Subareolar Sclerosing Ductal Hyperplasia: Further Characterization of a Distinctive Clinicopathological Entity

Esther Cheng, Timothy M. D'Alfonso, Maria Arafah, Rebecca Marrero Rolon, Paula S. Ginter, Syed A. Hoda

Research output: Contribution to journalReview articlepeer-review

4 Scopus citations

Abstract

Subareolar sclerosing duct hyperplasia (SSDH) remains to be fully characterized nearly 20 years after initial description. Thirty-five SSDH cases diagnosed over a 16-year period (January 2000 to December 2015) were reviewed. All patients were female (mean age = 59 years, range = 18-80) who had presented with a unilateral solitary lesion (left 22, right 13) with a mean size of 1.3 cm (range = 0.4-3.0 cm), and showed florid and papillary epithelial hyperplasia with dense sclerosis without involvement of nipple or areolar epidermis. Significant lesions concurrent within SSDH included low-grade adenosquamous carcinoma (n = 1), ductal carcinoma in situ (DCIS; n = 1), lobular carcinoma in situ (LCIS; n = 1), and atypical ductal hyperplasia (ADH; n = 13). No case of SSDH recurred in a mean follow-up of 44 months (range = 6-189). Subsequent significant lesions occurred in 6 patients: DCIS (n = 3; ipsilateral 2, contralateral 1), ipsilateral ADH (n = 2), and ipsilateral atypical lobular hyperplasia (n = 1). Long-term follow-up for patients with SSDH is indicated as DCIS can occur subsequently in either breast.

Original languageEnglish (US)
Pages (from-to)4-11
Number of pages8
JournalInternational Journal of Surgical Pathology
Volume25
Issue number1
DOIs
StatePublished - Feb 1 2017
Externally publishedYes

Keywords

  • breast
  • epithelial hyperplasia
  • nipple
  • radial scar
  • subareolar

ASJC Scopus subject areas

  • Anatomy
  • Surgery
  • Pathology and Forensic Medicine

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