Literature DB >> 24346888

Phacomatosis pigmentovascularis type IIa--case report.

Majoriê Mergen Segatto1, Eloísa Unfer Schmitt2, Laura Netto Hagemann2, Roberta Castilhos da Silva2, Cristiane Almeida Soares Cattani2.   

Abstract

Phacomatosis Pigmentovascularis is a rare syndrome characterized by capillary malformation and pigmentary nevus. A case of a 2-year-old patient is reported, who presented extensive nevus flammeus and an aberrant Mongolian spot, without systemic disease, manifestations that allow us to classify this case as type IIa Phacomatosis Pigmentovascularis, according to Hasegawa's classification.

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Year:  2013        PMID： 24346888      PMCID： PMC3875999          DOI： 10.1590/abd1806-4841.20132248

Source DB:  PubMed          Journal:  An Bras Dermatol        ISSN： 0365-0596            Impact factor:   1.896


  7 in total

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

Authors:  B P-H Chang; C-H Hsu; H-C Chen; J-W Hsieh
Journal:  Br J Dermatol       Date:  2007-03-13       Impact factor: 9.302

Review 2.  Phacomatosis pigmentovascularis revisited and reclassified.

Authors:  Rudolf Happle
Journal:  Arch Dermatol       Date:  2005-03

3.  Cutis marmorata telangiectatica congenita and extensive mongolian spots: type 5 phacomatosis pigmentovascularis.

Authors:  A Torrelo; A Zambrano; R Happle
Journal:  Br J Dermatol       Date:  2003-02       Impact factor: 9.302

Review 4.  Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber syndrome and Klippel-Trenaunay syndrome.

Authors:  Lindsey B Finklea; Melinda R Mohr; Molly M Warthan; David H Darrow; Judith V Williams
Journal:  Pediatr Dermatol       Date:  2010 May-Jun       Impact factor: 1.588

5.  Treatment of phacomatosis pigmentovascularis: a combined multiple laser approach.

Authors:  Taro Kono; Ali Riza Erçöçen; Henry H L Chan; Yuji Kikuchi; Keijiro Hori; Shoichi Uezono; Motohiro Nozaki
Journal:  Dermatol Surg       Date:  2003-06       Impact factor: 3.398

6.  Phakomatosis pigmentovascularis type IVa.

Authors:  Y Hasegawa; M Yasuhara
Journal:  Arch Dermatol       Date:  1985-05

Review 7.  Phakomatosis pigmentovascularis: Clinical findings in 15 patients and review of the literature.

Authors:  Montse Fernández-Guarino; Pablo Boixeda; Elena de Las Heras; Sonsoles Aboin; Cristina García-Millán; Pedro Jaén Olasolo
Journal:  J Am Acad Dermatol       Date:  2007-11-28       Impact factor: 11.527
  7 in total
  3 in total

1.  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.

Authors:  Han Ma; Mengsi Liao; Shu Qiu; Ruijun Luo; Rongbiao Lu; Chun Lu
Journal:  An Bras Dermatol       Date:  2015 May-Jun       Impact factor: 1.896

Review 2.  Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review.

Authors:  Akash Kumar; Diane B Zastrow; Elijah J Kravets; Daniah Beleford; Maura R Z Ruzhnikov; Megan E Grove; Annika M Dries; Jennefer N Kohler; Daryl M Waggott; Yaping Yang; Yong Huang; Katherine M Mackenzie; Christine M Eng; Paul G Fisher; Euan A Ashley; Joyce M Teng; David A Stevenson; Joseph T Shieh; Matthew T Wheeler; Jonathan A Bernstein
Journal:  Am J Med Genet A       Date:  2019-03-28       Impact factor: 2.802

3.  Phacomatosis pigmentovascularis of cesioflammea type.

Authors:  Delky Johanna Villarreal Villarreal; Fabiano Leal
Journal:  An Bras Dermatol       Date:  2016 Sep-Oct       Impact factor: 1.896
  3 in total

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