Results 11 to 20 of about 785 (150)

Acute generalized livedo racemosa caused by Capnocytophaga canimorsus identified by MALDI-TOF MS

International Journal of Infectious Diseases, 2015
Independent of the size of the dog and the type of injury, serious infections may follow a dog bite and these may result in the abrupt onset of multiorgan failure.
Eleni E Magira
exaly   +3 more sources

Cutaneous metastasis of urothelial carcinoma resulting in vascular occlusion and livedo racemosa [PDF]

JAAD Case Reports, 2020
Anita S. Savell, BS, Bryn Morris, BS, Michael R. Heaphy, Jr., MD   +2 more
doaj   +2 more sources

A case series of Sneddon syndrome: clinical features, diagnostic workup, and literature review [PDF]

BMC Neurology
Background Sneddon syndrome, a rare, non-inflammatory thrombotic vasculopathy characterized by livedo racemosa and cerebrovascular disease. Case presentation We present a case series of six women diagnosed with Sneddon syndrome.
Bruno Henrique Carneiro Costa Filho, Victor Ting Po Chy, João Augusto de Macedo Cavalcanti de Albuquerque, Pedro Jatobá Arteiro, Davi Alexandre Soares Neves, Mário Luciano de Mélo Silva Júnior, Eduardo Sousa de Melo   +6 more
doaj   +2 more sources

Clinical Characteristics and Disease Course of Livedoid Vasculopathy: A 10-Year Retrospective Analysis [PDF]

Clinical, Cosmetic and Investigational Dermatology
Yali Gao,1 Yaling Li,2 Dilixiati Mairepati,1,3 Haijian Wu,4 Junfeng Liu,5 Jiande Han,1 Hui Zhou1 1Department of Dermatology, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, Guangdong, 510080, People’s Republic of China; 2Department of ...
Gao Y, Li Y, Mairepati D, Wu H, Liu J, Han J, Zhou H   +6 more
doaj   +2 more sources

Successful treatment of Sneddon Syndrome with high dose intravenous immunoglobulin

JEADV Clinical Practice
Sneddon Syndrome is an orphan disease characterized by the clinical presence of livedo racemosa and cerebrovascular ischaemia. Its pathophysiology remains inadequately understood and no validated treatment modality has been established.
Markus Reitmajer, Stephan Forchhammer, Toni Silber   +2 more
doaj   +2 more sources

The Validation of the 2023 ACR/EULAR Antiphospholipid Syndrome Classification Criteria in a Cohort from Turkey [PDF]

Diagnostics
Background/Objectives: Our aim was to validate the performance of the American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) classification criteria for antiphospholipid syndrome (APS), published in 2023, in an APS cohort ...
Salim Mısırcı, Ali Ekin, Burcu Yağız, Belkıs Nihan Coşkun, Ediz Dalkılıç, Yavuz Pehlivan   +5 more
doaj   +2 more sources

Cutaneous Vasculitis as a Covid‐19 Manifestation: A Cross‐Sectional Study With Detailed Histopathological Evaluation

JEADV Clinical Practice
Background Although coronavirus disease 2019 (Covid‐19) primarily affects the lungs, dermatologic lesions can present as one of the extrapulmonary manifestations.
Reem Diab, Azadeh Rakhshan, Mohammad Shahidi Dadras, Sareh Salarinejad, Ali Kaddah, Zahra Razzaghi, Marwa Akhdar, Roxanna Sadoughifar, Fahimeh Abdollahimajd   +8 more
doaj   +2 more sources

Amantadine-induced livedo racemosa. [PDF]

BMJ Case Rep
Chakraborty U, Banerjee S, Chandra A, Sil A.   +3 more
europepmc   +3 more sources

Livedo racemosa and spontaneous retinal detachment as presenting signs of paraneoplastic sarcoid vasculitis [PDF]

JAAD Case Reports
Nadean F. Alnajjar, BS, Olivia M.T. Davies, MD, Ashley Gochoco, DO, Stephen R. Lyle, MD, PhD, Christopher Iriarte, MD   +4 more
doaj   +2 more sources

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

Romanian 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, Andreea Lili Barbulescu, Paulina Lucia Ciurea, Roxana Mihaela Dumitrascu, Beatrice Andreea Chisalau, Cristina Dorina Parvanescu, Sineta Cristina Firulescu, Florentin Ananu Vreju   +7 more
doaj   +1 more source