ChloroquineV1, Main, Exploration, bibRecord, 001730

Cutaneous polyarteritis nodosa: a comprehensive review

Identifieur interne : 001730 ( Main/Exploration ); précédent : 001729; suivant : 001731

Cutaneous polyarteritis nodosa: a comprehensive review

Auteurs : Aaron Joseph Morgan [États-Unis] ; Robert A. Schwartz [États-Unis]

Source :

International Journal of Dermatology [ 0011-9059 ] ; 2010-07.

RBID : ISTEX:95E12FA7378379705147E6538D12179BC01EF198

English descriptors

Teeft :
- Acad, Acad dermatol, Arch dermatol, Arthralgia, Arthritis rheum, Case report, Clinical course, Complement levels, Constitutional symptoms, Corticosteroid, Cpan, Cutaneous, Cutaneous periarteritis nodosa, Cutaneous polyarteritis nodosa, Cutaneous vasculitis, Dermatol, Dermatol venereol, Dermatology, Dermatology morgan, Erythema, Erythema nodosum, Erythrocyte sedimentation rate, International journal, International society, Livedo, Livedo reticularis, Lower extremities, Mild cases, Myalgia, Ndings, Nodosa, Nodule, Periarteritis, Periarteritis nodosa, Polyarteritis, Polyarteritis nodosa, Reticularis, Review cutaneous polyarteritis nodosa, Rheum, Skin ulcers, Subcutaneous, Subcutaneous nodules, Subcutaneous tissue, Systemic, Systemic polyarteritis nodosa, Tender subcutaneous nodules, Ulceration, Urticarial vasculitis, Vasculitis.

Abstract

Cutaneous polyarteritis nodosa is a rare form of vasculitis relating to small‐to‐medium‐sized arteries. Its etiology is unknown. Clinical manifestations include tender subcutaneous nodules, livedo reticularis, cutaneous ulcers and necrosis. Although it is distinct from systemic polyarteritris nodosa in that it lacks significant internal organ involvement, extra‐cutaneous manifestations may be evident. Commonly encountered symptoms include fever, malaise, myalgias, arthralgias, and paresthesias. Exclusion of systemic polyarteritis nodosa is essential in diagnosis. The clinical course is chronic with remissions, relapses, and a favorable prognosis. Mild cases may resolve with nonsteroidal anti‐inflammatory drugs. If more severe, treatment with systemic corticosteroids generally achieves adequate response; however, adjunctive therapy is often necessary to allow reduction in steroid dosage.

Url:

https://api.istex.fr/ark:/67375/WNG-JL6VG5XM-G/fulltext.pdf

DOI: 10.1111/j.1365-4632.2010.04522.x

Affiliations:

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Le document en format XML

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<front><div type="abstract" xml:lang="en">Cutaneous polyarteritis nodosa is a rare form of vasculitis relating to small‐to‐medium‐sized arteries. Its etiology is unknown. Clinical manifestations include tender subcutaneous nodules, livedo reticularis, cutaneous ulcers and necrosis. Although it is distinct from systemic polyarteritris nodosa in that it lacks significant internal organ involvement, extra‐cutaneous manifestations may be evident. Commonly encountered symptoms include fever, malaise, myalgias, arthralgias, and paresthesias. Exclusion of systemic polyarteritis nodosa is essential in diagnosis. The clinical course is chronic with remissions, relapses, and a favorable prognosis. Mild cases may resolve with nonsteroidal anti‐inflammatory drugs. If more severe, treatment with systemic corticosteroids generally achieves adequate response; however, adjunctive therapy is often necessary to allow reduction in steroid dosage.</div>
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Cutaneous polyarteritis nodosa: a comprehensive review

Cutaneous polyarteritis nodosa: a comprehensive review

Source :

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri