Malignant Atrophic Papulosis(Degos's Syndrome)
نویسندگان
چکیده
منابع مشابه
Malignant atrophic papulosis.
Malignant atrophic papulosis (MAP) is a rare disorder and only a few cases have been reported in blacks and Asians. A 38-year old male with typical cutaneous lesions of MAP which were confirmed histopathologically is reported.
متن کاملOlanzapine-Induced Neuroleptic Malignant Syndrome
Neuroleptic malignant syndrome (NMS) is a rare but life-threatening idiosyncratic side effect resulting from neuroleptic drugs. NMS mainly occurs in patients treated with high-potency typical antipsychotics, but rarely caused by atypical antipsychotics. Although NMS is less common with atypical antipsychotic, but it seems that its incidence is rising due to increased administration of such drug...
متن کاملDegos disease – malignant atrophic papulosis or cutaneointestinal lethal syndrome: rarity of the disease
BACKGROUND Degos disease is a very rare syndrome with a rare type of multisystem vasculopathy of unknown cause that affects the skin, gastrointestinal tract, and central nervous system. Other organs such as the kidneys, lungs, pleura, liver, heart, and eyes, can also be involved. OBJECTIVE To highlight the incidence of Degos disease with regard to age and sex, discuss the necessity of its acc...
متن کاملKöhlmeier-Degos Disease (malignant atrophic papulosis) and neurologic involvement.
Dr. Felipe Slaviero – Serviço de Neurologia e Neurocirurgia Rua Teixeira Soares 640 99010-901 Passo Fundo RS Brasil. E-mail: [email protected] The malignant atrophic papulosis (MAP) was first described by Köhlmeier in 1941 and recognized as a specific entity by Degos in 1942. This rare disorder is an obstructive vasculopathy of unknown origin, characterized by vascular lesions of the s...
متن کاملMalignant atrophic papulosis (Köhlmeier-Degos disease) - A review
UNLABELLED DEFINITION OF THE DISEASE: Malignant atrophic papulosis (MAP), described independently by Köhlmeier and Degos et al., is a rare, chronic, thrombo-obliterative vasculopathy characterized by papular skin lesions with central porcelain-white atrophy and surrounding teleangiectatic rim. EPIDEMIOLOGY Less than 200 cases have been described in the literature. The first manifestation of M...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1964
ISSN: 0035-9157
DOI: 10.1177/003591576405700632