1986
DOI: 10.1111/j.1600-0560.1986.tb01644.x
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Immunohistochemical markers of sweat gland tumors

Abstract: Using immunoperoxidase methods, normal sweat glands, 44 benign and 4 malignant sweat gland tumors were tested for the presence of carcinoembryonic antigen (CEA), pregnancy-specific-B1-glycoprotein (SP1) and actin (ACT). CEA and SP1 stained the secretory and duct-lining cells of normal eccrine glands. Among benign tumors, 74% were positive for CEA and 44% for SP1. The staining reaction was found mainly in luminal secretions and surrounding cells. Staining by SP1 was reduced, but not suppressed, after absorption… Show more

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Cited by 55 publications
(22 citation statements)
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“…[18][19][20][21][22][23] However, other authors have described the findings of decapitation secretion in tubular structures of this neoplasm, which supports an apocrine differentiation, 22,[24][25][26][27] an opinion that we share. 28 In our study, calretinin immunostaining was not found in apocrine hidradenoma, with only focal positivity in the basal layer of some neoplastic aggregations.…”
Section: Discussionmentioning
confidence: 58%
“…[18][19][20][21][22][23] However, other authors have described the findings of decapitation secretion in tubular structures of this neoplasm, which supports an apocrine differentiation, 22,[24][25][26][27] an opinion that we share. 28 In our study, calretinin immunostaining was not found in apocrine hidradenoma, with only focal positivity in the basal layer of some neoplastic aggregations.…”
Section: Discussionmentioning
confidence: 58%
“…Since anti-CEA antibody reacts with the inner surface of ductal lumina and intercellular canaliculi of the cccrine gland, this antibody may be used as a marker of the tumor cells differentiating toward the cccrine gland. It has been reported that normal apocrine glandular epithelium [8,10] and apocrine adenocarci noma 1111 arc not stained for CEA. However, these find ings contradict those of other investigators [ 12.…”
Section: Discussionmentioning
confidence: 99%
“…However, other authors have not found myoepithelial cells by ultrastuctural and histochemical studies. Furthermore, immunohistochemistry has failed to demonstrate myoepithelial differentiation (6). To clarify the nature of the cells of which is composed, we performed immunohistochemical stainings using various monoclonal antibodies for cytokeratins (CKs: CK, CK7, CK20, Cam5.2), epithelial membrane antigen (EMA), and carcinoembryonic antigen (CEA).…”
Section: Introductionmentioning
confidence: 99%