Serveur d'exploration sur le lymphœdème

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Pseudosarcoma: massive localized lymphedema of the morbidly obese.

Identifieur interne : 003B09 ( PubMed/Corpus ); précédent : 003B08; suivant : 003B10

Pseudosarcoma: massive localized lymphedema of the morbidly obese.

Auteurs : Parviz Goshtasby ; John Dawson ; Nikhilesh Agarwal

Source :

RBID : pubmed:16417764

English descriptors

Abstract

Massive localized lymphedema is a term used to describe a benign overgrowth of lymphoproliferative tissue in morbidly obese patients, which is characterized by fibrotic and edematous fibroadipose tissue. Because of its large size and similar appearance to sarcomas, it has often been termed a pseudosarcoma. Patients tend to seek treatment only when the masses reach a sufficient size to alter their activities of daily living or have problems with excoriation or wound breakdown. Resection is indicated in these cases or if there is any question as to underlying malignancy of the lesion. Although recurrence is common, overall prognosis is good, with only anecdotal reports of transformation to angiosarcoma in the literature. We report a patient afflicted with this unique disorder.

DOI: 10.1381/096089206775222014
PubMed: 16417764

Links to Exploration step

pubmed:16417764

Le document en format XML

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<name sortKey="Goshtasby, Parviz" sort="Goshtasby, Parviz" uniqKey="Goshtasby P" first="Parviz" last="Goshtasby">Parviz Goshtasby</name>
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<nlm:affiliation>Department of General and Trauma Surgery, York Hospital, York, PA 17405, USA. parvizmd75@yahoo.com</nlm:affiliation>
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<name sortKey="Dawson, John" sort="Dawson, John" uniqKey="Dawson J" first="John" last="Dawson">John Dawson</name>
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<name sortKey="Agarwal, Nikhilesh" sort="Agarwal, Nikhilesh" uniqKey="Agarwal N" first="Nikhilesh" last="Agarwal">Nikhilesh Agarwal</name>
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<div type="abstract" xml:lang="en">Massive localized lymphedema is a term used to describe a benign overgrowth of lymphoproliferative tissue in morbidly obese patients, which is characterized by fibrotic and edematous fibroadipose tissue. Because of its large size and similar appearance to sarcomas, it has often been termed a pseudosarcoma. Patients tend to seek treatment only when the masses reach a sufficient size to alter their activities of daily living or have problems with excoriation or wound breakdown. Resection is indicated in these cases or if there is any question as to underlying malignancy of the lesion. Although recurrence is common, overall prognosis is good, with only anecdotal reports of transformation to angiosarcoma in the literature. We report a patient afflicted with this unique disorder.</div>
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