IgG4-related Disease with Bone Marrow Involvement

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Pericardial Involvement in IgG4-related Disease.

We herein report the case of a 65-year-old man with pericardial involvement associated with autoimmune pancreatitis. Chest CT imaging showed pericardial thickening. The patient responded to corticosteroid therapy, and the pericardial thickening resolved. Multiple organs are involved in immunoglobulin G4 (IgG4)-related disease (IgG4-RD); however, only a few cases of IgG4-related chronic constric...

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Kidney involvement by IgG4-related sclerosing disease

A 54-year-old Caucasian woman was admitted due to persistent febrile syndrome, sweating and abdominal pain. Fever marked the onset of the patient’s medical history 10 years earlier. The physical examination revealed normal findings. Laboratory data showed normal white blood cell count, mild microcytic anaemia with a normal reticulocyte count, important inflammatory syndrome (C-reactive protein ...

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Large vessel involvement by IgG4-related disease

OBJECTIVES IgG4-related disease (IgG4-RD) is an immune-mediated fibroinflammatory condition that can affect multiple organs and lead to tumefactive, tissue-destructive lesions. Reports have described inflammatory aortitis and periaortitis, the latter in the setting of retroperitoneal fibrosis (RPF), but have not distinguished adequately between these 2 manifestations. The frequency, radiologic ...

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Sarcoidosis with bone marrow involvement.

427 virus, hepatitis B virus, hepatitis C virus, cyto‐ megalovirus, and Epstein–Barr virus) were ex‐ cluded. Blood and urine cultures were negative. Tuberculosis was excluded. Serum iron and fo‐ lic acid levels were normal, while a moderate vi‐ tamin B12 deficiency was detected (101 pg/ml; normal range, 157–1057 pg/ml). A small propor‐ tion of erythroblasts had dysplastic features on bone marro...

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IgG4-related disease presenting as panuveitis without scleral involvement

BACKGROUND The following case emphasizes the importance of including IgG4-related disease (RD) in the differential diagnosis of intraocular inflammation and multiple cranial nerve palsies. RESULTS A 33-year-old man, with a history of idiopathic bilateral panuveitis, presented with a new right pupillary-sparing partial third nerve palsy, which spontaneously resolved in 2 weeks, but was followe...

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ژورنال

عنوان ژورنال: Internal Medicine

سال: 2016

ISSN: 0918-2918,1349-7235

DOI: 10.2169/internalmedicine.55.6749