Dabska tumor arising in lymphangioma circumscriptum
Identifieur interne : 004D22 ( Istex/Corpus ); précédent : 004D21; suivant : 004D23Dabska tumor arising in lymphangioma circumscriptum
Auteurs : Patrick O. Emanuel ; Robert Lin ; Lester Silver ; Miriam B. Birge ; Helen Shim ; Robert G. PhelpsSource :
- Journal of Cutaneous Pathology [ 0303-6987 ] ; 2008-01.
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:
DOI: 10.1111/j.1600-0560.2007.00765.x
Links to Exploration step
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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.
--></abstract>
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<name type="personal"><namePart type="given">Patrick O.</namePart>
<namePart type="family">Emanuel</namePart>
<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>
<namePart type="family">Lin</namePart>
<affiliation>Department of Pathology</affiliation>
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<name type="personal"><namePart type="given">Lester</namePart>
<namePart type="family">Silver</namePart>
<affiliation>Department of Plastic Surgery, Mount Sinai Medical Center, New York, NY, USA</affiliation>
<role><roleTerm type="text">author</roleTerm>
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<name type="personal"><namePart type="given">Miriam B.</namePart>
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<affiliation>Department of Dermatopathology</affiliation>
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<name type="personal"><namePart type="given">Helen</namePart>
<namePart type="family">Shim</namePart>
<affiliation>Department of Dermatopathology</affiliation>
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<name type="personal"><namePart type="given">Robert G.</namePart>
<namePart type="family">Phelps</namePart>
<affiliation>Department of Dermatopathology</affiliation>
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<dateIssued encoding="w3cdtf">2008-01</dateIssued>
<edition>Accepted for publication February 26, 2007</edition>
<copyrightDate encoding="w3cdtf">2008</copyrightDate>
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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>
<relatedItem type="host"><titleInfo><title>Journal of Cutaneous Pathology</title>
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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>
<identifier type="PublisherID">CUP</identifier>
<part><date>2008</date>
<detail type="volume"><caption>vol.</caption>
<number>35</number>
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<extent unit="pages"><start>65</start>
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