Preprint Review Version 1 Preserved in Portico This version is not peer-reviewed

Multidisciplinary Aproach: A Goal For The Management Of Complications In Systemic Scleroderma. Literature Review And Case Scenario

Version 1 : Received: 13 October 2023 / Approved: 18 October 2023 / Online: 18 October 2023 (17:05:56 CEST)

A peer-reviewed article of this Preprint also exists.

Pătrîntașu, D.-E.; Sárközi, H.K.; Lupușor, E.; Vlangăr, I.E.; Rotariu, G.-M.; Rența, I.-A.; Nan, A.-N.; Budin, C.E. A Multidisciplinary Approach as A Goal for the Management of Complications in Systemic Scleroderma: A Literature Review and Case Scenario. Diagnostics 2023, 13, 3332. Pătrîntașu, D.-E.; Sárközi, H.K.; Lupușor, E.; Vlangăr, I.E.; Rotariu, G.-M.; Rența, I.-A.; Nan, A.-N.; Budin, C.E. A Multidisciplinary Approach as A Goal for the Management of Complications in Systemic Scleroderma: A Literature Review and Case Scenario. Diagnostics 2023, 13, 3332.

Abstract

Systemic sclerosis (also known as scleroderma) is a chronic fibrosing autoimmune disease with both skin and multisystem organ involvement. Scleroderma has the highest mortality among all rheumatic diseases. The pathophysiology mechanism of systemic sclerosis is a progressive self-amplifying process, which implicates the widespread microvascular damage, followed by a dysregulation of innate and adaptive immunity and inflammation, and diffuse fibrosis of the skin and visceral organs. Fibrosis of internal organs is a hint for systemic sclerosis, moreover associated with interstitial lung disease (SSc-ILD) is a complex process. We report a case of a 56 years old female, diagnosed with Systemic Sclerosis 16 years ago. The systemic and clinical manifestations, respiratory functional tests, radiological aspects and specific therapy were discussed.

Keywords

systemic sclerosis; interstitial lung disease; lung diseases; Raynaud’s syndrome

Subject

Medicine and Pharmacology, Pathology and Pathobiology

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