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Phacomatosis pigmentovascularis type IIIb.

作者信息

Seckin Dilek, Yucelten Deniz, Aytug Ayse, Demirkesen Cuyan

机构信息

Department of Dermatology, Marmara University School of Medicine, Istanbul, Turkey.

出版信息

Int J Dermatol. 2007 Sep;46(9):960-3. doi: 10.1111/j.1365-4632.2007.03121.x.

DOI:10.1111/j.1365-4632.2007.03121.x
PMID:17822502
Abstract

Phacomatosis pigmentovascularis (PPV) is a group of syndromes comprising coexistent vascular and pigmentary nevi, which is first classified into five subtypes and then further categorized according to the absence or presence of associated systemic findings as type (a) and (b), respectively. This case report is of an 11-year-old Turkish girl with extensive vascular nevus and nevus spilus. Because of coexistent scoliosis, the patient represents an example of PPV type IIIb. Including the present case, a total of eight cases of PPV type IIIb have been reported to date. The case is discussed in view of the new classification proposed by Happle.

摘要

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引用本文的文献

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Indian J Dermatol. 2019 May-Jun;64(3):217-223. doi: 10.4103/ijd.IJD_385_18.
2
Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review.色素性外胚叶发育不良伴大理石皮肤和斑状皮肤色素沉着症的皮肤外表现:病例系列及文献复习。
Am J Med Genet A. 2019 Jun;179(6):966-977. doi: 10.1002/ajmg.a.61134. Epub 2019 Mar 28.
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A Neonatal Case of Phacomatosis Pigmentovascularis Type IIa.
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Balkan Med J. 2015 Jan;32(1):129-30. doi: 10.5152/balkanmedj.2015.15448. Epub 2015 Jan 1.