Congenital Triangular Alopecia in Phakomatosis Pigmentovascularis: Report of 3 Cases

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Bilateral Temporal Triangular Alopecia Associated with Phakomatosis Pigmentovascularis Type IV Successfully Treated with Follicular Unit Transplantation

Temporal triangular alopecia (TTA), also known as congenital triangular alopecia, is a nonscarring, noninflammatroy, circumscribed form of alopecia. TTA has been associated with several disorders, such as Phakomatosis Pigmentovascularis. Hair restoration surgery using follicular unit transplantation has been a successful treatment modality for TTA. Herein we report such a success that was susta...

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Phakomatosis Pigmentovascularis: A case report

An eighteen-year old man is reported who had a large nevus spilus on the right side of his body with port wine stain on the anterior and posterior sides of his trunk without any systemic involvement. Considering the clinical signs and skin biopsy report of the patient, the diagnosis of phakomatosis pigmentovascularis type IIIa was made.

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Congenital triangular alopecia.

To cite: Lacarrubba F, Micali G. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013202918 DESCRIPTION A 4-year-old Caucasian girl presented with a 1-year history of asymptomatic, localised alopecia. Examination revealed a 3.5×3.0 cm area of alopecia over the right frontotemporal region of the scalp, with its apex towards the vertex (figure 1). There was no scali...

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Incidence of congenital triangular alopecia*

To the Editor, We read with interest the excellent article titled “Use of dermoscopy in the diagnosis of temporal triangular alopecia” by Campos et al.1 However, we take issue with their statement that the incidence of congenital triangular alopecia has been estimated at 0.11%.2 Taken at face value, readers may assume that 0.11% of the general population have congenital triangular alopecia. The...

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Phakomatosis pigmentovascularis type IIa

Phakomatosis Pigmentovascularis (PPV) is a rare cutaneous congenital malformation syndrome, defined as simultaneous occurrence of congenital cutaneous vascular and pigmentary anomalies. As most of the reported cases are from Far East countries, especially Japan, we reported a case of PPV type IIa in an Iranian patient. This case was unusual because of the coexistence of unilateral extensive por...

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ژورنال

عنوان ژورنال: Acta Dermato-Venereologica

سال: 2000

ISSN: 0001-5555

DOI: 10.1080/000155500750043041