CT-guided biopsy in the differential diagnosis of Sjogren syndrome associated cystic lung disease: A case of lung nodular AL-

Amyloidosis CT guided fine needle aspiration biopsy Cystic lung disease Sjogren syndrome

Journal

Radiology case reports
ISSN: 1930-0433
Titre abrégé: Radiol Case Rep
Pays: Netherlands
ID NLM: 101467888

Informations de publication

Date de publication:
Nov 2020
Historique:
received: 21 06 2020
revised: 01 08 2020
accepted: 05 08 2020
entrez: 30 9 2020
pubmed: 1 10 2020
medline: 1 10 2020
Statut: epublish

Résumé

Pulmonary involvement in Sjogren syndrome (SS) could manifest as cystic lung disease (CLD). CLD in SS includes lymphocytic interstitial pneumonia (LIP) and pulmonary amyloidosis. Differential diagnosis usually requires surgical lung biopsy, whereas CT-guided percutaneous fine needle aspiration biopsy (CT-FNAB) has not yet explored. We describe the case of a 63-year-old never smoker Caucasian female with a SS diagnosis who displayed a newly detected diffuse CLD at high-resolution computed tomography, though totally asymptomatic. Given the favorable location of one big lesion at the superior left lobe, a CT-FNAB was proposed instead of a more invasive SLB. At histology examination a diagnosis of pulmonary nodular AL kappa amyloidosis in the context of SS was established. In conclusion, CT-FNAB might represent an alternative and less invasive diagnostic procedure than SLB in the differential diagnosis of CLD, even if further research is needed. Moreover, this case presents an unusual association between SS and pulmonary nodular AL kappa amyloidosis, with pulmonary nodules and cysts without systemic manifestations.

Identifiants

pubmed: 32994835
doi: 10.1016/j.radcr.2020.08.012
pii: S1930-0433(20)30403-9
pmc: PMC7501412
doi:

Types de publication

Case Reports

Langues

eng

Pagination

2331-2334

Informations de copyright

© 2020 Published by Elsevier Inc. on behalf of University of Washington.

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Auteurs

Claudio Tirelli (C)

Department of Internal Medicine and Therapeutics, Division of Respiratory Diseases, University of Pavia and IRCCS Policlinico San Matteo Foundation, Pavia, Italy.

Giovanni Zanframundo (G)

Division of Rheumatology, University and IRCCS Policlinico S. Matteo Foundation, Pavia, Italy.

Adele Valentini (A)

Division of Radiology, IRCCS Policlinico S. Matteo Foundation, Pavia, Italy.

Chandra Bortolotto (C)

Division of Radiology, IRCCS Policlinico S. Matteo Foundation, Pavia, Italy.

Roberto Dore (R)

Radiology Unit, Istituti Clinici Città di Pavia, Pavia, Italy.

Tiberio Oggionni (T)

Division of Respiratory Diseases, IRCCS Policlinico San Matteo Foundation, Pavia, Italy.

Paolo Milani (P)

Department of Molecular Medicine, Amyloidosis Research and Treatment Center, Foundation "Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo", University of Pavia, Pavia, Italy.

Elena Bravi (E)

Unit of Rheumatology, Guglielmo da Saliceto Hospital, Piacenza, Italy.

Zamir Kadija (Z)

Division of Internal Medicine, Azienda Sanitaria dell'Alto Adige, Brunico Hospital, Brunico, Italy.

Francesca Mariani (F)

Division of Respiratory Diseases, IRCCS Policlinico San Matteo Foundation, Pavia, Italy.

Veronica Codullo (V)

Division of Rheumatology, University and IRCCS Policlinico S. Matteo Foundation, Pavia, Italy.

Patrizia Morbini (P)

Pathology Unit, University and IRCCS Policlinico S. Matteo Foundation, Pavia, Italy.

Giovanni Palladini (G)

Department of Molecular Medicine, Amyloidosis Research and Treatment Center, Foundation "Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo", University of Pavia, Pavia, Italy.

Federica Meloni (F)

Department of Internal Medicine and Therapeutics, Division of Respiratory Diseases, University of Pavia and IRCCS Policlinico San Matteo Foundation, Pavia, Italy.

Lorenzo Cavagna (L)

Division of Rheumatology, University and IRCCS Policlinico S. Matteo Foundation, Pavia, Italy.

Classifications MeSH