| Recurrent nodular haemangiomas in Klippel-Trénaunay syndrome. | |
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MedLine Citation:
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PMID: 1323362 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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A one-year-old child had hypertrophy of the left leg and an unusual constellation of a naevus flammeus and superficial enlarged veins of the trunk together with successive appearance and involution since birth of numerous nodular elements located in the naevus and in the surrounding normal skin. Microscopic examination of these elements showed haemangiomas with capillaries, cavernous channels and lymphangiomatous components. The benign nature of transient nodular elements located to the trunk and the lack of associated visceral vascular malformations in the Klippel-Trénaunay syndrome are documented. |
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Authors:
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N Illum; H Winther Nielsen; B Guldhammer Skov |
Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Acta paediatrica (Oslo, Norway : 1992) Volume: 81 ISSN: 0803-5253 ISO Abbreviation: Acta Paediatr. Publication Date: 1992 May |
Date Detail:
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Created Date: 1992-09-16 Completed Date: 1992-09-16 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 9205968 Medline TA: Acta Paediatr Country: NORWAY |
Other Details:
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Languages: eng Pagination: 456-8 Citation Subset: IM |
Affiliation:
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Department of Paediatrics, Hvidovre Hospital, Copenhagen, Denmark. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Hemangioma
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complications*,
pathology Humans Infant, Newborn Klippel-Trenaunay-Weber Syndrome / complications*, pathology Male Neoplasm Recurrence, Local Skin Neoplasms / complications*, pathology |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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