Basal cell proliferations of the prostate other than usual basal cell hyperplasia

A clinicopathologic study of 23 cases, including four carcinomas, with a proposed classification

Jesse K. McKenney, Mahul B. Amin, John R. Srigley, Rafael E. Jimenez, Jae Y. Ro, David Grignon, Robert H. Young

Research output: Contribution to journalArticle

47 Citations (Scopus)

Abstract

Basaloid proliferations of the prostate with morphologic patterns other than usual basal cell hyperplasia are rare, and the distinction between benign and malignant lesions has been difficult. We describe 23 such lesions and classify them into two groups: adenoid cystic-like hyperplasia and adenoid cystic or basaloid carcinoma. Adenoid cystic-like hyperplasia (n = 19) was characterized by an older age at presentation (mean, 71.8 years), transition zone location with background of nodular hyperplasia, multifocality, lobulation, circumscription, and small acini with occasional hyalinization. A cribriform pattern limited to small- and medium-sized glands, squamous metaplasia, and hypercellular myxoid stroma were occasionally seen. Adenoid cystic carcinoma (n = 3) was characterized by a younger age at presentation (mean, 46.0 years), peripheral zone involvement, and large acini that were often dilated and exhibited extensive interanastomoses, prominent intraglandular hyalinization, perineural invasion, and extraprostatic extension. Basaloid carcinoma (n = 1) showed infiltration between normal glands, perineural invasion, and extraprostatic extension but lacked a cribriform architecture. The degree of cytologic atypia and mitotic rate overlapped between the hyperplasia and carcinoma cases. Both hyperplastic lesions and adenoid cystic carcinomas showed a basal cell phenotype with strong immunoreactivity to cytokeratins 14 and 34βE12, but the basaloid carcinoma was negative for these markers. In all cases, the proliferating basal cells were nonreactive for myoepithelial and prostatic secretory cell markers. The 8 patients with adenoid cystic-like hyperplasia with available follow-up information had no progression of disease (mean follow-up period, 8.6 years). One patient with adenoid cystic carcinoma died with widespread metastases, but the 3 other patients with carcinomas had no disease progression (mean follow-up period, 7.0 years). In conclusion, most florid basaloid proliferations of the prostate fall into one of two categories. In the first, there is a clear association with nodular hyperplasia (adenoid cystic-like hyperplasia) and, although cytologie atypia and mitoses may be seen, they are present within a lesion that retains an orderly, vaguely nodular (noninfiltrative) pattern. The second group of cases (adenoid cystic and basaloid carcinoma) shows a widespread, haphazard infiltrative growth pattern. This study suggests that adenoid cystic carcinomas are biologically indolent following prostatectomy but have a low risk of distant metastasis.

Original languageEnglish (US)
Pages (from-to)1289-1298
Number of pages10
JournalAmerican Journal of Surgical Pathology
Volume28
Issue number10
DOIs
StatePublished - Oct 2004
Externally publishedYes

Fingerprint

Hyperplasia
Prostate
Adenoids
Adenoid Cystic Carcinoma
Cell Proliferation
Carcinoma
Disease Progression
Keratin-14
Neoplasm Metastasis
Metaplasia
Prostatectomy
Mitosis
Phenotype
Growth

Keywords

  • Adenoid basal tumor
  • Adenoid cystic carcinoma
  • Adenoid cystic-like hyperplasia
  • Adenoid cystic-like tumor
  • Basal cell carcinoma
  • Basal cell hyperplasia
  • Basaloid carcinoma
  • Immunohistochemistry
  • Prostate gland

ASJC Scopus subject areas

  • Anatomy
  • Pathology and Forensic Medicine

Cite this

Basal cell proliferations of the prostate other than usual basal cell hyperplasia : A clinicopathologic study of 23 cases, including four carcinomas, with a proposed classification. / McKenney, Jesse K.; Amin, Mahul B.; Srigley, John R.; Jimenez, Rafael E.; Ro, Jae Y.; Grignon, David; Young, Robert H.

In: American Journal of Surgical Pathology, Vol. 28, No. 10, 10.2004, p. 1289-1298.

Research output: Contribution to journalArticle

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