Lipedema, a rare disease.
Identifieur interne : 002422 ( PubMed/Checkpoint ); précédent : 002421; suivant : 002423Lipedema, a rare disease.
Auteurs : Bae Wook Shin [Corée du Sud] ; Young-Joo Sim ; Ho Joong Jeong ; Ghi Chan KimSource :
- Annals of rehabilitation medicine [ 2234-0653 ] ; 2011.
Abstract
Lipedema is a chronic disease of lipid metabolism that results in the symmetrical impairment of fatty tissue distribution and storage combined with the hyperplasia of individual fat cells. Lipedema occurs almost exclusively in women and is usually associated with a family history and characteristic features. It can be diagnosed based on clinical history and physical examination. Lipedema is usually symmetrical, but spares the feet, is often painful to palpation, and is negative for Stemmer's sign. Additionally, lipedema patients can present with microangiopathies and lipomas. The well-known therapies for lipedema include complex decongestive therapy, pneumatic compression, and diet modifications. However, whether these treatments help reduce swelling is debatable. We encountered a case of lipedema that was initially misdiagnosed as lymphedema. The patient's clinical features and history were different from those typical of lymphedema, prompting a diagnosis of lipedema and she was treated with a complex decongestive therapy program.
DOI: 10.5535/arm.2011.35.6.922
PubMed: 22506222
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Lipedema occurs almost exclusively in women and is usually associated with a family history and characteristic features. It can be diagnosed based on clinical history and physical examination. Lipedema is usually symmetrical, but spares the feet, is often painful to palpation, and is negative for Stemmer's sign. Additionally, lipedema patients can present with microangiopathies and lipomas. The well-known therapies for lipedema include complex decongestive therapy, pneumatic compression, and diet modifications. However, whether these treatments help reduce swelling is debatable. We encountered a case of lipedema that was initially misdiagnosed as lymphedema. The patient's clinical features and history were different from those typical of lymphedema, prompting a diagnosis of lipedema and she was treated with a complex decongestive therapy program.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">22506222</PMID><DateCreated><Year>2012</Year><Month>04</Month><Day>16</Day></DateCreated><DateCompleted><Year>2012</Year><Month>08</Month><Day>23</Day></DateCompleted><DateRevised><Year>2017</Year><Month>02</Month><Day>20</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">2234-0653</ISSN><JournalIssue CitedMedium="Internet"><Volume>35</Volume><Issue>6</Issue><PubDate><Year>2011</Year><Month>Dec</Month></PubDate></JournalIssue><Title>Annals of rehabilitation medicine</Title><ISOAbbreviation>Ann Rehabil Med</ISOAbbreviation></Journal><ArticleTitle>Lipedema, a rare disease.</ArticleTitle><Pagination><MedlinePgn>922-7</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.5535/arm.2011.35.6.922</ELocationID><Abstract><AbstractText>Lipedema is a chronic disease of lipid metabolism that results in the symmetrical impairment of fatty tissue distribution and storage combined with the hyperplasia of individual fat cells. Lipedema occurs almost exclusively in women and is usually associated with a family history and characteristic features. It can be diagnosed based on clinical history and physical examination. Lipedema is usually symmetrical, but spares the feet, is often painful to palpation, and is negative for Stemmer's sign. Additionally, lipedema patients can present with microangiopathies and lipomas. The well-known therapies for lipedema include complex decongestive therapy, pneumatic compression, and diet modifications. However, whether these treatments help reduce swelling is debatable. We encountered a case of lipedema that was initially misdiagnosed as lymphedema. The patient's clinical features and history were different from those typical of lymphedema, prompting a diagnosis of lipedema and she was treated with a complex decongestive therapy program.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Shin</LastName><ForeName>Bae Wook</ForeName><Initials>BW</Initials><AffiliationInfo><Affiliation>Department of Physical Medicine and Rehabilitation, Kosin University College of Medicine, Busan 602-702, Korea.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sim</LastName><ForeName>Young-Joo</ForeName><Initials>YJ</Initials></Author><Author ValidYN="Y"><LastName>Jeong</LastName><ForeName>Ho Joong</ForeName><Initials>HJ</Initials></Author><Author ValidYN="Y"><LastName>Kim</LastName><ForeName>Ghi Chan</ForeName><Initials>GC</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2011</Year><Month>12</Month><Day>30</Day></ArticleDate></Article><MedlineJournalInfo><Country>Korea (South)</Country><MedlineTA>Ann Rehabil Med</MedlineTA><NlmUniqueID>101573065</NlmUniqueID><ISSNLinking>2234-0645</ISSNLinking></MedlineJournalInfo><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Lymphology. 2008 Mar;41(1):40-4</RefSource><PMID Version="1">18581957</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Plast Reconstr Surg. 1994 Nov;94(6):841-7; discussion 848-9</RefSource><PMID Version="1">7972431</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Surg Clin North Am. 2003 Jun;83(3):639-58</RefSource><PMID Version="1">12822730</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Dermatol Online J. 2010 Sep 15;16(9):4</RefSource><PMID Version="1">20875325</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Am J Med Genet A. 2010 Apr;152A(4):970-6</RefSource><PMID Version="1">20358611</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Lymphology. 2008 Dec;41(4):161-6</RefSource><PMID Version="1">19306662</PMID></CommentsCorrections></CommentsCorrectionsList><OtherID Source="NLM">PMC3309375</OtherID><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Complex decongestive therapy</Keyword><Keyword MajorTopicYN="N">Lipedema</Keyword><Keyword MajorTopicYN="N">Lymphedema</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2011</Year><Month>08</Month><Day>28</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2011</Year><Month>11</Month><Day>11</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2012</Year><Month>4</Month><Day>17</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2012</Year><Month>4</Month><Day>17</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2012</Year><Month>4</Month><Day>17</Day><Hour>6</Hour><Minute>1</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">22506222</ArticleId><ArticleId IdType="doi">10.5535/arm.2011.35.6.922</ArticleId><ArticleId IdType="pmc">PMC3309375</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Corée du Sud</li></country></list><tree><noCountry><name sortKey="Jeong, Ho Joong" sort="Jeong, Ho Joong" uniqKey="Jeong H" first="Ho Joong" last="Jeong">Ho Joong Jeong</name><name sortKey="Kim, Ghi Chan" sort="Kim, Ghi Chan" uniqKey="Kim G" first="Ghi Chan" last="Kim">Ghi Chan Kim</name><name sortKey="Sim, Young Joo" sort="Sim, Young Joo" uniqKey="Sim Y" first="Young-Joo" last="Sim">Young-Joo Sim</name></noCountry><country name="Corée du Sud"><noRegion><name sortKey="Shin, Bae Wook" sort="Shin, Bae Wook" uniqKey="Shin B" first="Bae Wook" last="Shin">Bae Wook Shin</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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