The Unveiled Triad: Clinical, Radiological and Pathological Insights into Hypersensitivity Pneumonitis.

BAL HRCT IIP ILD IPF artificial intelligence high-resolution computed tomography hypersensitivity pneumonitis idiopathic interstitial pneumonia idiopathic pulmonary fibrosis

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
30 Jan 2024
Historique:
received: 28 11 2023
revised: 10 01 2024
accepted: 25 01 2024
medline: 10 2 2024
pubmed: 10 2 2024
entrez: 10 2 2024
Statut: epublish

Résumé

Hypersensitivity pneumonitis (HP) is a diffuse parenchymal lung disease (DLPD) characterized by complex interstitial lung damage with polymorphic and protean inflammatory aspects affecting lung tissue targets including small airways, the interstitium, alveolar compartments and vascular structures. HP shares clinical and often radiological features with other lung diseases in acute or chronic forms. In its natural temporal evolution, if specific therapy is not initiated promptly, HP leads to progressive fibrotic damage with reduced lung volumes and impaired gas exchange. The prevalence of HP varies considerably worldwide, influenced by factors like imprecise disease classification, diagnostic method limitations for obtaining a confident diagnosis, diagnostic limitations in the correct processing of high-resolution computed tomography (HRCT) radiological parameters, unreliable medical history, diverse geographical conditions, heterogeneous agricultural and industrial practices and occasionally ineffective individual protections regarding occupational exposures and host risk factors. The aim of this review is to present an accurate and detailed 360-degree analysis of HP considering HRCT patterns and the role of the broncho-alveolar lavage (BAL), without neglecting biopsy and anatomopathological aspects and future technological developments that could make the diagnosis of this disease less challenging.

Identifiants

pubmed: 38337490
pii: jcm13030797
doi: 10.3390/jcm13030797
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Auteurs

Gaetano Rea (G)

Department of Radiology, Monaldi Hospital, Azienda Ospedaliera dei Colli, 80131 Naples, Italy.

Marialuisa Bocchino (M)

Department of Clinical Medicine and Surgery, Section of Respiratory Diseases, University Federico II, Monaldi Hospital, Azienda Ospedaliera dei Colli, 80131 Naples, Italy.

Roberta Lieto (R)

Department of Radiology, Monaldi Hospital, Azienda Ospedaliera dei Colli, 80131 Naples, Italy.

Roberta Eufrasia Ledda (RE)

Section of Radiology, Unit of Surgical Science, Department of Medicine and Surgery (DiMeC), University of Parma, 43121 Parma, Italy.

Michele D'Alto (M)

Department of Cardiology, University "L. Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.

Marco Sperandeo (M)

Interventional Ultrasound Unit, Department of Internal Medicine, IRCCS "Casa Sollievo Della Sofferenza" Hospital, San Giovanni Rotondo, 71013 Foggia, Italy.

Raffaella Lucci (R)

Department of Pathology, Monaldi Hospital, Azienda Ospedaliera dei Colli, 80131 Naples, Italy.

Patrizio Pasquinelli (P)

Italian Federation of Pulmonary Fibrosis and Rare Pulmonary Diseases "FIMARP", 00185 Rome, Italy.
Department of Pulmonary Diseases, San Camillo-Forlanini Hospital, 00152 Rome, Italy.

Stefano Sanduzzi Zamparelli (S)

Department of Translational Medical Sciences, University "L. Vanvitelli", 80131 Naples, Italy.

Giorgio Bocchini (G)

Department of Radiology, Monaldi Hospital, Azienda Ospedaliera dei Colli, 80131 Naples, Italy.

Tullio Valente (T)

Department of Radiology, Monaldi Hospital, Azienda Ospedaliera dei Colli, 80131 Naples, Italy.

Giacomo Sica (G)

Department of Radiology, Monaldi Hospital, Azienda Ospedaliera dei Colli, 80131 Naples, Italy.

Classifications MeSH