{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,28]],"date-time":"2025-08-28T12:31:42Z","timestamp":1756384302727,"version":"3.40.5"},"reference-count":9,"publisher":"FapUNIFESP (SciELO)","issue":"6 suppl 1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["An. Bras. Dermatol."],"published-print":{"date-parts":[[2013,12]]},"abstract":"<jats:p>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.<\/jats:p>","DOI":"10.1590\/abd1806-4841.20132248","type":"journal-article","created":{"date-parts":[[2014,1,30]],"date-time":"2014-01-30T19:47:10Z","timestamp":1391111230000},"page":"85-88","source":"Crossref","is-referenced-by-count":5,"title":["Phacomatosis pigmentovascularis type IIa - case report"],"prefix":"10.1590","volume":"88","author":[{"given":"Majori\u00ea Mergen","family":"Segatto","sequence":"first","affiliation":[{"name":"Federal University for Health Sciences,  Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Elo\u00edsa Unfer","family":"Schmitt","sequence":"additional","affiliation":[{"name":"Sanitary Dermatology Outpatient Clinic,  Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Laura Netto","family":"Hagemann","sequence":"additional","affiliation":[{"name":"Sanitary Dermatology Outpatient Clinic,  Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Roberta Castilhos da","family":"Silva","sequence":"additional","affiliation":[{"name":"Sanitary Dermatology Outpatient Clinic,  Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cristiane Almeida Soares","family":"Cattani","sequence":"additional","affiliation":[{"name":"Sanitary Dermatology Outpatient Clinic,  Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"530","reference":[{"key":"ref1","doi-asserted-by":"crossref","first-page":"1068","DOI":"10.1111\/j.1365-2133.2007.07798.x","article-title":"An infant with extensive Mongolian spot, naevus flammeus and cutis marmorata telangiectatica congenita: a unique case of phakomatosis pigmentovascularis","volume":"156","author":"Chang BP","year":"2007","journal-title":"Br J Dermatol"},{"key":"ref2","first-page":"1","article-title":"Phakomatosis pigmentovascularis","volume":"57","author":"Ota N","year":"1947","journal-title":"Jpn J Dermatol B"},{"key":"ref3","doi-asserted-by":"crossref","first-page":"651","DOI":"10.1001\/archderm.1985.01660050103025","article-title":"Phakomatosis pigmentovascularis type VIa","volume":"121","author":"Hasegawa Y","year":"1985","journal-title":"Arch Dermatol"},{"key":"ref4","doi-asserted-by":"crossref","first-page":"342","DOI":"10.1046\/j.1365-2133.2003.05118.x","article-title":"Cutis marmorata telangiectasica congenita and extensive Mongolian spots: type V phakomatosis pigmentovascularis","volume":"148","author":"Torrelo A","year":"2003","journal-title":"Br J Dermatol"},{"key":"ref5","doi-asserted-by":"crossref","first-page":"88","DOI":"10.1016\/j.jaad.2007.08.012","article-title":"Phakomatosis pigmentovascularis: Clinical findings in 15 patients and review of the literature","volume":"58","author":"Fern\u00e1ndez-Guarino M","year":"2008","journal-title":"J Am Acad Dermatol"},{"key":"ref6","doi-asserted-by":"crossref","first-page":"385","DOI":"10.1001\/archderm.141.3.385","article-title":"Phakomatosis pigmentovascularis revisited and reclassified","volume":"141","author":"Happle R","year":"2005","journal-title":"Arch Dermatol"},{"key":"ref7","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1111\/j.1525-1470.2010.01144.x","article-title":"Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber Syndrome and Klippel-Trenaunay Syndrome","volume":"27","author":"Finklea LB","year":"2010","journal-title":"Pediatr Dermatol"},{"key":"ref8","first-page":"163","article-title":"Facomatose Pigmentovascular: relato de caso","volume":"72","author":"Ribas J","year":"1997","journal-title":"An Bras Dermatol"},{"key":"ref9","first-page":"642","article-title":"Treatment of Phacomatosis Pigmentovascularis: A Combined Multiple Laser Approach","volume":"29","author":"Kono T","year":"2003","journal-title":"Dermatol Surg"}],"container-title":["Anais Brasileiros de Dermatologia"],"original-title":[],"link":[{"URL":"http:\/\/www.scielo.br\/pdf\/abd\/v88n6s1\/0365-0596-abd-88-06-s1-0085.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,5,19]],"date-time":"2025-05-19T15:00:42Z","timestamp":1747666842000},"score":1,"resource":{"primary":{"URL":"http:\/\/www.scielo.br\/scielo.php?script=sci_arttext&pid=S0365-05962013000800085&lng=en&tlng=en"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,12]]},"references-count":9,"journal-issue":{"issue":"6 suppl 1","published-print":{"date-parts":[[2013,12]]}},"alternative-id":["S0365-05962013000800085"],"URL":"https:\/\/doi.org\/10.1590\/abd1806-4841.20132248","relation":{},"ISSN":["0365-0596"],"issn-type":[{"type":"electronic","value":"0365-0596"}],"subject":[],"published":{"date-parts":[[2013,12]]}}}