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An infant with extensive Mongolian spot, naevus flammeus and cutis marmorata telangiectatica congenita: a unique case of phakomatosis pigmentovascularis.

作者信息

Chang B P-H, Hsu C-H, Chen H-C, Hsieh J-W

出版信息

Br J Dermatol. 2007 May;156(5):1068-71. doi: 10.1111/j.1365-2133.2007.07798.x. Epub 2007 Mar 13.

DOI:10.1111/j.1365-2133.2007.07798.x
PMID:17355231
Abstract
摘要

相似文献

1
An infant with extensive Mongolian spot, naevus flammeus and cutis marmorata telangiectatica congenita: a unique case of phakomatosis pigmentovascularis.一名患有广泛蒙古斑、鲜红斑痣和先天性毛细血管扩张性大理石样皮肤的婴儿：色素血管性斑痣性错构瘤病的一个独特病例。
Br J Dermatol. 2007 May;156(5):1068-71. doi: 10.1111/j.1365-2133.2007.07798.x. Epub 2007 Mar 13.
2
Large aberrant Mongolian spots coexisting with cutis marmorata telangiectatica congenita (phacomatosis pigmentovascularis type V or phacomatosis cesiomarmorata).巨大异常蒙古斑与先天性网状青斑并存（色素血管性错构瘤综合征V型或大理石样皮肤血管扩张症）。
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The case of a boy with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita: a unique instance of phacomatosis pigmentovascularis.一名患有太田痣、广泛蒙古斑、鲜红斑痣、贫血痣和先天性毛细血管扩张性大理石样皮肤的男孩病例：色素血管性斑痣性错构瘤病的一个独特实例。
An Bras Dermatol. 2015 May-Jun;90(3 Suppl 1):10-2. doi: 10.1590/abd1806-4841.20153466.
4
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A case of phakomatosis pigmentovascularis type II: port-wine stain and dermal melanocytosis with cutis marmorata telangiectatica congenita-like lesions.II型色素血管性斑痣性错构瘤病1例：葡萄酒色斑与皮肤黑素细胞增多症伴先天性网状青斑样损害
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New case of phacomatosis cesio-flammeo-marmorata: the time is right to review the classification for phacomatosis pigmentovascularis.新的蓝褐色大理石样错构瘤病例：是时候重新审视色素血管性错构瘤的分类了。
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[Nevus flammeus, aberrant mongolian spot and neurological symptoms].
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引用本文的文献

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Cutis marmorata telangiectatica congenita: a literature review.先天性大理石样皮肤毛细血管扩张症：文献回顾。
Orphanet J Rare Dis. 2019 Dec 4;14(1):283. doi: 10.1186/s13023-019-1229-8.
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 female infant with phacomatosis pigmentovascularis and congenital chylous ascites: A case report.
一名患有色素血管性母斑病和先天性乳糜性腹水的女婴：病例报告。
Medicine (Baltimore). 2018 Aug;97(34):e12012. doi: 10.1097/MD.0000000000012012.
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Phacomatosis Cesioflammea with Cutis Marmorata-like Lesions and Unusual Extracutaneous Abnormalities: Is It a Distinct disorder?伴有大理石样皮肤样损害及异常皮肤外表现的焰色痣：它是一种独特的疾病吗？
Indian J Dermatol. 2017 Mar-Apr;62(2):207-209. doi: 10.4103/0019-5154.201760.
5
Cutis marmorata telangiectatica congenita and aberrant Mongolian spots: Type V phacomatosis pigmentovascularis or phacomatosis cesiomarmorata.先天性大理石样皮肤毛细血管扩张症与异常蒙古斑：V型色素血管性错构瘤病或大理石样皮肤错构瘤病。
JAAD Case Rep. 2016 Jan 23;2(1):28-30. doi: 10.1016/j.jdcr.2015.10.006. eCollection 2016 Jan.
6
The case of a boy with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita: a unique instance of phacomatosis pigmentovascularis.一名患有太田痣、广泛蒙古斑、鲜红斑痣、贫血痣和先天性毛细血管扩张性大理石样皮肤的男孩病例：色素血管性斑痣性错构瘤病的一个独特实例。
An Bras Dermatol. 2015 May-Jun;90(3 Suppl 1):10-2. doi: 10.1590/abd1806-4841.20153466.
7
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An Bras Dermatol. 2013 Nov-Dec;88(6 Suppl 1):85-8. doi: 10.1590/abd1806-4841.20132248.
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