Results 31 to 40 of about 4,331 (188)

Síndroma antifosfolipídica associado a síndroma de Sneddon com envolvimento cardíaco: um diagnóstico desafiante

open access: yesRevista Portuguesa de Cardiologia, 2014
Resumo: A síndroma de Sneddon é uma entidade rara caracterizada pela associação de doença cerebrovascular isquémica e livedo reticularis. Os autores apresentam um caso de acidente vascular cerebral isquémico e enfarte do miocárdio em doente com síndroma ...
Ana Faustino   +6 more
doaj   +1 more source

Oxalosis and Livedo Reticularis

open access: yesActas Dermo-Sifiliográficas (English Edition), 2013
Oxalosis is a disease caused by the deposition of calcium oxalate in extrarenal tissues, most commonly bone, myocardium, retina, blood vessels, and skin, causing the clinical manifestations of the disease. Involvement of the blood vessels of the skin can give rise to livedo reticularis, acrocyanosis, ulcers, and gangrene.
E, Jorquera-Barquero   +3 more
openaire   +2 more sources

Nicolau Syndrome in a Child Caused by Penicillin Injection [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2022
A wide range of side effects can occur during drug administration. Nicolau Syndrome (NS) is a rare iatrogenic side effect of medications injected Intramuscularly (i.m.). The clinical manifestations range from localised pain and erythema to total necrosis
Rafat Abdulroof Alkadi   +3 more
doaj   +1 more source

Livedo reticularis in type 2 lepra reaction: A rare presentation

open access: yesIndian Dermatology Online Journal, 2014
Type 2 lepra reaction or erythema nodosum leprosum (ENL) is an immune complex syndrome that occurs mostly in lepromatous leprosy and sometimes in borderline lepromatous leprosy patients.
Kikkeri Narayanasetty Naveen   +3 more
doaj   +1 more source

Distal phalangeal erythema in an infant with biallelic PDSS1 mutations: Expanding the phenotype of primary Coenzyme Q10 deficiency

open access: yesJIMD Reports, 2021
We report a detailed clinical examination in a patient with primary coenzyme Q10 deficiency caused by biallelic mutations in the PDSS1 gene who presented clinical features of mitochondrial encephalopathy associated with pulmonary hypertension, livedo ...
Marcello Bellusci   +3 more
doaj   +1 more source

Livedoid vasculopathy – A diagnostic and therapeutic challenge

open access: yesFrontiers in Medicine, 2022
Livedoid vasculopathy is a rare, chronic-recurrent occlusive disorder in the microcirculation of dermal vessels. The clinical appearance is characterized by Livedo racemosa, painful ulceration, located in the distal parts of the lower extremities ...
Maria Rosa Burg   +3 more
doaj   +1 more source

A retrospective study on the prevalence of anti-phospholipid antibodies, thrombotic events and cutaneous signs of vasculopathy in 173 hospitalized COVID-19 patients

open access: yesInternational Journal of Immunopathology and Pharmacology, 2021
Background Hypercoagulability is a risk factor of thromboembolic events in COVID-19. Anti-phospholipid (aPL) antibodies have been hypothesized to be involved.
Giulia Gasparini MD   +8 more
doaj   +1 more source

LIVEdoid vasculopathy – benefit of intravenous immunoglobulin in a refractory case [PDF]

open access: yesRomanian Journal of Rheumatology, 2021
Livedoid vasculopathy is a rare vascular disease which typically manifests as recurrent ulcerative lesions on the lower extremities. It is classified as a vasculopathy, not a true vasculitis, and defined as a vasooclusive syndrome, caused by non ...
Stefan Cristian Dinescu   +7 more
doaj   +1 more source

Unilateral Livedoid Hyperpigmentation of the Lower Extremity

open access: yesGraduate Medical Education Research Journal, 2021
Mentor: Ashley Wysong Program: Dermatology Type: Case Report Background: Erythema ab igne is a clinical diagnosis that comes with a broad differential diagnosis.
Dillon Clarey   +2 more
doaj   +1 more source

Epithelioid angiosarcoma revealed by livedoid distal vascular emboli

open access: yesHuman Pathology: Case Reports, 2018
Angiosarcomas are rare malignant mesenchymal tumours with endothelial differentiation, which may arise in any organ. Angiosarcoma of the aorta is even more exceptional.
Annika Fournier, MD   +6 more
doaj   +1 more source

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