Thyroid transcription factor-1 (TTF-1) positivity has been reported in tumors of many organs such as lung, thyroid and gastrointestinal tractus but it is rarely seen in prostate. The reported cases are TTF-1 positive small cell neuroendocrine cell carcinoma accompanied by acinar prostate adenocarcinoma[7-9]. We report a case of acinar adenocarcinoma with predominant non-neuroendocrine TTF-1 positive small cell intraductal component.
Sectioning, hematoxylin–eosin staining and immunohistochemistry of the tumor were performed according to standard protocols. Chromogranin A (Neomarker, cocktail), p63 (Neomarker, 4A4), synaptophysin (Novocastro, 27G12), CD56 (Cell Marque, 123C3.D5), thyroid transcription factor-1 (Novocastro, SPT24) and Ki- 67 (DAKO, MIB-1) were detected by mouse monoclonal antibodies, whereas AMACR (Neomarker, 13H4) was detected by monoclonal rabbit antibody. IHC staining process took place on the BenchMark XT fully automatic immunohistochemistry staining device.
Prostate carcinoma was identified in 10 of the 12 core biopsy specimens. Tumor was characterized by two separate histological features: (1) high grade infiltrating acinar adenocarcinoma with Gleason score 8 or 9 (2) intraductal carcinoma which was characterized by malign epithelial cells filling dilated ductal-acinar structures surrounded by basal cells (Figure 1A-B). Interestingly, the cells in the center of dilated ducts were smaller and more benign-looking than the cells of the peripheral parts of the dilated duct (Figure 1C). Immunhistochemical analysis with chromogranin, synaptophysin and CD56 failed to show a neuroendocrine differentiation in these cell and the peripheral parts of IDC-P as well as acinar adenocarcinoma component. Ki67 was also negative in the small cell areas of IDC-P. The peripheral located neoplastic cells exhibited positivity for only AMACR (Figure 1D,E) while the neoplastic cells within the center were only positive for TTF-1 (Figure 1F). Basal cells showed p63 positivity in the IDC-P component (Figure 1D,E). Also some cells in the acinar adenocarcinoma component exhibited positivity for TTF-1 (Figure 1F).
Recent studies have revealed the TMPRSS2-ERG gene fusion in prostate cancers. This gene fusion is seen IDC-P and more aggressive prostate cancer which are all favoring the first theory.[12-14] In a large core needle biopsy series, Guo and Epstein reported 27 pure IDC-P cases without infiltrative adenocarcinoma, six of which were diagnosed as Gleason score 8 or 9 high grade infiltrative cancer in their subsequent radical prostatectomies[6]. Among these 27 cases, nine showed similar central located small cell component as in our case. Regarding the second hypothesis, Cohen et al reported a distinct variant of IDC-P accompanying extensive HG-PIN[15]. They found a close spatial association between IDC-P and HG-PIN with continuing lumens suggestive of a IDC-P arising in areas of HG-PIN.[15]. However, the mechanisms of carcinogenesis in prostate carcinoma as well as how HG-PIN progress to IDC-P is still unclear[16].
In our case, we observed a high grade prostatic acinar adenocarcinoma accompanied by an extensive morphologically and immunhistochemically similar to intraductal component. Intraductal component showed prominent small cells. Both components expressed TTF-1 positivity but lacked neuroendocrine differentiation. According to Wang and Epstein, negative stains for neuroendocrine markers should not exclude the diagnosis of small cell carcinoma as long as the morphology on routinely stained sections is diagnostic[7]. However, in our case, small cell carcinoma was excluded by both negativity of neuroendocrine markers and also on morphological grounds as the central located small cells lacked the histologic malignancy criteria described for these tumors. There are few reports related to TTF1 expression in the tumors of prostate tissue. Leite et al found that TTF-1 was moderately positive in mucinous differentiation areas of two cases[17].
The SPT24 clone has a stronger affinity for TTF-1 protein but may lead to TTF-1 positivity in cancer cells other than pulmonary and thyroid carcinomas. Another explanation may be the aberrant expression in these small cells caused by amplification of the chromosomal region of the TTF-1 gene[18].
TTF-1 positivity was previously reported in small cell prostate adenocarcinomas along with other neuroendocrine markers as reported by Yao and Agoff[9,19]. However, Ordonez et al. reported on the contrary[20]. To our knowledge there is no information in the literature regarding TTF-1 positivity of this particular variant. Additionally TTF-1 positivity may serve as a surrogate marker for this particular variant of intraductal carcinoma. This observation should be supported by future studies.