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Nobukazu Ishizaka - One of the best experts on this subject based on the ideXlab platform.

  • Immunoglobulin G4 related coronary periarteritis in a patient presenting with myocardial ischemia
    Human Pathology, 2012
    Co-Authors: Jun Tanigawa, Motomu Tsuji, Masahiro Daimon, Motonobu Murai, Takahiro Katsumata, Nobukazu Ishizaka
    Abstract:

    Summary Recent studies suggest that the cardiovascular system might be a possible target of Immunoglobulin G4–related disease. Here we present a 66-year-old man who was admitted to our hospital because of chest symptoms suggestive of acute coronary syndrome. Besides luminal narrowing of the coronary arteries, marked periarterial thickening around the coronary artery was observed by computed tomography coronary angiography. Serum Immunoglobulin G4 levels of this patient were elevated (564 mg/dL). The patient underwent coronary bypass surgery. After incision of the pericardium, a glittery white-yellowish, elastic-hard periarterial mass surrounding the left circumflex artery could be seen. Histologic analysis of the biopsy specimen showed the formation of lymphoid follicles and the presence of Immunoglobulin G4–positive plasma cells; therefore, the diagnosis was Immunoglobulin G4–related coronary periarteritis accompanied by physiologically significant myocardial ischemia.

  • Sarcoidosis does not belong to or overlap with Immunoglobulin G4-related diseases based on an assessment of serum Immunoglobulin G4 levels in cardiac and noncardiac sarcoidosis.
    Human Pathology, 2011
    Co-Authors: Fumio Terasaki, Motomu Tsuji, Shun Kizawa, Shuichi Fujita, Yumiko Kanzaki, Yasushi Kitaura, Nobukazu Ishizaka
    Abstract:

    Summary Although sarcoidosis may exhibit histopathologic features similar to those of a newly emerging clinical entity, Immunoglobulin G4–related sclerosing disease, sarcoidosis is currently not considered to be associated with Immunoglobulin G4–related immunoinflammation. Not many studies on this association have been reported. We investigated serum Immunoglobulin G4 levels among patients with sarcoidosis with or without cardiac involvement (cardiac sarcoidosis and non–cardiac sarcoidosis patients). The mean serum Immunoglobulin G4 level among the 65 patients with sarcoidosis was 56.8 ± 43.0 mg/dL, which did not significantly differ between patients with cardiac sarcoidosis (54 ± 48 mg/dL, n=12) and patients without cardiac sarcoidosis (58 ± 42 mg/dL; n=53). Serum level of soluble interleukin 2 receptor, a potent marker that may reflect sarcoidosis activity, was elevated in cardiac sarcoidosis (910 ± 683 U/L) and noncardiac sarcoidosis (689 ± 399 U/L) but did not significantly differ between the groups. Immunohistochemistry of cardiac or lymph node specimens from patients with cardiac sarcoidosis showed only sparse or no infiltration of Immunoglobulin G4–positive lymphocytes, in contrast to the moderate to severe infiltration of CD68-positive macrophages and CD45-positive lymphocytes. Although the number of study subjects was small, these findings collectively suggest that regardless of the presence or absence of cardiac involvement, sarcoidosis does not belong to or overlap with Immunoglobulin G4–related sclerosing disease.

Hirohiko Kakizaki - One of the best experts on this subject based on the ideXlab platform.

Yasuni Nakanuma - One of the best experts on this subject based on the ideXlab platform.

Audrey B. Erman - One of the best experts on this subject based on the ideXlab platform.

  • Immunoglobulin G4-related sclerosing disease Mimicking sjogren's syndrome: A case report.
    The Laryngoscope, 2016
    Co-Authors: Hilary C. Mccrary, Erynne A. Faucett, Audrey B. Erman
    Abstract:

    Immunoglobulin G4-related sclerosing disease (IgG4-RSD) is a fibroinflammatory condition that has the potential to affect nearly every organ system. Classic histological findings include storiform fibrosis and lymphoplasmacytic infiltrates of Immunoglobulin G4 (IgG4)-positive plasma cells. The clinical features of IgG4-RSD may be an under-recognized disease process that can mimic other autoimmune disorders, including Sjogren's syndrome. We describe a rare case of IgG4-RSD involving the salivary glands, initially misdiagnosed as Sjogren's syndrome. Clinical features of IgG4-RSD can mimic those of other autoimmune disorders affecting the head and neck. Therefore, otolaryngologists should have IgG4-RSD on their differential when evaluating patients with diffuse salivary gland swelling. Laryngoscope, 126:2242-2245, 2016.

Yasuhiro Takahashi - One of the best experts on this subject based on the ideXlab platform.