Publication:
Acquired lymphangiectasis: A case report (major hallmarks in its differential diagnosis from lymphangioma circumscriptum)

dc.contributor.authorsMidi A., Ayabakan Ö., Sav A.
dc.date.accessioned2022-03-28T14:54:04Z
dc.date.accessioned2026-01-11T18:14:36Z
dc.date.available2022-03-28T14:54:04Z
dc.date.issued2007
dc.description.abstractAcquired lymphangiectasis is a superficial lymphatic dilatation caused by a wide range of scarring processes. Histologically indistinguishable from lymphangioma circumscriptum and commonly occurs in adults as a late sequel of surgery and radiation therapy. Patients usually present with numerous translucent vesicles in a chronic lymph edematous area several years after surgery with or without radiation therapy. We report a case of acquired lymphangiectasis, happened 17 years after the surgical intervention. Lesions were located the left subaxillary region. This is the first case that is reported so late in the literature after the surgery.
dc.identifier.issn10191941
dc.identifier.urihttps://hdl.handle.net/11424/256091
dc.language.isoeng
dc.relation.ispartofMarmara Medical Journal
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAcquired
dc.subjectLymphangiectasis
dc.subjectLymphangioma circumscriptum
dc.titleAcquired lymphangiectasis: A case report (major hallmarks in its differential diagnosis from lymphangioma circumscriptum)
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage46
oaire.citation.issue1
oaire.citation.startPage43
oaire.citation.titleMarmara Medical Journal
oaire.citation.volume20

Files