Sarcoidosis is a multisystem inflammatory disorder characterized by noncaseating granulomas. The diagnosis of sarcoidosis is based on three criteria: clinical history, consistent imaging findings, and histopathology. Radiologists play an important role for the diagnosis and follow-up evaluation of patients with sarcoidosis, which often require a multimodal approach. This imaging essay will explore the typical and atypical imaging manifestations of sarcoidosis at chest radiography, CT, PET/CT, and MRI, provide imaging examples, and discuss relevant differential diagnoses for clinical practice. Thorax, MR-Imaging, Staging, PET/CT, CT, Conventional Radiography, Sarcoidosis, Thoracic Imaging, Scintigraphy © RSNA, 2025.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1148/ryct.240294 | DOI Listing |
Pediatr Rheumatol Online J
March 2025
Paediatric Clinical Immunology, Pellegrin Hospital, INSERM CICP, University Hospital Centre of Bordeaux, Bordeaux, CIC1401, France.
Background: Non-infectious paediatric granulomatous uveitis (PGU) is a rare disease that is idiopathic in more than half of affected children. The diagnosis of definite ocular sarcoidosis (OS) must be supported by the presence of non-caseating granulomas detected in biopsy, and is therefore a challenge in children with PGU. This study investigated the utility of minor salivary gland biopsy (MSGB) in the diagnosis of definite OS in PGU.
View Article and Find Full Text PDFCureus
February 2025
Internal Medicine, AdventHealth, Orlando, USA.
Establishing the diagnosis of miliary tuberculosis (TB) can be challenging due to the heterogeneous clinical presentations and low sensitivity of diagnostic tests. Miliary TB shares overlapping clinical, radiological, and histopathological features with other chronic granulomatous diseases, such as sarcoidosis, often posing a significant diagnostic challenge for clinicians. A 36-year-old male from Haiti presented with a four-month history of recurrent fever, dry cough, night sweats, and weight loss.
View Article and Find Full Text PDFJ Nucl Cardiol
March 2025
Department of Nuclear Medicine, Shandong Provincial Hospital affiliated to Shandong First Medical University, Jinan, Shandong, China. Electronic address:
JACC Case Rep
March 2025
Division of Cardiology, Department of Medicine, Queen's University, Kingston, Canada. Electronic address:
Background: Amyloid transthyretin (ATTR) cardiac amyloidosis is a progressive cardiomyopathy characterized by misfolded transthyretin deposition, resulting in ventricular stiffening which may cause cardiac dysfunction.
Case Summary: An 86-year-old man with history of pulmonary sarcoidosis presented with progressive dyspnea and emesis. An electrocardiogram demonstrated complete heart block and he underwent permanent pacemaker implantation.
Radiol Cardiothorac Imaging
April 2025
University of Florida College of Medicine, 1600 SW Archer Rd, Gainesville, FL 32608.
Sarcoidosis is a multisystem inflammatory disorder characterized by noncaseating granulomas. The diagnosis of sarcoidosis is based on three criteria: clinical history, consistent imaging findings, and histopathology. Radiologists play an important role for the diagnosis and follow-up evaluation of patients with sarcoidosis, which often require a multimodal approach.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!