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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 1
1964 1
1973 1
1976 1
1980 2
1982 2
1983 2
1986 1
1987 1
1989 2
1990 8
1991 2
1992 1
1993 2
1994 10
1995 12
1996 6
1997 3
1998 8
1999 4
2000 2
2001 4
2002 1
2003 7
2004 4
2005 3
2006 1
2007 8
2008 3
2009 2
2010 4
2011 1
2012 3
2013 7
2014 3
2015 3
2016 7
2017 8
2018 5
2019 10
2020 5
2021 5
2022 4
2023 4

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164 results

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Page 1
Polyarteritis nodosa revisited: a review of historical approaches, subphenotypes and a research agenda.
Karadag O, Jayne DJ. Karadag O, et al. Clin Exp Rheumatol. 2018 Mar-Apr;36 Suppl 111(2):135-142. Epub 2018 Feb 20. Clin Exp Rheumatol. 2018. PMID: 29465365 Free article. Review.
Polyarteritis nodosa (PAN) is a rare form of primary systemic vasculitis with heterogeneous presentations, treatments and disease course. ...Monogenic disorders similar to PAN have been described (familial Mediterranean fever, Adenosine Deaminase-2 deficiency), and …
Polyarteritis nodosa (PAN) is a rare form of primary systemic vasculitis with heterogeneous presentations, treatments and dise …
Management of cutaneous vasculitis.
Micheletti RG, Pagnoux C. Micheletti RG, et al. Presse Med. 2020 Oct;49(3):104033. doi: 10.1016/j.lpm.2020.104033. Epub 2020 Jul 6. Presse Med. 2020. PMID: 32645416 Review.
Cutaneous vasculitis encompasses cutaneous components of systemic vasculitides, skin-limited variants of systemic vasculitides, such as IgA vasculitis or cutaneous polyarteritis nodosa, and single-organ cutaneous vasculitis, as individual …
Cutaneous vasculitis encompasses cutaneous components of systemic vasculitides, skin-limited variants of systemic vasculitides …
VEXAS syndrome (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) for the dermatologist.
Sterling D, Duncan ME, Philippidou M, Salisbury JR, Kulasekararaj AG, Basu TN. Sterling D, et al. J Am Acad Dermatol. 2023 Dec;89(6):1209-1214. doi: 10.1016/j.jaad.2022.01.042. Epub 2022 Feb 2. J Am Acad Dermatol. 2023. PMID: 35121074 Review.
There have already been 141 confirmed published cases since original publication, 126 of which had documented cutaneous signs.(1-34) A wide range of skin presentations are reported, including Sweet-like urticated and tender erythematous nodules, cartilaginous involvement w …
There have already been 141 confirmed published cases since original publication, 126 of which had documented cutaneous signs.(1-34) …
[Cutaneous polyarteritis nodosa].
Turska M, Parada-Turska J. Turska M, et al. Wiad Lek. 2018;71(1 pt 1):73-77. Wiad Lek. 2018. PMID: 29558355 Review. Polish.
Cutaneous polyarteritis nodosa is a rare disease that affects vessels of the deep skin and the subcutaneous tissue. ...Cutaneous polyarteritis nodosa can also cause extracutaneous symptoms (fever, malaise, myalgias, arthralgias, neuropath …
Cutaneous polyarteritis nodosa is a rare disease that affects vessels of the deep skin and the subcutaneous tissue. ... …
Polyarteritis nodosa.
Forbess L, Bannykh S. Forbess L, et al. Rheum Dis Clin North Am. 2015;41(1):33-46, vii. doi: 10.1016/j.rdc.2014.09.005. Rheum Dis Clin North Am. 2015. PMID: 25399938 Review.
Polyarteritis nodosa (PAN) is a systemic disease, but variants are cutaneous PAN and single-organ disease. ...
Polyarteritis nodosa (PAN) is a systemic disease, but variants are cutaneous PAN and single-organ disease. ...
Polyarteritis Nodosa Neurologic Manifestations.
de Boysson H, Guillevin L. de Boysson H, et al. Neurol Clin. 2019 May;37(2):345-357. doi: 10.1016/j.ncl.2019.01.007. Epub 2019 Mar 16. Neurol Clin. 2019. PMID: 30952413 Review.
Polyarteritis nodosa (PAN) is a necrotizing vasculitis affecting medium-sized vessels whose main manifestations are weight loss, fever, peripheral neuropathy, renal, musculoskeletal, gastrointestinal tract and/or cutaneous involvement(s), hypertension and/or …
Polyarteritis nodosa (PAN) is a necrotizing vasculitis affecting medium-sized vessels whose main manifestations are weight los …
Cutaneous polyarteritis nodosa.
Díaz-Pérez JL, De Lagrán ZM, Díaz-Ramón JL, Winkelmann RK. Díaz-Pérez JL, et al. Semin Cutan Med Surg. 2007 Jun;26(2):77-86. doi: 10.1016/j.sder.2007.02.003. Semin Cutan Med Surg. 2007. PMID: 17544958 Review.
The term polyarteritis nodosa (PAN) presently includes classic systemic PAN, cutaneous PAN, and microscopic PAN (microscopic polyangeiitis). ...Histopathologically, cutaneous PAN shows a single artery involved with diagnostic inflammatory changes. ...
The term polyarteritis nodosa (PAN) presently includes classic systemic PAN, cutaneous PAN, and microscopic PAN (micros …
Granulomatous Vasculitis.
Sharma A, Dogra S, Sharma K. Sharma A, et al. Dermatol Clin. 2015 Jul;33(3):475-87. doi: 10.1016/j.det.2015.03.012. Dermatol Clin. 2015. PMID: 26143427 Review.
This group includes granulomatous vasculitides, namely, granulomatosis with polyangiitis (GPA), eosinophilic granulomatosis with polyangiitis (EGPA), and nongranulomatous vasculitis, namely, microscopic polyangiitis (MPA). Classic polyarteritis nodosa (PAN) is a gra …
This group includes granulomatous vasculitides, namely, granulomatosis with polyangiitis (GPA), eosinophilic granulomatosis with polyangiiti …
Cutaneous polyarteritis nodosa: a comprehensive review.
Morgan AJ, Schwartz RA. Morgan AJ, et al. Int J Dermatol. 2010 Jul;49(7):750-6. doi: 10.1111/j.1365-4632.2010.04522.x. Int J Dermatol. 2010. PMID: 20618492 Review.
Cutaneous polyarteritis nodosa is a rare form of vasculitis relating to small-to-medium-sized arteries. ...Clinical manifestations include tender subcutaneous nodules, livedo reticularis, cutaneous ulcers and necrosis. Although it is distinct from syst …
Cutaneous polyarteritis nodosa is a rare form of vasculitis relating to small-to-medium-sized arteries. ...Clinical man …
Lymphocytic Thrombophilic Arteritis: A Review.
Vakili S, Zampella JG, Kwatra SG, Blanck J, Loss M. Vakili S, et al. J Clin Rheumatol. 2019 Apr;25(3):147-152. doi: 10.1097/RHU.0000000000000846. J Clin Rheumatol. 2019. PMID: 30044260 Review.
Macular lymphocytic arteritis or lymphocytic thrombophilic arteritis (LTA) is a recently described cutaneous arteritis that is characterized by asymptomatic macules and patches of the extremities associated with lymphocytic arteritis at the deep dermal/subcuticular junctio …
Macular lymphocytic arteritis or lymphocytic thrombophilic arteritis (LTA) is a recently described cutaneous arteritis that is charac …
164 results