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http://dx.doi.org/10.1159/000117142 | DOI Listing |
Ann Med Surg (Lond)
June 2024
Department of Gastroenterology and Hepatology.
Introduction And Importance: Buerger's disease is an uncommon segmental nonatherosclerotic vasculitis essentially affecting small to medium-sized arteries and veins of upper and lower extremities and can lead to limb amputation. Visceral vessel involvement is quite rare accounting for 2% of cases presenting with acute abdomen due to mesenteric ischemia. Moreover, isolated visceral involvement is even rare.
View Article and Find Full Text PDFCirc J
February 2024
Division of Rheumatology, Department of Internal Medicine, Tokyo Women's Medical University School of Medicine.
J Med Case Rep
January 2023
The College of Physicians and Surgeons of Nova Scotia, Halifax, Canada.
Background: Peripheral manifestations secondary to progressive vascular occlusions are characteristic of the rare condition termed thromboangiitis obliternas (TAO) or Buerger's disease. The central manifestations of this disease are however poorly characterized, particularly those of psychiatric nature, and their prevalence is largely unknown. Speculations have been made around the polymorphic nature and triggers of observed psychopathology in TAO; much however remains to be unraveled in this area.
View Article and Find Full Text PDFRespirol Case Rep
March 2022
Department of Respiratory Medicine Fujita Health University, School of Medicine Toyoake Japan.
Secondary fungal infections are a critical problem that accompany immunosuppressive therapy for severe coronavirus disease 2019 (COVID-19). We report a fatal case of COVID-19 with disseminated mucormycosis diagnosed during autopsy. A 58-year-old man with diabetes was hospitalized for severe COVID-19 and treated with remdesivir, systemic steroids and tocilizumab.
View Article and Find Full Text PDFAlzheimer Dis Assoc Disord
May 2022
Forensic Medicine, Pusan National University School of Medicine, Yangsan, Republic of Korea.
Young-onset dementia (YOD, age at onset below 45 y) has a broad differential diagnosis. We describe a 41-year-old man with atypical manifestations of YOD syndrome in cerebral thromoboangiitis obliterans (CTAO). Extensive antemortem workup including clinical assessment, laboratory investigations, neuroimaging, and genetic testing did not elucidate a diagnosis.
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