Literature DB >> 24767183

Sarcoidosis as a systemic disease.

Virendra N Sehgal1, Najeeba Riyaz2, Kingshuk Chatterjee3, Pradeep Venkatash4, Sonal Sharma5.   

Abstract

Sarcoidosis is a systemic disease, where for the abnormal localized collections of chronic inflammatory cells, the granuloma is cardinal, which may result in the formation of nodule(s) in the tissue of any organ of the body, with lungs and lymph nodes involvement being the most common. The granulomas are nonnecrotizing. The disease may either be asymptomatic or chronic. Its onset is gradual and may improve or clear up spontaneously. Clinical features of specific and nonspecific cutaneous lesions are described, emphasizing their role as a prelude to its systemic manifestations, afflicting respiratory, liver, spleen, musculoskeletal, ocular, cardiac, and neurologic systems. The salient briefs of diagnostic procedures are outlined, in addition to historical background and etiopathogenesis. Several currently available treatment modalities are outlined for instant reference.
Copyright © 2014 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 24767183     DOI: 10.1016/j.clindermatol.2013.11.002

Source DB:  PubMed          Journal:  Clin Dermatol        ISSN: 0738-081X            Impact factor:   3.541


  4 in total

1.  Ocular involvement in sarcoidosis.

Authors:  Vinay Kansal; Michael Dollin
Journal:  CMAJ       Date:  2017-04-24       Impact factor: 8.262

Review 2.  [Facial manifestations of granulomatous diseases].

Authors:  F Butsch
Journal:  Hautarzt       Date:  2017-07       Impact factor: 0.751

Review 3.  Sarcoidosis and the heart: A review of the literature.

Authors:  Emrah Ipek; Selami Demirelli; Emrah Ermis; Sinan Inci
Journal:  Intractable Rare Dis Res       Date:  2015-11

Review 4.  Sarcoid Uveitis: An Intriguing Challenger.

Authors:  Pia Allegri; Sara Olivari; Federico Rissotto; Roberta Rissotto
Journal:  Medicina (Kaunas)       Date:  2022-07-04       Impact factor: 2.948

  4 in total

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