Generalized keratosis pilaris associated with erythromelanosis follicularis faciei et colli: A rare coexistence
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چکیده
منابع مشابه
Erythromelanosis follicularis faciei et colli with reticulated hyperpigmentation of the extremities
Erythromelanosis follicularis faciei et colli (EFFC) is a distinct, rare, and underdiagnosed condition of unknown etiology that is characterized by well-demarcated erythema, hyperpigmentation, and follicular papules. The pigmentation is usually on both maxillary, preauricular regions, and the cheeks. We report a case of a 12-year-old boy with EFFC that was associated with reticulated pigmentati...
متن کاملErythrosis pigmentosa mediofacialis (Brocq) and erythromelanosis follicularis faciei et colli in the same patient.
Erythrosis pigmentosa peribuccalis (Brocq) (or erythrosis pigmentosa mediofacialis) and erythromelanosis follicularis faciei et colli, have been regarded as different disorders, mainly because the first occurs on the mediofacial area and is common in women and the second mostly occurs pre-auricularly in men. Both conditions show histological signs of abnormal follicular keratinization with tele...
متن کاملErythromelanosis Follicularis Faciei: A Case Report and Review of the Literature.
Erythromelanosis follicularis faciei is a rare sporadic condition of unknown etiology characterized by reddish-brownish patches and follicular papules that appear commonly on the face and rarely on the neck. Herein, we report a 16-year-old male who had asymptomatic facial skin lesions since early childhood. His family history revealed a similar case in his younger brother. His parents are not c...
متن کاملLong-pulsed dye laser for the treatment of erythromelanosis follicularis faciei: report of two clinical cases.
Two Japanese men complained of redness of their jowls and requested treatment of those areas. Examination revealed welldemarcated reddish-brown pigmentation with granular texture on both sides of the cheeks. The redness of the lesion was mainly caused by dilation of superficial vessels and vanished when pressure was applied. Both patients were diagnosed as EFF by the classical triad, which is c...
متن کاملRare ocular manifestations in keratosis follicularis (Darier–White disease)
Keratosis follicularis (Darier's disease) is a rare (1 in 30,000-100,000) genetic autosomal-dominant predominantly dermatological disorder characterized by hyperkeratosis and acantholysis due to a defective calcium transport in the cells. Ocular findings, if present, are very rare in this condition. Here, we are reporting a case of keratosis follicularis (Darier's disease) with ocular manifesta...
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ژورنال
عنوان ژورنال: Indian Journal of Paediatric Dermatology
سال: 2015
ISSN: 2319-7250
DOI: 10.4103/2319-7250.160665