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[Shrinking lung syndrome in systemic lupus erythematosus: A study of 9 patients]. / Síndrome del pulmón encogido asociado a lupus eritematoso sistémico: estudio de 9 pacientes.
Casey, Alberto; Enghelmayer, Juan I; Legarreta, Cora G; Berón, Ana María; Perín, María Marta; Dubinsky, Diana.
Afiliación
  • Casey A; División de Neumonología, Hospital de Clínicas, Universidad de Buenos Aires, Buenos Aires, Argentina.
  • Enghelmayer JI; División de Neumonología, Hospital de Clínicas, Universidad de Buenos Aires, Buenos Aires, Argentina. Electronic address: jiedsn@gmail.com.
  • Legarreta CG; División de Neumonología, Hospital de Clínicas, Universidad de Buenos Aires, Buenos Aires, Argentina.
  • Berón AM; División de Reumatología, Hospital de Clínicas, Universidad de Buenos Aires, Buenos Aires, Argentina.
  • Perín MM; División de Neumonología, Hospital de Clínicas, Universidad de Buenos Aires, Buenos Aires, Argentina.
  • Dubinsky D; División de Reumatología, Hospital de Clínicas, Universidad de Buenos Aires, Buenos Aires, Argentina.
Med Clin (Barc) ; 162(7): 350-353, 2024 04 12.
Article en En, Es | MEDLINE | ID: mdl-38195280
ABSTRACT

INTRODUCTION:

Shrinking lung syndrome (SLS) is a rare manifestation of systemic lupus erythematosus. Our aim was to describe the clinical, radiological, and functional characteristics of a cohort with SLS and its evolution over time.

METHODS:

A retrospective study was conducted between 2009 and 2018. Demographic, clinical, functional, radiological, and treatment data were collected.

RESULTS:

Out of a total of 225 patients, 11 presented with SLS (prevalence of 4.8%). Two patients were excluded. The mean age was 39.33±16 years, and 6 were female. The main symptoms were dyspnea and pleuritic pain. The mean forced vital capacity was 49%, total lung capacity was 60%, carbon monoxide diffusing capacity was 66%, carbon monoxide transference factor was 128%, maximal inspiratory pressure was 66%, and maximal expiratory pressure was 82%. All patients received corticosteroids. After a median follow-up of 19 months, 4 cases showed improvement, and 4 cases remained stable.

CONCLUSIONS:

SLS should be considered in every lupus patient with unexplained dyspnea. Although it often shows improvement, many cases experience persistent deterioration despite treatment.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades del Sistema Digestivo / Enfermedades Pulmonares / Lupus Eritematoso Sistémico / Enfermedades Musculares Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En / Es Revista: Med Clin (Barc) Año: 2024 Tipo del documento: Article País de afiliación: Argentina Pais de publicación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades del Sistema Digestivo / Enfermedades Pulmonares / Lupus Eritematoso Sistémico / Enfermedades Musculares Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En / Es Revista: Med Clin (Barc) Año: 2024 Tipo del documento: Article País de afiliación: Argentina Pais de publicación: España