Osseous sarcoidosis: A multicenter retrospective case-control study of 48 patients.


Journal

Joint bone spine
ISSN: 1778-7254
Titre abrégé: Joint Bone Spine
Pays: France
ID NLM: 100938016

Informations de publication

Date de publication:
Nov 2019
Historique:
received: 11 03 2019
accepted: 16 07 2019
pubmed: 3 8 2019
medline: 24 6 2020
entrez: 3 8 2019
Statut: ppublish

Résumé

To describe the clinical presentation, distribution of lesions, treatment, and outcomes of osseous sarcoidosis. A French retrospective multicenter study of patients with biopsy-proven sarcoidosis analyzed patients with 1) a biopsy-proven granuloma without caseous necrosis, and either 2) osseous clinical manifestations, or 3) abnormal osseous imaging. Sarcoidosis patients with osseous involvement (cases) were compared with 264 age- and sex-matched sarcoidosis patients with no osseous manifestations (controls). In the osseous sarcoidosis group (n=88), forty-two (48%) patients had osseous-related symptoms involving the axial (69%) and/or appendicular (58%) skeleton. On imaging, the most commonly affected bones were in the spine (52%), pelvis (42%), hands (22%) and femur (19%). Compared with controls, cases had higher rates of mediastinal (93% vs. 47%) and extra-thoracic lymph node involvement (66% vs. 21%), pulmonary (90% vs. 65%) and cutaneous involvement (44% vs. 23%) (all P<0.0001), and hypercalcemia (8.5% vs. 2%, P=0.014). Spleen/liver and gastrointestinal involvement were less frequent in the osseous sarcoidosis group (29% vs. 45%, and 1% vs. 17%, respectively, P<0.0001). Response rates to with glucocorticoids alone, glucocorticoids plus methotrexate or glucocorticoids plus hydroxychloroquine were 23/44 (52%), 9/13 (69%) and 4/6 (67%), respectively. In patients with osseous sarcoidosis the spine and pelvis were the most commonly affected bones. Compared with controls, cases with osseous sarcoidosis have higher rates of thoracic and extra-thoracic lymph node involvement, pulmonary and cutaneous involvement, and hypercalcemia. Most patients with osseous sarcoidosis had a good response to glucocorticoids in combination with methotrexate or hydroxychloroquine.

Identifiants

pubmed: 31374357
pii: S1297-319X(19)30115-0
doi: 10.1016/j.jbspin.2019.07.009
pii:
doi:

Substances chimiques

Glucocorticoids 0
Hydroxychloroquine 4QWG6N8QKH
Methotrexate YL5FZ2Y5U1

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

789-793

Informations de copyright

Copyright © 2019 Société française de rhumatologie. All rights reserved.

Auteurs

Imen Ben Hassine (I)

Sorbonne Universités, UPMC Univ Paris 06, UMR 7211, and Inflammation-Immunopathology-Biotherapy Department (DHU i2B), 75005 Paris, France; AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Department of Internal Medicine and Clinical Immunology, 75013 Paris, France.

Christopher Rein (C)

Service de Médecine Interne et Rhumatologie, HIA Legouest, Metz, France.

Cloé Comarmond (C)

Sorbonne Universités, UPMC Univ Paris 06, UMR 7211, and Inflammation-Immunopathology-Biotherapy Department (DHU i2B), 75005 Paris, France; INSERM, UMR_S 959, 75013 Paris, France; CNRS, FRE3632, 75005 Paris, France; AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Department of Internal Medicine and Clinical Immunology, 75013 Paris, France.

Camille Glanowski (C)

Hôpital d'instruction des armées de Bégin, Saint-Mandé, France.

Nathalie Saidenberg-Kermanac'h (N)

AP-HP, Groupe Hospitalier Avicenne-Jean Verdier-René Muret, Service de Rhumatologie, et Sorbonne Paris Cité, Université Paris 13, INSERM U1125, Bobigny, France.

Benoît Meunier (B)

Service de Médecine Interne, CHU La Timone, Aix-Marseille Université, Marseille, France.

Nicolas Schleinitz (N)

Service de Médecine Interne, CHU La Timone, Aix-Marseille Université, Marseille, France.

Noémie Chanson (N)

Service de Médecine Interne, CHU Bichat, Paris, France.

Karim Sacré (K)

Service de Médecine Interne, CHU Bichat, Paris, France.

Marc Scherlinger (M)

Service de Rhumatologie, CHU de Bordeaux, Bordeaux, France.

Christophe Richez (C)

Service de Rhumatologie, CHU de Bordeaux, Bordeaux, France.

Sandrine Hirschi (S)

Service de Pneumologie, CHU de Strasbourg, Strasbourg, France.

Matthieu Groh (M)

Service de Médecine Interne, CH Foch, Suresnes, France.

Hervé Devilliers (H)

Service de Médecine Interne, CHU Dijon Bourgogne, Dijon, France.

Philip Bielefeld (P)

Service de Médecine Interne, CHU Dijon Bourgogne, Dijon, France.

David Saadoun (D)

Sorbonne Universités, UPMC Univ Paris 06, UMR 7211, and Inflammation-Immunopathology-Biotherapy Department (DHU i2B), 75005 Paris, France; INSERM, UMR_S 959, 75013 Paris, France; CNRS, FRE3632, 75005 Paris, France; AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Department of Internal Medicine and Clinical Immunology, 75013 Paris, France.

Catherine Chapelon-Abric (C)

AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Department of Internal Medicine and Clinical Immunology, 75013 Paris, France.

Laurent Arnaud (L)

Service de Rhumatologie, Hôpitaux Universitaires de Strasbourg, Centre de Référence RESO, INSERM UMR-S1109, Université de Strasbourg, 67000 Strasbourg, France.

Patrice Cacoub (P)

Sorbonne Universités, UPMC Univ Paris 06, UMR 7211, and Inflammation-Immunopathology-Biotherapy Department (DHU i2B), 75005 Paris, France; INSERM, UMR_S 959, 75013 Paris, France; CNRS, FRE3632, 75005 Paris, France; AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Department of Internal Medicine and Clinical Immunology, 75013 Paris, France. Electronic address: patrice.cacoub@aphp.fr.

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Classifications MeSH