Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2011:2011:702494.
doi: 10.1155/2011/702494. Epub 2011 Jul 13.

Sarcomatoid carcinoma of the prostate: ductal adenocarcinoma and stromal sarcoma-like appearance: a rare association

Affiliations
Case Reports

Sarcomatoid carcinoma of the prostate: ductal adenocarcinoma and stromal sarcoma-like appearance: a rare association

David Parada et al. Case Rep Urol. 2011.

Abstract

Sarcomatoid carcinoma (SC) of prostate gland is a rare biphasic tumour. In about half of cases, initial diagnosis is acinar adenocarcinoma, followed by nonsurgical therapy, with a subsequent diagnosis of SC. The survival rate is lower. We report a case of an 59-years-old man with unusual histopathologic finding of prostate sarcomatoid carcinoma, showing characteristics of ductal prostatic adenocarcinoma and prostatic stromal sarcoma-like appearance. Ductal adenocarcinoma was characterized by tall columnar cells with abundant amphophilic to eosinophil cytoplasm. Pleomorphic sarcoma was characterized to have overall glandular growth pattern, simulating a malignant phyllodes tumour. Estrogen and progesterone receptors showed nuclear immunostaining in mesenchymal multinucleated giant cells. In conclusion, SC of the prostate is an exceedingly rare tumour. Retrospective analyses render prostate SC as one of the most aggressive prostate malignancies. The prognosis is dismal regardless of other histologic or clinical findings.

PubMed Disclaimer

Figures

Figure 1
Figure 1
(a) Pelvic MRI considered suspicious for extracapsular extension of the tumour. (b) Pelvic TC scan showed tumour with extents hypodense zones, consistent with necrosis.
Figure 2
Figure 2
Microscopic finding. (a) Typical histopathologic aspect of prostatic ductal adenocarcinoma, showing a cribiform pattern. (b) Stroma with giant cells. (H-E, 50x–100x). (c, d, and e) Pleomorphic sarcoma characterized to have overall glandular growth pattern (H-E, 50x-100x-200x). (f) Malignant stroma showed increased cellularity and pleomorphism. Note: no spindled, fascicular, or heterologous growth pattern were presents. (H-E, 400x).
Figure 3
Figure 3
Immunohistochemical profile. (a) Cytokeratin AE1/ae3 stain showing a strong reactivity in epithelial component and focal expression is present at mesenchymal component (DAB, 100x). (b) Ki-67 nuclear positivity in both epithelial and mesenchymal component (DAB, 100x). (c and d) Estrogen and progesterone receptor expression. Multinucleated stromal cells showing nuclear positivity (Circle) (DAB, 400x). (e and f) p63 immunoreactivity in epithelial and stromal elements (DAB, 100x-200x).

Similar articles

Cited by

References

    1. World Health Organization Classification of Tumours: Pathology and Genetics of Tumours of the Urinary System and Male Genital Organs. IARC Press, Lyon, France, 2004.
    1. Humphrey PA. Variants of Prostatic Carcinoma in Prostate Pathology. Chicago, Ill, USA: ASCP Press; 2003.
    1. Grignon DJ. Unusual subtypes of prostate cancer. Modern Pathology. 2004;17(3):316–327. - PubMed
    1. Mazzucchelli R, Lopez-Beltran A, Cheng L, Scarpelli M, Kirkali Z, Montironi R. Rare and unusual histological variants of prostatic carcinoma: clinical significance. BJU International. 2008;102(10):1369–1374. - PubMed
    1. Shannon RL, Ro JY, Grignon DJ, et al. Sarcomatoid carcinoma of the prostate: a clinicopathologic study of 12 patients. Cancer. 1992;69(11):2676–2682. - PubMed

Publication types

LinkOut - more resources