scholarly journals 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

2015 ◽  
Vol 90 (3 suppl 1) ◽  
pp. 10-12 ◽  
Author(s):  
Han MA ◽  
Mengsi Liao ◽  
Shu Qiu ◽  
Ruijun Luo ◽  
Rongbiao Lu ◽  
...  
2013 ◽  
Vol 88 (6 suppl 1) ◽  
pp. 85-88 ◽  
Author(s):  
Majoriê Mergen Segatto ◽  
Eloísa Unfer Schmitt ◽  
Laura Netto Hagemann ◽  
Roberta Castilhos da Silva ◽  
Cristiane Almeida Soares Cattani

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.


Dermato ◽  
2021 ◽  
Vol 1 (2) ◽  
pp. 35-42
Author(s):  
Yujin Han ◽  
Se-Hoon Lee ◽  
Minah Cho ◽  
Sang-Hyun Cho ◽  
Jeong-Deuk Lee ◽  
...  

Dermal melanocytic disorders present as bluish pigmentation on the skin. Several entities including Mongolian spot, aberrant Mongolian spot, nevus of Ota, and nevus of Ito have been reported. It is often difficult to distinguish between the different entities from their overlapping features. Although they share similar etiologies and histologic findings, their co-morbidities and prognosis differ. In this paper, we report four cases of dermal melanocytic disorders of which we were not able to make a clear-cut diagnosis. Also, we briefly review the dermal melanocytic disorders.


2015 ◽  
Vol 43 (2) ◽  
pp. 225-226 ◽  
Author(s):  
Shujiro Hayashi ◽  
Tomoko Kaminaga ◽  
Iliana Tantcheva-Poor ◽  
Yoichiro Hamasaki ◽  
Atsushi Hatamochi

1954 ◽  
Vol 22 (3) ◽  
pp. 225-236 ◽  
Author(s):  
C.S. Dorsey ◽  
Hamilton Montgomery

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