Distal Extremity Necrosis as a Manifestation of Cutaneous Polyarteritis Nodosa: Case Report and Review of the Acute Management of a Pediatric Patient

2012 ◽  
Vol 29 (4) ◽  
pp. 473-478 ◽  
Author(s):  
Victoria L. Williams ◽  
Ricardo Guirola ◽  
Kristy Flemming ◽  
Gunjan M. Modi ◽  
Cecilia Rosales ◽  
...  
Keyword(s):  
Case Report ◽  
Pediatric Patient ◽  
Polyarteritis Nodosa ◽  
Acute Management ◽  
Distal Extremity ◽  
Cutaneous Polyarteritis Nodosa

scholarly journals Case report and review of minocycline-induced cutaneous polyarteritis nodosa

2005 ◽  
Vol 53 (3) ◽  
pp. 468-470 ◽  
Author(s):  
Brent Culver ◽  
Aleksandr Itkin ◽  
Ken Pischel
Keyword(s):  
Case Report ◽  
Polyarteritis Nodosa ◽  
Cutaneous Polyarteritis Nodosa

scholarly journals Acute Management of Tension Pneumocephalus in a Pediatric Patient: A Case Report

2018 ◽  
Vol 54 (1) ◽  
pp. 112-115
Author(s):  
Lauren M. L'Hommedieu ◽  
Michael W. Dingeldein ◽  
Krystal L. Tomei ◽  
Brendan J. Kilbane
Keyword(s):  
Case Report ◽  
Pediatric Patient ◽  
Acute Management ◽  
Tension Pneumocephalus

scholarly journals Cutaneous Polyarteritis Nodosa (cPAN) in ab 5 Years Old Girl

2018 ◽  
Vol 2 (5) ◽  
Author(s):  
Lubna Nazir
Keyword(s):  
Case Report ◽  
Skin Biopsy ◽  
Polyarteritis Nodosa ◽  
Clinical Course ◽  
Systemic Vasculitis ◽  
Separate Entity ◽  
Rare Form ◽  
Cutaneous Polyarteritis Nodosa ◽  
True Incidence ◽  
Hands And Feet

Polyarteritis nodosa is a rare form of systemic vasculitis. Cutaneous polyarteritis nodosa (cPAN) is subtype of systemic PAN which predominantly affects the skin, extra-cutaneous findings include fever, malaise, myalgias, arthralgias, and neuropathy. The true incidence of cutaneous PAN is unknown. cPAN is recognized as a separate entity and is essentially a benign disorder which should be distinguished from systemic PAN, as the clinical course and management of the two conditions is different. In this case report, we have described a patient with fever and gangrene of both hands and feet. The patient underwent a very extensive workup in order to determine the cause of her condition, which finally turned out cPAN on skin biopsy

Destructive arthritis with cutaneous polyarteritis nodosa requiring surgical intervention: a case report and review of the literature

2020 ◽  
Vol 4 (2) ◽  
pp. 272-277
Author(s):  
Takahiro Iwata ◽  
Hiromu Ito ◽  
Moritoshi Furu ◽  
Masahiro Ishikawa ◽  
Masayuki Azukizawa ◽  
...  
Keyword(s):  
Case Report ◽  
Polyarteritis Nodosa ◽  
Surgical Intervention ◽  
Review Of The Literature ◽  
Cutaneous Polyarteritis Nodosa

Case Report of Empagliflozin-Induced Cutaneous Polyarteritis Nodosa

2018 ◽  
Vol 22 (5) ◽  
pp. 516-518 ◽  
Author(s):  
Derek To ◽  
Scott Bradshaw ◽  
Jennifer Lipson
Keyword(s):  
Case Report ◽  
Polyarteritis Nodosa ◽  
Cutaneous Polyarteritis Nodosa ◽  
Subcutaneous Nodules ◽  
Full Resolution ◽  
First Case ◽  
Clinical Variant

Polyarteritis nodosa (PAN) is a rare vasculitis affecting medium-sized vessels. Cutaneous PAN is a clinical variant, and we report the first case of empagliflozin-induced cutaneous PAN in a 69-year-old man. After starting empagliflozin, the patient presented with tender subcutaneous nodules on his legs, which showed a medium-sized vessel vasculitis on histopathology. Upon cessation of this medication, he had full resolution of these nodules. This case illustrates that empagliflozin can induce cutaneous PAN, and further attention to this medication’s association with cutaneous PAN is warranted.

scholarly journals Cutaneous polyarteritis nodosa and tuberculosis in a child: a very rare case report

2021 ◽  
Author(s):  
Reinan Tavares Campos ◽  
Lucia Maria Mattei Arruda Campos ◽  
Clovis Arthur A Silva ◽  
Pedro Vale Bede ◽  
Maria Fernanda Badue Pereira ◽  
...  
Keyword(s):  
Case Report ◽  
Polyarteritis Nodosa ◽  
Rare Case ◽  
Cutaneous Polyarteritis Nodosa ◽  
Rare Case Report

scholarly journals Cutaneous polyarteritis nodosa and concurrent pseudoxanthoma elasticum–like phenotype: A case report

2020 ◽  
Vol 8 ◽  
pp. 2050313X2095311
Author(s):  
Roxana Mititelu ◽  
Larry W Cheung ◽  
Denis Sasseville
Keyword(s):  
Case Report ◽  
Genetic Testing ◽  
Comparative Genomic Hybridization ◽  
Polyarteritis Nodosa ◽  
Array Comparative Genomic Hybridization ◽  
Pseudoxanthoma Elasticum ◽  
Comparative Genomic ◽  
Unique Case ◽  
Cutaneous Polyarteritis Nodosa ◽  
Normal Limits

We report a unique case of a patient presenting with histologically confirmed pseudoxanthoma elasticum–like phenotype and cutaneous polyarteritis nodosa. Cardiac, gastroenterological, and ophthalmologic evaluations were within normal limits. Genetic evaluation was pertinent for absent ABCC6, ENPP1, and GGCX mutations and a normal array comparative genomic hybridization. Extensive workup revealed skin-limited cutaneous polyarteritis nodosa, and further genetic testing for ADA2 deficiency was negative. The cutaneous polyarteritis nodosa lesions had an excellent response to hydroxychloroquine and methotrexate. Pseudoxanthoma elasticum and polyarteritis nodosa are relatively uncommon, and our patient is among the first reported cases presenting with both pseudoxanthoma elasticum–like and polyarteritis nodosa. Furthermore, this case emphasizes the importance of a thorough cutaneous exam, as the patient had the lesions consistent with pseudoxanthoma elasticum–like since childhood and had previously gone undiagnosed.

A case report of cutaneous polyarteritis nodosa in siblings

2016 ◽  
Vol 28 (6) ◽  
pp. 1049-1052 ◽  
Author(s):  
Toshitaka Kizawa ◽  
Yuko Yoto ◽  
Miyako Mizukami ◽  
Takeshi Tsugawa ◽  
Takako Takeuchi ◽  
...  
Keyword(s):  
Case Report ◽  
Polyarteritis Nodosa ◽  
Cutaneous Polyarteritis Nodosa
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