Primary cutaneous anaplastic large cell lymphoma with intralymphatic involvement associated with chronic lymphedema.
Identifieur interne : 000289 ( PubMed/Corpus ); précédent : 000288; suivant : 000290Primary cutaneous anaplastic large cell lymphoma with intralymphatic involvement associated with chronic lymphedema.
Auteurs : Peiyuan Fan ; Lin Nong ; Jingru Sun ; Xiaoqing Liu ; Marshall E. Kadin ; Ting Li ; Ping Tu ; Yang WangSource :
- Journal of cutaneous pathology [ 1600-0560 ] ; 2017.
Abstract
Chronic lymphedema predisposes to develop malignant cutaneous tumors, including angiosarcoma, Kaposi's sarcoma and B-cell lymphoma. T-cell malignancy has rarely been associated with chronic lymph stasis. Here, we report a case of primary cutaneous anaplastic large cell lymphoma (pcALCL) with lymphatic spread associated with chronic lymphedema. The patient is a 56-year-old man who received orchiectomy and right inguinal lymphadenectomy for malignant seminoma 10 years ago, which led to prominent lymphedema of the right leg. He developed extensive skin nodules on the lymphedematous area for 3 months. Histopathology findings confirmed a diagnosis of pcALCL, which is a subtype of cutaneous T-cell lymphoma characterized by the presence of CD30+ T cells. Intralymphatic infiltration of malignant cells is prominent. The pathogenesis of intralymphatic cutaneous anaplastic large cell lymphoma is largely unknown. Our case suggests that chronic lymphedema resulted in persistent CD4+ T-cell inflammation, which then may contribute to the development of pcALCL.
DOI: 10.1111/cup.12933
PubMed: 28337783
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Primary cutaneous anaplastic large cell lymphoma with intralymphatic involvement associated with chronic lymphedema.</title><author><name sortKey="Fan, Peiyuan" sort="Fan, Peiyuan" uniqKey="Fan P" first="Peiyuan" last="Fan">Peiyuan Fan</name><affiliation><nlm:affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author><author><name sortKey="Nong, Lin" sort="Nong, Lin" uniqKey="Nong L" first="Lin" last="Nong">Lin Nong</name><affiliation><nlm:affiliation>Department of Pathology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author><author><name sortKey="Sun, Jingru" sort="Sun, Jingru" uniqKey="Sun J" first="Jingru" last="Sun">Jingru Sun</name><affiliation><nlm:affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author><author><name sortKey="Liu, Xiaoqing" sort="Liu, Xiaoqing" uniqKey="Liu X" first="Xiaoqing" last="Liu">Xiaoqing Liu</name><affiliation><nlm:affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author><author><name sortKey="Kadin, Marshall E" sort="Kadin, Marshall E" uniqKey="Kadin M" first="Marshall E" last="Kadin">Marshall E. Kadin</name><affiliation><nlm:affiliation>Department of Dermatology and Skin Surgery, Boston University School of Medicine, Providence, Rhode Island.</nlm:affiliation></affiliation></author><author><name sortKey="Li, Ting" sort="Li, Ting" uniqKey="Li T" first="Ting" last="Li">Ting Li</name><affiliation><nlm:affiliation>Department of Pathology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author><author><name sortKey="Tu, Ping" sort="Tu, Ping" uniqKey="Tu P" first="Ping" last="Tu">Ping Tu</name><affiliation><nlm:affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author><author><name sortKey="Wang, Yang" sort="Wang, Yang" uniqKey="Wang Y" first="Yang" last="Wang">Yang Wang</name><affiliation><nlm:affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2017">2017</date><idno type="RBID">pubmed:28337783</idno><idno type="pmid">28337783</idno><idno type="doi">10.1111/cup.12933</idno><idno type="wicri:Area/PubMed/Corpus">000289</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000289</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Primary cutaneous anaplastic large cell lymphoma with intralymphatic involvement associated with chronic lymphedema.</title><author><name sortKey="Fan, Peiyuan" sort="Fan, Peiyuan" uniqKey="Fan P" first="Peiyuan" last="Fan">Peiyuan Fan</name><affiliation><nlm:affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author><author><name sortKey="Nong, Lin" sort="Nong, Lin" uniqKey="Nong L" first="Lin" last="Nong">Lin Nong</name><affiliation><nlm:affiliation>Department of Pathology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author><author><name sortKey="Sun, Jingru" sort="Sun, Jingru" uniqKey="Sun J" first="Jingru" last="Sun">Jingru Sun</name><affiliation><nlm:affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author><author><name sortKey="Liu, Xiaoqing" sort="Liu, Xiaoqing" uniqKey="Liu X" first="Xiaoqing" last="Liu">Xiaoqing Liu</name><affiliation><nlm:affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author><author><name sortKey="Kadin, Marshall E" sort="Kadin, Marshall E" uniqKey="Kadin M" first="Marshall E" last="Kadin">Marshall E. Kadin</name><affiliation><nlm:affiliation>Department of Dermatology and Skin Surgery, Boston University School of Medicine, Providence, Rhode Island.</nlm:affiliation></affiliation></author><author><name sortKey="Li, Ting" sort="Li, Ting" uniqKey="Li T" first="Ting" last="Li">Ting Li</name><affiliation><nlm:affiliation>Department of Pathology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author><author><name sortKey="Tu, Ping" sort="Tu, Ping" uniqKey="Tu P" first="Ping" last="Tu">Ping Tu</name><affiliation><nlm:affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author><author><name sortKey="Wang, Yang" sort="Wang, Yang" uniqKey="Wang Y" first="Yang" last="Wang">Yang Wang</name><affiliation><nlm:affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Journal of cutaneous pathology</title><idno type="eISSN">1600-0560</idno><imprint><date when="2017" type="published">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Chronic lymphedema predisposes to develop malignant cutaneous tumors, including angiosarcoma, Kaposi's sarcoma and B-cell lymphoma. T-cell malignancy has rarely been associated with chronic lymph stasis. Here, we report a case of primary cutaneous anaplastic large cell lymphoma (pcALCL) with lymphatic spread associated with chronic lymphedema. The patient is a 56-year-old man who received orchiectomy and right inguinal lymphadenectomy for malignant seminoma 10 years ago, which led to prominent lymphedema of the right leg. He developed extensive skin nodules on the lymphedematous area for 3 months. Histopathology findings confirmed a diagnosis of pcALCL, which is a subtype of cutaneous T-cell lymphoma characterized by the presence of CD30+ T cells. Intralymphatic infiltration of malignant cells is prominent. The pathogenesis of intralymphatic cutaneous anaplastic large cell lymphoma is largely unknown. Our case suggests that chronic lymphedema resulted in persistent CD4+ T-cell inflammation, which then may contribute to the development of pcALCL.</div></front></TEI><pubmed><MedlineCitation Status="Publisher" Owner="NLM"><PMID Version="1">28337783</PMID><DateCreated><Year>2017</Year><Month>03</Month><Day>24</Day></DateCreated><DateRevised><Year>2017</Year><Month>05</Month><Day>05</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1600-0560</ISSN><JournalIssue CitedMedium="Internet"><PubDate><Year>2017</Year><Month>Mar</Month><Day>23</Day></PubDate></JournalIssue><Title>Journal of cutaneous pathology</Title><ISOAbbreviation>J. Cutan. Pathol.</ISOAbbreviation></Journal><ArticleTitle>Primary cutaneous anaplastic large cell lymphoma with intralymphatic involvement associated with chronic lymphedema.</ArticleTitle><ELocationID EIdType="doi" ValidYN="Y">10.1111/cup.12933</ELocationID><Abstract><AbstractText>Chronic lymphedema predisposes to develop malignant cutaneous tumors, including angiosarcoma, Kaposi's sarcoma and B-cell lymphoma. T-cell malignancy has rarely been associated with chronic lymph stasis. Here, we report a case of primary cutaneous anaplastic large cell lymphoma (pcALCL) with lymphatic spread associated with chronic lymphedema. The patient is a 56-year-old man who received orchiectomy and right inguinal lymphadenectomy for malignant seminoma 10 years ago, which led to prominent lymphedema of the right leg. He developed extensive skin nodules on the lymphedematous area for 3 months. Histopathology findings confirmed a diagnosis of pcALCL, which is a subtype of cutaneous T-cell lymphoma characterized by the presence of CD30+ T cells. Intralymphatic infiltration of malignant cells is prominent. The pathogenesis of intralymphatic cutaneous anaplastic large cell lymphoma is largely unknown. Our case suggests that chronic lymphedema resulted in persistent CD4+ T-cell inflammation, which then may contribute to the development of pcALCL.</AbstractText><CopyrightInformation>© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Fan</LastName><ForeName>Peiyuan</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Nong</LastName><ForeName>Lin</ForeName><Initials>L</Initials><AffiliationInfo><Affiliation>Department of Pathology, Peking University First Hospital, Beijing, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sun</LastName><ForeName>Jingru</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Liu</LastName><ForeName>Xiaoqing</ForeName><Initials>X</Initials><AffiliationInfo><Affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kadin</LastName><ForeName>Marshall E</ForeName><Initials>ME</Initials><AffiliationInfo><Affiliation>Department of Dermatology and Skin Surgery, Boston University School of Medicine, Providence, Rhode Island.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Li</LastName><ForeName>Ting</ForeName><Initials>T</Initials><AffiliationInfo><Affiliation>Department of Pathology, Peking University First Hospital, Beijing, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Tu</LastName><ForeName>Ping</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Yang</ForeName><Initials>Y</Initials><Identifier Source="ORCID">http://orcid.org/0000-0001-7805-2861</Identifier><AffiliationInfo><Affiliation>Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2017</Year><Month>03</Month><Day>23</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Cutan Pathol</MedlineTA><NlmUniqueID>0425124</NlmUniqueID><ISSNLinking>0303-6987</ISSNLinking></MedlineJournalInfo><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">immunosuppression</Keyword><Keyword MajorTopicYN="N">inflammation</Keyword><Keyword MajorTopicYN="N">lymphedema</Keyword><Keyword MajorTopicYN="N">pathogenesis</Keyword><Keyword MajorTopicYN="N">primary cutaneous anaplastic large cell lymphoma</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2016</Year><Month>08</Month><Day>27</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2017</Year><Month>03</Month><Day>01</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2017</Year><Month>03</Month><Day>21</Day></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2017</Year><Month>3</Month><Day>25</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2017</Year><Month>3</Month><Day>25</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2017</Year><Month>3</Month><Day>25</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>aheadofprint</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">28337783</ArticleId><ArticleId IdType="doi">10.1111/cup.12933</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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