نتایج جستجو برای: embolia cutis medicamentosa
تعداد نتایج: 2813 فیلتر نتایج به سال:
Two unrelated patients of different sexes are described, both presenting with congenital redundant skin (cutis laxa), growth deficiency, mental retardation and bone dystrophy. Parental consanguinity in both families and a more pronounced severity of the neurological disease in the male patient were present. Both patients were diagnosed in infancy as having De Barsy syndrome, but clinical follow...
INTRODUCTION Calcinosis circumscripta is a form of ectopic mineralization characterized by single or multiple cutaneous nodules containing calcium salts. Calcinosis cutis circumscripta is a very rare form of idiopathic calcinosis cutis arising in the second half oflife. It typically involves the extremities and is associated with prior trauma and scleroderma. We dealt with a very rare form of c...
Aleukemic leukemia cutis is a rare condition in which patients have skin lesions containing leukemic cells before evidence of leukemia can be detected in the peripheral blood. There are only 23 cases of this phenomenon documented in the English literature. We describe a 62-year-old woman who developed a diffuse, clinically benign-appearing cutaneous eruption, which histologically showed an atyp...
The cutis laxa syndromes are multisystem disorders that share loose redundant inelastic and wrinkled skin as a common hallmark clinical feature. The underlying molecular defects are heterogeneous and 13 different genes have been involved until now, all of them being implicated in elastic fiber assembly. We provide here molecular and clinical characterization of three unrelated patients with a v...
522 Ann Dermatol Received November 15, 2012, Revised January 25, 2013, Accepted for publication January 28, 2013 Corresponding author: Hans Jürgen Hoffmann, Allergy Center for West Denmark, Department of Pulmonary Medicine, Health: Aarhus University, Building 2b, Nørrebrogade 44, DK 8000 Aarhus C, Denmark. Tel: 45-78462107, Fax: 45-78462110, E-mail: hans.jurgen.hoffmann @ki.au.dk This is an Ope...
Nearly 68% of patients with cutis marmorata have a congenital abnormality, the most common being body asymmetry. Cutis marmorata has also been shown to be associated with the chiari malformations, macrocephaly, hemimegalencephaly, bilateral cortical dysplasia, calvarial haemangioma and cavum septi pellucidum cysts.2 In fact, this subset of patients may have developmental delay and are now class...
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