Idiopathic Granulomatous Mastitis and Elastosis Perforans Serpiginosa: An Undescribed Association
نویسندگان
چکیده
منابع مشابه
Elastosis Perforans Serpiginosa
Elastosis perforans serpiginosa is a rare skin disease characterized by transepidermal elimination of abnormal elastic fibers. This condition classically presents as small papules arranged in serpiginous or annular patterns on the neck, face, arms, or other flexural areas. While these lesions may spontaneously resolve, they often persist for longer periods of time. Though numerous treatment mod...
متن کاملDrug-induced elastosis perforans serpiginosa.
To cite: Menzies S, Kirby B. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2015-212482 DESCRIPTION A 42-year-old woman presented with a 5-year history of multiple enlarging skin lesions. Her medical history was significant for Wilson’s disease, for which she had taken penicillamine for approximately 20 years. She had multiple small erythaematous keratotic papul...
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A 14-year-old girl was first seen with an 8-month history of an asymptomatic “rash” on her chin and a “wart” on her right hand. At physical examination, she had several pink papules coalescing into annular and arcuate plaques on the central aspect of her chin (Figure 1). She was also noted to have a single flesh-colored verrucous papule on her right palm, which was treated with liquid nitrogen ...
متن کاملD-penicillamine-induced Elastosis Perforans Serpiginosa
To the Editor: Elastosis perforans serpiginosa (EPS) is part of different kinds of perforating diseases that are dependent on factors such as idiopathic, reactive, or drug induced. We report here a case of a patient who presented with multiple reddish‐brown keratinized papules coalescing to form serpiginous plaques in the anterior and posterior of the neck, which was found to be typical D‐penic...
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A 22-year-old woman presented with a 2-year history of an eruption on the anterior aspect of her neck and right arm that was relatively asymptomatic. She had a history of cystinuria, which had been treated with D-penicillamine for several years, but the D-penicillamine therapy had been discontinued 2 years before the onset of the eruption. A biopsy was performed approximately 1 year before her ...
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ژورنال
عنوان ژورنال: American Journal of Clinical Pathology
سال: 2018
ISSN: 0002-9173,1943-7722
DOI: 10.1093/ajcp/aqy090.069