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Cervical Pre-cancers: Biopsy and Immunohistochemistry
How to cite this article: How to cite this article: Kamal M. Cervical pre-cancers: Biopsy and immunohistochemistry. CytoJournal 2022;19:38.
The existence of precursor lesions for invasive cervical cancer has been recognized for more than 50 years. Our understanding of the pathobiology and behavior of cervical cancer precursors has evolved considerably over the past five decades. Furthermore, the terminology used to classify pre-invasive lesions of the cervix has frequently changed. The realization that human papillomavirus (HPV) infections constitute a morphologic continuum has prompted efforts to include them within a single classification system, specifically the squamous intraepithelial lesions (SILs) which have now been embraced by the surgical pathologists. The reduced number of specific pathological categories has made clinical decision-making more straightforward. The generic criteria for SIL have two important histological parameters: Alterations in the density of superficial epithelial cells and superficial squamous atypia. The flat condyloma or cervical intraepithelial neoplasia (CIN) I is generally associated with intermediate and high-risk HPV types as against the low-risk viruses that cause exophytic/papillary growth patterns of condylomas. The diagnosis of low-grade SIL (LSIL) (flat and exophytic condylomas) requires first excluding benign mimics of LSIL and second to confirm the characteristic cytologic atypia. For high-grade SILs (HSILs), the extent and degree of atypia generally exceed the limits of that described in flat or exophytic condylomas (LSILs). Less maturation, abnormal cell differentiation, loss of cell polarity, and increased mitotic index with abnormal mitotic figures occupying increasing thickness of the epithelium define a lesion as CIN II or CIN III. Atypical immature metaplasia associated with inflammation and atrophy is a challenge in cervical biopsy interpretation. Careful attention to the growth pattern of the epithelium, the distribution of the atypia, nuclear spacing, and the degree of anisokaryosis and the presence of enlarged hyperchromatic nuclei help in differentiating a non-neoplastic from a neoplastic process. This chapter describes in depth the diagnostic difficulties in the interpretation of cervical biopsies. It also provides useful criteria in distinguishing benign mimics from true precancerous lesions and the role of biomarkers such as the p16ink4 and Ki-67 in the differential diagnosis of precursor lesions and the reactive and metaplastic epithelium.
Atypical Immature metaplasia
biomarkers in cervical precancers
Mitosis in cervical biopsy
pseudokoilocytes in cervical biopsies
SILs-diagnostic difficulties in cervical biopsy
INTRODUCTION AND TERMINOLOGY
It was known for long that there are epithelial abnormalities adjoining the invasive carcinoma cervix. The term dysplasia came into being for cervical abnormalities which showed features midway between those of carcinoma in situ and normal cervical epithelium. There have been rapid advances in research on cervical carcinoma over the past few decades. Human papillomavirus (HPV) is now known as the causative agent of cervical cancer and has been found in almost all cervical cancers. The term cervical intraepithelial neoplasia (CIN) was introduced by Richart who used it to describe all lesions which were precursors of squamous cell carcinoma. Cervical squamous intraepithelial neoplasia refers to all squamous alterations that occur in or near the transformation zone in association with HPV infection, thereby encompassing the terms condyloma, CIN, dysplasia, and squamous intraepithelial lesions (SILs).
With better understanding of the biology and pathogenesis of these lesions, we now have categories of precancerous lesions that are fewer in number and are also very specific. These have helped us define these lesions in a better way, leading to better clinical decision-making. The most widely used, “twotiered” classification of the Bethesda System (TBS) for cervical cytology, that is, low-grade SIL (LSIL) and high-grade (HSIL), is now being used for histopathological description also. The SIL terminology has gained wide acceptance, but there are still many who prefer the CIN terminology, in most instances, primarily because of customary usage. However, it is recommended to use the diagnostic terminology proposed by the LAST (Lower Anogenital Squamous Terminology) committee which is based on TBS of classification, for surgical pathology specimens. The LAST recommendations are of providing a two-part diagnosis, with SIL first and the equivalent CIN in parenthesis thereafter. LSIL will thus appear as “LSIL (CIN 1).” The distinction between CIN2 and CIN3 is arbitrary and not significant from management point of view and so both are considered under HSIL and written as “HSIL (CIN2/CIN3).”
In general, while diagnosing CIN in cervical biopsies, one should focus on maturation of the squamous epithelium, an overall cellular disorganization, loss of cell polarity, presence of nuclear atypia in lower and upper layers, increased mitotic index (MI) with mitosis in upper half of the epithelium, and abnormal mitotic figures in some cases. Broadly, CIN1 is used when these features occupy the lower one-third of the cervical epithelium. CIN 2 is used when these are seen in the lower one-third to two-thirds of the epithelium and CIN 3 when two-thirds or the entire thickness of the epithelium is showing atypical basaloid cells.
LOW-GRADE SILS-LSIL (CIN1)
LSIL (CIN1) may be identified at any age following the onset of sexual activity which also marks the beginning of chances of acquiring various sexually transmitted infections, one of them being the HPV infection. The HPV causes three different types of clinical diseases – warts, dysplasia, and cancer – mostly in or around the genital area. The HPVs are highly epitheliotropic and have an affinity for the squamous epithelium of the lower genital tract, but the HR HPV types, in particular, have a tropism for the metaplastic squamous cells at the squamocolumnar junction.[8,9] This has very important consequences related to cytology screening as most precursor lesions and cancers arise at this site, which is amenable to sampling with a brush or spatula.
Clinically, “elevated warty” lesions also known as Condyloma acuminatum are less common on the cervix and are generally pure warty lesions. These are induced by the HPV-types 6 and 11 in 70–90% of the cases, but occasionally other types – such as HPV-16 and 18 are encountered. When the latter is the case, high-grade cytologic atypia is often found. Much more common are the “subclinical condylomas” that can be flat, spiked, or inverted condylomas or show simply warty atypia. These are of more concern as they are non-exophytic, and can only be identified during colposcopy as they turn white after application of 5% acetic acid. Koilocytic viral cytopathic effect is the pathognomonic feature of both exophytic and flat condylomas. Both these lesions, particularly the subclinical HPV lesions, can be (i) pure constellation of koilocytes in the middle and upper layers of the squamous epithelium or they can be (ii) pure CIN1 lesions without koilocytosis. It is doubtful whether LSIL (CIN1), as an indicator of HPV infection, can be reproducibly diagnosed in the absence of koilocytotic change. Therefore, the practice of reporting whether or not there is dysplasia within this condyloma (i.e., condyloma ± CIN1) is no longer followed.
The normal cervical epithelium has a basket weave appearance with equidistant regular proliferating capillaries at the SCJ. Glands are seen beneath the squamous epithelium [Figure 1]
Histopathology of exophytic lesions exhibits thickening of the epithelium (acanthosis) with variable papillomatosis [Figure 2] and viral cytopathic effect. As compared to the inflamed or metaplastic cervical squamous epithelium, the proliferation rate of condyloma is higher and is particularly elevated in the presence of HR HPV types[11-13]
Microscopically, these clinically different lesions share the following features: Relatively normal basal cell layer, expanded or hyperplastic parabasal cell layer [Figure 3a and b], orderly maturation, mitotic activity (but few or no abnormal mitoses), and koilocytosis [Figure 4]
The abnormal maturation, abnormal cell proliferation, and atypia (in SIL) are exemplified by nuclear enlargement, hyperchromatic nuclei, increased N/C ratio, abnormal chromatin distribution with coarse chromatin, irregular and wrinkled nuclear membrane, and nuclear pleomorphism
Koilocytotic atypia is seen in the middle and upper portions of the epithelium [Figure 5]. Keep in mind, the “atypia on the surface epithelium” as it avoids overdiagnosis
Koilocytotic atypia is a constellation of cellular changes that include marked variation in nuclear size (3 fold) and shape, wrinkled nuclei, hyperchromasia, binucleation or multinucleation, and perinuclear halos. Multinucleated cells are due to changes in mitosis [Figure 6]
Uneven spacing of the nuclei is characteristic giving the impression of “clones” as seen in cartilage [Figure 7]
Nuclear atypia and perinuclear halos are characteristic features of koilocytes. There is perinuclear cytoplasmic vacuolation with thickening of cytoplasmic membrane or peripheral condensation of cytoplasm. We see these perinuclear halos in the superficial layers and they are better appreciated in cytology smears
Flat lesions with features of LSILs (flat condylomata) without koilocytotic atypia, that is, pure CIN1 lesions, show mitosis in the lower one-third of the epithelium, loss of polarity of nuclei, and marked nuclear atypia and mitosis in the basal layer [Figure 9a-c]
However, LSIL do not harbor many abnormal mitotic figures and therefore a lesion with high MI must be carefully evaluated to decide whether it can be upgraded to HSIL [Figure 10].
Although CIN1 is also induced by HPV infection, it takes a morphologic backseat in many cases. However, biopsies may show features of both CIN1 and HPV cytopathic effects [Figure 11]
Clinically, HSILs, when extensive, present as an unhealthy cervix that bleeds on touch, but are best appreciated and evaluated colposcopically.
Microscopically, these lesions are distinguished from LSIL by the presence of mild to marked cytologic atypia encompassing the lower 2/3rds of the squamous epithelium
There are nuclear crowding and loss of polarity of cells
There are loss of normal maturation and thereby accumulation of primitive basaloid appearing cells. However, a variable degree of surface maturation may be observed [Figure 13]
Some lesions exhibit surface koilocytotic change and epithelial maturation and make it difficult to distinguish LSIL from HSIL that corresponds to CIN II [Figure 14]. Those lesions that show little or no maturation correspond to CIN III. Basaloid (immature) cells are seen in more than one-third of the epithelium [Figure 15a]
These cells are round to oval and have an increased N: C ratio
There is nuclear atypia in the form of hyperchromasia, coarse chromatin, membrane irregularities, and variable degree of nuclear pleomorphism, which generally exceeds that of LSIL and is present in all layers of epithelium. The atypia is often bizarre
There is prominent mitotic activity and an increase in MI is seen. Atypical mitotic figures are typically present and may be seen in the upper layers of the epithelium
At times, it is required to decide whether the lesion is LSIL or HSIL. In such situations, p16 immunostaining can help resolve the dilemma. However, please remember that morphological diagnosis using H & E stain is the mainstay and adjunctive studies using p16 are useful only in selected few borderline cases. If there is strong and diffuse block positivity, a diagnosis of HSIL (CIN1/2) can be rendered.
Once the pathologist has made the diagnosis of HSIL (CIN1/2) in a cervical biopsy, it is the responsibility of the gynecologist to determine the presence or absence of invasive carcinoma
Variants of HSIL keratinizing HSIL are characterized by superficial keratinization in addition to atypia
Atypical keratinized cells may be seen in smears in some benign cellular reactions such as hyperkeratosis or parakeratosis, atypia of undetermined significance, some LSILs and HSILs, and invasive squamous cell carcinomas
HSILs with immature metaplastic differentiation comprise immature cells which appear uniform with variable cytoplasmic differentiation and rounded or undulating epithelial stromal interface. These retain certain features of immature metaplasia [Figure 16]
In contrast to conventional metaplasia, these HSILs with a metaplastic phenotype exhibit reduced superficial cell maturation, maintain a relatively high nuclear density on the surface with hyperchromasia, and lack uniform cytoplasmic borders in these cells
SILS – DIAGNOSTIC DIFFICULTIES IN CERVICAL BIOPSIES
Although it is important not to miss SILs, the overdiagnosis of benign atypia also has important clinical implications and can result in undue physical and psychological distress, to both the patient and the team of doctors. However, there are instances, however, in which a clear interpretation is not possible because of cell changes that are difficult to classify.
When the histopathologic features of HPV infection (namely, koilocytosis, multinucleation, acanthosis, papillomatosis, parakeratosis, individual cell keratinization, mitosis in the lower basal third of the epithelium, hyperplasia of basal layers, and absence of distinct basal cell layer) are either less striking of SIL or are inconsistently present or they are only mildly/focally evident, such lesions result in a report of questionable importance for the treating gynecologist. Diverse nomenclature has been used like atypical squamous lesions (ASL) or atypical lesions (AL) for the subset of biopsies for which the histologic diagnosis is of unclear significance.[18,19] The biologic behavior of ASL and its relationship to HPV infections is still not well understood and also not well-defined.[20-23] The diagnosis of ASL often is used by pathologists to describe histologically borderline conditions, including neoplastic and non-neoplastic processes in the uterine cervix.[24,25] The various conditions included in the category of ASL are atypical repair or reactive changes, atrophy, atypical immature metaplasia (AIM), transitional metaplasia, and dysplasia or carcinoma with metaplastic changes. The word “atypical” is a common denominator in these terminologies meaning that which is not typical of a pathology. The term atypia may also be used by some as a defensive measure to avoid a potential legal entanglement.
From the colposcopist point of view, both, that is, AL and metaplastic/reactive lesions and SILs appear as acetowhite foci, and hence biopsied and represent one of the most frequent challenges in routine surgical pathology practice. The colposcopist takes a punch biopsy either when he wants to confirm histologically an undeniable CIN of any grade so that he can proceed with ablative procedures such as loop electrosurgical excision procedure (LEEP) or cold knife conization OR when the colposcopic findings are ambiguous. Moreover, therefore, while taking a biopsy, it requires real sufficient experience to differentiate a benign from atypical or premalignant lesion in the acetowhite spectrum of an “atypical transformation zone.”
In cytological diagnosis, the borderline category or the gray lesions of atypical squamous cells of undetermined significance (ASC-US) of cervical lesions have been widely accepted. In contrast, leave apart the introduction of a borderline category in histological diagnosis, even the term atypia is not acceptable and is strongly criticized for several reasons.[26-28] First, everyone thinks that biopsy is the final answer to all clinical differentials and the pathologist will narrow down ambiguous results of all previous investigations. Second, there is high rate of intra- and inter-observer disagreement in distinguishing reactive lesions on one hand and pre-cancers on the other. Third, cervical reactive/metaplastic conditions and SILs can also be present adjacently, making the diagnosis all the more difficult. In addition, a clear trend to overdiagnose normal, metaplastic, or reactive cervical biopsies as HPV-associated LSIL has been reported, with therapeutic, reproductive, sexual, and social consequences.[29,30]
In the ALTS study, biopsy specimens were obtained because of a cytologic diagnosis of ASCUS or LSIL and were triaged with HPV DNA test. The biopsies were reviewed independently by five experienced pathologists. The rate of dysplasia ranged from 23% to 51%. All pathologists agreed in 28%. Point is that, in spite of the fact that straightforward criteria for reactive and precancerous lesions are clearly defined, we must accept that subjectivity is universal in reporting pre-cancers and specially LSIL (CIN1).
To improve the diagnosis and management of histological AL, it would be important to identify among them those lesions that are really HPV associated and above all, that they are harboring hrHPV DNA. Continuous efforts have been made to evaluate various histologic and cytologic features in the original samples of ASL for their ability to differentiate neoplastic from non-neoplastic lesions as determined by subsequent tissue diagnoses or sufficient follow-up with multiple cytologic tests.[32,33] Attempts have been made not only to make a clear distinction between neoplastic and nonneoplastic groups but also to eliminate the ASL category, for lesions in the uterine cervix, through the application of morphologic and immunohistochemical criteria. The immunostaining patterns for p16 and Ki-67 of the original ASL samples were evaluated with an easy and clearly defined method by determining the presence or absence of positive cells in the upper two-thirds of the squamous epithelial layer. The histologic and cytologic features that potentially could separate neoplastic (or malignant) from non-neoplastic (or benign) groups in ASLs are as follows:
These criteria are most useful and also most necessary in – distinguishing LSIL from benign reactive atypia and HSIL from atrophy and immature metaplasia.
Mitosis: Any mitotic figure, normal or abnormal, present or absent, in the squamous epithelium
Nuclear appearance: Predominantly hyperchromatic (>50%) without recognizable nucleoli or predominantly vesicular (>50%) with recognizable nucleoli or nuclear grooves
Nuclear growth pattern: Predominantly horizontal (>50%) or predominantly vertical (>50%)
Perinuclear halo: Present or absent with a dense cytoplasmic rim
Cell border: Distinct or indistinct in more than 50% of the squamous cells
Primitive cells: Cells with a nuclear/cytoplasmic ratio of more than 50%, present or absent, in the upper third of the squamous cell layer
Inflammation: Neutrophils or lymphocytes present or absent, within the epithelial layer.
DIFFERENTIATING LSIL FROM REACTIVE EPITHELIAL CHANGES (NON-SPECIFIC)
The presence of mitosis is one of the most important histologic indicators for the neoplastic group. To eliminate subjectivity of observations – making a genuine search for mitosis is often rewarding
In a normal cervix, the normal basal cells hardly ever show a mitotic figure and parabasal cells of a reactive epithelium may rarely show mitosis. Therefore, just the presence or absence of a normal or abnormal mitosis may be as much as necessary to label the lesion as favoring neoplastic. Although, only abnormal mitotic figures are considered indicators of CIN in some reports[15,34,35]
Even if the nuclear atypia in the surrounding cells is not marked presence of many mitotic figure favors a neoplastic process [Figure 18]
However, the atypical areas where one wants to look for mitosis sometimes are so limited in the original sections that practically it is not possible to identify and quantify the mitotic figures per microscopic field. In such situations, go ahead with serial and deep sections [Figure 19]. This way one can improve the diagnosis of LSIL in additional 20% of cases. A mitotic count of 6/10 high-power fields favors LSIL. Furthermore, taking additional or multiple biopsies during colposcopy improve significantly the detection rate of SILs
In fact, when mitotic figures are identified easily, it is recommended that such mitotically active CIN I may be upgraded to CIN II when it is positive for high-risk (HR) HPV DNA. Increasing CIN grade is associated with increasing MI [Figure 20]. Earlier studies have observed that the capability of pathologists to differentiate between CIN1 and CIN2 is poor and there is a school of thoughts who recommended that CIN2 should be considered among the low-grade abnormalities rather than high-grade ones. Even from natural history point of view, very few of the CIN2 lesions progress further
Primarily differences in size and staining of intermediate and superficial cells and a combination of cytoplasmic features, nuclear features, and the growth pattern helps one distinguish nonspecific changes from SILs. In LSIL, cytoplasm is capable of maturation but nuclei retain the karyokinetic abilities of younger cells. Nucleomegaly with hyperchromasia in mature looking cells with or without perinuclear halo is what one has to look for to call it a LSIL
The most important discriminating feature between benign and neoplastic lesion is absence of variance, in either cell size or staining intensity and nuclear abnormalities in the cell population [Figure 21]
Technically, there should be 3-fold differences in size of cells with variable staining in SIL. Approximately 90% of LSILs show binucleation. Presence of two or more binucleate cells in one high-power field is strongly supportive of diagnosis of LSIL [Figure 22].
Benign mimics of koilocytes or “pseudo-koilocytosis” are most troublesome and most common in acute or chronic inflammatory lesions. They are as a result of irritation of the epithelium because of variety of factors such as infections due to Candida, Trichomonas, and Gardnerella vaginalis
Koilocytosis resulting from inflammatory cell changes may cause slight nuclear abnormalities and narrow perinuclear clear zones
The halos are usually regular, round, and uniform in appearance, with centrally placed nuclei. Narrowness and regular appearance of the perinuclear zone along with fairly well-preserved horizontal stratification of nuclei is seen in nonneoplastic lesions. These features are at a substantial variance with classic koilocytotic atypia [Figure 23]
Presence of only perinuclear halos without peripheral condensation of the cytoplasm can be seen in reactive conditions also, therefore, nuclear atypia along with perinuclear halos should be looked for while diagnosing LSIL[39-41]
Another common source of pseudo-koilocytes is the intermediate squamous cells, filled with glycogen. However, they lack the hyperchromasia, overall enlargement of size of nuclei >3 times the nuclei of corresponding normal layer, and they also lack thick rim of cytoplasm. Under higher magnification, the nuclei are vesicular and are not hyperchromatic and nuclear grooves are seen
Vesicular nuclei with prominent nucleoli are most unusual of dysplastic epithelium. Nuclei showing hyperchromasia or vesicular appearance – although important – is not statistically significant in differentiating neoplastic from non-neoplastic lesions [Figures 24 and 25]
The abnormalities in a true neoplastic lesion are generally striking and focal
However, focal and few abnormalities with mild nuclear atypia may create a suspicion of CIN I. Such minor abnormalities are the source of maximum subjective variation. If these abnormalities are seen in >50% of the tissue provided, one may report it as favoring a neoplastic process or LSIL
The overall growth pattern of the epithelium with mild nuclear abnormalities shows a horizontal and fairly regular stratification of nuclei that favors a nonneoplastic lesion
A vertical orientation of nuclei in more than 50% areas, in the biopsy provided, is an indication of immaturity of cells and favor a neoplastic lesion [Figure 26]
Quite often normal slides are miscategorized as LSIL and vice versa as a result of focal loss of a regular basal layer. Hyperplasia of basal layers and absence of a distinct basal cell layer are considered as features of HPV infection. However, the converse is also reported. It is reported that a normal basal cell layer is usually maintained both in a condyloma and in CIN 1.
At times, especially in cases of atrophy, there are only one or two para basal layers with mild-to-moderate atypia and with focal absence of a distinct basal cell layer [Figure 27]
On the other hand, it may be difficult to categorize focal basal cell hyperplasia (one of the features of HPV infection). Remember, focal basal cell hyperplasia may also be associated with the use of oral contraceptives or intrauterine device, pregnancy, healing erosions, inflammations, and infections [Figure 28a-c].
These focal and few abnormalities with mild nuclear atypia may create a suspicion of CIN1. However, if these abnormalities are seen in >50% of the tissue provided, one may report it as favoring a neoplastic process or LSIL.
In general, in infection, considerable numbers of inflammatory cells are seen within the epithelium or in adjacent areas and this favors a reactive process [Figure 24].
DIFFERENTIATING HSIL FROM AIM AND ATROPHY
Atypical Immature Metaplasia (AIM)
The proposed categories of AIM[22,24] and transitional metaplasia[23,25] of the uterine cervix are considered borderline lesions histologically. These are fraught with two facts, one is that their biologic and clinical characteristics are yet to be determined and second is the fact that there is substantial interobserver variability in the interpretation of their histopathologic findings
Most immature squamous metaplasia have no cytologic atypia (typical immature metaplasia), while a small percentage can show mild atypia (so-called atypical immature squamous metaplasia or AIM)
The term AIM was introduced in 1983 to describe cervical lesions with uniform full-thickness basal proliferation with high nuclear density but without sufficient criteria for CIN III (now HSIL)
AIM refers to a full-thickness intraepithelial basaloid lesion in the uterine cervix that features both metaplasia and atypia and is, therefore, difficult to distinguish from CIN III
Atypical or immature metaplasia is an ill-defined histologic entity that is either benign, neoplastic ab initio, or may be a step in the development of low- or high-grade lesions of metaplastic type. Possibility of LSIL in immature or atypical metaplasia must be entertained or cannot be ruled out when the basal layers start showing all features of CIN I and there is marked atypia with mitosis. Immature metaplasia is a fertile soil for HPV infection and integration. It may evolve to both LSIL and HSIL. HPV DNA test is positive in 70–80% of cases [Figure 29a and b]
AIM represents a heterogeneous group of lesions and is characterized by absent or minimal maturation of metaplastic squamous epithelium, absent or minimal koilocytosis, and mild nuclear pleomorphism
Ancillary testing using a panel of CK17, p16ink4 may help resolve the issue. p16 is a marker for HPV-induced dysplasia. Cytokeratin (CK) 17 is a marker for cervical reserve (stem) cells, which give rise to metaplasia.
Microscopic (histologic) description
To differentiate AIM from HSIL in cervical biopsies, it is recommended to make use of these three modalities:
Appropriate selection of histologic and cytologic criteria, seven criteria described by Chisa and Ayoma [Table 1] with a determination to consistently apply them to selected lesions can resolve many of our diagnostic problems
Second, we have the facility of HPV DNA testing to validate our findings. hrHPV DNA testing, when possible should be done as it does help to clarify the clinical significance of ASL/AIM. The presence of HR oncogenic viral types (e.g., HPV-16 and 18) would confer a different clinical importance, compared to low-risk types (e.g., HPV-6 and 11)
Third, a host of molecular markers for tissue diagnosis is available and IHC can be helpful in differentiating benign from neoplastic lesions, for example, Ki-67+ cells (nuclear staining) usually show scattered staining and are evenly distributed throughout the squamous epithelium of neoplastic ASLs.
|Typical immature metaplasia||Atypical immature metaplasia||HSIL|
|Monotonous population of cells with a high N: C ratio that lacks cytoplasmic maturation in the superficial layers. Nucleoli are seen||Monotonous population of cells with a high N: C ratio that lacks cytoplasmic maturation in the superficial layers. Nucleoli may be seen||Monotonous population of cells with a high N: C ratio that lacks cytoplasmic maturation in the superficial layers
Nucleoli generally not seen
|Minimal or no cell crowding, the nuclei are evenly spaced, mild-to-moderate enlargement, minimal anisokaryosis, uniform, and vertical orientation of nuclei||cell crowding present, anisokaryosis may or may not be seen||surface atypia and nuclear crowding are observed|
|The cytoplasmic margins and desmosomal junctions are recognized||The cytoplasmic margins and desmosomal junctions are not recognized||The cytoplasmic margins and desmosomal junctions are not recognized|
|Mitoses are uncommon, if present, are typical, and confined to basal layers||Mitosis are seen and at times in the upper third of the epithelium||Mitosis are seen and at times in the upper third of the epithelium and mitotic index may be high|
|In addition, these changes will be accompanied by acute and chronic inflammatory cells and spongiosis.||Inflammation may be present in the stroma but inflammatory cells are generally seen encroaching the epithelium||Inflammatory cells are generally seen encroaching not seen within the epithelium|
|Ki67 may be negative or positive with scattered patterns||Ki67 is positive with scattered patterns||Positive and evenly distributed all cases of HG-SIL are positive for Ki67|
|CK17 can be positive||CK17 can be positive||CK17 can be positive in immature squamous metaplasia and in some CIN|
|Typical IM and mature squamous metaplasia is consistently negative for p16||Immunoreactivity to p16 is not seen||In contrast, immunoreactivity to p16 is seen|
|hrHPV DNA is negative||hrHPV DNA may be positive||hrHPV DNA is generally positive|
When Atypical Immature squamous metaplasia is composed of a monotonous population of cells with a high N:C ratio, cell crowding and a high mitotic index, the closest differential is HSIL. As against a typical immature metaplasia (IM), that has minimal cell crowding, the nuclei are evenly spaced with mild-to-moderate enlargement but minimal anisokaryosis and uniform and vertical orientation of nuclei are seen and the cytoplasmic margins and desmosomal junctions are recognized [Figure 30a and b].
Atrophy is exceedingly difficult to distinguish from HSIL. Features that are helpful are as follows:
Presence of hyperchromatic but generally uniform nuclei. The epithelium is thin or with very few layers of cells that are with maintained polarity. The nuclear appearance is predominantly smudgy, hyperchromatic without recognizable nucleoli and often their internal structure is no longer discernible [Figure 31]
The diagnosis is reached mainly by careful comparison of the abnormal cells with adjacent dry, but normal, squamous cells and an assessment of the relative nuclear hyperchromasia and altered nucleocytoplasmic ratio. In spite of the accumulated experience, there are situations where lingering doubts will persist as to whether an atrophic smear is benign or contains cells suspicious of cancer
In atrophy, at times, the SILs are derived from reserve or basal cells of the endocervical epithelium. It is composed of small round atypical cells which replace the epithelium lining the endocervical canal. The lesion may extend to the transformation zone located higher up in the canal and, therefore, represents a diagnostic challenge to the colposcopist. The lesion is beyond the reach of the colposcope and is often detected in the specimen of endocervical curettage [Figure 32]
In the presence of inflammation, whether this is a HSIL of the small cell type or immature metaplasia with atypia is extremely difficult to qualify
A positive p16 immunostain is of significance to differentiate between metaplasia and HSIL small cell type found high up in the canal
Morphologically atrophy also shows immature parabasal and basal cells with no differentiation. And stripping away of the fragile epithelial cells from the surface gives a false impression of HSIL, and therefore, surface maturation in AIM is not appreciated. Ki 67 is negative because overall proliferation is very low in atrophy [Figure 33a and b]
No nuclear pleomorphism or atypia is seen and there is no mitosis
p16 and Ki67 can help distinguish atrophy from HSIL. It has low Ki67 index and is negative for p16.
BIOMARKERS IN THE DIAGNOSIS OF SQUAMOUS LESIONS/ IMMUNOHISTOCHEMISTRY
Biomarkers are more helpful in identifying SILs that have a higher probability of progressing to HSIL or invasive carcinomas. It is important to remember that there is not a single biomarker on which a decision to proceed to LEEP or cone biopsy can be made. Biomarkers are less useful in sorting out minor abnormalities and more important for the confirmation of SIL that is most likely a HSIL.
p16INK4a and Ki-67 immunohistochemistry assist in the histological differential diagnosis of precursor lesions and the reactive and metaplastic epithelium
Ki-67 indicates cellular multiplication and is a marker of cellular proliferation. Most LSIL will have an increased Ki-67 labeling index. Mib1 is a highly sensitive and specific marker for identifying LSIL and is helpful in verifying the diagnosis of equivocal cases. Mib 1 immunostaining as an adjunct test can be used to increase diagnostic accuracy of LSILs. Normally, only one or two parabasal layers take nuclear positivity for Ki-67 and rarely in the basal layer of the cervical squamous epithelium. A cluster of at least two stained nuclei in the upper two-thirds of the epithelial thickness is taken as an HPV-related lesion which is responsible for inducing cell cycle activity in these cells [Figure 34a-d].  All Mib1-positive cases are generally HPV positive
Another marker is Pro-Ex-C, the distribution of this has been shown to be similar to Ki-67. It is less pronounced in benign proliferations and more conspicuous in many SILs with less background staining relative to p16
p16ink4, a cyclin-dependent kinase inhibitor. Overexpression of p16 is linked with the continued expression of HPV oncogene E7 and acts as a reliable biomarker for HPV.[44,45] It is absent in normal squamous epithelium and inflammatory benign conditions
It can be increased in reactive conditions as well
It is strongly expressed in lesions associated with intermediate and HR HPV types in contrast to low-risk HPV infections
Approximately one-third of LSIL will show strong diffuse staining of the lower portion of the epithelium with p16INK4a. The presence of strong diffuse staining in the lower half of the epithelium indicates HPV and LSIL [Figure 35]. It is recommended to always correlate morphology with p16 staining
In immature metaplasia and atrophy, disparity in p16 and Ki-67 staining can occur. An explanatory note may be added taking into consideration the morphology, clinical, and colposcopic findings [Figure 36 a and b].
I acknowledge the help of Dr. Jasvinder Kaur Bhatia in the completion of this chapter.
LIST OF ABBREVIATIONS (In Alphabetic Order)
AIM - Atypical Immature Metaplasia
AL - Atypical lesions
ALTS - ASC-US /LSIL Triage Study
ASC - Atypical Squamous cells
ASC-US - Atypical squamous cells of undetermined significance
CIN - Cervical Intraepithelial Neoplasia
CK – Cytokeratin
H&E - Hematoxylin & Eosin
HPV - Human papilloma virus
HPV DNA - Deoxyribonucleic acid
HR HPV - high risk Human papilloma virus
HSIL - High grade squamous intraepithelial lesion
IM - Immature Metaplasia
LAST - Lower Anogenital Squamous Terminology
LEEP - Loop Electric Excision Procedure
LSIL - Low grade squamous intraepithelial lesion
MI - Mitotic index
N/C - Nuclear/Cytoplasmic ratio
SILs - Squamous intraepithelial lesions
TBS - The Bethesda System
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