Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Aug;95(33):e4626.
doi: 10.1097/MD.0000000000004626.

Shrinking lung syndrome in systemic lupus erythematosus: A case series and review of the literature

Affiliations
Review

Shrinking lung syndrome in systemic lupus erythematosus: A case series and review of the literature

Helena Borrell et al. Medicine (Baltimore). 2016 Aug.

Abstract

Shrinking lung syndrome (SLS) is a rare and less known complication mainly associated with systemic lupus erythematosus (SLE). In this study, we analyze the clinical features, investigation findings, approaches to management, and outcome in a case series of 9 adult patients with SLE and SLS diagnosed during a 35-year period in 3 referral tertiary care hospitals in Spain. Additionally, we reviewed 80 additional cases previously reported (PubMed 1965-2015). These 80 cases, together with our 9 patients, form the basis of the present analysis.The overall SLS prevalence in our SLE population was 1.1% (9/829). SLS may complicate SLE at any time over its course, and it usually occurs in patients without previous or concomitant major organ involvement. More than half of the patients had inactive lupus according to SELENA-systemic lupus erythematosus disease activity index (SLEDAI) scores. Typically, it presents with progressive exertional dyspnea of variable severity, accompanied by pleuritic chest pain in 76% of the cases.An important diagnostic delay is common. The diagnostic tools that showed better yield for SLS detection are the imaging techniques (chest x-ray and high-resolution computed tomography) along with pulmonary and diaphragmatic function tests. Evaluation of diaphragm dome motion by M-mode ultrasonography and phrenic nerve conduction studies are less useful.There are no standardized guidelines for the treatment of SLS in SLE. The majority of patients were treated with medium or high doses of glucocorticoids. Several immunosuppressive agents have been used in conjunction with steroids either if the patient fails to improve or since the beginning of the treatment. Theophylline and beta-agonists, alone or in combination with glucocorticoids, have been suggested with the intent to increase diaphragmatic strength.The overall long-term prognosis was good. The great majority of patients had significant clinical improvement and stabilization, or mild to moderate improvement on pulmonary function tests. The mortality rate was very low.

PubMed Disclaimer

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1
MEDLINE search: process selection.

Similar articles

Cited by

References

    1. Ahmed S, Herrick A, O’Driscoll BR. Shrinking lung syndrome in patients without systemic lupus erythematosus. Arthritis Rheum 2001; 44:243–245. - PubMed
    1. Blanco Pérez JJ, Pérez González A, Guerra Vales JL, et al. Shrinking lung in primary Sjögren's syndrome successfully treated with rituximab. Arch Bronconeumol 2015; 51:475–476. - PubMed
    1. Tavoni A, Vitali C, Cirigliano G, et al. Shrinking lung in primary Sjögren's syndrome. Arthritis Rheum 1999; 42:2249–2255. - PubMed
    1. Scirè CA, Caporali R, Zanierato M, et al. Shrinking lung syndrome in systemic sclerosis. Arthritis Rheum 2003; 48:2999–3000. - PubMed
    1. Hochberg MC. for the Diagnostic, Therapeutic Criteria Committee of the American College of Rheumatology. Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum 1997; 40:1725. - PubMed