Axillary apocrine carcinoma with benign apocrine tumours: a case report involving a pathological and immunohistochemical study and review of the literature
Background: Apocrine carcinoma is rare and often occurs in the axilla. This is the second apocrine carcinoma arising in bilateral axillae with associated apocrine hyperplasia to be reported. Aims/Methods: Because benign apocrine tumours may be precursors of cancer, this case was investigated immunoh...
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description | Background: Apocrine carcinoma is rare and often occurs in the axilla. This is the second apocrine carcinoma arising in bilateral axillae with associated apocrine hyperplasia to be reported. Aims/Methods: Because benign apocrine tumours may be precursors of cancer, this case was investigated immunohistochemically and histologically, and a literature (English and Japanese) review undertaken of cases with coexistent malignant and benign apocrine tumours in the axilla to elucidate the relation between apocrine carcinoma and benign apocrine tumours. Results: Only four cases of axillary apocrine carcinoma with benign apocrine tumours were identified in the literature. In each case, benign apocrine hyperplasia was situated within and surrounding the adenocarcinomatous nests. Staining for epithelial membrane antigen revealed three patterns: (1) poorly differentiated tumour cells showing strong cytoplasmic staining; (2) combined luminal surface and cytoplasmic staining of glandular cells; and (3) a strongly positive lineal staining pattern at the luminal membrane surface, comprising one or two apocrine hyperplastic secretory cells. The basal lesions of apocrine hyperplasia were strongly positive for α smooth muscle actin, whereas the periphery of adenomatous lesions showed weaker positive staining, even though the periphery of adenocarcinomatous lesions was negative. Conclusions: All five apocrine carcinomas with benign apocrine tumours occurred in elderly Japanese men who had bilateral benign apocrine tumours even if affected by unilateral axillary apocrine carcinoma. The immunohistochemical results support the notion that apocrine hyperplasia is a precursor of cancer and that apocrine carcinoma, adenoma, and hyperplasia may be successive steps in the linear progression to carcinoma. |
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This is the second apocrine carcinoma arising in bilateral axillae with associated apocrine hyperplasia to be reported. Aims/Methods: Because benign apocrine tumours may be precursors of cancer, this case was investigated immunohistochemically and histologically, and a literature (English and Japanese) review undertaken of cases with coexistent malignant and benign apocrine tumours in the axilla to elucidate the relation between apocrine carcinoma and benign apocrine tumours. Results: Only four cases of axillary apocrine carcinoma with benign apocrine tumours were identified in the literature. In each case, benign apocrine hyperplasia was situated within and surrounding the adenocarcinomatous nests. Staining for epithelial membrane antigen revealed three patterns: (1) poorly differentiated tumour cells showing strong cytoplasmic staining; (2) combined luminal surface and cytoplasmic staining of glandular cells; and (3) a strongly positive lineal staining pattern at the luminal membrane surface, comprising one or two apocrine hyperplastic secretory cells. The basal lesions of apocrine hyperplasia were strongly positive for α smooth muscle actin, whereas the periphery of adenomatous lesions showed weaker positive staining, even though the periphery of adenocarcinomatous lesions was negative. Conclusions: All five apocrine carcinomas with benign apocrine tumours occurred in elderly Japanese men who had bilateral benign apocrine tumours even if affected by unilateral axillary apocrine carcinoma. The immunohistochemical results support the notion that apocrine hyperplasia is a precursor of cancer and that apocrine carcinoma, adenoma, and hyperplasia may be successive steps in the linear progression to carcinoma.</description><identifier>ISSN: 0021-9746</identifier><identifier>EISSN: 1472-4146</identifier><identifier>DOI: 10.1136/jcp.2004.019794</identifier><identifier>PMID: 15976347</identifier><identifier>CODEN: JCPAAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>Adenocarcinoma, Papillary - pathology ; Adenoma, Sweat Gland - pathology ; Aged ; Aged, 80 and over ; Antigens ; apocrine carcinoma ; Apocrine Glands - pathology ; Axilla ; benign apocrine tumour ; Biological and medical sciences ; Breast cancer ; Calcification ; Cytoplasm ; EMA ; epithelial membrane antigen ; Humans ; Hyperplasia ; Immunoglobulins ; immunohistochemical study ; Investigative techniques, diagnostic techniques (general aspects) ; Lymphatic system ; Male ; Medical sciences ; Original ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Precancerous Conditions - pathology ; Sweat Gland Neoplasms - pathology ; Tumors ; α smooth muscle actin ; αSMA</subject><ispartof>Journal of clinical pathology, 2005-07, Vol.58 (7), p.757-761</ispartof><rights>Copyright 2005 Journal of Clinical Pathology</rights><rights>2005 INIST-CNRS</rights><rights>Copyright: 2005 Copyright 2005 Journal of Clinical Pathology</rights><rights>Copyright © Copyright 2005 Journal of Clinical Pathology 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b522t-5042788dd55913f842a10b6b710f4aaf02b6dc3abb8f97952170e02aa97f9d063</citedby><cites>FETCH-LOGICAL-b522t-5042788dd55913f842a10b6b710f4aaf02b6dc3abb8f97952170e02aa97f9d063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1770727/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1770727/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16945444$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15976347$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miyamoto, T</creatorcontrib><creatorcontrib>Hagari, Y</creatorcontrib><creatorcontrib>Inoue, S</creatorcontrib><creatorcontrib>Watanabe, T</creatorcontrib><creatorcontrib>Yoshino, T</creatorcontrib><title>Axillary apocrine carcinoma with benign apocrine tumours: a case report involving a pathological and immunohistochemical study and review of the literature</title><title>Journal of clinical pathology</title><addtitle>J Clin Pathol</addtitle><description>Background: Apocrine carcinoma is rare and often occurs in the axilla. This is the second apocrine carcinoma arising in bilateral axillae with associated apocrine hyperplasia to be reported. Aims/Methods: Because benign apocrine tumours may be precursors of cancer, this case was investigated immunohistochemically and histologically, and a literature (English and Japanese) review undertaken of cases with coexistent malignant and benign apocrine tumours in the axilla to elucidate the relation between apocrine carcinoma and benign apocrine tumours. Results: Only four cases of axillary apocrine carcinoma with benign apocrine tumours were identified in the literature. In each case, benign apocrine hyperplasia was situated within and surrounding the adenocarcinomatous nests. Staining for epithelial membrane antigen revealed three patterns: (1) poorly differentiated tumour cells showing strong cytoplasmic staining; (2) combined luminal surface and cytoplasmic staining of glandular cells; and (3) a strongly positive lineal staining pattern at the luminal membrane surface, comprising one or two apocrine hyperplastic secretory cells. The basal lesions of apocrine hyperplasia were strongly positive for α smooth muscle actin, whereas the periphery of adenomatous lesions showed weaker positive staining, even though the periphery of adenocarcinomatous lesions was negative. Conclusions: All five apocrine carcinomas with benign apocrine tumours occurred in elderly Japanese men who had bilateral benign apocrine tumours even if affected by unilateral axillary apocrine carcinoma. The immunohistochemical results support the notion that apocrine hyperplasia is a precursor of cancer and that apocrine carcinoma, adenoma, and hyperplasia may be successive steps in the linear progression to carcinoma.</description><subject>Adenocarcinoma, Papillary - pathology</subject><subject>Adenoma, Sweat Gland - pathology</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antigens</subject><subject>apocrine carcinoma</subject><subject>Apocrine Glands - pathology</subject><subject>Axilla</subject><subject>benign apocrine tumour</subject><subject>Biological and medical sciences</subject><subject>Breast cancer</subject><subject>Calcification</subject><subject>Cytoplasm</subject><subject>EMA</subject><subject>epithelial membrane antigen</subject><subject>Humans</subject><subject>Hyperplasia</subject><subject>Immunoglobulins</subject><subject>immunohistochemical study</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Lymphatic system</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Original</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Precancerous Conditions - pathology</subject><subject>Sweat Gland Neoplasms - pathology</subject><subject>Tumors</subject><subject>α smooth muscle actin</subject><subject>αSMA</subject><issn>0021-9746</issn><issn>1472-4146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkUFv1DAQhSMEokvhzA1ZQnBAynbsOHHMAalaAUUqcAHEzXIcZ-MlsYPtbNvfwp_F2111gQsnS_M-P828l2VPMSwxLqqzjZqWBIAuAXPG6b1sgSkjOcW0up8tAAjOOaPVSfYohA0ALhguHmYnuOSsKihbZL_Or80wSH-D5OSUN1YjJb0y1o0SXZnYo0Zbs7ZHOc6jm314jWQig0ZeT85HZOzWDVtj12k-ydi7wa2NkgOStkVmHGfrehOiU70eb-chzu3Nrer11ugr5DoUe40GE7WXcfb6cfagk0PQTw7vafb13dsvq4v88vP7D6vzy7wpCYl5CZSwum7bsuS46GpKJIamahiGjkrZAWmqVhWyaeouhVQSzEADkZKzjrdQFafZm73vNDejbpW20ctBTN6MKRjhpBF_K9b0Yu22AjMGjLBk8PJg4N3PWYcoRhOUTrla7eYgKsYZ8BoS-PwfcJOytOm45FVjILSucaLO9pTyLgSvu7tVMIhd7SLVLna1i33t6cezPy848oeeE_DiAMiQwu-8tMqEI1dxWlK6M8r3XKpKX9_p0v9IRxSsFJ--rcTHC_wdKK3Fjn-155tx898tfwN37NXc</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Miyamoto, T</creator><creator>Hagari, Y</creator><creator>Inoue, S</creator><creator>Watanabe, T</creator><creator>Yoshino, T</creator><general>BMJ Publishing Group Ltd and Association of Clinical Pathologists</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><general>Copyright 2005 Journal of Clinical Pathology</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20050701</creationdate><title>Axillary apocrine carcinoma with benign apocrine tumours: a case report involving a pathological and immunohistochemical study and review of the literature</title><author>Miyamoto, T ; Hagari, Y ; Inoue, S ; Watanabe, T ; Yoshino, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b522t-5042788dd55913f842a10b6b710f4aaf02b6dc3abb8f97952170e02aa97f9d063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adenocarcinoma, Papillary - pathology</topic><topic>Adenoma, Sweat Gland - pathology</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antigens</topic><topic>apocrine carcinoma</topic><topic>Apocrine Glands - pathology</topic><topic>Axilla</topic><topic>benign apocrine tumour</topic><topic>Biological and medical sciences</topic><topic>Breast cancer</topic><topic>Calcification</topic><topic>Cytoplasm</topic><topic>EMA</topic><topic>epithelial membrane antigen</topic><topic>Humans</topic><topic>Hyperplasia</topic><topic>Immunoglobulins</topic><topic>immunohistochemical study</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Lymphatic system</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Original</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. 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This is the second apocrine carcinoma arising in bilateral axillae with associated apocrine hyperplasia to be reported. Aims/Methods: Because benign apocrine tumours may be precursors of cancer, this case was investigated immunohistochemically and histologically, and a literature (English and Japanese) review undertaken of cases with coexistent malignant and benign apocrine tumours in the axilla to elucidate the relation between apocrine carcinoma and benign apocrine tumours. Results: Only four cases of axillary apocrine carcinoma with benign apocrine tumours were identified in the literature. In each case, benign apocrine hyperplasia was situated within and surrounding the adenocarcinomatous nests. Staining for epithelial membrane antigen revealed three patterns: (1) poorly differentiated tumour cells showing strong cytoplasmic staining; (2) combined luminal surface and cytoplasmic staining of glandular cells; and (3) a strongly positive lineal staining pattern at the luminal membrane surface, comprising one or two apocrine hyperplastic secretory cells. The basal lesions of apocrine hyperplasia were strongly positive for α smooth muscle actin, whereas the periphery of adenomatous lesions showed weaker positive staining, even though the periphery of adenocarcinomatous lesions was negative. Conclusions: All five apocrine carcinomas with benign apocrine tumours occurred in elderly Japanese men who had bilateral benign apocrine tumours even if affected by unilateral axillary apocrine carcinoma. The immunohistochemical results support the notion that apocrine hyperplasia is a precursor of cancer and that apocrine carcinoma, adenoma, and hyperplasia may be successive steps in the linear progression to carcinoma.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and Association of Clinical Pathologists</pub><pmid>15976347</pmid><doi>10.1136/jcp.2004.019794</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma, Papillary - pathology Adenoma, Sweat Gland - pathology Aged Aged, 80 and over Antigens apocrine carcinoma Apocrine Glands - pathology Axilla benign apocrine tumour Biological and medical sciences Breast cancer Calcification Cytoplasm EMA epithelial membrane antigen Humans Hyperplasia Immunoglobulins immunohistochemical study Investigative techniques, diagnostic techniques (general aspects) Lymphatic system Male Medical sciences Original Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Precancerous Conditions - pathology Sweat Gland Neoplasms - pathology Tumors α smooth muscle actin αSMA |
title | Axillary apocrine carcinoma with benign apocrine tumours: a case report involving a pathological and immunohistochemical study and review of the literature |
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