Inverted (hobnail) high‑grade prostatic intraepithelial neoplasia and invasive inverted pattern

  • Authors:
    • Meltem Öznur
    • Sevim Baykal Koca
    • Pelin Yıldız
    • Burak Bahadır
    • Kemal Behzatoğlu
  • View Affiliations

  • Published online on: August 10, 2015     https://doi.org/10.3892/ol.2015.3584
  • Pages: 2395-2399
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Abstract

High‑grade prostatic intraepithelial neoplasia (HGPIN) is considered to be an important precursor for prostatic adenocarcinoma. The present study aimed to investigate the histological features of the uncommon inverted (hobnail) pattern of HGPIN in transrectal ultrasonographic (TRUS) prostatic needle biopsies from 13 cases. These 13 diagnosed cases of inverted HGPIN were identified out of a total of 2,034 TRUS biopsies (0.63%), obtained from patients suspected to have prostate cancer. The hobnail pattern is comprised of secretory cell nuclei, which are histologically localized at the luminal surface of the prostate gland, rather than the periphery, and exhibit reverse polarity. Histological examinations were performed and the results demonstrated that 5 of the 13 cases exhibited pure inverted histology, while HGPIN was observed to be histologically associated with other patterns in the remaining 8 patients. In addition, an association with adenocarcinoma was identified in 7 of the 13 cases. All 7 carcinomas accompanied by inverted HGPIN were conventional acinar adenocarcinoma cases; of note, for these 7 cases, the Gleason score was 7 for each. One acinar adenocarcinoma case accompanying inverted HGPIN demonstrated hobnail characteristics in large areas of the invasive component. It was observed that nuclei were proliferated in the invasive cribriform glands, which was comparable to that of inverted HGPIN, and were located on the cytoplasmic luminal surface; a similar morphology was also observed in individual glands. In conclusion, the results of the present study suggested that the hobnail HGPIN pattern may be of diagnostic importance due to its high association with adenocarcinoma and the high Gleason scores in the accompanying carcinomas.

Introduction

Intraepithelial neoplasia describes the atypical proliferations observed in the squamous epithelium, such as in the uterine cervix, and has been reported to have ‘precancerous’ characteristics (1). Therefore, intraepithelial neoplasia has been used to indicate cancer precursors and lesions with high risk for cancer in certain types of adenocarcinomas, including those of the breast, pancreas and endometrium (24). The typical histological appearance of intraepithelial neoplasia is characterized by the cytological features of cancer, for which it is a precursor, with atypical cell proliferation in anatomical structures, including normal ducti and acini (15).

Prostatic intraepithelial neoplasia (PIN) is a well-defined entity, which exhibits cytological changes and the proliferation of secretory cells, features which are comparable to those of cancer cells within the prostatic ducti and acini (58). Although PIN is defined as low- or high-grade, low-grade is generally not considered relevant due to its low prognostic significance and low degree of interobserver agreement among pathologists (7,9). Therefore, only the expression of high-grade PIN (HGPIN) was investigated in the present study. The acinar type of HGPIN is known to be closely associated with prostate adenocarcinoma, as HGPIN was reported to be observed in 85–100% of the materials examined following prostatectomies performed due to adenocarcinoma (9). In addition, a close association was reported between PIN and atypical glandular foci suspicious for malignancy (10). Furthermore, it was determined that the risk of malignancy increases in core prostate biopsies with the increased number of cores with PIN (11).

PIN has four basic architectural patterns: Tufting, micropapillary, cribriform and flat; in addition, other less common patterns, such as signet-ring cell, small-cell neuroendocrine, foamy, mucinous, squamous differentiation and inverted patterns have been reported (512). The inverted (hobnail) pattern is composed of secretory cell nuclei, which are histologically localized at the luminal surface of the prostate gland, rather than the periphery, and exhibit reverse polarity (12). The hobnail PIN pattern (variant) is a rare histological type in the prostate; at present, only one previous study has investigated this pattern, which evaluated a total of 15 cases of hobnail HGPIN (12). This inverted pattern was found to be primarily localized in the peripheral zone and was associated with adenocarcinoma in 45% of the cases (12).

The aim of the present study was to discuss the frequency of the hobnail PIN variant/pattern in core needle biopsies of prostate glands as well as to investigate the histological features and association with adenocarcinoma.

Materials and methods

Patients and histological samples

In the present study, a total of 2,034 prostate transrectal ultrasonographic (TRUS) biopsy samples were evaluated for the presence of the hobnail PIN pattern. The samples were evaluated at the Pathology Clinic of the Istanbul Education and Research Hospital (Istanbul, Turkey) between January 2010 and 2014. Out of the 2,034 TRUS biopsy samples, 13 cases of inverted HGPIN were identified. A total of 12 core biopsies were performed for each of the 13 patients. Tissue samples (4–6 µm) were fixed in formalin, paraffin-embedded onto glass slides and stained with hematoxylin and eosin for histological evaluation. The slides were then examined under a light microscope (BW51; Olympus Corporation Tokyo, Japan). The following criteria were required for the positive diagnosis of hobnail PIN: Localization of the nuclei on the luminal surface of the prostate gland, rather than the periphery, which indicates reverse polarity in the proliferated cells of the acini and ducts; and observation of less prominent nucleoli in the nuclei of cells compared with adjacent non-inverted cell nuclei. Cases diagnosed with hobnail PIN were then categorized according to whether the PIN was pure or associated with other variants or prostate adenocarcinoma (13). In addition, the Gleason score (14) was determined for cases with prostatic adenocarcinoma accompanying hobnail PIN. The Gleason grading system is used to score the histological growth pattern and glandular differentiation of prostatic adenocarcinoma cells. It includes five basic grade patterns ranging from grade 1–5 (grade 1, well-differentiated tumor pattern; grade 5, no glandular differentiation). The final Gleason score, which ranges from 2–10, is calculated by the addition of the two most common grades: the primary (most common) pattern and the secondary (second most common) pattern. Thus, the most well-differentiated tumors exhibit a Gleason score of 2, and the least-differentiated tumors exhibit a score of 10 (14). Written informed consent was obtained from all patients and the study was approved by the ethics committee of Istanbul Education and Research Hospital.

Immunohistochemical analysis

Immunohistochemical studies were performed for p63, 34βE12 and α-methylacyl-coenzyme A racemase (AMACR) for the differential diagnosis with adenocarcinoma in cases diagnosed with inverted PIN. Immunohistochemistry was conducted using the Benchmark XT staining system (Ventana Medical Systems, Inc., Tucson, AZ, USA) and antibodies against 34βE12 (monoclonal mouse anti-human; cat. no. CM 127 AC; 1:50; Biocare Medical Inc., Concord, CA, USA), AMACR (monoclonal rabbit anti-human; cat. no. 504S-14; 1:100; Cell Marque Corporation, Rocklin, CA, USA) and p63 (monoclonal mouse anti-human; cat. no. VP 163 GG25; 1:200; Biocare Medical Inc.). Briefly, the tissue sections were deparaffinized with EZ Prep solution (Ventana Medical Systems, Inc.) at 75°C, pretreated with cell conditioning 1 (CC1) solution (Ventana Medical Systems, Inc.) for antigen retrieval at 95°C, and incubated with hydrogen peroxide (Ventana Medical Systems, Inc.) for 4 min to block endogenous peroxidase activity. The sections were then incubated with the AMACR, p63 and 34βE12 primary antibodies for 32 min at 37°C. Next, the sections were blocked using the Endogenous Biotin Blocking Kit (Ventana Medical Systems, Inc.) followed by incubation with a streptavidin-horseradish peroxiade-conjugated secondary antibody (monoclonal goat anti-rat; cat. no. 760-500; 1:200; Ventana Medical Systems, Inc.) for 8 min at 37°C. The immunolocalized AMACR, p63 and 34βE12 were visualized using a copper-enhanced DAB reaction. The slides were counterstained with hematoxylin II (Ventana Medical Systems, Inc.) for 4 min and Bluing Reagent (Ventana Medical Systems, Inc.) for 4 min and coverslips were applied using an automated coverslipper (Tissue-Tek Film Automated Coverslipper; Sakura Finetek Japan Co., Ltd., Tokyo, Japan). Cytoplasmic staining for AMACR and 34βE12, and nuclear staining for p63 were considered positive. The clinical data of the patients, including age and medical history, were obtained from the patient charts. None of the cases involved in the present study with adenocarcinoma underwent surgery at the hospitals affiliated with the authors; therefore, radical prostatectomy materials were not examined.

Results

Identification of hobnail PIN

Out of the 2,034 biopsy samples that were examined in the present study, the hobnail PIN pattern was identified in a total of 13 (0.63%) samples. The age range of the 13 patients was 53–83 years, with a mean age of 64 years. Hobnail PIN was observed in 4 cores in 3 patients, 2 cores in 5 patients and 1 core in 5 patients. In addition, prostatic acinar type adenocarcinoma was identified in 7 cases. The Gleason score was 7 in all of the adenocarcinoma cases.

Histological examinations of hobnail PIN

Proliferation in the form of micropapillary projections and mounds (tufting), particularly in the acini, was observed via microscopy in all 13 patients. However, nuclei localized on the luminal surface of the glands and not on the periphery (reverse polarity) were the most notable features (Fig. 1). In addition, inverted cell nuclei frequently demonstrated less prominent nucleoli compared with adjacent non-inverted cell nuclei (Fig. 2). Certain acini demonstrated the inverted feature in all parts, while others only partially demonstrated this feature (Fig. 2). Micropapillary projections and tufting patterns were also accompanied by cribriform and flat patterns in certain inverted PIN cases (Fig. 3). Furthermore, inverted morphology and intracytoplasmic mucin were observed in certain acini in one case (Fig. 4). Pure inverted histology was present in 4 of the 13 cases and PIN with other patterns was identified in 9 patients.

Gleason scores

All 7 carcinomas accompanied by inverted PIN were conventional acinar adenocarcinoma cases with a Gleason score of 7. These scores were of 3+4 in 6 cases and 4+3 in the other case.

Invasive features of hobnail PIN associated with invasive adenocarcinoma

One case of acinar adenocarcinoma accompanying inverted PIN revealed large hobnail areas in the invasive component. The nuclei in the invasive cribriform structures had proliferated and were located on the luminal aspect of the cytoplasm, which was comparable to that of the inverted HGPIN sections. In addition, similar characteristics were observed in the separate invasive glands as well (Figs. 58). A cribriform pattern and single glandular structures were prominent in the invasive component (Fig. 5). Similar patterns were also observed surrounding inverted PIN areas (Fig. 6). Immunohistochemical 34βE12 expression was evident along the basal cell layer in glands with inverted PIN (Fig. 7). Typical inverted features were also identified in tumoral glandular structures surrounding the peripheral nerves (Fig. 8).

Immunohistochemical analysis

Basal cell markers, p63 and 34βE12, were found to be positively expressed in the hobnail PIN areas, indicating the presence of a basal cell layer and the absence of carcinoma. In addition, cytoplasmic staining with AMACR was observed in all 13 cases following immunohistochemical study, confirming the presence of both PIN and carcinoma.

Discussion

HGPIN requires much consideration due to its frequent association with prostate cancer in prostatic core biopsies; increased risk of cancer has been associated with an increased number of HGPIN-positive cores. In addition, at the molecular level, HGPIN displays the characteristics of a precursor cancerous lesion (512,1517). PIN has four well-defined primary architectural patterns, including tufting, micropapillary, cribriform and flat, which do not carry prognostic significance (12). In addition, the signet-ring cell, small-cell neuroendocrine, foamy, mucinous, squamous differentiation and inverted patterns are less commonly observed (12).

The inverted (hobnail) pattern is rare and has only been reported by one previous study (12). Argani and Epstein (12) reported the incidence rate of hobnail PIN as 0.43% in their study. In the present study, an incidence rate of 0.63% was determined; however, the present study was prospective and actively searched for this entity in all TRUS biopsies, which may account for the increase in reported incidence rate.

A hobnail appearance is the typical feature of clear cell adenocarcinoma, which is predominantly observed in the genital system (18). The distinguishing features of hobnail from other patterns include the polarization of enlarged cell nuclei towards the lumen of the glands. This pattern may be missed as it is rare in prostate biopsies and resembles the central zone acini of the prostate; however, it may be distinguished from the central zone acini with features such as enlarged nuclei and with the known localization of the biopsy (12).

An association with prostate adenocarcinoma was identified in almost half of the cases in a previous study on inverted PIN (12). In the present study, it was observed that 7 of the 13 cases were associated with acinar adenocarcinoma. The Gleason score was 7 in all the adenocarcinoma-associated cases in the present study, which was higher than those reported in the Argani and Epstein study: The Gleason score was 6 (3+3) in 80% of the cases with adenocarcinoma accompanying PIN in the Argani and Epstein (12) study of 15 cases. The high association with carcinoma and high Gleason score may therefore have interesting prognostic significance for inverted PIN.

In the present study, histological features of conventional prostatic acinar adenocarcinoma were identified in 6 of the 7 cases with adenocarcinoma accompanying hobnail PIN. The remaining case exhibited a different adenocarcinoma histology and demonstrated features similar to that of the accompanying hobnail PIN. Therefore, it was difficult to distinguish the invasive carcinoma cribriform pattern areas with PIN morphology from the actual hobnail PIN regions in certain areas. The negative immunohistochemical results of the basal cell markers, p63 and 34βE12, in the carcinoma areas and positive results in the hobnail PIN areas aided the differential diagnosis. In addition, most of the individual invasive glands outside the cribriform pattern demonstrated inverted features. The Gleason score of this case was 7 (4+3) and tumor was present in all 12 core biopsies. In a study by Arkani and Epstein (12), no adenocarcinoma cases with inverted features were reported. Thus, to the best of our knowledge, the current study reports the first case of prostatic adenocarcinoma with hobnail histological features in the invasive component in the English literature.

In conclusion, the present study identified the histological features of the uncommonly diagnosed hobnail PIN. The high rate of association with prostatic acinar adenocarcinoma (54%) and the high Gleason score (7) of the carcinomas were noteworthy. However, further studies are required in order to determine whether the hobnail pattern is aggressive. In addition, the present study identified inverted pattern histological features in the invasive component of an associated adenocarcinoma in one case of hobnail PIN.

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October-2015
Volume 10 Issue 4

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Spandidos Publications style
Öznur M, Koca SB, Yıldız P, Bahadır B and Behzatoğlu K: Inverted (hobnail) high‑grade prostatic intraepithelial neoplasia and invasive inverted pattern. Oncol Lett 10: 2395-2399, 2015.
APA
Öznur, M., Koca, S.B., Yıldız, P., Bahadır, B., & Behzatoğlu, K. (2015). Inverted (hobnail) high‑grade prostatic intraepithelial neoplasia and invasive inverted pattern. Oncology Letters, 10, 2395-2399. https://doi.org/10.3892/ol.2015.3584
MLA
Öznur, M., Koca, S. B., Yıldız, P., Bahadır, B., Behzatoğlu, K."Inverted (hobnail) high‑grade prostatic intraepithelial neoplasia and invasive inverted pattern". Oncology Letters 10.4 (2015): 2395-2399.
Chicago
Öznur, M., Koca, S. B., Yıldız, P., Bahadır, B., Behzatoğlu, K."Inverted (hobnail) high‑grade prostatic intraepithelial neoplasia and invasive inverted pattern". Oncology Letters 10, no. 4 (2015): 2395-2399. https://doi.org/10.3892/ol.2015.3584