Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Y.-L. Pennec"'
Publikováno v:
La Revue de Médecine Interne. 26:S253-S255
[Bacteremia and pneumonia due to Yersinia enterocolitica serotype O:3 in an immunocompetent patient]
Publikováno v:
Medecine et maladies infectieuses. 35(6)
The authors report a rare case of Yersinia enterocolitica O:3 pneumonia in an immunocompetent 70-year old man. There was no evidence of acute gastrointestinal disease. Diagnosis was confirmed by blood cultures. He responded with resolution of the inf
Publikováno v:
Clinical and experimental rheumatology. 22(5)
The association of kerato-conjunctivitis sicca and xerostomia has been termed Sjogren's syndrome (SS). Although this disease is referred to as a non-organ-specific autoimmune condition, the vast majority of the deleterious effects of primary SS are r
Publikováno v:
La Revue de medecine interne. 23(9)
Systemic vasculitis presenting as a tumorlike lesion are unusual and affect mainly the uro-genital system and breast. Muscle-localized tumorlike periarteritis nodosa are scarce.We report localized tumorlike polyarteritis nodosa affecting the forearm
Publikováno v:
Annales de medecine interne. 149(1)
Serum IgG and IgA are glycoprotein and significant glycoform abnormalities have been established in primary Sjögren's syndrome. The proportion of asialylated IgG is abnormally high in the patients, whereas IgA1 and IgA2 appear to be over-sialylated.
Publikováno v:
La Revue de medecine interne. 22(2)
Orbital myositis is a subtype of nonspecific orbital inflammation confined to one or more of the extraocular muscles.Three female patients presented presumed orbital myositis, in each of whom the diagnosis was suspected clinically and confirmed by th
Publikováno v:
Annales de medecine interne. 151(6)
Involvement of the temporal arteries, considered to be the hallmark of giant cell arteritis, is rather rare in other pathologic processes. We describe a patient with lymphoma involving temporal artery. A 68-year-old man has been followed closely with
Publikováno v:
Joint bone spine. 67(4)
Classic polyarteritis nodosa is a multisystem inflammatory disease associated with necrotizing vasculitis of small and medium arteries. In most cases, the causes of polyarteritis nodosa remain unknown, but viruses (HBV, HCV, HIV) and microbes (especi
Publikováno v:
Histology and histopathology. 15(2)
CD45RO+ T cells are referred to as memory or helper-inducer while CD45RA+ T cells are regarded as naive or suppressor-inducer T cells. The former population predominates in the peripheral blood and even more in the synovial fluid of patients with rhe
Publikováno v:
La Revue de medecine interne. 20(12)
Polyarteritis nodosa is a disease process with a wide clinical spectrum, ranging from a severe generalized multisystem disorder to a more benign condition which may remain limited to the skin, muscles and peripheral nerves, and is termed cutaneous po