Beta‐hCG–producing malignant phyllodes tumour
Phyllodes tumours (PTs) of the breasts are rare fibroepithelial tumours accounting for less than 1% of all breast tumours. They have a wide range of presentations, ranging from benign‐natured tumours that behave similarly to fibroadenomas, to aggressive malignant tumours that can rapidly advance bot...
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Veröffentlicht in: | Surgical practice 2024-08, Vol.28 (3), p.170-172 |
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description | Phyllodes tumours (PTs) of the breasts are rare fibroepithelial tumours accounting for less than 1% of all breast tumours. They have a wide range of presentations, ranging from benign‐natured tumours that behave similarly to fibroadenomas, to aggressive malignant tumours that can rapidly advance both locally and distally. Histologically, PTs are classified into benign, borderline, or malignant based on a combination of the following five features: degree of stromal cellularity, stromal cell atypia, mitotic activity, infiltrative or circumscribed margins, and presence or absence of stromal overgrowth. Malignant tumours demonstrate high levels of stromal cellularity and atypia, infiltrative margins, high mitotic rate (>10 mitoses per 10 high‐power fields), and the presence of stromal overgrowth. Treatment predominantly relies on complete excision of the lesion, although treatment regimens for malignant PTs with adjuvant chemoradiation lack standardization as a result of its rarity. Malignant tumours are also often associated with paraneoplastic syndromes such as recurrent hypoglycaemia and hypertrophic osteoarthropathy. Here, we report a case of recurrent malignant PT with serum beta‐human chorionic gonadotrophin secretion. |
doi_str_mv | 10.1111/1744-1633.12694 |
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They have a wide range of presentations, ranging from benign‐natured tumours that behave similarly to fibroadenomas, to aggressive malignant tumours that can rapidly advance both locally and distally. Histologically, PTs are classified into benign, borderline, or malignant based on a combination of the following five features: degree of stromal cellularity, stromal cell atypia, mitotic activity, infiltrative or circumscribed margins, and presence or absence of stromal overgrowth. Malignant tumours demonstrate high levels of stromal cellularity and atypia, infiltrative margins, high mitotic rate (>10 mitoses per 10 high‐power fields), and the presence of stromal overgrowth. Treatment predominantly relies on complete excision of the lesion, although treatment regimens for malignant PTs with adjuvant chemoradiation lack standardization as a result of its rarity. Malignant tumours are also often associated with paraneoplastic syndromes such as recurrent hypoglycaemia and hypertrophic osteoarthropathy. Here, we report a case of recurrent malignant PT with serum beta‐human chorionic gonadotrophin secretion.</description><identifier>ISSN: 1744-1625</identifier><identifier>EISSN: 1744-1633</identifier><identifier>DOI: 10.1111/1744-1633.12694</identifier><language>eng</language><publisher>Melbourne: Wiley Publishing Asia Pty Ltd</publisher><subject>Adjuvants ; Biomarkers ; Breast cancer ; Histology ; Medical prognosis ; Tumors</subject><ispartof>Surgical practice, 2024-08, Vol.28 (3), p.170-172</ispartof><rights>2024 College of Surgeons of Hong Kong.</rights><rights>2024 College of Surgeons of Hong Kong</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2694-682cbd3abfbea53661d4798a58de6eb3be03e02e0e0c9a93b555c374a5e617663</cites><orcidid>0000-0002-0672-5518</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1744-1633.12694$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1744-1633.12694$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,27933,27934,45583,45584</link.rule.ids></links><search><creatorcontrib>Leung, Laura Lok Wa</creatorcontrib><creatorcontrib>Marabi, Monalyn</creatorcontrib><creatorcontrib>Tsoi, Violet Yee Kei</creatorcontrib><title>Beta‐hCG–producing malignant phyllodes tumour</title><title>Surgical practice</title><description>Phyllodes tumours (PTs) of the breasts are rare fibroepithelial tumours accounting for less than 1% of all breast tumours. They have a wide range of presentations, ranging from benign‐natured tumours that behave similarly to fibroadenomas, to aggressive malignant tumours that can rapidly advance both locally and distally. Histologically, PTs are classified into benign, borderline, or malignant based on a combination of the following five features: degree of stromal cellularity, stromal cell atypia, mitotic activity, infiltrative or circumscribed margins, and presence or absence of stromal overgrowth. Malignant tumours demonstrate high levels of stromal cellularity and atypia, infiltrative margins, high mitotic rate (>10 mitoses per 10 high‐power fields), and the presence of stromal overgrowth. Treatment predominantly relies on complete excision of the lesion, although treatment regimens for malignant PTs with adjuvant chemoradiation lack standardization as a result of its rarity. Malignant tumours are also often associated with paraneoplastic syndromes such as recurrent hypoglycaemia and hypertrophic osteoarthropathy. Here, we report a case of recurrent malignant PT with serum beta‐human chorionic gonadotrophin secretion.</description><subject>Adjuvants</subject><subject>Biomarkers</subject><subject>Breast cancer</subject><subject>Histology</subject><subject>Medical prognosis</subject><subject>Tumors</subject><issn>1744-1625</issn><issn>1744-1633</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFUMtOwzAQtBBIlMKZayTOaf2IneRYKmiRKnEAzpbtbNpUeREnQrn1Eyrxh_0SHIJ6ZS-7Ws3szA5C9wTPiKs5CYPAJ4KxGaEiDi7Q5Ly5PM-UX6Mba_cYszAK2QSRR2jV6XDcLVenw3fdVElnsnLrFSrPtqUqW6_e9XleJWC9tiuqrrlFV6nKLdz99Sn6eH56X679zevqZbnY-GaQ90VEjU6Y0qkGxZkQJAnCOFI8SkCAZhowA0wBAzaxipnmnBsWBoqDIKEQbIoexrvO1GcHtpV7p146SckIjSnGOI4caj6iTFNZ20Aq6yYrVNNLguWQixw-l0MK8jcXx-Aj4yvLof8PLhdv65H3Az4-ZXE</recordid><startdate>202408</startdate><enddate>202408</enddate><creator>Leung, Laura Lok Wa</creator><creator>Marabi, Monalyn</creator><creator>Tsoi, Violet Yee Kei</creator><general>Wiley Publishing Asia Pty Ltd</general><general>Blackwell Publishing Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><orcidid>https://orcid.org/0000-0002-0672-5518</orcidid></search><sort><creationdate>202408</creationdate><title>Beta‐hCG–producing malignant phyllodes tumour</title><author>Leung, Laura Lok Wa ; Marabi, Monalyn ; Tsoi, Violet Yee Kei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2694-682cbd3abfbea53661d4798a58de6eb3be03e02e0e0c9a93b555c374a5e617663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adjuvants</topic><topic>Biomarkers</topic><topic>Breast cancer</topic><topic>Histology</topic><topic>Medical prognosis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leung, Laura Lok Wa</creatorcontrib><creatorcontrib>Marabi, Monalyn</creatorcontrib><creatorcontrib>Tsoi, Violet Yee Kei</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Surgical practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leung, Laura Lok Wa</au><au>Marabi, Monalyn</au><au>Tsoi, Violet Yee Kei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Beta‐hCG–producing malignant phyllodes tumour</atitle><jtitle>Surgical practice</jtitle><date>2024-08</date><risdate>2024</risdate><volume>28</volume><issue>3</issue><spage>170</spage><epage>172</epage><pages>170-172</pages><issn>1744-1625</issn><eissn>1744-1633</eissn><abstract>Phyllodes tumours (PTs) of the breasts are rare fibroepithelial tumours accounting for less than 1% of all breast tumours. They have a wide range of presentations, ranging from benign‐natured tumours that behave similarly to fibroadenomas, to aggressive malignant tumours that can rapidly advance both locally and distally. Histologically, PTs are classified into benign, borderline, or malignant based on a combination of the following five features: degree of stromal cellularity, stromal cell atypia, mitotic activity, infiltrative or circumscribed margins, and presence or absence of stromal overgrowth. Malignant tumours demonstrate high levels of stromal cellularity and atypia, infiltrative margins, high mitotic rate (>10 mitoses per 10 high‐power fields), and the presence of stromal overgrowth. Treatment predominantly relies on complete excision of the lesion, although treatment regimens for malignant PTs with adjuvant chemoradiation lack standardization as a result of its rarity. Malignant tumours are also often associated with paraneoplastic syndromes such as recurrent hypoglycaemia and hypertrophic osteoarthropathy. Here, we report a case of recurrent malignant PT with serum beta‐human chorionic gonadotrophin secretion.</abstract><cop>Melbourne</cop><pub>Wiley Publishing Asia Pty Ltd</pub><doi>10.1111/1744-1633.12694</doi><tpages>3</tpages><orcidid>https://orcid.org/0000-0002-0672-5518</orcidid></addata></record> |
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subjects | Adjuvants Biomarkers Breast cancer Histology Medical prognosis Tumors |
title | Beta‐hCG–producing malignant phyllodes tumour |
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