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A retrospective analysis was performed to describe the cytomorphological and histopathological findings and human papillomavirus (HPV) genotypes for glassy cell carcinoma (GCC) of the uterine cervix. Five cases of cervical GCC, in which the glassy cell features constituted at least 95% of the specimen, were included. Four patients had stage IIB GCCs and one had stage IIIB GCC. All patients underwent concurrent chemoradiation therapy. Based on pretreatment cytology, only 1 of the 5 cases was correctly diagnosed as GCC. The remaining cases were diagnosed as carcinoma of undetermined type, adenocarcinoma, poorly differentiated carcinoma, or unsatisfactory for evaluation. Cytological specimens had moderate cellularity and contained small clusters of tumor cells admixed with amphophilic, granular tumor diathesis. The tumor cells possessed large, round to oval nuclei and abundant, granular, ground-glass cytoplasm. The nuclei exhibited prominent eosinophilic nucleoli. The cytoplasm displayed sharp margins and molding, resulting in “intercellular windows” between neighboring attached cells. HPV genotyping revealed that high-risk HPV types 18, 16, and 31 were detected in 3, 1, and 1 cases, respectively. Consistent with this finding, all cases exhibited block p16 positivity, confirming the association of HPV infection with GCC. In conclusion, a distinct cytoplasmic margin, the characteristic histopathological feature of GCC, was observed in liquid-based cytological preparations. We suggest that sharp cytoplasmic outlines with molding and intercellular windows are characteristic cytomorphological features of GCC. Detection of high-risk HPV in all cases strongly supported the notion that high-risk HPV is involved in the pathogenesis of GCC.
Glassy cell carcinoma (GCC) of the uterine cervix is a rare pathological form of cervical carcinoma that occurs in 1-2% of all cases [1–3]. The World Health Organization Classification currently considers this tumor to be a subtype of “other epithelial tumors” . The mean patient age of those with GCC is ~10 years less than that of patients with squamous cell carcinoma or adenocarcinoma of the cervix [1, 2, 5]. GCC was first described by Cherry and Glucksmann  in 1956 as a specific and distinctive entity of the most poorly differentiated adenosquamous carcinoma. They defined the histological diagnostic criteria and indicated that this tumor was uncommon and associated with poor prognosis. Two decades later, Littman et al.  described GCC tumors in detail, redefining and amplifying the histological criteria. Since then, interest in GCC has expanded and a number of studies have been conducted [1–3, 7–22]. However, cervical GCC is not yet widely recognized. Furthermore, because of GCC rarity there have been no clinical trials or large cohort studies.
Early detection of cervical cancer greatly increases the successful treatment rate. In countries with established early detection programs, the impact of cytology-based cervical screening is reflected in the substantial reduction in the cervical cancer incidence over the past 50 years [23–27]. Although the aggressive clinical course of GCC encourages the use of early detection methods because data on the cytological features of GCC are limited, a cytological diagnosis can be difficult, despite characteristic histopathological features [1–4, 17]. Liquid-based cytology can improve specimen quality by providing a standardized method of collecting cervicovaginal material, and dispersing cells in a thin layer that is relatively inflammation-free [28–30]. This reduces the likelihood of unsatisfactory smears and increases the cytomorphological abnormality detection rate [31–37]. Although liquid-based cytology has become a common screening method for cervical cancer, limited information is available on the liquid-based cytology findings of GCC.
The aim of the present study was to describe the cytomorphological and histopathological features and immunophenotypes of cervical GCC. In addition, human papillomavirus (HPV) infection status in cervical GCCs was evaluated. We found characteristic cytomorphological features, and verified that those are consistent with typical histopathological features of GCC. We observed high-risk HPV infection and block p16 positivity in all examined cases.
During the period from July 2007 to June 2016, 675 patients were diagnosed as having primary cervical carcinoma. Thirty-three (4.9%) cases of poorly differentiated carcinoma were collected from computerized patient records. Based on the rarity of GCC, we reviewed the 9 (1.3%) cases of cervical poorly differentiated adenosquamous carcinoma. Among the 9 cases, 2 cases that presented glassy cell features but that also had squamous (1 case) or glandular (1 case) differentiation, and 2 cases that had diffuse, strong p40 expression were excluded. The remaining 5 (0.7%) cases were cervical GCCs. Five patients with cervical GCC were included in a retrospective analysis. The median and mean patients ages at diagnosis were 38 and 48.2 years, respectively (range, 36-67 years). Four (80.0%) of the 5 patients had International Federation of Gynecology and Obstetrics (FIGO) stage IIB GCCs and the remaining 1 (20.0%) had FIGO stage IIIB GCC. None of the patients were pregnant or had a recent history of pregnancy. All patients underwent concurrent chemoradiation therapy.
The clinicopathological characteristics of the 5 patients with cervical GCC are summarized in Table Table1.1. Based on pretreatment cytology, only 1 (20.0%) of the 5 cases was correctly diagnosed as GCC (case 4), although for the case with an unsatisfactory cytological specimen on the first examination, a cytological diagnosis of GCC was obtained from the recurrent tumor (case 3). The remaining cases were diagnosed as carcinoma, type undetermined (case 1), adenocarcinoma (case 2), or poorly differentiated carcinoma (case 5). There were no false negative results. Liquid-based cytology specimens displayed moderate cellularity and contained small clusters of polygonal tumor cells admixed with amphophilic, granular necrotic debris (tumor diathesis; Figure Figure1A).1A). Most cellular clusters had < 20 cells. Even though most tumor cells were cohesive, individual tumor cells were frequently observed. A background of tumor diathesis was common (Figure (Figure1B).1B). Some tumor cells assumed a pseudocolumnar shape, resembling endocervical cells (Figure (Figure1C),1C), but there was no definitive evidence of glandular differentiation. Rarely, cellular clusters showing vague acinar architecture and nuclear polarization were noted, but insufficient for diagnosis of adenocarcinoma. There was no evidence of dyskeratosis or intercellular bridge formation. The tumor cells possessed large, round to oval nuclei with a thin, irregular nuclear membrane. Although most tumor cells had finely dispersed chromatin, some had coarse chromatin and thick nuclear membranes with dense parachromatin. A moderate to large amount of tumor cell cytoplasm stained faintly blue with Papanicolaou stain, giving a fine ground-glass appearance (Figure (Figure1D).1D). The cytoplasm displayed distinct outlines with molding and clear, slit-like spaces between neighboring attached cells (“intercellular windows”; Figure Figure1E).1E). The tumor cells were 3–7 fold larger than lymphocytes, and the majority of their nuclei contained prominent nucleoli (Figure (Figure1F).1F). Occasionally, tumor cell phagocytosis of apoptotic neutrophils was observed. There was a mixed population of inflammatory cells, mainly plasma cells and lymphocytes, in the background. Eosinophils, though present, were not easily detected. An intimate admixture of neutrophils and tumor cells, a so-called granuloepithelial complex , was often identified (Figures 1G-1I). Cytoplasmic molding and intercellular windows were often seen in these complexes. Frequent mitoses (Figures 1J-1K) and atypical mitotic figures (Figures (Figures1L)1L) were detected.
Histopathologically, the tumor tissue consisted of nests, cords, or sheets of large polygonal cells with a moderate to large amount of pale, evenly spread, finely granular or ground glass-appearing cytoplasm (Figure (Figure2A).2A). The tumor cell nests were separated by thin, delicate fibrovascular septa, containing a cellular infiltrate, which consisted predominantly of plasma cells and lymphocytes admixed with eosinophils (Figure (Figure2B).2B). The individual tumor cells exhibited sharp cytoplasmic outlines and large, pleomorphic nuclei with prominent nucleoli (Figure (Figure2C).2C). Mitotic figures were numerous and included abnormal forms (Figure (Figure2D).2D). Under high-power magnification (×400), the distinct cytoplasmic margins that were seen on the cytological specimens were often observed. Cell shape variation associated with cytoplasmic molding and intercellular windows was consistent with that found on the cytology (Figures 2E-2F). Some tumor cells displayed cytoplasmic microvacuolation. Bizarre multinucleated giant cells were commonly seen (Figure (Figure2G).2G). There was no evidence of squamous pearl formation, dyskeratosis, or intercellular bridge formation. Although a pseudocolumnar arrangement of the tumor cells that was observed on the cytological specimens was also found (Figure (Figure2H),2H), there was no evidence of gland formation or mucin production. A few microscopic foci of coagulative tumor cell necrosis were present.
Immunohistochemical staining results are shown in Table Table1.1. Estrogen (ER; Figure Figure2I)2I) and progesterone (PgR; Figure Figure2J)2J) receptors were focally positive in 1 case. None of the cases showed p40 (Figure (Figure2K)2K) or carcinoembryonic antigen (CEA; Figure Figure2L)2L) expression. In contrast, all cases exhibited diffuse and strong nuclear and cytoplasmic p16 immunoreactivity (block positivity; Figure Figure2M2M).
HPV genotype was analyzed using HPV DNA chip assay. High-risk HPV was detected in all cases (Table (Table1).1). This result was in agreement with the block p16 positivity observed in all cases. The genotype was variable; type 18 was detected in three (60.0%) cases, and type 16 (20.0%) and type 31 (20.0%) was detected in 1 case for each. Multiple HPV genotypes were not observed.
It has been documented that GCC does not have a distinctive cytological appearance [2, 3, 17]. In the present study, a pretreatment cytological diagnosis of GCC was made in only 1 case examined. Similar to our observation, in a previous study, 1 of 9 (11.1%) GCC cases were correctly diagnosed on a cervicovaginal smear . The remaining cases were diagnosed as squamous cell carcinoma (3 cases), adenocarcinoma (1 case), adenosquamous carcinoma (1 case), or carcinoma, unknown type (3 cases). The reason for such a low diagnostic accuracy in cytology might be attributed to the lack of differentiation and a low suspicion index for GCC. However, pathologists should be aware of the cytomorphological features of GCC because it not only has relatively unique cytomorphology but also diagnostic pitfalls, leading to occasional misdiagnosis. In our series, the established histopathological findings of GCC were verified in the cytological specimens. Clusters of tumor cells with abundant, granular cytoplasm, pleomorphic nuclei, and prominent nucleoli were consistent with GCC histomorphology. In addition, sharp cytoplasmic outlines of GCC cells associated with cytoplasmic molding and intercellular window formation were apparent in liquid-based cytological preparations, and these were confirmed on histopathological examination. Although sharp cytoplasmic margins have been suggested as a histopathological characteristic of GCC, there have been no reports concerning cytoplasmic molding and intercellular windows as cytomorphological features. Since these 2 features are typically found in reactive or neoplastic mesothelial lesions, it is difficult to conclude that they are pathognomonic for cervical GCC. However, because cytoplasmic molding and intercellular windows are not found in liquid-based cytology of common cervical neoplastic lesions such as high-grade squamous intraepithelial lesion, squamous cell carcinoma, adenocarcinoma in situ, and endocervical adenocarcinoma, it could be inferred that at least cytoplasmic molding and distinct intercellular windows could be useful cytological features to diagnose GCC.
Previous studies have found a strong association between cervical GCC and high-risk HPV infection [3, 7–12], which would be consistent with the findings in the present study. According to an accumulation of the present and previous data, the overall prevalence of high-risk HPV infection would be 51.3% (20/39; Table Table2).2). Interestingly, 3 previous cases showed multiple high- and low-risk HPV infections , whereas in the present study high-risk HPV alone was noted. In the present study, 3 (60.0%) cases had HPV type 18, which was the most common type detected in previous studies (10/15; 75.0%). HPV type 18 is most commonly associated with glandular tumors of the uterine cervix [4, 7, 8], which leads to the argument that GCC should be identified as a subtype of adenocarcinoma rather than of squamous cell carcinoma; however, the GCC glandular lineage cannot be proven because HPV type 18 is not specific to glandular lesions. In fact, HPV type 18 is the second most common HPV types in cervical squamous epithelial lesions and is strongly associated with high-grade neuroendocrine carcinomas . Therefore, it is reasonable to assume that HPV type 18 has an ability to make a target cell differentiate in variable directions . Although the pathogenetic importance of high-risk HPV infection in cervical GCC could not be determined definitively because of the small number of cases reported, based on the results of the present and previous studies there is a high possibility that it is involved in GCC carcinogenesis. Further studies are needed for a full evaluation of HPV infection status in GCC of the uterine cervix.
In the present study, all the five cases we examined expressed block p16 positivity, which was consistent with the presence of high-risk HPV. In addition, focal ER and PgR positivity in 1 case was consistent with a previous study that detected ER (2 cases) and PgR (1 case) among 11 cases of GCC . However, considering that the remaining 4 cases were negative for both ER and PgR, and most cervical carcinomas does not express these hormone receptors, their expression may be unusual in GCC.
Cytological differential diagnoses of cervical GCC include atypical reparative cells, nonkeratinizing squamous cell carcinoma with severe inflammation, lymphoepithelioma-like carcinoma, and malignant melanoma. Pak et al.  reported a false-negative rate of 33% when performing a cytological diagnosis of GCC. In GCC, frequently appearing syncytial tumor cell arrangements and abundant cytoplasm may deceive cytopathologists. In typical repair, cells occur primarily in monolayer sheets and syncytia and contain prominent nucleoli. However, nuclear piling, significant anisonucleosis, and irregularities in chromatin distribution that exceed changes in typical repair, can result in the false exclusion of carcinoma. Nevertheless, atypical reparative reactions lack both tumor diathesis and nuclear hyperchromasia. Moreover, isolated atypical tumor cells in reparative reactions are uncommon . Compared with nonkeratinizing squamous cell carcinoma with inflammation, GCC tumor cells are larger and more polygonal with larger nuclei and distinct cell membranes. Nonkeratinizing squamous cell carcinoma has more oval nuclei with coarser chromatin, which is frequent distributed along the nuclear membrane. In lymphoepithelial-like carcinoma, cell membranes are indistinct, and the nuclear chromatin is distributed peripherally, marginating the nuclear membrane. Although eosinophils are often observed in GCC, in lymphoepithelial-like carcinoma the majority of infiltrating inflammatory cells are lymphocytes and plasma cells, which might be useful for differentiation. However, it is not clear if there is a significant difference in proportion of the inflammatory cells between these 2 diseases because in the present cases, lymphoplasmacytic infiltrates were dominant. A misdiagnosis of malignant melanoma might be avoided by the absence of cytoplasmic melanin pigments and epithelial marker immunoreactivity. GCC neither expresses HMB-45 nor Melan A.
In conclusion, we have described the cytomorphology, histopathology, immunophenotype, and HPV genotypes of cervical GCC. We demonstrated that distinct cytoplasmic margins are a major cytomorphological and histopathological feature of GCC. Cytoplasmic molding and intercellular window formation might be useful cytomorphological characteristics for a differential diagnosis of GCC, especially in liquid-based preparations. In addition, high-risk HPV infection in all cases supported the notion that high-risk HPV is involved in the pathogenesis of GCC.
Glassy cell features were defined based on the 3 main criteria originally reported by Cherry and Glucksmann  and amplified by Littman et al.  as: (1) cells with a moderate amount of ground-glass or finely granular cytoplasm that stains faintly blue with hematoxylin and eosin, (2) distinct cytoplasmic borders that stain with eosin and periodic acid-Schiff, and (3) large nuclei with conspicuous nucleoli. The present study was restricted to cases in which the glassy cell features constituted at least 95% of the specimen. All available slides of 9 poorly differentiated adenosquamous carcinoma cases were reviewed. Five cases of cervical GCCs were included in the present study. Pretreatment cytological specimens were available for all 5 cases. The present study was reviewed and approved by the Institutional Review Board of Severance Hospital, Yonsei University Health System, Seoul, Republic of Korea (2016-1010-001).
For liquid-based cytological smears, samples were taken from the fornix, portio, and endocervix. The ThinPrep test (Hologic Inc., Marlborough, MA, USA) was performed using an automated liquid-based monolayer cell preparation system (ThinPrep 2000 system; Hologic Inc.), according to manufacturer's recommendations. Briefly, the samples were immersed in CytoLyt buffer (Hologic Inc.) and then transferred to a PreservCyt bowl (Hologic Inc.). Cells were released by pushing the brush to the bottom, forcing the bristles apart, and swirling the brush in the fluid. A cylinder containing a filtration membrane was placed in the bowl and rotated to ensure homogeneous cell distribution. Erythrocytes and mucus were allowed to penetrate the filtration membrane under negative pressure, leaving the cell membranes on the filtration membrane. Each ThinPrep slide was fixed in ethanol and stained using the Papanicolaou method. Tumor diathesis, cellular composition, and cellular arrangement of the specimens were evaluated.
The biopsied specimens were fixed in 10% neutral-buffered formalin and embedded in paraffin blocks. From each formalin-fixed, paraffin-embedded block, 4-μm sections were cut and stained with hematoxylin and eosin. A variable number of hematoxylin and eosin-stained slides from each case were available for review. Among these, the most representative slide, containing an appropriate volume of tumor and possibly normal cervical tissue, was chosen for immunohistochemical staining and HPV genotyping.
The formalin-fixed, paraffin-embedded sections were deparaffinized and rehydrated using xylene and alcohol. Immunohistochemical staining was performed using the Ventana Benchmark XT automated staining system (Ventana Medical Systems, Tucson, AZ, USA) or the Dako Omnis (Dako, Agilent Technologies, Carpinteria, CA, USA), according to the manufacturer's instructions. Antigen retrieval was performed using Cell Conditioning Solution (CC1; Ventana Medical Systems) or EnVision FLEX Target Retrieval Solution, High pH (Dako, Agilent Technologies). Sections were incubated with primary antibodies (Table (Table3).3). After chromogenic visualization, using ultraView Universal DAB Detection Kits (Ventana Medical Systems) or EnVision FLEX /HRP (Dako, Agilent Technologies), slides were counterstained with hematoxylin. Appropriate positive and negative controls were stained concurrently to validate the staining method.
We performed polymerase chain reaction (PCR)-based microarray for HPV genotyping, using a commercially available HPV 9G DNA chip (BMT HPV 9G DNA Chip; Biometrix Technology, Chuncheon, Republic of Korea) . The 9G test examined the presence of 14 high-risk (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68) and 5 low-risk (6, 11, 34, 40, 42) HPV types; analyses were performed according to the manufacturer's instructions . Briefly, the PCR mixture consisted of 10 μL of the extracted target DNA, 10 μL of the primer set (provided by the manufacturer), and PCR premix (provided by the manufacturer), which contained dNTP and Taq DNA polymerase in an amplification buffer. Amplification was performed using the following steps: predenaturation for 5 min at 94°C; 40, 30-s denaturation cycles at 94°C; 40, 30-s annealing cycles at 45°C; 40, 30-s elongation cycles at 72°C; and a final 5-min elongation step at 72°C. PCR products were electrophoresed in a 2% agarose gel to confirm successful amplification. Each hybridization chamber of the 9G was covered with a mixture of the hybridization solution (35 μL) and PCR product (15 μL), followed by incubation at 23–26°C for 30 min. After washing, array images were scanned and imaged using a fluorescent scanner (ScanArray GX Microarray Scanner, PerkinElmer Life and Analytical Sciences, Waltham, MA, USA).
This study was supported by a faculty research grant of Yonsei University College of Medicine for 2016 (6-2016-0130).
CONFLICTS OF INTEREST
The authors declare that they have no conflicts of interest.