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http://dx.doi.org/10.1111/bdi.13262 | DOI Listing |
J Med Virol
September 2025
Department of Pathology, West China Hospital, Sichuan University, Chengdu, China.
Systemic chronic active Epstein-Barr virus disease (sCAEBVD) can primarily involve skeletal muscle to form CAEBV-myopathy (CAEBV-M), which may resemble idiopathic inflammatory myopathies (IIMs). This study reports an 11-patient, 10-year cohort of CAEBV-M to summarize clinicoseropathologic features. CAEBV-M typically affects young adults (median: 29 years), with universal limb swelling, frequent disseminated muscle involvement (73%), and systemic symptoms like fever (82%), splenomegaly (82%), and hemophagocytic lymphohistiocytosis (55%).
View Article and Find Full Text PDFSpine (Phila Pa 1976)
September 2025
Department of Health Sciences, University of Jaén, Campus Las Lagunillas s/n, 23071 Jaén, Spain.
Study Design: Systematic review and meta-analysis of observational studies.
Objective: This systematic review and meta-analysis aimed to assess the possible relationship between atypical laterality curves and NAA.
Summary: Idiopathic scoliosis (IS) is a three-dimensional spinal deformity of unknown origin.
Diagnostics (Basel)
August 2025
Department of Maxillofacial and Oral Surgery, Dubrava University Hospital, 10000 Zagreb, Croatia.
Cocaine-induced vasculitis (CIV), especially when associated with PR3-ANCA positivity, can be very similar both clinically and serologically to idiopathic granulomatosis with polyangiitis (GPA). The distinction between these entities is crucial due to the different etiologies, treatment strategies, and prognoses. We present a unique case of CIV that manifested exclusively in a previously dissected neck area-an example of the locus minoris resistance phenomenon-and was initially misinterpreted as skin melanoma recurrence.
View Article and Find Full Text PDFDiagnostics (Basel)
August 2025
Center for Clinical and Translational Science, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua Medicine, Tsinghua University, Beijing 102218, China.
: Retroperitoneal fibrosis (RPF), a rare fibroinflammatory disorder, is classified into idiopathic (iRPF) and secondary (sRPF) forms, with the latter posing significant diagnostic challenges in routine clinical pathway due to atypical presentations, especially in malignancy-associated (maRPF) cases. : Here, we report a 38-year-old female with congenital pancreatic hypoplasia presenting with elusive hypometabolic retroperitoneal masses, initially suggestive of iRPF. Persistent CA19-9 elevation prompted histopathological evaluation, revealing poorly differentiated adenocarcinoma of indeterminate origin.
View Article and Find Full Text PDFParkinsonism Relat Disord
August 2025
Department of Neurology, Tri-Service General Hospital, National Defense Medical University, Taipei, Taiwan. Electronic address:
Background: Vascular parkinsonism (VP) is a heterogeneous syndrome caused by cerebrovascular pathology. While generally distinguishable from Parkinson's disease (PD), overlap may occur in some cases. The genetic basis of VP remains unclear.
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