High-Emergency Lung Transplantation for Interstitial Lung Disease Associated With Anti-MDA5 Dermatomyositis: A Case Report.


Journal

Transplantation proceedings
ISSN: 1873-2623
Titre abrégé: Transplant Proc
Pays: United States
ID NLM: 0243532

Informations de publication

Date de publication:
Oct 2021
Historique:
received: 28 04 2021
accepted: 07 08 2021
pubmed: 14 9 2021
medline: 26 11 2021
entrez: 13 9 2021
Statut: ppublish

Résumé

Rapidly progressive interstitial lung disease (RPILD) associated with the anti-melanoma differentiation-associated gene 5 antibody-positive (anti-MDA5ab+) dermatomyositis (DM) is a rare but life-threatening condition despite immunosuppressive treatment. We report the case of a 44-year-old woman who was diagnosed with severe RPILD associated with anti-MDA5ab+ DM 1 week before her admission in the intensive care unit. The patient underwent a successful double-lung transplant after she failed treatment with immunosuppressive therapy, including tofacitinib. At 1-year follow-up, she had experienced no relapse of the disease. This case includes a patient recently diagnosed with RPILD for whom no treatment showed efficacy, including glucocorticoids, cyclophosphamide, plasma exchanges, tofacitinib, and tacrolimus. She was placed under mechanical ventilation and venovenous extracorporeal membrane oxygenation 2 weeks after diagnosis in a bridge-to-transplant process. She was successfully transplanted 20 days later after having been registered on the French National Lung Transplant Waiting List with high priority. One year after surgery, her pulmonary function tests were good, and she showed no sign of relapse of anti-MDA5ab+ DM. Lung transplantation can be a life-saving procedure in RPILD related to anti-MDA5ab+ DM. High-emergency allocation priority on the transplant list reduced the time between diagnosis and surgery. Patients without comorbidities should be promptly referred to specialized centers to rapidly assess the feasibility of transplantation in this context.

Sections du résumé

BACKGROUND BACKGROUND
Rapidly progressive interstitial lung disease (RPILD) associated with the anti-melanoma differentiation-associated gene 5 antibody-positive (anti-MDA5ab+) dermatomyositis (DM) is a rare but life-threatening condition despite immunosuppressive treatment. We report the case of a 44-year-old woman who was diagnosed with severe RPILD associated with anti-MDA5ab+ DM 1 week before her admission in the intensive care unit. The patient underwent a successful double-lung transplant after she failed treatment with immunosuppressive therapy, including tofacitinib. At 1-year follow-up, she had experienced no relapse of the disease.
CASE REPORT METHODS
This case includes a patient recently diagnosed with RPILD for whom no treatment showed efficacy, including glucocorticoids, cyclophosphamide, plasma exchanges, tofacitinib, and tacrolimus. She was placed under mechanical ventilation and venovenous extracorporeal membrane oxygenation 2 weeks after diagnosis in a bridge-to-transplant process. She was successfully transplanted 20 days later after having been registered on the French National Lung Transplant Waiting List with high priority. One year after surgery, her pulmonary function tests were good, and she showed no sign of relapse of anti-MDA5ab+ DM.
CONCLUSIONS CONCLUSIONS
Lung transplantation can be a life-saving procedure in RPILD related to anti-MDA5ab+ DM. High-emergency allocation priority on the transplant list reduced the time between diagnosis and surgery. Patients without comorbidities should be promptly referred to specialized centers to rapidly assess the feasibility of transplantation in this context.

Identifiants

pubmed: 34511249
pii: S0041-1345(21)00543-1
doi: 10.1016/j.transproceed.2021.08.012
pii:
doi:

Substances chimiques

Autoantibodies 0
Interferon-Induced Helicase, IFIH1 EC 3.6.4.13

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2613-2615

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Antoine Marchiset (A)

Réanimation Polyvalente, Hôpital Foch, Suresnes, France.

Mathilde Neuville (M)

Réanimation Polyvalente, Hôpital Foch, Suresnes, France. Electronic address: m.neuville@hopital-foch.com.

Guillaume Voiriot (G)

Sorbonne Université, Médecine Intensive Réanimation, Hôpital Tenon, Paris, France.

Julien De Wolf (J)

Chirurgie Thoracique, Hôpital Foch, Suresnes, France.

Matthieu Glorion (M)

Chirurgie Thoracique, Hôpital Foch, Suresnes, France.

François Parquin (F)

Unité de Soins Intensifs Respiratoires, Hôpital Foch, Suresnes, France.

Antoine Roux (A)

Pneumologie, Hôpital Foch, Suresnes, France.

Morgan Le Guen (ML)

Département d'Anesthésie, Hôpital Foch, Suresnes, France.

Yves Allenbach (Y)

Département de Médecine interne et Immunologie Clinique, Hôpital Pitié-Salpêtrière, Paris, France.

Benjamin Zuber (B)

Réanimation Polyvalente, Hôpital Foch, Suresnes, France.

Charles Cerf (C)

Réanimation Polyvalente, Hôpital Foch, Suresnes, France.

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Classifications MeSH