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Micropapillary carcinoma: new variant of prostatic acinar adenocarcinoma

Authors :
Mneimneh, Wadad S.
Linos, Konstantinos
Shah, Paras
Jennings, Timothy A.
Fisher, Hugh
Nazeer, Tipu
Source :
Archives of Pathology & Laboratory Medicine. November 1, 2012, Vol. 136 Issue 11, 1447
Publication Year :
2012

Abstract

Since its establishment in 1966, the Gleason grading system for prostatic adenocarcinoma has undergone several modifications to enhance the correlation between histologic findings and clinical outcome. (1) The most recent [...]<br />A micropapillary variant of prostatic acinar adenocarcinoma has not been reported in the literature. Herein, we report a case of a 50-year-old patient who presented with an elevated prostate-specific antigen concentration and was subsequently diagnosed with prostatic acinar adenocarcinoma on biopsy. Radical prostatectomy specimen revealed prostatic carcinoma with Gleason score 4 + 5 = 9/10, with micropapillary component constituting 80% of tumor volume. Immunohistochemical studies of the prostate carcinoma showed a homogeneously positive prostate-specific antigen and α-methylacyl-CoA racemase, high-molecular-weight cytokeratin, and p63 protein cocktail pattern of staining in both micropapillary and conventional components. Pelvic lymph nodes were negative for metastatic disease. In contrast to the aggressive behavior of micropapillary carcinomas of other organs, the disease in our patient has thus far followed a more benign course, with low stage on presentation and a 2-year follow-up free of disease. However, prognostic correlation should be established on large series in order to assign this variant to a grade category within the Gleason scheme. (Arch Pathol Lab Med. 2012; 136:1447-1450; doi: 10.5858/arpa.2011-0359-CR)

Subjects

Subjects :
Diseases
Keratin
Adenocarcinoma

Details

Language :
English
ISSN :
15432165
Volume :
136
Issue :
11
Database :
Gale General OneFile
Journal :
Archives of Pathology & Laboratory Medicine
Publication Type :
Academic Journal
Accession number :
edsgcl.331169323
Full Text :
https://doi.org/10.5858/arpa.2011-0359-CR)