include cytology as an accepted method for the diagnosis of this malignancy.[6 7] The article describes the consensus of opinions of the authors on how cytology together with ancillary testing can be used to establish a reliable diagnosis of MM.

Keywords

Cytology

effusion

guidelines

mesothelioma

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INTRODUCTION

The diagnosis of malignant mesothelioma (MM) can in the majority of cases be based on the evaluation of the effusion,[8] and diagnostic criteria are readily available and illustrated in textbooks.[9 10 11 12] In such cases, the morbidity of the patient is significantly decreased since a definitive cytological diagnosis negates the need for more invasive diagnostic procedures and eliminates the necessity for a biopsy, which has a higher potential for morbidity and a documented increased risk of tumor seeding.[13 14] Definitive treatment can also be immediately initiated avoiding delay. However, when effusion cytology is inconclusive for the diagnosis of MM, tissue core biopsy should be performed as previously recommended. The two techniques are complementary.

It should be emphasized that the important measure here is the reliability of the cytological diagnosis, that is, the positive predictive value, which has been shown to be equal to that of histopathology for use in both clinical and medico-legal contexts. Although the history of exposure to asbestos can be significant and reinforces the suspicion for MM, it is not mandatory for the diagnosis. Nor can the diagnosis of MM rely on the location of the tumour in the pleura or peritoneum or on the gender of the patient.

The diagnosis of MM on cytology includes two steps: The establishment that the effusion is malignant, and then a diagnosis of the mesothelial origin of the malignant cells.

Cytopathology is rightfully recognized as a subspecialty of pathology in its own right and the accuracy of the procedure for the diagnosis of cancer on cytological grounds in experienced hands carries the same weight as that of a tissue biopsy. Proficiency in cytological diagnosis can be achieved through knowledge, training and experience obtained by fellowship programs and daily practice. With such training in cytopahology, the experienced cytopathologists can often recognize MM based on a routinely stained specimen.[4] The accurate diagnosis should, however, always be verified by the use of ancillary techniques. Immunocytochemistry (ICC) or immunohistochemistry (IHC) will in most cases be sufficient, while other techniques such as molecular biology, electron microscopy (EM) and biomarker analyses may add further support and even improve sensitivity. Because of the medico-legal ramifications and with the availability of many mesothelial and adenocarcinoma markers we strongly recommend that all cases should be confirmed with ICC/IHC.

A MM diagnosis can in a majority of cases be achieved based on the cytomorphology and ancillary testing. The main obstacles for the diagnosis are: (i) The low yield of the diagnostic cells due to hypocellularity, bleeding or inflammation; (ii) a cytopathologist's lack of experience; and (iii) lack of awareness of this diagnostic possibility. Low yield of diagnostic cells can be circumvented by concentration techniques such as liquid base cytology and the cell block technique.[15]

Frequently the diagnosis of MM can be established on the first effusion, making a follow-up biopsy redundant, particularly in inoperable cases where adjuvant therapy can be initiated. However, a negative finding does not exclude this diagnosis. This is especially common when the tumor is dominated by a sarcomatoid component, and core biopsy is indicated in these cases in line with the previous guidelines, particularly when surgery is considered, because the presence of a sarcomatoid component may influence therapeutic management.[14]

HOW TO HANDLE THE MATERIAL

The effusion is preferably sent to the laboratory fresh if possible with anticoagulants (heparin ethylenediaminetetraacetic acid or sodium citrate) present, but without added fixatives and it should be refrigerated at 4°C until processing. When longer transportation times are needed, a volume of 50% ethanol can be added as a preservative.

Upon arrival in the laboratory, the fluid should be processed without delay. Refrigerated samples should be brought to room temperature, particularly when using preparation techniques associated with liquid-based cytology (LBC). To prepare a cell pellet, the material is centrifuged at 1000 g or more for 10 min. For the cytomorphological evaluation, it is recommended that both air dried and wet fixed smears or cytospins are prepared to be stained with Papanicolaou (Pap), and either Diff-Quick or May-Grünewald-Giemsa (MGG). Cytospins or cellblocks are prepared for ICC or IHC, respectively. When effusions are bloody, hemolysis should be attempted prior to slide preparation.

Where EM is available, an aliquot of the cell pellet should be transferred to buffered glutaraldehyde without delay. The cells can then be kept at 4°C for later embedding if the case subsequently requires this. A 2–5 mL aliquot of the cell-free supernatant can be stored at −20°C for later biomarker analyses if these are available. EM can sometimes also be applied to paraffin embedded tissue when a fresh specimen is not available, and the diagnosis of mesothelioma depends solely on the existence of the archival material.[16]

BASIC CYTOMORPHOLOGY

Serous effusions from patients with MM at any location can be divided into three groups:

Those cases that are malignant on cytomorphological criteria;
Those cases where the cytological material requires some form of ancillary testing to establish malignancy;
Those cases that cannot be diagnosed by cytology. This category includes cases with minimal cell shedding, typically almost all sarcomatoid and desmoplastic MM, and also those epithelioid MM that do not have malignant cytomorphology or diagnostic positive ancillary tests.

In addition to cytomorphology, the first two categories generally require ancillary techniques such as ICC or IHC and in rare cases EM, to confirm the phenotype as of mesothelial origin. The main differential diagnosis in this setting is usually between MM and metastatic adenocarcinoma. The third category will require some form of histological material.

Cytomorphological features of malignancy in effusions

The first basic question in evaluating the cytomorphology of pleural effusions is whether the cells are malignant or not. A malignant condition can in many cases be diagnosed, based on routinely stained cell preparations [Table 1].

Overtly malignant cells with diagnostic nuclear malignant features may be seen in various anaplastic tumors, and in this setting establishing phenotype may be difficult. Such cells are less common in MM than in adenocarcinoma and other metastatic malignancies. Attempts to establish a malignant diagnosis should be undertaken, when the sample contains exceptionally large numbers of mesothelial cells even when the nuclear atypia is less apparent. Fluorescent in situ hybridization (FISH) and/or ICC or IHC will often confirm the presence of malignant cells.

Cytomorphological features suggesting malignant mesothelioma but requiring some form of ancillary confirmation

The main cytologic findings of MM in effusions have been well described in the literature,[8 17] and the criteria have recently been re-evaluated.[18] The experienced cytopathologist will in many cases recognize the MM effusion, but the definite diagnosis should be supported by ancillary techniques. It is the experience of several laboratories of the authors that the diagnosis is completely reliable when this approach is used.

At low power, the first indication of MM is often a highly cellular slide with numerous tissue fragments [Table 2]. Although pleomorphic, the cells appear monotonous at scanning magnification and there is a lack of a second “alien” cell population. It should be remembered that some cases are extremely discohesive[19] and high cellularity should be enough to motivate further ancillary tests to diagnose a possible MM. These cellular cases, with or without papillary tissue fragments, are sometimes difficult to distinguish from reactive mesothelial hyperplasia, which has been called in the past “mesotheliosis.” On the other hand, in less differentiated MM the nuclear atypia is evident, and the malignancy is diagnosed on nuclear criteria of malignancy while the mesothelial phenotype can be less obvious. A suggestive finding that establishes the mesothelial origin is the occurrence of intercellular clear slits or “windows” between the cells in the tissue fragments. Minute tissue fragments can show cell-within-cell arrangements known previously as “cell cannibalism” or cellular clasping and pinching [Figures 1-3].

Examining the cytoplasmic periphery and the cell membrane can also shed light on the mesothelial origin of cells. In well-fixed Pap-stained slides, a brush border often can be detected corresponding to the microvilli seen at EM, and there is differential staining between the central and peripheral cytoplasm, that is, there is endoectoplasmic demarcation or two-tone staining. This finding can, however, be less obvious in LBC preparations. In MGG-stained MM cells, a diffuse pinkish haze close to the cell border is frequently noted [Figure 3]. This may represent hyaluronan, which is attached during its synthesis in the cell membrane and therefore not extracted during staining. A common finding in MM cells is also “blebbing” with rounded cytoplasmic protrusions extending from the plasma membrane. The MM cytoplasm often contains glycogen deposits, which manifest as elongated yellowish vacuoles or deposits beneath the cell membrane and are best seen in Pap-stained slides.

Background features may also raise the suspicion of MM. The MGG stain often shows a red or pink granular background, a finding that correlates with high concentrations of hyaluronan in the effusion [Figure 2]. As well, pink extracellular material can be found in pockets between cells in papillary tissue fragments in the MGG. This water-soluble glycosaminoglycan is extracted and thus not seen in the Pap-stained material.

Another cytoplasmic feature indicative of MM is the presence of numerous small lipid-containing vacuoles [Figure 3]. They can be seen in the entire cytoplasm of MGG-stained air-dried preparations and when overlapping the nucleus they appear as “punched out holes.” These vacuoles represent a degenerative process and increase with time if the effusion is kept unfixed.[20 21] These droplets are extracted by ethanol fixation for the Pap stain, but they are easily demonstrated in MGG-stained slides.

IMMUNOCYTOCHEMISTRY AND IMMUNOHISTOCHEMISTRY

The main differential diagnoses of MM are adenocarcinoma and reactive mesothelial proliferations, so called “mesotheliosis,” and the diagnosis in the majority of cases can be resolved using ICC on cytospins or IHC on cell blocks. Ancillary testing must be available in laboratories diagnosing MM based on effusions.

Mesothelial phenotype of tumor cells

It is recommended that a panel of at least four antibodies should be used, two in favor and two against MM. The diagnosis should never be based on one single ICC or IHC reaction. Numerous antibodies for MM are commercially available, but most are not entirely specific and may show cross-reactivity with other tumors such as ovarian carcinomas.

The antibodies and epitopes used for cytological samples are the same as those recommended for formalin fixed histological material.[1 2] In cell blocks as well as in cytospin preparations epithelial membrane antigen (EMA) with accentuated reactivity at the cell membrane is often used to support the diagnosis of MM.[22] However, EMA is not a specific mesothelial marker, and the typical cell membrane reactivity may also be seen in adenocarcinomas. Other antibodies supporting the diagnosis of a MM are calretinin, podoplanin (D2-40), WT-1, CK5/6 and mesothelin. Calretinin can, however, also be expressed in breast carcinomas[23] and CK5/6 and mesothelin are sometimes also expressed in ovarian and pancreatic adenocarcinoma [Figure 4].

Recommended antibodies for excluding a mesothelial origin include carcinoembryonic antigen (CEA), BerEp4 and MOC-31, thyroid transcription factor-1 (TTF-1), CD15 and Sialyl-TN. Among the different anti-CEA antibodies available to exclude a MM, the best performing reagent seems to be a monoclonal preparation (No. A0115, DAKO).[24] Although reactivity to the DAKO monoclonal CEA antibody is rarely, if ever, seen in MM, a proportion of MM will express BerEp4 or MOC-31. Double staining with calretinin and BerEp4 will help in most MM cases, as the calretinin reactivity will override that of BerEp4 [Figures 4 and 5].

In summary, to demonstrate the mesothelial origin of a tumor cell population, it is recommended that two of the above antibodies in favor of MM and two excluding the diagnosis be used in a panel: EMA (membranous staining pattern) and calretinin, CEA and BerEp4 will show typical reactivity for MM (the first two positive and the second two negative) in most cases and will exclude adenocarcinomas (the first two negative and the second two positive).[25] If the results are equivocal, additional MM positive antibodies such as podoplanin and WT-1 may be useful, provided the adenocarcinoma markers are negative. As well, additional MM negative antibodies such as CD15 and/or B72.3 can be considered. If there is a known history of another malignancy such as breast, intestinal or lung carcinomas, it is worth including specific markers for such malignancies, such as estrogen receptor or GATA3, CDX2 and TTF-1, respectively.

Malignant mesothelioma versus reactive mesothelium (“mesotheliosis”)

It is more difficult to distinguish reactive mesothelial cells from malignant ones based on IHC or ICC and at least two antibodies should be used in a panel. Benign mesothelial cells are known to contain muscle filaments and they express desmin. The mesothelial cell loses this reactivity to desmin early during the oncogenic process, and the absence of such immunoreactivity is a commonly recommended criterion for MM. In the same way, the typical cell membrane reactivity to EMA in the mesothelial cell is a strong indicator of malignancy, but the specificity for MM may vary between different anti-EMA antibodies. Data indicate that the E29 clone (DAKO) has superior performance in distinguishing malignant from reactive mesothelial cells.[26] This is even better seen when performed as a double stain for desmin together with EMA [Figure 5]. Similar use has also been described with antibodies against CD146, Imp3 and Glut-1.[27 28 29] Furthermore, a general accumulation of p53 in cell tumor nuclei can in some cases be used as further supporting evidence of malignancy.[30]

Peritoneal and pericardial malignant mesothelioma

Since the majority of MM occurs in the pleural cavity, most diagnostic methods have been validated on pleural effusions. MM may also arise in the other serous cavities, where they can show a different clinical spectrum indicating biological differences. Peritoneal MM generally affects younger patients and has a comparable incidence among women and men. A particular papillary neoplasm with superficial spread and bland cytology is designated “well-differentiated papillary mesothelioma”[31] and usually occurs in the peritoneal cavity of women as multifocal lesions.[32]

The challenging differential diagnosis in the peritoneum is between MM and ovarian or peritoneal serous carcinoma.[33] These tumors have common histogenesis, may be difficult to differentiate morphologically and co-express many of the diagnostic markers discussed in the previous section. However, the serous carcinomas of ovary and uterus and peritoneal origin stain positive for BerEp4, PAX8, B72.3, BG8, CA 19-9, Leu-M1 (CD15), MUC4 and estrogen receptor, all of which are rarely or never expressed in MM [Figure 6].[20 33 34]

Pericardial MM are less common. The diagnosis is based on the same criteria as pleural and peritoneal MM, but pericardial fluids are often associated with inflammatory conditions, and here the challenge is to distinguish the MM from mesothelial reactive changes. Malignancy must in these cases be established and verified with caution, using ICC and IHC, and possibly other techniques such as analysis of ploidy by FISH (see below).

OPTIONAL ANCILLARY TECHNIQUES

The diagnostic sensitivity of MM in effusions can be improved further by the use of other ancillary techniques, such as molecular biology, EM and chemical analyses of soluble biomarkers in the effusion supernatant. Equipment for EM is not generally available while other techniques, such as ELISA and FISH are more widely available.

Analysis of soluble biomarkers

Tumor-specific markers can be demonstrated by ICC or IHC in the tumor cell, and are also found in the effusion supernatant, either as secretory products or as a result of tumor cell decay. These tests can be run in parallel with the morphologic evaluations on all effusions with the malignancy of unknown origin, those suspicious for malignancy and those with plentiful mesothelial cells.

The two best-established biomarkers are hyaluronan and mesothelin.[35 36 37 38 39 40] Additional possible MM biomarkers are reported in the recent literature[41 42 43] and are awaiting further evaluation and validation for clinical practice. Hyaluronan is a glycosaminoglycan often secreted in large amounts into MM effusions: A concentration exceeding 250 g/L is only seen in MM effusions[40 44] and appears to be specific for this diagnosis, but such high levels are only obtained in 50–60% of MM effusions.

The mesothelin family of proteins is one of the most investigated soluble biomarkers to aid MM diagnosis, both in sera and effusions. The protein is cleaved into a C-terminal ~ 40 kDa protein, which is commonly referred to as “mesothelin” or C-ERC/mesothelin, while the solubilized, N-terminal, 30 kDa part is referred to as “megakaryocyte potentiating factor” or N-ERC/mesothelin. Both these fragments can be analyzed in the effusion supernatant, and high levels indicate malignancy with sensitivity similar to that of hyaluronan.

The analysis of hyaluronan and mesothelin can be performed in two steps, with the second analysis only performed when the first marker shows moderately elevated values. The high specificity of hyaluronan for MM makes this glycosaminoglycan the best choice for the first analysis. Concentrations exceeding 250 mg/L indicate a MM, while samples with 60–249 mg/L can be analyzed for their concentration of mesothelin. A value exceeding 20 nM (0.8 mg/L) of C-ERK/mesothelin or 50 nM (1.5 mg/L) of N-ERK/mesothelin likewise will indicate the MM diagnosis, although this marker can be produced by carcinomas particularly ovarian and pancreatic carcinomas and is therefore not entirely specific. Intermediate values can be applied to a logistic interpretation model to support the diagnosis of MM in additional cases.[40] The levels of hyaluronan and mesothelin correlate and tend to identify the same cases, but this is not absolute, and the combined use in a logistic battery will improve the sensitivity.

Electron microscopy

When available, EM can be of help when ICC and IHC are not entirely conclusive or when the biomarkers indicate a MM in spite of inconclusive cytomorphology. Effusions are well suited for EM, provided a portion of the cell pellet is properly fixed early in the process. This requires that an aliquot of the first fresh cell pellet is fixed in glutaraldehyde without delay. The ultrastructural analysis can then be performed on demand.

The ultrastructure of MM cells is well known, and EM is considered the gold standard for the diagnosis of MM [Figure 7]. The finding of apical cell membranes with microvilli at basolateral surfaces, forming “extracellular neolumina,” and/or forming an intracellular vesicle or “intracellular neolumina” is pathognomonic for a malignant cell [Figure 7c and d]. To be certain that the group of cells represent a tissue fragment of the tumor and not just an aggregate of cells, desmosomes should be present between the cells [Figure 7d], and the reliable diagnosis of MM is best based on cell tissue fragments and not on an entirely dissociated cell population.

Apart from criteria seen in cytomorphology including nuclear pleomorphism and atypical nucleoli, the nuclear morphology of the MM cell in EM is often highly irregular in a way never seen in the light microscope [Figure 7a]. The characteristic feature of the MM cell is the presence of long slender microvilli without any core rootlets and glycocalyx formation on the surface [Figure 7d]. These microvilli are distinctly different from those seen in adenocarcinoma, in which the cell villi are coarser with a stiffer rod-like appearance and often with a distinct glycocalyx. Although not as abundant, long slender microvilli may appear also on reactive mesothelial cells, and it is important that the malignant nature of these cells is established by the presence of extra and intracellular neolumina. Furthermore, the MM cell often contains glycogen deposits, and microtubules are often present as a “scarf” around the nucleus [Figure 7e and f].

Electron microscopy, when all criteria are demonstrated, clearly distinguishes MM from adenocarcinomas, but a conclusive MM diagnosis can only be expected in some 50% of the cases; the main limiting factors are the need for well-preserved cellular material and the presence of papillary and other tissue fragments. However, the analysis is useful, particularly when ICC and IHC fail to confirm the diagnosis and molecular testing is not available, and it may also be helpful in diagnosing unusual rare variants such as small cell, deciduoid, and clear cell variants.

Molecular biology

A malignant condition can also be demonstrated by the presence of an aneuploid cell population. This can be performed by FISH analysis, and the use of 4 target sequences, such as in the Abbot Urovysion^® kit are sufficient in most cases.[45] Three probes of this kit label centromeric sequences on chromosomes 3, 7 and 17, thus showing gains or losses of the chromosome while the fourth probe labels the 9p21 band containing the p16INK gene. Finding a homozygous deletion of the 9p21 band is virtually always associated with malignancy and is particularly common in certain malignancies, among them MM, while it occurs much less in carcinomas metastatic to the serous cavities [Figure 8]. The deletion will therefore support the diagnosis of a MM although it is not pathognomonic.

A second criterion for malignancy, that cells with gains in at least two of the probed centromeric sequences, must be interpreted with care, and caution is advised when interpreting tri-or tetraploid signals from benign cells in S-or G2-phase.

Demonstration of telomerase activity is a promising general marker of malignancy, and has been shown to assist the diagnosis of MM in cases not resolved by morphology, ICC/IHC or hyaluronan analysis.[46] The best results so far have been achieved using the in situ telomere repeat amplification protocol assay,[47] but this has not yet been established in routine practice.

SUMMARY OF DIFFERENTIAL DIAGNOSES

The two main differential diagnoses of MM are adenocarcinoma and benign, reactive mesothelial cells. The distinction of MM from metastatic carcinoma is in most cases made with the help of ICC or IHC. Metastatic adenocarcinomas react with BerEp4, B72.3, CEA and/or CD15. MMs are positive to calretinin (stronger than to BerEp4), podoplanin (D2-40), mesothelin, EMA accentuated on the cell membrane and WT1, although the last three are common also in ovarian carcinomas. Antibodies indicating a specific primary site greatly assist the diagnosis of metastatic carcinomas, and include TTF-1 in most lung adenocarcinomas, PAX-8 in ovarian and renal carcinomas, CDX2 in colorectal carcinoma and estrogen receptor and GATA3 in breast carcinoma.

An often more challenging task is to differentiate between reactive, benign mesothelial cells and MM. ICC and IHC are often helpful. The most often recommended epitope is desmin, which is lost early during the malignant transformation of mesothelial cells, but some reactivity may remain in the malignant cell population and the effusion may be a mixture of malignant and benign mesothelial cells. Reactivity to EMA in most cases overrides the weaker reactivity to desmin in the malignant cells, and the use of desmin/EMA double stains is recommended. In some cases, there is also a general reactivity to p53 indicating a malignant condition. The use of ploidy analysis by Urovysion^® FISH will in most cases indicate malignancy.[48]

As with pleural MM, the overwhelming majority of peritoneal MM are epithelioid[34] and the main differential diagnosis for MM in ascitic fluids is gastrointestinal cancer of pancreatic, gastric or primarily colonic colorectal origin or, in women, primary peritoneal, tubal or ovarian carcinoma, mainly of the serous type.

For further test panels applicable in ICC and IHC for particular differential diagnostic challenges, see the appendix section of “serous effusions,” edited by Davidson et al.[11]

MEDICO-LEGAL ASPECTS

Medico-legal implications constitute a significant preanalytical consideration when contemplating the cytological diagnosis of MM. The connection between the lethal malignancy MM and its deadly etiological agent asbestos, whose source is usually easily traceable, resulted in a worldwide wave of litigation, which is far from subsiding. The litigation process requires an unequivocal diagnosis based on a variety of specimens and raises a number of issues for the pathologist who first considers the diagnosis of MM. All cytopathological diagnoses may be scrutinized by expert witnesses, debated by numerous attorneys and end up in a court of law, but this is particularly so in MM. The diagnosis of MM must be made based on solid grounds including cytomorphology and ancillary techniques such as ICC and IHC, and in most countries a definitive diagnosis of MM on this basis is currently accepted in everyday medical practice and in courts of law with or without a concurrent histopathological diagnosis.

The long latency period ensures that MM is far from disappearing. Despite severe regulation and banning of the mining and use of asbestos in the U.S., Australia, South Africa and Europe, it is expected that the incidence of MM will continue to increase for sometime in these countries and also in newly industrialized, less regulated societies throughout the world, where mining and various industrial applications of asbestos occur. Litigation, therefore, will be a fact of life as long as patients and their lawyers succeed in linking MM to asbestos exposure in their cases in courts of law.

CONCLUSIONS

Although the sensitivity of cytology for the diagnosis of mesothelioma may vary with the experience of cytopathologist, its accuracy is unquestioned, following these guidelines. MM can thus be specifically diagnosed with a positive predictive value 100% based on the examination of an effusion, using cytology with appropriate ancillary techniques.[5] The diagnosis can in this way be obtained earlier and with less invasive techniques. In addition, a positive pleural cytology is a reliable indicator of visceral pleural invasion.[49]

There is agreement regarding: (1) The means to distinguish benign reactive mesothelial proliferations from MM; (2) the key cytologic features of pleural and peritoneal MM cells in effusions; (3) the use of ancillary techniques in the diagnosis and differential diagnosis of MM; and (4) the use, where necessary, of EM on effusion cell pellets.

The accurate diagnosis can in the majority of cases be obtained earlier, making further invasive diagnostic measures unnecessary, but it is recognized that sarcomatoid or “nonepithelioid” MM are not detected in this way, and MM in effusions with a heavy admixture of blood and inflammatory cells pose diagnostic difficulties.

These guidelines are meant to be a practical reference for the pathologist trained in cytopathology, and for the physician managing patients with possible MM.

GENERAL RECOMMENDATIONS

The cytological diagnosis of MM in effusions should fulfill one of the following criteria

Indisputable malignant cells on cytomorphological criteria which demonstrate a mesothelial phenotype, which should be verified by ancillary techniques
Cytomorphological features which are not unequivocally malignant, but ancillary techniques confirm malignancy and a mesothelial phenotype.

When evaluated in clinical practice these two options can make the specific diagnosis of MM with a high degree of sensitivity and accuracy,[5] while noting that the diagnosis of sarcomatoid MM can rarely be established by effusion cytology.

COMPETING INTERESTS STATEMENT BY ALL AUTHORS

The authors declare that they have no competing interests.

AUTHORSHIP STATEMENT BY ALL AUTHORS

All authors have contributed to this publication.

We agree to publish this manuscript as Open Access article under Creative Commons Legal Code (http://creativecommons.org/licenses/by/2.0/) so that the intellectual property (IP) of this manuscript would be retained in public domain. Under this license authors have published this article in multiple journals.

ETHICS STATEMENT BY ALL AUTHORS

This is a paper without original data.

LIST OF ABBREVIATIONS (In alphabetic order)

CEA - Carcinoembryonic Antigen

EM - Electron Microscopy

EMA - Epithelial Membrane Antigen

FISH - Fluorescent in situ Hybridization

IAC - International Academy of Cytology

ICC - Immunocytochemistry

IHC - Immunohistochemistry

IMIG - International Mesothelioma Interest Group

LBC - Liquid-Based Cytology

MGG - May-Grunewald-Giemsa

MM - Malignant Mesothelioma

Pap - Papanicolaou

EDITORIAL/PEER-REVIEW STATEMENT

This article is published in multiple Journals and authors have agreed to publish this also in CytoJournal as Open Access article under Creative Commons Legal Code.(http://creativecommons.org/licenses/by/2.0/) so that the intellectual property.(IP) of this manuscript would be retained in public domain.

Available FREE in open access from: http://www.cytojournal.com/text.asp?2015/12/1/26/170726

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