[Cutaneous angiosarcoma following conservative surgery and radiotherapy for breast carcinoma. A case report].
Identifieur interne : 007038 ( Main/Exploration ); précédent : 007037; suivant : 007039[Cutaneous angiosarcoma following conservative surgery and radiotherapy for breast carcinoma. A case report].
Auteurs : K. Kajo [Slovaquie] ; J. Lúcan ; K. Macháleková ; Z. BeratsováSource :
- Ceskoslovenska patologie [ 1210-7875 ] ; 2007.
Descripteurs français
- KwdFr :
- Adulte d'âge moyen, Femelle, Humains, Hémangiosarcome (anatomopathologie), Hémangiosarcome (étiologie), Mastectomie partielle, Région mammaire, Seconde tumeur primitive (anatomopathologie), Tumeurs cutanées (anatomopathologie), Tumeurs cutanées (étiologie), Tumeurs du sein (), Tumeurs du sein (radiothérapie), Tumeurs radio-induites (anatomopathologie).
- MESH :
- anatomopathologie : Hémangiosarcome, Seconde tumeur primitive, Tumeurs cutanées, Tumeurs radio-induites.
- radiothérapie : Tumeurs du sein.
- étiologie : Hémangiosarcome, Tumeurs cutanées.
- Adulte d'âge moyen, Femelle, Humains, Mastectomie partielle, Région mammaire, Tumeurs du sein.
English descriptors
- KwdEn :
- Breast, Breast Neoplasms (radiotherapy), Breast Neoplasms (surgery), Female, Hemangiosarcoma (etiology), Hemangiosarcoma (pathology), Humans, Mastectomy, Segmental, Middle Aged, Neoplasms, Radiation-Induced (pathology), Neoplasms, Second Primary (pathology), Skin Neoplasms (etiology), Skin Neoplasms (pathology).
- MESH :
- etiology : Hemangiosarcoma, Skin Neoplasms.
- pathology : Hemangiosarcoma, Neoplasms, Radiation-Induced, Neoplasms, Second Primary, Skin Neoplasms.
- radiotherapy : Breast Neoplasms.
- surgery : Breast Neoplasms.
- Breast, Female, Humans, Mastectomy, Segmental, Middle Aged.
Abstract
Breast angiosarcomas (AS) are very rare neoplasms, which can be divided into primary (or sporadic), and secondary AS, the latter arising either on the base of lymphoedema after mastectomy (so called AS with Stewart-Treves syndrome- ASSTS), or skin AS after breast conservation surgery with subsequent radiotherapy for breast cancer (KPRAS). The authors present a case of a 55-year-old female patient with a 17mm tumour in nipple region, developing 8 years after primary diagnosis of tubulolobular carcinoma of the breast which was treated by breast conservation surgery and radiotherapy. A probatory bioptic examination of the lesion proved well-differentiated KPRAS. The patient underwent mastectomy. The authors analyse the basic clinical and morphological features of KPRAS, which distinguish it from other forms of AS, e.g. occurrence in older age, shorter period of latency after radiation therapy when compared to ASSTS, absence of lymphoedema, and rare involvement of the breast tissue. Prognosis of this entity is very poor; today the most reliable prognostic marker is histological grading. However, it will be needed to assess in the future new indicators of prognosis of patients with this rare disease.
PubMed: 17623978
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 003597
- to stream PubMed, to step Curation: 003597
- to stream PubMed, to step Checkpoint: 003597
- to stream Ncbi, to step Merge: 002794
- to stream Ncbi, to step Curation: 002794
- to stream Ncbi, to step Checkpoint: 002794
- to stream Main, to step Merge: 007157
- to stream Main, to step Curation: 007038
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">[Cutaneous angiosarcoma following conservative surgery and radiotherapy for breast carcinoma. A case report].</title><author><name sortKey="Kajo, K" sort="Kajo, K" uniqKey="Kajo K" first="K" last="Kajo">K. Kajo</name><affiliation wicri:level="1"><nlm:affiliation>Ustav patologickej anatómie, Jesseniovej lekárskej fakulty, Martinskej fakultnej nemocnice, Martin. karol.kajo@post.sk</nlm:affiliation><country wicri:rule="url">Slovaquie</country></affiliation></author><author><name sortKey="Lucan, J" sort="Lucan, J" uniqKey="Lucan J" first="J" last="Lúcan">J. Lúcan</name></author><author><name sortKey="Machalekova, K" sort="Machalekova, K" uniqKey="Machalekova K" first="K" last="Macháleková">K. Macháleková</name></author><author><name sortKey="Beratsova, Z" sort="Beratsova, Z" uniqKey="Beratsova Z" first="Z" last="Beratsová">Z. Beratsová</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2007">2007</date><idno type="RBID">pubmed:17623978</idno><idno type="pmid">17623978</idno><idno type="wicri:Area/PubMed/Corpus">003597</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">003597</idno><idno type="wicri:Area/PubMed/Curation">003597</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">003597</idno><idno type="wicri:Area/PubMed/Checkpoint">003597</idno><idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">003597</idno><idno type="wicri:Area/Ncbi/Merge">002794</idno><idno type="wicri:Area/Ncbi/Curation">002794</idno><idno type="wicri:Area/Ncbi/Checkpoint">002794</idno><idno type="wicri:doubleKey">1210-7875:2007:Kajo K:cutaneous:angiosarcoma:following</idno><idno type="wicri:Area/Main/Merge">007157</idno><idno type="wicri:Area/Main/Curation">007038</idno><idno type="wicri:Area/Main/Exploration">007038</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">[Cutaneous angiosarcoma following conservative surgery and radiotherapy for breast carcinoma. A case report].</title><author><name sortKey="Kajo, K" sort="Kajo, K" uniqKey="Kajo K" first="K" last="Kajo">K. Kajo</name><affiliation wicri:level="1"><nlm:affiliation>Ustav patologickej anatómie, Jesseniovej lekárskej fakulty, Martinskej fakultnej nemocnice, Martin. karol.kajo@post.sk</nlm:affiliation><country wicri:rule="url">Slovaquie</country></affiliation></author><author><name sortKey="Lucan, J" sort="Lucan, J" uniqKey="Lucan J" first="J" last="Lúcan">J. Lúcan</name></author><author><name sortKey="Machalekova, K" sort="Machalekova, K" uniqKey="Machalekova K" first="K" last="Macháleková">K. Macháleková</name></author><author><name sortKey="Beratsova, Z" sort="Beratsova, Z" uniqKey="Beratsova Z" first="Z" last="Beratsová">Z. Beratsová</name></author></analytic><series><title level="j">Ceskoslovenska patologie</title><idno type="ISSN">1210-7875</idno><imprint><date when="2007" type="published">2007</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Breast</term><term>Breast Neoplasms (radiotherapy)</term><term>Breast Neoplasms (surgery)</term><term>Female</term><term>Hemangiosarcoma (etiology)</term><term>Hemangiosarcoma (pathology)</term><term>Humans</term><term>Mastectomy, Segmental</term><term>Middle Aged</term><term>Neoplasms, Radiation-Induced (pathology)</term><term>Neoplasms, Second Primary (pathology)</term><term>Skin Neoplasms (etiology)</term><term>Skin Neoplasms (pathology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Femelle</term><term>Humains</term><term>Hémangiosarcome (anatomopathologie)</term><term>Hémangiosarcome (étiologie)</term><term>Mastectomie partielle</term><term>Région mammaire</term><term>Seconde tumeur primitive (anatomopathologie)</term><term>Tumeurs cutanées (anatomopathologie)</term><term>Tumeurs cutanées (étiologie)</term><term>Tumeurs du sein ()</term><term>Tumeurs du sein (radiothérapie)</term><term>Tumeurs radio-induites (anatomopathologie)</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Hémangiosarcome</term><term>Seconde tumeur primitive</term><term>Tumeurs cutanées</term><term>Tumeurs radio-induites</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Hemangiosarcoma</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Hemangiosarcoma</term><term>Neoplasms, Radiation-Induced</term><term>Neoplasms, Second Primary</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" qualifier="radiotherapy" xml:lang="en"><term>Breast Neoplasms</term></keywords><keywords scheme="MESH" qualifier="radiothérapie" xml:lang="fr"><term>Tumeurs du sein</term></keywords><keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Breast Neoplasms</term></keywords><keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Hémangiosarcome</term><term>Tumeurs cutanées</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Breast</term><term>Female</term><term>Humans</term><term>Mastectomy, Segmental</term><term>Middle Aged</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Femelle</term><term>Humains</term><term>Mastectomie partielle</term><term>Région mammaire</term><term>Tumeurs du sein</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Breast angiosarcomas (AS) are very rare neoplasms, which can be divided into primary (or sporadic), and secondary AS, the latter arising either on the base of lymphoedema after mastectomy (so called AS with Stewart-Treves syndrome- ASSTS), or skin AS after breast conservation surgery with subsequent radiotherapy for breast cancer (KPRAS). The authors present a case of a 55-year-old female patient with a 17mm tumour in nipple region, developing 8 years after primary diagnosis of tubulolobular carcinoma of the breast which was treated by breast conservation surgery and radiotherapy. A probatory bioptic examination of the lesion proved well-differentiated KPRAS. The patient underwent mastectomy. The authors analyse the basic clinical and morphological features of KPRAS, which distinguish it from other forms of AS, e.g. occurrence in older age, shorter period of latency after radiation therapy when compared to ASSTS, absence of lymphoedema, and rare involvement of the breast tissue. Prognosis of this entity is very poor; today the most reliable prognostic marker is histological grading. However, it will be needed to assess in the future new indicators of prognosis of patients with this rare disease.</div></front></TEI><affiliations><list><country><li>Slovaquie</li></country></list><tree><noCountry><name sortKey="Beratsova, Z" sort="Beratsova, Z" uniqKey="Beratsova Z" first="Z" last="Beratsová">Z. Beratsová</name><name sortKey="Lucan, J" sort="Lucan, J" uniqKey="Lucan J" first="J" last="Lúcan">J. Lúcan</name><name sortKey="Machalekova, K" sort="Machalekova, K" uniqKey="Machalekova K" first="K" last="Macháleková">K. Macháleková</name></noCountry><country name="Slovaquie"><noRegion><name sortKey="Kajo, K" sort="Kajo, K" uniqKey="Kajo K" first="K" last="Kajo">K. Kajo</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 007038 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 007038 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= LymphedemaV1
|flux= Main
|étape= Exploration
|type= RBID
|clé= pubmed:17623978
|texte= [Cutaneous angiosarcoma following conservative surgery and radiotherapy for breast carcinoma. A case report].
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:17623978" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \
| NlmPubMed2Wicri -a LymphedemaV1
| This area was generated with Dilib version V0.6.31. |  |