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

Year Number of Results
1976 1
1977 1
1978 1
1979 1
1980 1
1981 1
1983 3
1984 2
1985 1
1986 2
1987 1
1988 1
1989 2
1990 3
1991 2
1992 1
1993 2
1994 1
1995 5
1996 1
1997 6
1998 3
1999 6
2000 5
2001 5
2002 7
2003 6
2004 4
2005 5
2006 8
2007 11
2008 13
2009 10
2010 12
2011 7
2012 18
2013 16
2014 14
2015 16
2016 15
2017 15
2018 19
2019 19
2020 20
2021 18
2022 12
2023 15
2024 7

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308 results

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Page 1
Henoch-Schönlein Purpura (IgA Vasculitis): Rapid Evidence Review.
Reamy BV, Servey JT, Williams PM. Reamy BV, et al. Am Fam Physician. 2020 Aug 15;102(4):229-233. Am Fam Physician. 2020. PMID: 32803924 Free article. Review.
Henoch-Schonlein purpura, now called immunoglobulin A (IgA) vasculitis, is a systemic, immune complex-mediated, small-vessel leukocytoclastic vasculitis characterized by nonthrombocytopenic palpable purpura, arthritis, and abdominal pain. It is the most common vascu …
Henoch-Schonlein purpura, now called immunoglobulin A (IgA) vasculitis, is a systemic, immune complex-mediated, small-vessel leukocytoclasti …
Diagnosis and management of leukocytoclastic vasculitis.
Fraticelli P, Benfaremo D, Gabrielli A. Fraticelli P, et al. Intern Emerg Med. 2021 Jun;16(4):831-841. doi: 10.1007/s11739-021-02688-x. Epub 2021 Mar 13. Intern Emerg Med. 2021. PMID: 33713282 Free PMC article. Review.
Leukocytoclastic vasculitis (LCV) is a histopathologic description of a common form of small vessel vasculitis (SVV), that can be found in various types of vasculitis affecting the skin and internal organs. The leading clinical presentation of LCV is palpable purpura
Leukocytoclastic vasculitis (LCV) is a histopathologic description of a common form of small vessel vasculitis (SVV), that can be found in v …
Henoch-Schönlein Purpura in Children: An Updated Review.
Leung AKC, Barankin B, Leong KF. Leung AKC, et al. Curr Pediatr Rev. 2020;16(4):265-276. doi: 10.2174/1573396316666200508104708. Curr Pediatr Rev. 2020. PMID: 32384035 Review.
Approximately 90% of cases occur in children between 2 and 10 years of age, with a peak incidence at 4 to 7 years. The diagnosis should be based on the finding of palpable purpura in the presence of at least one of the following criteria, namely, diffuse abdominal p …
Approximately 90% of cases occur in children between 2 and 10 years of age, with a peak incidence at 4 to 7 years. The diagnosis should be b …
Diagnosing and treating ANCA-associated vasculitis: an updated review for clinical practice.
Chevet B, Cornec D, Casal Moura M, Cornec-Le Gall E, Fervenza FC, Warrington KJ, Specks U, Berti A. Chevet B, et al. Rheumatology (Oxford). 2023 May 2;62(5):1787-1803. doi: 10.1093/rheumatology/keac623. Rheumatology (Oxford). 2023. PMID: 36315063 Review.
When a diagnosis of AAV is suspected, as in patients with multisystem organ dysfunction or those with features such as chronic recurrent rhinosinusitis, cavitated lung nodules, palpable purpura or acute kidney injury, then appropriate further investigations are need …
When a diagnosis of AAV is suspected, as in patients with multisystem organ dysfunction or those with features such as chronic recurrent rhi …
Vasculitis-What Do We Have to Know? A Review of Literature.
Shavit E, Alavi A, Sibbald RG. Shavit E, et al. Int J Low Extrem Wounds. 2018 Dec;17(4):218-226. doi: 10.1177/1534734618804982. Epub 2018 Dec 3. Int J Low Extrem Wounds. 2018. PMID: 30501545 Review.
Therefore, the clinical presentation of vasculitis (most commonly palpable purpura on the lower extremities) dictates a thorough history, review of systems, and a meticulous physical examination. ...
Therefore, the clinical presentation of vasculitis (most commonly palpable purpura on the lower extremities) dictates a thorou …
IgA vasculitis.
Pillebout E, Sunderkötter C. Pillebout E, et al. Semin Immunopathol. 2021 Oct;43(5):729-738. doi: 10.1007/s00281-021-00874-9. Epub 2021 Jun 25. Semin Immunopathol. 2021. PMID: 34170395 Review.
The dominant clinical features include round or oval and retiform palpable purpura predominantly on the lower legs, arthralgia or arthritis, gastrointestinal bleeding or pain and glomerulonephritis with mesangial IgA deposits (IgAVN). ...
The dominant clinical features include round or oval and retiform palpable purpura predominantly on the lower legs, arthralgia …
Cutaneous Vasculitis: Review on Diagnosis and Clinicopathologic Correlations.
Frumholtz L, Laurent-Roussel S, Lipsker D, Terrier B. Frumholtz L, et al. Clin Rev Allergy Immunol. 2021 Oct;61(2):181-193. doi: 10.1007/s12016-020-08788-4. Clin Rev Allergy Immunol. 2021. PMID: 32378145 Review.
Involvement of small superficial vessels results mostly in urticarial, but relatively persistent plaques, papules, and palpable purpura. Involvement of vessels in the dermohypodermic junction or hypodermis results in ulcers, nodules, or livedo. ...
Involvement of small superficial vessels results mostly in urticarial, but relatively persistent plaques, papules, and palpable pu
Palpable Purpura.
Novotny RW, Trinh LN, Gowan AJ, Lomeli MC MD. Novotny RW, et al. Am Fam Physician. 2024 Mar;109(3):265-267. Am Fam Physician. 2024. PMID: 38574218 No abstract available.
Cryofibrinogen-Associated Glomerulonephritis.
Sethi S, Yachoui R, Murray DL, Radhakrishnan J, Alexander MP. Sethi S, et al. Am J Kidney Dis. 2017 Feb;69(2):302-308. doi: 10.1053/j.ajkd.2016.08.031. Epub 2016 Nov 17. Am J Kidney Dis. 2017. PMID: 27866967
Both patients presented with proteinuria and hematuria. One had significant cutaneous ulcers and palpable purpura. Kidney biopsy in both cases showed membranoproliferative glomerulonephritis with no immunoglobulin deposition. ...
Both patients presented with proteinuria and hematuria. One had significant cutaneous ulcers and palpable purpura. Kidney biop …
Small-vessel vasculitis.
Iglesias-Gamarra A, Restrepo JF, Matteson EL. Iglesias-Gamarra A, et al. Curr Rheumatol Rep. 2007 Aug;9(4):304-11. doi: 10.1007/s11926-007-0049-3. Curr Rheumatol Rep. 2007. PMID: 17688840 Review.
The classical clinical phenotype is leukocytoclastic vasculitis with palpable purpura, but manifestations vary widely depending upon the organs involved. ...
The classical clinical phenotype is leukocytoclastic vasculitis with palpable purpura, but manifestations vary widely dependin …
308 results