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A 32-year-old man presented with the symptoms of a floating sensation, weakness on the right side of the body, and tremor of the right hand. Head MRI was performed, and T-weighted images showed high-signal lesions around the lateral ventricles, subcortical white matter, and dorsal medulla oblongata. Moreover, MRI of the cervical spine showed multiple high-signal lesions without contrast enhancement. Based on these findings, the patient was diagnosed with primary progressive multiple sclerosis (PPMS) and was treated with steroid pulse therapy, plasma exchange, and oral fingolimod. However, the patient's condition deteriorated slowly, and he died at the age of 43 years. An autopsy revealed multiple demyelinating lesions in the central nervous system. No inflammatory cell infiltration or macrophage accumulation was observed, and there was no evidence of an active lesion. Herein, we present this rare autopsy case of PPMS in Japan with a review of the literature.
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http://dx.doi.org/10.5692/clinicalneurol.cn-002092 | DOI Listing |
Intern Med
September 2025
Fujita Health University School of Medicine, Department of Nephrology, Japan.
An 81-year-old man was treated with prednisolone, avacopan, and rituximab for microscopic polyangiitis and sulfamethoxazole/trimethoprim (SMX/TMP) and vonoprazan for prophylaxis. The liver enzyme levels were elevated 42 days after avacopan administration. Avacopan, SMX/TMP, and vonoprazan treatment were discontinued.
View Article and Find Full Text PDFLeg Med (Tokyo)
August 2025
Department of Legal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu 431-3192, Japan.
Reports on the quantification of fluvoxamine (FLV) in human tissues have been quite limited, although FLV has been used as an antidepressant since 1986. Fluvoxamine acid (FLA) was shown to be the major metabolite of FLV in human urine in 1983, but its quantification is also limited to only three works using human plasma. The existence of desmethyl fluvoxamine (FLD) in human specimens was recently reported in 2025; therefore, its quantification has not yet been performed.
View Article and Find Full Text PDFAm J Forensic Med Pathol
September 2025
Department of Pathology, St Louis University School of Medicine, Office of the Medical Examiner - City of St. Louis, St. Louis, MO.
Myotonic dystrophy type 1, or dystrophia myotonica type 1 (DM1), is a multisystem disorder inherited in an autosomal dominant manner. It is caused by a CTG tri-nucleotide expansion in the 3'-untranslated region (3'-UTR) of the dystrophia myotonia protein kinase (DMPK) gene. Core clinical features include progressive skeletal muscle weakness, myotonia, and systemic complications, with premature mortality most often due to respiratory or cardiac dysfunction.
View Article and Find Full Text PDFAlzheimers Dement
September 2025
Department of Neurology, University Hospitals Cleveland Medical Center, Cleveland, Ohio, USA.
Introduction: Little is known about factors influencing indecision or changes in brain donation program (BDP) enrollment status among Alzheimer's disease and related dementias research participants. This study examined demographic features associated with these decisions in participants from the Cleveland Alzheimer's Disease Research Center (CADRC).
Methods: Demographics and BDP status were extracted from the CADRC database and analyzed based on initial and current BDP enrollment status.
Am J Forensic Med Pathol
September 2025
Forensic Pathology and Coronial Services, Pathology Queensland, Queensland Health.
Predation by domestic pigs is unusual but not unheard of. However, predation by a herd of pigs is rare and has not been previously reported in the literature. We present a case report of an individual with predation by a herd of domestic pigs.
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