Article: Kaposiform hemangioendothelioma: Five patients with cutaneous lesion and long follow-up
| Title | Kaposiform hemangioendothelioma: Five patients with cutaneous lesion and long follow-up |
|---|---|
| Authors | MacMoune Lai, F4 To, KF4 Choi, PCL4 Leung, PC4 Kumta, SM4 Yuen, PPM4 Lam, WY1 Cheung, ANY2 Allen, PW3 |
| Issue Date | 2001 |
| Publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/modpathol/ |
| Citation | Modern Pathology, 2001, v. 14 n. 11, p. 1087-1092 [How to Cite?] DOI: http://dx.doi.org/10.1038/modpathol.3880441 |
| Abstract | Kaposiform hemangioendothelioma is a rare locally aggressive vascular tumor of the skin, deep soft tissue, and bone in children, characterized by infiltrating nodules and sheets of spindle cells, and unmistakable resemblance to Kaposi's sarcoma. More than 60 patients with such tumor have been reported so far, and while many have died as a result of extensive disease and severe coagulopathy, the long-term biologic behavior of this tumor remains undetermined. We describe five patients with kaposiform hemangioendothelioma and a mean follow-up of 19 years, ranging from 8 to 35 years. This report emphasizes on the importance of cutaneous lesions being the most commonly affected site, but also for its clinical diversity. Early diagnosis is possible even for a small skin lesion, which may be critical for the treatment of a potentially fatal deep-seated extensive tumor. All five patients are well, and three of them with persistent vascular tumor, which has carried two patients from childhood to adult. Although the behavior of this tumor might have been modified by radiation or interferon in three patients, this series indicates that kaposiform hemangioendothelioma is incapable of metastasis, despite a protracted course of many decades with no tendency for spontaneous regression. |
| ISSN | 0893-3952 2011 Impact Factor: 4.792 2011 SCImago Journal Rankings: 0.565 |
| DOI | http://dx.doi.org/10.1038/modpathol.3880441 |
| References | References in Scopus |
| dc.contributor.author | MacMoune Lai, F |
|---|---|
| dc.contributor.author | To, KF |
| dc.contributor.author | Choi, PCL |
| dc.contributor.author | Leung, PC |
| dc.contributor.author | Kumta, SM |
| dc.contributor.author | Yuen, PPM |
| dc.contributor.author | Lam, WY |
| dc.contributor.author | Cheung, ANY |
| dc.contributor.author | Allen, PW |
| dc.date.accessioned | 2010-09-06T09:41:15Z |
| dc.date.available | 2010-09-06T09:41:15Z |
| dc.date.issued | 2001 |
| dc.description.abstract | Kaposiform hemangioendothelioma is a rare locally aggressive vascular tumor of the skin, deep soft tissue, and bone in children, characterized by infiltrating nodules and sheets of spindle cells, and unmistakable resemblance to Kaposi's sarcoma. More than 60 patients with such tumor have been reported so far, and while many have died as a result of extensive disease and severe coagulopathy, the long-term biologic behavior of this tumor remains undetermined. We describe five patients with kaposiform hemangioendothelioma and a mean follow-up of 19 years, ranging from 8 to 35 years. This report emphasizes on the importance of cutaneous lesions being the most commonly affected site, but also for its clinical diversity. Early diagnosis is possible even for a small skin lesion, which may be critical for the treatment of a potentially fatal deep-seated extensive tumor. All five patients are well, and three of them with persistent vascular tumor, which has carried two patients from childhood to adult. Although the behavior of this tumor might have been modified by radiation or interferon in three patients, this series indicates that kaposiform hemangioendothelioma is incapable of metastasis, despite a protracted course of many decades with no tendency for spontaneous regression. |
| dc.description.nature | Link_to_subscribed_fulltext |
| dc.identifier.citation | Modern Pathology, 2001, v. 14 n. 11, p. 1087-1092 [How to Cite?] DOI: http://dx.doi.org/10.1038/modpathol.3880441 |
| dc.identifier.citeulike | 10924596 |
| dc.identifier.doi | http://dx.doi.org/10.1038/modpathol.3880441 |
| dc.identifier.epage | 1092 |
| dc.identifier.hkuros | 83963 |
| dc.identifier.issn | 0893-3952 2011 Impact Factor: 4.792 2011 SCImago Journal Rankings: 0.565 |
| dc.identifier.issue | 11 |
| dc.identifier.openurl | ![]() |
| dc.identifier.pmid | 11706068 |
| dc.identifier.scopus | eid_2-s2.0-0035163732 |
| dc.identifier.spage | 1087 |
| dc.identifier.uri | http://hdl.handle.net/10722/88278 |
| dc.identifier.volume | 14 |
| dc.language | eng |
| dc.publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/modpathol/ |
| dc.publisher.place | United Kingdom |
| dc.relation.ispartof | Modern Pathology |
| dc.relation.references | References in Scopus |
| dc.subject.mesh | Adult |
| dc.subject.mesh | Child |
| dc.subject.mesh | Diagnosis, Differential |
| dc.subject.mesh | Female |
| dc.subject.mesh | Follow-Up Studies |
| dc.subject.mesh | Hemangioendothelioma - pathology |
| dc.subject.mesh | Humans |
| dc.subject.mesh | Infant |
| dc.subject.mesh | Male |
| dc.subject.mesh | Sarcoma, Kaposi - pathology |
| dc.subject.mesh | Skin - pathology |
| dc.subject.mesh | Skin Neoplasms - pathology |
| dc.subject.mesh | Time Factors |
| dc.title | Kaposiform hemangioendothelioma: Five patients with cutaneous lesion and long follow-up |
| dc.type | Article |
Author Affiliations
- Tuen Mun Hospital
- The University of Hong Kong
- Flinders Medical Centre
- Chinese University of Hong Kong


