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Ophthalmic vascular manifestations in eosinophil-associated diseases: a comprehensive analysis of 57 patients from the CEREO and EESG networks and a literature review.
Chapuis, Elisa; Bousquet, Elodie; Viallard, Jean-François; Terrier, Benjamin; Amoura, Zahir; Batani, Veronica; Brézin, Antoine; Cacoub, Patrice; Caminati, Marco; Chazal, Thibaud; Comarmond, Cloé; Durieu, Isabelle; Ebbo, Mikael; Grall, Maximilien; Ledoult, Emmanuel; Losappio, Laura; Mattioli, Irene; Mékinian, Arsène; Padoan, Roberto; Regola, Francesca; Schroeder, Jan; Seluk, Lior; Trefond, Ludovic; Wechsler, Michael E; Lefevre, Guillaume; Kahn, Jean-Emmanuel; Sève, Pascal; Groh, Matthieu.
Afiliación
  • Chapuis E; National Reference Center for Hypereosinophilic Syndromes, CEREO, Suresnes, France.
  • Bousquet E; Department of Internal Medicine, Bichat Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Viallard JF; Department of Ophthalmology, Lariboisière Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Terrier B; National Reference Center for Hypereosinophilic Syndromes, CEREO, Suresnes, France.
  • Amoura Z; Department of Internal Medicine, Bordeaux University Hospital, Bordeaux, France.
  • Batani V; Department of Internal Medicine, National Referral Center for Systemic and Autoimmune Diseases, Cochin Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Brézin A; Department of Internal Medicine, Autoimmune and systemic diseases, La Pitié Salpetrière Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Cacoub P; Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS Ospedale San Raffaele, Milan, Italy.
  • Caminati M; Department of Ophthalmology, Cochin Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Chazal T; Department of Internal Medicine and Clinical Immunology, La Pitié Salpetrière Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Comarmond C; Asthma Center and Allergy Unit, Center for Hyper-Eosinophilic Dysimmune Conditions, Department of Medicine, University of Verona, Verona, Italy.
  • Durieu I; Department of Internal Medicine, Hospital Fondation Adolphe de Rothschild, Paris, France.
  • Ebbo M; Department of Internal Medicine, Competence Center for Rare Autoimmune and Inflammatory Diseases, Lariboisière Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Grall M; Department of Internal Medicine, Centre Hospitalier Universitaire Lyon Sud, Pierre-Bénite, France.
  • Ledoult E; National Reference Center for Hypereosinophilic Syndromes, CEREO, Suresnes, France.
  • Losappio L; Internal Medicine Department, Hopital La Timone, APHM, Aix Marseille University, Marseille, France.
  • Mattioli I; Department of Internal Medicine, CHU Rouen, Rouen, France.
  • Mékinian A; National Reference Center for Hypereosinophilic Syndromes, CEREO, Suresnes, France.
  • Padoan R; Department of Internal Medicine and Clinical Immunology, CHU Lille, Lille, France.
  • Regola F; Department of Clinical Immunology, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Schroeder J; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
  • Seluk L; Department of Internal Medicine, St Antoine Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Trefond L; Unit of Rheumatology, Department of Medicine DIMED, University of Padua, Padua, Italy.
  • Wechsler ME; Rheumatology and Clinical Immunology Unit, Department of Clinical and Experimental Sciences, ASST Spedali Civili and University of Brescia, Brescia, Italy.
  • Lefevre G; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
  • Kahn JE; Department of Medicine, National Jewish Health, Denver, CO, United States.
  • Sève P; National Reference Center for Hypereosinophilic Syndromes, CEREO, Suresnes, France.
  • Groh M; Department of Internal Medicine, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.
Front Immunol ; 15: 1379611, 2024.
Article en En | MEDLINE | ID: mdl-38720897
ABSTRACT

Introduction:

Eosinophils have widespread procoagulant effects. In daily practice, eosinophil-related cardiovascular toxicity consists of endomyocardial damage, eosinophilic vasculitis and arterial or venous thrombosis. Here we aim to report on the clinical features and treatment outcomes of patients with unexplained ophthalmic vascular manifestations and eosinophilia.

Methods:

We conducted a retrospective, multicenter, observational study and a literature review of patients with eosinophilia (≥0.5 x109/L) and concomitant ophthalmic vascular manifestations independent of the underlying eosinophilic disease but with no alternative cause for ophthalmic manifestations.

Results:

Fifty-seven patients were included (20 from the observational study and 37 from the literature review). Ophthalmic vascular features were the initial manifestation of eosinophil-related disease in 34 (59%) patients and consisted of 29 central retinal artery occlusions, six branch retinal artery occlusions, five central retinal vein occlusions, two branch retinal vein occlusions, seven retinal vasculitides, two retinal vasospasms, 12 Purtscher's retinopathies, 13 anterior ischemic optic neuropathies and two posterior ischemic optic neuropathies. The median [IQR] absolute eosinophil count at onset of ophthalmic vascular manifestations was 3.5 [1.7-7.8] x109/L. Underlying eosinophil-related diseases included eosinophilic granulomatosis with polyangiitis (n=32), clonal hypereosinophilic syndrome (HES) (n=1), idiopathic HES (n=13), lymphocytic HES (n=2), adverse drug reactions (n=3), parasitosis (n=2), polyarteritis nodosa (n=1), IgG4-related disease (n=1), eosinophilic fasciitis (n=1) and primary sclerosing cholangitis (n=1). Other extra-ophthalmologic arterial or venous thromboses related to eosinophilia were reported in four (7%) and nine (16%) patients, respectively. Visual prognosis was poor only eight (10%) patients achieved full recovery of ophthalmologic symptoms. After a median follow-up of 10.5 [1-18] months, one patient (3%) had a recurrence of an ophthalmic vascular manifestation, and three patients (10%) had a recurrence of other vascular symptoms (deep vein thrombosis in two and pulmonary embolism in one patient). At the time of recurrence, absolute eosinophil counts were above 0.5 x109/L in all cases (n=4).

Discussion:

This study broadens the spectrum of vascular manifestations associated with hypereosinophilia by adding ophthalmic vascular manifestations. In patients with ophthalmological vascular manifestations and hypereosinophilia, aggressive treatment of the underlying pathology (and normalization of blood count) should be implemented.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Eosinofilia / Eosinófilos Idioma: En Revista: Front Immunol Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Eosinofilia / Eosinófilos Idioma: En Revista: Front Immunol Año: 2024 Tipo del documento: Article