Literature DB >> 24121179

Cystic hypersecretory (in situ) carcinoma of the breast: a clinicopathologic and immunohistochemical characterization of 10 cases with clinical follow-up.

Timothy M D'Alfonso1, Paula S Ginter, Yi-Fang Liu, Sandra J Shin.   

Abstract

Cystic hypersecretory carcinoma (CHC) is an uncommon variant of ductal carcinoma in situ characterized by, among other features, the presence of luminal secretion resembling thyroidal colloid. CHC is thought to behave in an indolent manner but has the potential to give rise to invasive carcinoma, which is often poorly differentiated. We studied the immunohistochemical, clinical, and morphologic features of 10 cases of CHC. All patients were women averaging 62.8 years in age (range, 47 to 79 y). The clinical/radiographic presentation was a mass (5/10), calcifications (3/10), bloody nipple discharge (1/10), and unknown (1/10). Microscopic size of CHC ranged from 0.2 to 2.7 cm (mean, 0.9 cm). Micropapillary growth was present in all cases. Nuclear grade was intermediate (5/10) or high (5/10). One case also showed microinvasive carcinoma. All cases arose in a background of cystic hypersecretory hyperplasia (CHH) and/or CHH with atypia. CHC was ER in 8/10 cases (ER+/PR+, 4/10; ER+/PR+, 4/10). Two cases were ER-/PR-, including the case with microinvasive carcinoma. All were HER2-. Androgen receptor was expressed in 3/10 (30%) cases. Myoepithelial stains p63, smooth muscle myosin, and CK5 showed circumferential staining in 9/10 (90%) cases, whereas 1 case was negative for p63, smooth muscle myosin, and CK5 in both CHC and adjacent CHH. Basal-like carcinoma markers EGFR, CK14, and CK5 were negative in all cases, with the exception of 1 case that was positive for EGFR. Four patients with follow-up information showed no evidence of disease (mean, 5.5 y). CHC is a distinct variant of ductal carcinoma in situ that arises in a background of CHH and is characterized by micropapillary growth, intermediate-grade to high-grade nuclei, and luminal colloid-like secretion. CHC is usually ER and HER2-. Negative or discontinuous reactivity with myoepithelial markers may be seen, despite its in situ nature. CHC usually behaves in a nonaggressive manner as was seen in our patients who were all free from disease at last follow-up.

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Year:  2014        PMID: 24121179     DOI: 10.1097/PAS.0b013e31829fc47b

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  4 in total

Review 1.  Invasive cystic hypersecretory carcinoma of the breast: a case report.

Authors:  Juan Liu; Wenjun Yang; Xiangyan Wu; Xiangrong Hu
Journal:  Int J Clin Exp Pathol       Date:  2015-06-01

2.  Invasive Cystic Hypersecretory Carcinoma of Breast: A Rare and Under Diagnosed Variant of Ductal Carcinoma.

Authors:  Nibedita Sahoo; Pritinanda Mishra; Susama Patra; Prakash Kumar Sasmal
Journal:  J Clin Diagn Res       Date:  2017-06-01

3.  Invasive cystic hypersecretory carcinoma of the breast.

Authors:  Srilata Chitti; Sunayana Misra; Arvind Ahuja; Nikhil Gupta; Raghav Yelamanchi
Journal:  Autops Case Rep       Date:  2022-04-28

4.  lnvasive cystic hypersecretory carcinoma of the breast associated with papillary pattern: a rare and poorly recognised variant of ductal carcinoma of the breast.

Authors:  Parul Gupta; Sonal Dhingra; Osman Musa; An Srivastava
Journal:  Ecancermedicalscience       Date:  2014-11-04
  4 in total

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