Dabska tumor arising in lymphangioma circumscriptum
Identifieur interne : 006E76 ( Main/Exploration ); précédent : 006E75; suivant : 006E77Dabska tumor arising in lymphangioma circumscriptum
Auteurs : Patrick O. Emanuel [États-Unis] ; Robert Lin ; Lester Silver [États-Unis] ; 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
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml: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.</div>
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