LymphedemaV1, Istex, Corpus, bibRecord, 004D22

Dabska tumor arising in lymphangioma circumscriptum

Identifieur interne : 004D22 ( Istex/Corpus ); précédent : 004D21; suivant : 004D23

Dabska tumor arising in lymphangioma circumscriptum

Auteurs : Patrick O. Emanuel ; Robert Lin ; Lester Silver ; Miriam B. Birge ; Helen Shim ; Robert G. Phelps

Source :

Journal of Cutaneous Pathology [ 0303-6987 ] ; 2008-01.

RBID : ISTEX:A44C2E74B6B860596528C5193B7C3201460CFFCF

Abstract

We describe a case of Dabska tumor (DT) occurring within a large congenital lymphangioma circumscriptum on the thigh of a 14‐year‐old female. Diagnostic biopsy showed numerous intravascular papillary projections lined by atypical endothelial cells within the anastomosing vascular channels of a lymphangioma circumscriptum. DT is regarded as a vascular tumor of intermediate malignant potential, most probably of lymphatic origin. Although it has been described in pre‐existing lymphangiomas, to the best of our knowledge this is the first case to be described in a pre‐existing lymphangioma circumscriptum. During a follow‐up of 9 years, the lymphangioma circumscriptum has recurred, but there has been no evidence of DT recurrence or metastasis.

Url:

https://api.istex.fr/document/A44C2E74B6B860596528C5193B7C3201460CFFCF/fulltext/pdf

DOI: 10.1111/j.1600-0560.2007.00765.x

Links to Exploration step

ISTEX:A44C2E74B6B860596528C5193B7C3201460CFFCF

Le document en format XML

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<abstractGroup><abstract type="main" xml:lang="en"><p>We describe a case of Dabska tumor (DT) occurring within a large congenital lymphangioma circumscriptum on the thigh of a 14‐year‐old female. Diagnostic biopsy showed numerous intravascular papillary projections lined by atypical endothelial cells within the anastomosing vascular channels of a lymphangioma circumscriptum. DT is regarded as a vascular tumor of intermediate malignant potential, most probably of lymphatic origin. Although it has been described in pre‐existing lymphangiomas, to the best of our knowledge this is the first case to be described in a pre‐existing lymphangioma circumscriptum. During a follow‐up of 9 years, the lymphangioma circumscriptum has recurred, but there has been no evidence of DT recurrence or metastasis.</p><!--

          Emanuel PO, Lin R, Silver L, Birge MB, Shim H, Phelps RG. Dabska tumor arising in lymphangioma circumscriptum.

J Cutan Pathol 2008; 35: 65–69. © Blackwell Munksgaard 2007.
        
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<name type="personal"><namePart type="given">Patrick O.</namePart>
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<affiliation>Department of Dermatopathology</affiliation>
<affiliation>E-mail: patrick.emanuel@mssm.edu</affiliation>
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<name type="personal"><namePart type="given">Robert</namePart>
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<name type="personal"><namePart type="given">Lester</namePart>
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<name type="personal"><namePart type="given">Miriam B.</namePart>
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<name type="personal"><namePart type="given">Helen</namePart>
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<name type="personal"><namePart type="given">Robert G.</namePart>
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<abstract lang="en">We describe a case of Dabska tumor (DT) occurring within a large congenital lymphangioma circumscriptum on the thigh of a 14‐year‐old female. Diagnostic biopsy showed numerous intravascular papillary projections lined by atypical endothelial cells within the anastomosing vascular channels of a lymphangioma circumscriptum. DT is regarded as a vascular tumor of intermediate malignant potential, most probably of lymphatic origin. Although it has been described in pre‐existing lymphangiomas, to the best of our knowledge this is the first case to be described in a pre‐existing lymphangioma circumscriptum. During a follow‐up of 9 years, the lymphangioma circumscriptum has recurred, but there has been no evidence of DT recurrence or metastasis.</abstract>
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<identifier type="ISSN">0303-6987</identifier>
<identifier type="eISSN">1600-0560</identifier>
<identifier type="DOI">10.1111/(ISSN)1600-0560</identifier>
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<part><date>2008</date>
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Dabska tumor arising in lymphangioma circumscriptum

Dabska tumor arising in lymphangioma circumscriptum

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