Hypopigmented macules of the limbs in two sisters: report on familial Bier spots*
نویسندگان
چکیده
Bier spots are asymptomatic, small, irregular, hypopigmented macules characterized by a normal histological appearance, which are usually found on the arms and legs of young adults. We describe the simultaneous presence of Bier spots in two siblings. This finding is unusual since, to the best of our knowledge, concurrent familial cases have never been reported in the literature.
منابع مشابه
Bier’s spots with onset in childhood*
Bier spots are small, irregular, hypopigmented macules that are usually found on the arms and legs. The macules disappear when the limb is raised. Bier spots have been reported in association with a number of conditions but there is no consistent association to specific desease. Although they usually affect young adults, we report a case of Bier spots that began in childhood. As an asymptomatic...
متن کاملBier spots: a benign vascular anomaly.
To cite: He A, Kwatra SG, Kim N, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2016214761 DESCRIPTION A 26-year-old woman with a reported history of tinea versicolour presented for persistent hypopigmentation on her bilateral forearms. Detailed examination revealed multiple small (5–10 mm), irregularly shaped white macules on the extensor surfaces of the ...
متن کاملA report of two cases of sarcoidosis in a family(brother and sister):case report
sarcoidosis is a granulomatius disease of unknown etiology involving multiple body systems.approximately 10-35% of patients with systemic disease have cutaneous involvement.skin lesions commonly observed in sarcoidosis include:erythema nodosum,macular or parpular rashes,nodules,hypopigmented or hyperpigmented patches,scarsarcoid,lupus pernio,plaques,and rarely mocusal lesions.this report descri...
متن کاملگزارش یک مورد از تومورهای گرد در رتین به همراه هامارتومای بینی دریک بیمار مبتلا به توبروزاسکلروزیس
Introduction: Tuberous Sclerosis (TS) is an autosomal dominant disease that affects the brain, skin, eye, heart, kidney even bones. The commonest presentation is seizures in infancy or early childhood (in 80% of cases), mental retardation (in 44%of cases). Characteristic skin lesion includes facial angiofibromas, adenoma sebaceum, hypopigmented macules, shagreen patches ungual ungual fibromas...
متن کاملProgressive hyperpigmentation and generalized lentiginosis without associated systemic symptoms: a rare hereditary pigmentation disorder in south-east Germany.
Familial progressive hyperpigmentation is rarely described in the literature. We report on five patients from three different families presenting with a peculiar progressive pigmentary disorder. The patients show a progressive diffuse, partly blotchy, hyperpigmentation, intermixed with scattered small hypopigmented macules, a few large hypopigmented areas, occasional café-au-lait spots and, mos...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره 90 شماره
صفحات -
تاریخ انتشار 2015