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Objectives: This study aimed to identify imaging features of IgG4-related sialadenitis (IgG4-RS) and differentiate it from Sjögren's syndrome (SS) and chronic obstructive parotid/submandibular sialadenitis (COP/COS).
Study Design: A retrospective analysis of sialographic findings was conducted on 40 IgG4-RS patients. Two radiologists blindly evaluated sialographic features, including ductal dilation, wall smoothness, duct interruption, acinar patterns, and glandular emptying. A comparative analysis with SS and COP/COS was also performed.
Results: Sialograms of 40 IgG4-RS patients (82 glands), 61 SS patients (71 glands), and 69 COP/COS patients (95 glands) were analyzed. Sialographic findings were categorized into four types: Type I (diminished/interrupted ducts without dilation), Type II (diminished/interrupted ducts with dilation), Type III (dilated main/branch ducts), and Type IV (normal appearance). In IgG4-RS, Type I and III were predominant in parotid glands, while Type I was more frequent in submandibular glands. Type II was most common in SS, and Type III in COP/COS.
Conclusions: Sialography reveals distinct features in IgG4-RS, especially in submandibular glands, characterized by diminished or interrupted secondary and tertiary ducts without peripheral duct dilation, aiding differentiation from SS and COP/COS.
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http://dx.doi.org/10.1016/j.oooo.2025.07.005 | DOI Listing |
Scand J Rheumatol
September 2025
Department of Rheumatology and Clinical Immunology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Objective: To investigate the reliability of lacrimal gland ultrasound (LGUS) in patients with clinically suspected Sjögren's disease (SjD).
Method: Of 41 consecutive patients with clinically suspected SjD, 28 were diagnosed with SjD and 13 were classified as non-SjD. Forty patients were scored for bilateral lacrimal gland (LG) B-mode evaluation; LGs were 'not visible' in one case.
Allergol Immunopathol (Madr)
September 2025
Division of Immunology and Allergy, Department of Internal Medicine, Ankara University School of Medicine, Ankara, Türkiye.
Wiskott-Aldrich Syndrome (WAS) is an X-linked immunodeficiency characterized by eczema, microthrombocytopenia, and recurrent infections. Immunoglobulin G4-related disease (IgG4-RD) is a fibroinflammatory disorder involving various organs. We present a 34-year-old male with WAS who developed cervical lymphadenopathy and parotid gland swelling.
View Article and Find Full Text PDFBreast Cancer (Auckl)
September 2025
Allgemeine Pathologie und pathologische Anatomie, Pathologisches Institut, Universitätsklinikum Heidelberg, Heidelberg, Germany.
Juvenile fibroadenoma typically is seen in the adolescent patient and has distinctive clinical and histopathological features that are related to the early onset of the benign tumor. Only rarely can juvenile fibroadenoma occur as a prepubertal lesion or may be detected earlier in childhood, raising questions about differential diagnosis and management of the lesion. We present a case of very early first manifestation of juvenile fibroadenoma in a 2-year-old patient.
View Article and Find Full Text PDFEur J Pediatr
September 2025
Department of Paediatric Otolaryngology, Royal Hospital for Children, 1345 Govan Road, Glasgow, G51 4TF, UK.
Unlabelled: Drooling is a common problem in children with neurodisability, and refractory cases may require surgery. Our aim was to assess whether a child's response to salivary botulinum toxin injections would predict success or failure from subsequent surgical intervention. Retrospective case note review of all children undergoing drooling surgery between 1st January 2007 and 31st December 2023 at the Royal Hospital for Children, Glasgow.
View Article and Find Full Text PDFNat Microbiol
September 2025
Department of Rheumatology and Clinical Immunology, the First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Viral infections are implicated in the pathogenesis of autoimmune diseases, including Sjögren's disease (SjD), but the mechanisms linking viral antigens to disease development remain poorly understood. To address this, we conducted shotgun metagenomic sequencing of saliva samples from 35 patients with SjD and 25 healthy controls. The salivary virome of the patients with SjD, particularly those with high disease activity, had an expansion of Siphoviridae bacteriophages and increased eukaryotic viral sequences, including Vientovirus.
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