A Scary Onset of a Rare and Aggressive Type of Primary Breast Sarcoma: A Case Report
Identifieur interne : 001521 ( Main/Curation ); précédent : 001520; suivant : 001522A Scary Onset of a Rare and Aggressive Type of Primary Breast Sarcoma: A Case Report
Auteurs : Inês Ramalho ; Sara Campos ; Teresa Rebelo ; Margarida Figueiredo DiasSource :
- Case Reports in Oncology [ 1662-6575 ] ; 2016.
Abstract
Primary breast sarcoma, arising from connective tissue within the breast, is extremely rare, accounting for less than 1% of all primary breast malignancies and no more than 5% of all sarcomas. The rarity of this pathology limits most studies to case reports and small retrospective studies, which has led to a lack of consensus on the clinical management. We report a clinical case of a 52-year-old woman, perimenopausal, previously healthy, with regular breast surveillance, who presented with a large (>20 cm) and rapidly expanding hypervascularized tumor of the left breast developed over 10 days, with a very thin preulcerative skin over the last 4 days. There was no systemic dissemination. The patient was submitted to total mastectomy and excision of axillary adenopathy. The tumor was diagnosed histologically as malignant phyllodes tumor associated with areas of high-grade sarcoma. Due to rapid growth and aggressive histological characteristics, adjuvant chemotherapy and radiotherapy were performed. There is a lot of evidence that tumors larger than 5 cm are associated with a poor prognosis. Despite the poor prognosis associated with this aggressive entity, the patient had no recurrence during 5 years of follow-up. We review the relevant literature about primary breast sarcomas.
Url:
DOI: 10.1159/000452946
PubMed: 28101028
PubMed Central: 5216215
Links toward previous steps (curation, corpus...)
- to stream Pmc, to step Corpus: Pour aller vers cette notice dans l'étape Curation :002151
- to stream Pmc, to step Curation: Pour aller vers cette notice dans l'étape Curation :002150
- to stream Pmc, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :000C72
- to stream Ncbi, to step Merge: Pour aller vers cette notice dans l'étape Curation :008C27
- to stream Ncbi, to step Curation: Pour aller vers cette notice dans l'étape Curation :008C27
- to stream Ncbi, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :008C27
- to stream Main, to step Merge: Pour aller vers cette notice dans l'étape Curation :001523
Links to Exploration step
PMC:5216215Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">A Scary Onset of a Rare and Aggressive Type of Primary Breast Sarcoma: A Case Report</title>
<author><name sortKey="Ramalho, Ines" sort="Ramalho, Ines" uniqKey="Ramalho I" first="Inês" last="Ramalho">Inês Ramalho</name>
</author>
<author><name sortKey="Campos, Sara" sort="Campos, Sara" uniqKey="Campos S" first="Sara" last="Campos">Sara Campos</name>
</author>
<author><name sortKey="Rebelo, Teresa" sort="Rebelo, Teresa" uniqKey="Rebelo T" first="Teresa" last="Rebelo">Teresa Rebelo</name>
</author>
<author><name sortKey="Figueiredo Dias, Margarida" sort="Figueiredo Dias, Margarida" uniqKey="Figueiredo Dias M" first="Margarida" last="Figueiredo Dias">Margarida Figueiredo Dias</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">28101028</idno>
<idno type="pmc">5216215</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216215</idno>
<idno type="RBID">PMC:5216215</idno>
<idno type="doi">10.1159/000452946</idno>
<date when="2016">2016</date>
<idno type="wicri:Area/Pmc/Corpus">002151</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">002151</idno>
<idno type="wicri:Area/Pmc/Curation">002150</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Curation">002150</idno>
<idno type="wicri:Area/Pmc/Checkpoint">000C72</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Checkpoint">000C72</idno>
<idno type="wicri:Area/Ncbi/Merge">008C27</idno>
<idno type="wicri:Area/Ncbi/Curation">008C27</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">008C27</idno>
<idno type="wicri:Area/Main/Merge">001523</idno>
<idno type="wicri:Area/Main/Curation">001521</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">A Scary Onset of a Rare and Aggressive Type of Primary Breast Sarcoma: A Case Report</title>
<author><name sortKey="Ramalho, Ines" sort="Ramalho, Ines" uniqKey="Ramalho I" first="Inês" last="Ramalho">Inês Ramalho</name>
</author>
<author><name sortKey="Campos, Sara" sort="Campos, Sara" uniqKey="Campos S" first="Sara" last="Campos">Sara Campos</name>
</author>
<author><name sortKey="Rebelo, Teresa" sort="Rebelo, Teresa" uniqKey="Rebelo T" first="Teresa" last="Rebelo">Teresa Rebelo</name>
</author>
<author><name sortKey="Figueiredo Dias, Margarida" sort="Figueiredo Dias, Margarida" uniqKey="Figueiredo Dias M" first="Margarida" last="Figueiredo Dias">Margarida Figueiredo Dias</name>
</author>
</analytic>
<series><title level="j">Case Reports in Oncology</title>
<idno type="eISSN">1662-6575</idno>
<imprint><date when="2016">2016</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en"><p>Primary breast sarcoma, arising from connective tissue within the breast, is extremely rare, accounting for less than 1% of all primary breast malignancies and no more than 5% of all sarcomas. The rarity of this pathology limits most studies to case reports and small retrospective studies, which has led to a lack of consensus on the clinical management. We report a clinical case of a 52-year-old woman, perimenopausal, previously healthy, with regular breast surveillance, who presented with a large (>20 cm) and rapidly expanding hypervascularized tumor of the left breast developed over 10 days, with a very thin preulcerative skin over the last 4 days. There was no systemic dissemination. The patient was submitted to total mastectomy and excision of axillary adenopathy. The tumor was diagnosed histologically as malignant phyllodes tumor associated with areas of high-grade sarcoma. Due to rapid growth and aggressive histological characteristics, adjuvant chemotherapy and radiotherapy were performed. There is a lot of evidence that tumors larger than 5 cm are associated with a poor prognosis. Despite the poor prognosis associated with this aggressive entity, the patient had no recurrence during 5 years of follow-up. We review the relevant literature about primary breast sarcomas.</p>
</div>
</front>
<back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Al Benna, S" uniqKey="Al Benna S">S Al-Benna</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Wang, F" uniqKey="Wang F">F Wang</name>
</author>
<author><name sortKey="Jia, Y" uniqKey="Jia Y">Y Jia</name>
</author>
<author><name sortKey="Tong, Z" uniqKey="Tong Z">Z Tong</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Li, N" uniqKey="Li N">N Li</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Hefny, Af" uniqKey="Hefny A">AF Hefny</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Holm, M" uniqKey="Holm M">M Holm</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Yin, M" uniqKey="Yin M">M Yin</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Surov, A" uniqKey="Surov A">A Surov</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Rashmi Chugh, M" uniqKey="Rashmi Chugh M">M Rashmi Chugh</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Radovanovi, A" uniqKey="Radovanovi A">A Radovanović</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Hsu, C" uniqKey="Hsu C">C Hsu</name>
</author>
<author><name sortKey="Mccloskey, Sa" uniqKey="Mccloskey S">SA McCloskey</name>
</author>
<author><name sortKey="Peddi, Pf" uniqKey="Peddi P">PF Peddi</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Harris, Jr" uniqKey="Harris J">JR Harris</name>
</author>
<author><name sortKey="Lippman, Me" uniqKey="Lippman M">ME Lippman</name>
</author>
<author><name sortKey="Morrow, M" uniqKey="Morrow M">M Morrow</name>
</author>
<author><name sortKey="Osborne, Ck" uniqKey="Osborne C">CK Osborne</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Testori, A" uniqKey="Testori A">A Testori</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Srinivasamurthy, Bc" uniqKey="Srinivasamurthy B">BC Srinivasamurthy</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Trent, Ij" uniqKey="Trent I">IJ Trent</name>
</author>
<author><name sortKey="Benjamin, Rs" uniqKey="Benjamin R">RS Benjamin</name>
</author>
<author><name sortKey="Valero, V" uniqKey="Valero V">V Valero</name>
</author>
</analytic>
</biblStruct>
</listBibl>
</div1>
</back>
</TEI>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Main/Curation
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001521 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Curation/biblio.hfd -nk 001521 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Sante |area= LymphedemaV1 |flux= Main |étape= Curation |type= RBID |clé= PMC:5216215 |texte= A Scary Onset of a Rare and Aggressive Type of Primary Breast Sarcoma: A Case Report }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Curation/RBID.i -Sk "pubmed:28101028" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Curation/biblio.hfd \ | NlmPubMed2Wicri -a LymphedemaV1
![]() | This area was generated with Dilib version V0.6.31. | ![]() |