منابع مشابه
Idiopathic eruptive macular pigmentation.
We present the case of a 10-year-old girl with a six months history of disseminated asymptomatic, brown pigmented macules on the trunk and proximal parts of the extremities. The clinical picture, histological findings, and the course of disease were similar to those of idiopathic eruptive macular pigmentation. The cutaneous lesions gradually disappeared over the next two years without any treat...
متن کاملIdiopathic eruptive macular pigmentation with papillomatosis: Report of nine cases.
Nine patients, seven males and two females aged 6-14 years, presented with extensive, asymptomatic, brown-black macules and mildly elevated, pigmented lesions of a few months' duration. The sites affected were the face, trunk and proximal extremities. The skin lesions were discrete and individual lesions were less than 2 cm in size. The clinical diagnoses rendered by the referring physicians we...
متن کاملIdiopathic Eruptive Macular Pigmentation in an Indian Male
64 Indian Dermatology Online Journal | Volume 9 | Issue 1 | January‐February 2018 Sir, We laud Subhadarshini et al.[1] for publication of their interesting case of idiopathic eruptive macular pigmentation in an Indian male. As they have pointed out this case differs from others described earlier in two aspects, namely, the persistence of lesions unchanged for 16 years and an aggravation thereaf...
متن کاملIdiopathic Eruptive Macular Pigmentation with Papillomatosis: An Unfamiliar Entity
Sir, Idiopathic eruptive macular pigmentation (IEMP) is an uncommon condition characterized by the presence of asymptomatic pigmented macules that involve face, trunk, and proximal extremities in children and adolescents, which gradually resolve over months or years without any residual pigmentation or scarring. Few cases have been reported in literature. We present a case of a 20‐year‐old fema...
متن کاملIdiopathic hyperphosphatasia with dermal pigmentation. A twenty-year follow-up.
Hyperphosphatasia, or hereditary bone dysplasia with hyperphosphatasaemia, is a rare genetic disorder which is characterised by failure to transform woven into lamellar bone. Clinical, radiological and histological features establish the diagnosis, fractures, deformities, diffuse sclerosis on radiographs and high serum alkaline phosphatase being characteristic. We report the case of a 27-year-o...
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ژورنال
عنوان ژورنال: Indian Journal of Dermatology
سال: 2007
ISSN: 0019-5154
DOI: 10.4103/0019-5154.33296