1997
DOI: 10.1093/ajcp/108.4.450
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Kaposiform Hemangioendothelioma in Adults:Clinicopathologic and Immunohistochemical Analysis of Three Cases

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Cited by 113 publications
(64 citation statements)
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“…This finding is notable because both of these tumors have been postulated to show lymphatic endothelial differentiation, on the basis of their characteristic infiltration by lymphocytes (29,30), the association of the former with lymphangiomatosis (29,31), and their reported usual absence of vWF expression (29,31). We observed vWF expression in 80% of kaposiform hemangioendothelioma and all Dabska tumors; again, this difference may be the result of our use of heat-induced epitope retrieval.…”
Section: Discussionmentioning
confidence: 59%
“…This finding is notable because both of these tumors have been postulated to show lymphatic endothelial differentiation, on the basis of their characteristic infiltration by lymphocytes (29,30), the association of the former with lymphangiomatosis (29,31), and their reported usual absence of vWF expression (29,31). We observed vWF expression in 80% of kaposiform hemangioendothelioma and all Dabska tumors; again, this difference may be the result of our use of heat-induced epitope retrieval.…”
Section: Discussionmentioning
confidence: 59%
“…In our case, the histological appearance of the tumor had remarkable resemblance of the spindle cell proliferation of dog and human KHE [5,6]. The vascular origin was confirmed by its histological appearance with evident blood vessels (which contain numerous erythrocytes) and by its positivity to factor VIII-related antigen, a universally accepted marker for endothelial cells, also expressed in bovine endothelial cells [4].…”
mentioning
confidence: 51%
“…In humans, hemangioendotheliomas are classically tumors of "intermediate" or "borderline" malignancy and are classified into spindle cell, retiform, polymorphous and kaposiform hemangioendotheliomas [2,6]. The Kaposiform hemangioendothelioma (KHE) is a rare vascular tumor found almost exclusively in early childhood with a wide anatomical distribution.…”
mentioning
confidence: 99%
“…KHE typically occurs during infancy and in the first decade of life. Although KHE may also develop in adults, only approximately 20 adult KHE patients have been reported (table 1) [1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17]; most of them were not associated with KMS [6]. KHE rarely originates from bone without accompanying cutaneous changes.…”
Section: Introductionmentioning
confidence: 99%