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Year Number of Results
1985 1
1990 1
1993 1
1997 2
1999 1
2000 2
2002 1
2003 2
2004 1
2005 1
2006 1
2008 2
2009 2
2010 2
2011 1
2012 2
2013 1
2014 2
2015 1
2016 3
2017 2
2019 5
2020 5
2021 9
2022 5
2023 4
2024 0

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53 results

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Page 1
Sneddon Syndrome: A Comprehensive Overview.
Samanta D, Cobb S, Arya K. Samanta D, et al. J Stroke Cerebrovasc Dis. 2019 Aug;28(8):2098-2108. doi: 10.1016/j.jstrokecerebrovasdis.2019.05.013. Epub 2019 May 31. J Stroke Cerebrovasc Dis. 2019. PMID: 31160219 Review.
Sneddon syndrome (SS) is an episodic or chronic, slowly progressive disorder and characterized by generalized livedo racemosa (patchy, violaceous, skin discoloration) and recurrent cerebrovascular events. ...Neurological manifestations usually occur in 3 phases: (1) …
Sneddon syndrome (SS) is an episodic or chronic, slowly progressive disorder and characterized by generalized livedo racemosa …
Rivaroxaban Versus Vitamin K Antagonist in Antiphospholipid Syndrome: A Randomized Noninferiority Trial.
Ordi-Ros J, Sáez-Comet L, Pérez-Conesa M, Vidal X, Riera-Mestre A, Castro-Salomó A, Cuquet-Pedragosa J, Ortiz-Santamaria V, Mauri-Plana M, Solé C, Cortés-Hernández J. Ordi-Ros J, et al. Ann Intern Med. 2019 Nov 19;171(10):685-694. doi: 10.7326/M19-0291. Epub 2019 Oct 15. Ann Intern Med. 2019. PMID: 31610549 Clinical Trial.
Post hoc analysis suggested an increased risk for recurrent thrombosis in rivaroxaban-treated patients with previous arterial thrombosis, livedo racemosa, or APS-related cardiac valvular disease. LIMITATION: Anticoagulation intensity was not measured in the rivaroxa …
Post hoc analysis suggested an increased risk for recurrent thrombosis in rivaroxaban-treated patients with previous arterial thrombosis, …
UBA1 Variations in Neutrophilic Dermatosis Skin Lesions of Patients With VEXAS Syndrome.
Zakine E, Schell B, Battistella M, Vignon-Pennamen MD, Chasset F, Mahévas T, Cordoliani F, Adès L, Sébert M, Delaleu J, Jachiet M, Lepelletier C, Lemaire P, Chauvel C, Dhouaieb B, Kim R, Cassius C, Georgin-Lavialle S, Mekinian A, Bagot M, Braun T, Rousset L, Begon E, de Masson A, Fenaux P, Clappier E, Bouaziz JD. Zakine E, et al. JAMA Dermatol. 2021 Nov 1;157(11):1349-1354. doi: 10.1001/jamadermatol.2021.3344. JAMA Dermatol. 2021. PMID: 34495287 Free PMC article.
All patients had neutrophilic dermatosis skin lesions, including tender red or violaceous papules, sometimes edematous, without fever, arthralgia, recurrence or pathergy, inflammatory edematous papules on the neck and trunk (sometimes umbilicated), and firm erythematous purpuric …
All patients had neutrophilic dermatosis skin lesions, including tender red or violaceous papules, sometimes edematous, without fever, arthr …
Livedo Racemosa: Clinical, Laboratory, and Histopathological Findings in 33 Patients.
Pincelli MS, Echavarria AMJ, Criado PR, Marques GF, Morita TCAB, Valente NYS, de Carvalho JF. Pincelli MS, et al. Int J Low Extrem Wounds. 2021 Mar;20(1):22-28. doi: 10.1177/1534734619896938. Epub 2020 Jan 29. Int J Low Extrem Wounds. 2021. PMID: 31996060
Livedo racemosa is a cutaneous finding characterized by a persistent, erythematous, or violaceous discoloration of the skin, in a broken, branched, discontinuous, and irregular pattern. A retrospective review of 33 cases with clinical diagnosis of livedo r …
Livedo racemosa is a cutaneous finding characterized by a persistent, erythematous, or violaceous discoloration of the skin, i …
Livedo racemosa in neurological diseases: an update on the differential diagnoses.
Mitri F, Enk A, Bersano A, Kraemer M. Mitri F, et al. Eur J Neurol. 2020 Oct;27(10):1832-1843. doi: 10.1111/ene.14390. Epub 2020 Jul 2. Eur J Neurol. 2020. PMID: 32526049 Review.
The physiological livedo reticularis usually appears in cold conditions, whereas the pathological and irregular livedo, which persists in warm temperatures, is often labeled as 'livedo racemosa'. Some neurological pathologies are associated with livedo, most commonl …
The physiological livedo reticularis usually appears in cold conditions, whereas the pathological and irregular livedo, which persists in wa …
A clinicopathological description of COVID-19-induced chilblains (COVID-toes) correlated with a published literature review.
Kolivras A, Thompson C, Pastushenko I, Mathieu M, Bruderer P, de Vicq M, Feoli F, Harag S, Meiers I, Olemans C, Sass U, Dehavay F, Fakih A, Lam-Hoai XL, Marneffe A, Van De Borne L, Vandersleyen V, Richert B. Kolivras A, et al. J Cutan Pathol. 2022 Jan;49(1):17-28. doi: 10.1111/cup.14099. Epub 2021 Aug 9. J Cutan Pathol. 2022. PMID: 34272741 Free PMC article. Review.
Patients presenting with acral lesions should be isolated, and chilblains should be distinguished from thrombotic lesions (livedo racemosa, retiform purpura, or ischemic acral necrosis)....
Patients presenting with acral lesions should be isolated, and chilblains should be distinguished from thrombotic lesions (livedo …
A review of pediatric vasculitis with a focus on juvenile polyarteritis nodosa.
Kawakami T. Kawakami T. Am J Clin Dermatol. 2012 Dec 1;13(6):389-98. doi: 10.2165/11599660-000000000-00000. Am J Clin Dermatol. 2012. PMID: 22845169 Review.
The common cutaneous manifestations include cutaneous nodules and livedo racemosa. Our research group previously established an algorithm for the differential diagnosis of primary cutaneous vasculitis. ...
The common cutaneous manifestations include cutaneous nodules and livedo racemosa. Our research group previously established a …
Clinical classification of vasculitis.
Sunderkötter C, Sindrilaru A. Sunderkötter C, et al. Eur J Dermatol. 2006 Mar-Apr;16(2):114-24. Eur J Dermatol. 2006. PMID: 16581560 Review.
As such, panarteritis nodosa involves medium-sized vessels and presents on the skin with subcutaneous nodules and livedo racemosa, while it does not cause glomerulonephritis. Leukocytoclastic vasculitis (LcV) involves the small vessels, resulting in palpable purpura …
As such, panarteritis nodosa involves medium-sized vessels and presents on the skin with subcutaneous nodules and livedo racemosa …
The Spectrum of the Deficiency of Adenosine Deaminase 2: An Observational Analysis of a 60 Patient Cohort.
Barron KS, Aksentijevich I, Deuitch NT, Stone DL, Hoffmann P, Videgar-Laird R, Soldatos A, Bergerson J, Toro C, Cudrici C, Nehrebecky M, Romeo T, Jones A, Boehm M, Kanakry JA, Dimitrova D, Calvo KR, Alao H, Kapuria D, Ben-Yakov G, Pichard DC, Hathaway L, Brofferio A, McRae E, Moura NS, Schnappauf O, Rosenzweig S, Heller T, Cowen EW, Kastner DL, Ombrello AK. Barron KS, et al. Front Immunol. 2022 Jan 10;12:811473. doi: 10.3389/fimmu.2021.811473. eCollection 2021. Front Immunol. 2022. PMID: 35095905 Free PMC article.
The deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessively inherited disease that has undergone extensive phenotypic expansion since being first described in patients with fevers, recurrent strokes, livedo racemosa, and polyarteritis nodosa in 2014. …
The deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessively inherited disease that has undergone extensive phenotypic expans …
Clinical characteristics of Martorell hypertensive ischaemic leg ulcer.
Karppinen JJ, Kallio M, Lappalainen K, Lagus H, Matikainen N, Isoherranen K. Karppinen JJ, et al. J Wound Care. 2023 Dec 2;32(12):797-804. doi: 10.12968/jowc.2023.32.12.797. J Wound Care. 2023. PMID: 38060417
OBJECTIVE: We sought to characterise the clinical picture of Martorell hypertensive ischaemic leg ulcer (HYTILU) by describing the ulcer borders with three clinical features: 'the red lipstick sign'; purple border; and livedo racemosa. We also aimed to characterise …
OBJECTIVE: We sought to characterise the clinical picture of Martorell hypertensive ischaemic leg ulcer (HYTILU) by describing the ulcer bor …
53 results