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Chronic Cardiac Herniation: A Peculiar Diagnosis.
Cureus
March 2024
Radiology, Pablo Tobón Uribe, Medellín, COL.
The presented case describes a 56-year-old male with adult-onset Still's disease, exhibiting polyserositis in 2019, who underwent pleurectomy and pericardiectomy. Despite treatment with tocilizumab and methylprednisolone, the patient developed deep vein thrombosis and pulmonary embolism in 2022, managed with apixaban. A contrast-enhanced chest tomography revealed no recurrent thromboembolic events.
View Article and Find Full Text PDFAdult-onset systemic autoinflammatory disorders: a clinical approach.
Reumatismo
January 2020
Department of Internal Medicine, Trofa Saúde Hospital Privado de Gaia, Vila Nova de Gaia.
Autoinflammatory disorders (AIDs) are a subgroup of immune-mediated syndromes that result from a primary dysfunction of the innate immune system. AIDs can be either monogenic or polygenic diseases. Unlike organspecific AIDs, systemic AIDs are characterized by fever and/or elevation of acute-phase reactants.
View Article and Find Full Text PDFFamilial Mediterranean fever variant with repeated atypical skin eruptions.
J Dermatol
September 2015
Department of Dermatology, Gifu University Graduate School of Medicine, Gifu, Japan.
Familial Mediterranean fever (FMF) is characterized by self-limited bouts of fever and polyserositis. Skin involvement is not common in FMF, and erysipelas-like erythema is found to be the most frequent skin eruption which is often accompanied by arthritis and fever, and disappears within 12-72 h. We report a 40-year-old Japanese woman who presented with a 2-year history of recurrent fever with general fatigue, polyarthralgia and transient maculopapular eruptions on her lower extremities and trunk.
View Article and Find Full Text PDF[Chest pain, reduced physical activity, and polyserositis in a 35-year old patient with anticonvulsive medication].
Internist (Berl)
January 2006
Medizinische Klinik II--Kardiologie und Pulmologie, Campus Benjamin Franklin der Charité Universitätsmedizin, Hindenburgdamm 30, 12200 Berlin.
We report on a rare case of a late-onset drug-induced lupus erythematosus. A 35 year old male patient complained about dyspnea, chest pain and reduced physical activity for three months. His medical history consisted of epilepsy treated with carbamazepine for 20 years.
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