F-FDG PET/CT in bone sarcoidosis: an observational study.

Clin Rheumatol

AP-HP, Hôpital Bichat-Claude Bernard, Service de Rhumatologie, 46 rue Henri Huchard, 75018, Paris, France.

Published: September 2020

Objective: Bone sarcoidosis is usually rare. Imaging procedures such as fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography (F-FDG PET/CT) can reveal bone sarcoidosis with better sensitivity than conventional radiography. We aimed to describe bone sarcoidosis involvement detected with F-FDG PET/CT.

Methods: This was an observational retrospective study of individuals with pulmonary sarcoidosis who underwent F-FDG PET/CT. According to the ATS/ERS/WASOG criteria, sarcoidosis was diagnosed by the presence of clinical and/or imaging features of sarcoidosis and evidence of non-caseating epithelioid granulomas on a biopsy. We assessed clinical and F-FDG PET/CT characteristics.

Results: Data for 85 patients with sarcoidosis (56.5% female, median age 47 [range 21-80] years) were analyzed. The median follow-up was 4 years. Among 56 patients, sarcoidosis occurred in more than three organs. According to ATS/ERS/WASOG criteria, bone sarcoidosis was diagnosed in 12 (14%) patients. The spine was the most commonly affected location (92%, n = 11), followed by the pelvis (67%, n = 8), sternum (33%, n = 4), humerus (25%, n = 3), and fingers (17%, n = 2). Only peripheral adenopathy was associated with bone sarcoidosis (p = 0.04). Seven patients had a F-FDG PET/CT follow-up, all showing a decrease of bone lesions.

Conclusion: Bone sarcoidosis occurred in 14% of patients with sarcoidosis, affecting multiple bones and mostly the axial skeleton. F-FDG PET/CT seems a sensitive tool for diagnosis and follow-up of bone sarcoidosis.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10067-020-05022-6DOI Listing

Publication Analysis

Top Keywords

bone sarcoidosis
32
f-fdg pet/ct
24
sarcoidosis
14
patients sarcoidosis
12
bone
9
ats/ers/wasog criteria
8
sarcoidosis diagnosed
8
sarcoidosis occurred
8
14% patients
8
f-fdg
7

Similar Publications

Sarcoidosis is an inflammatory multisystem disease characterised by non-necrotising granulomas that typically affect the lungs, lymph nodes, eyes, skin, liver, spleen, heart, bones and joints. Although rare, necrotising granulomas can also occur. In this report, we present a case of a healthy woman in her 60s who presented with a 1-year history of fatigue and generalised body aches.

View Article and Find Full Text PDF

Rheumatic Manifestations of Sarcoidosis.

Diagnostics (Basel)

December 2024

North Bristol NHS Foundation Trust, Bristol BS10 5NB, UK.

Sarcoidosis is a multisystem granulomatous inflammatory disorder, of unknown aetiology, which causes a wide spectrum of clinical phenotypes. It can present at any age, most commonly between 20 and 60 years, with a roughly equal sex distribution. Diagnosis is often delayed due to multiple diagnostic mimics, particularly joint disease.

View Article and Find Full Text PDF

Osseous sarcoidosis is a rare manifestation of sarcoidosis, often mimicking other conditions like metastatic disease. Skeletal involvement occurs in only 3%-13% of cases (1), making diagnosis challenging. We present the case of a 63-year-old female with a 1-month history of inflammatory bone pain and multiple lytic and blastic lesions.

View Article and Find Full Text PDF

Chimeric antigen receptor T (CAR T) cell therapies have emerged as a valuable treatment modality for patients with plasma cell disorders. As the population of patients receiving CAR T therapies grows, the identification and management of associated rare toxicities become increasingly crucial. This study aims to identify safety signals associated with commercial anti-B-cell maturation antigen (BCMA) CAR T therapies using the Food and Drug Administration Adverse Event Reporting System (FAERS).

View Article and Find Full Text PDF

Nonspecific, or idiopathic, orbital inflammation (IOI) is a group of diseases characterized primarily by inflammation. Another term-pseudotumor-reflects its trait of mimicking oncological processes. Its clinical manifestations are highly polymorphic.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!