1.Thyroglobulin Synthesis of Oxyphilic Cells in Various Types of Neoplastic and Autoimmune Thyroid Diseases.
Tae Sook HWANG ; Jin Suk SUH ; Yong Il KIM ; Seong Hoe PARK ; Bo Youn CHO ; Chang Soon KOH
Journal of Korean Medical Science 1990;5(1):33-37
To determine the content of thyroglobulin in oxyphilic cells of the thyroid, which have been considered as non-thyroglobulin producing cells, the degree of stainability of the various oxyphilic cells for thyroglobulin was compared with that of non-oxyphilic follicular cells in either same or different lesion. A total of 13 oxyphilic lesions, including three follicular adenomas containing oxyphilic cell nodules, four pure oxyphilic cell adenomas, and six Hashimoto's thyroiditis were compared with 16 of non-oxyphilic lesions such as, seven follicular adenomas, four chronic lymphocytic thyroiditis, and five Graves' disease. Many oxyphilic cells stained positively for thyroglobulin regardless of their morphologic variation, but less intensely than the usual follicular cells in follicular adenomas, chronic lymphocytic thyroiditis, and Graves' disease. The stainability of oxyphilic cells for thyroglogulin did not show any significant correlation with morphologic features, whereas in follicular adenomas, the non-oxyphilic follicular cells forming microfollicles stained less strongly for thyroglobulin than the same cells lining large mature follicles in a reproducible way. With above findings, we concluded that oxyphilic cells maintain the functional activity in terms of thyroglobulin synthesis, although the content of the thyroglobulin is less than that of non-oxyphilic colloid forming follicular cells.
Adenoma/*metabolism/pathology
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Graves Disease/*metabolism/pathology
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Humans
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Staining and Labeling
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Thyroglobulin/*biosynthesis
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Thyroid Neoplasms/pathology
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Thyroiditis, Autoimmune/*metabolism/pathology
2.Expression of CD40 and Apoptosis Related Molecules in Autoimmune Thyroid Diseases.
Jeong Hae KIE ; Min Sun CHO ; Woo Ick YANG
Yonsei Medical Journal 2001;42(5):488-496
Apoptosis is responsible for the loss of thyrocytes in autoimmune thyroiditis. Recent investigations into the pathogenesis of apoptosis have revealed that the important roles of suicide molecules expression on both thyrocytes and cytotoxic T-lymphocytes. To study the mechanism of thyrocyte loss in various forms of thyroiditis, we evaluated in situ expression patterns of CD40, Fas, and Fas-L on thyrocytes and infiltrating inflammatory cells by immunohistochemical staining of thyroid samples obtained from 49 patients (Graves' disease, n=10 : Hashimoto's thyroiditis, n=14; nonspecific lymphocytic thyroiditis, n=11; subacute granulomatous thyroiditis, n=11; normal, n=3). The role of cytotoxic T-lymphocytes was also evaluated by analyzing the expression of granzyme B along with their phenotypic characteristics. CD40 was not expressed on thyrocytes of normal controls while they showed a diffuse expression of Fas and a scattered focal expression of Fas-L. The plump thyrocytes proximal to the inflammatory infiltrates showed more intense expressions of these three molecules in various forms of thyroiditis and a close correlation was found between CD40 and Fas-L expression on thyrocytes. Unlike Fas, which was expressed on infiltrating lymphocytes in all groups, Fas-L was not expressed on infiltrating lymphocytes, except those in subacute granulomatous thyroiditis. Granzyme B expressing activated cytotoxic T-lymphocytes occupied a negligible proportion of CD8+ T-lymphocytes in various forms of thyroiditis, and no difference was found in terms of their proportions according to the type of thyroiditis. These results show the acquisition of CD40, Fas and Fas-L molecules on thyrocytes proximal to inflammatory cell aggregates and the negligible expression of granzyme B and Fas-L on the infiltrating lymphocytes, and suggest that Fas and Fas-L mediated apoptosis of thyrocytes (fratricide) may be more important than T cell-mediated cytotoxicity in various forms of thyroiditis.
Antigens, CD40/*metabolism
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Antigens, CD95/metabolism
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Apoptosis/*physiology
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Graves' Disease/*metabolism/pathology
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Human
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Membrane Glycoproteins/metabolism
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Reference Values
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Thyroiditis, Autoimmune/*metabolism/pathology
3.Distribution of lymphocytic subpopulations infiltrated in thyroid glands of Graves' disease.
Hyeon Joo JEONG ; Mi Kyung LEE ; In Joon CHOI ; Yoo Bock LEE
Yonsei Medical Journal 1989;30(2):118-124
We studied ninety cases of thyroid glands both histopathologically and by immunohistochemical methods in patients with Graves' disease using B and T cell markers to evaluate the role of lymphocytic subpopulation. Females were affected more frequently than males with a ratio of 6.5:1, and usually the females were younger than the males at the time of surgery. The heavier the lymphocytic infiltration, the higher was the percentage of germinal center formation or fibrosis. The degree of lymphocytic infiltration was also related to the titers of antithyroglobulin or antimicrosomal antibodies. T cells were mostly scattered individually or in small groups between the follicles; however, in the severely infiltrated group, the major pattern was in clusters. T8 positive cells were more abundant than T4 positive cells, and their distribution pattern was accordant with T11 positive cells. Immunoglobulin synthesizing B cells were positively stained in 47 of 94 cases tested and IgG was the most predominant. In the mild and moderate lymphocytic infiltration groups, IgM was mostly stained at the mantle zone or in the lymphoid cluster of the interfollicular stroma, whereas IgM positive cells were present exclusively in the germinal center of the severely infiltrated group. The results of our study indicate that the major lymphocyte subpopulation in Graves' disease is B lymphocytes, and the degree of T lymphocytic infiltration correlated better with titers of antimicrosomal antibody than antithyroglobulin.
Adolescent
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Adult
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Child
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Female
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Graves' Disease/immunology/*pathology
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Human
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Immunoglobulins/metabolism
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Lymphocytes/immunology/pathology
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Male
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Middle Age
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Support, Non-U.S. Gov't
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Thyroid Gland/immunology/pathology
4.Propylthiouracil induced anti-neutrophil cytoplasmic antibody-associated vasculitis with bone marrow plasmacytosis and granulocytopenia.
Abdullah OZKOK ; Serpil SALMAN ; Mehmet AGAN ; A Selim YAVUZ ; Sema YARMAN ; Harika BOZTEPE ; Faruk ALAGOL ; Refik TANAKOL
Chinese Medical Journal 2009;122(9):1112-1114
Adult
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Agranulocytosis
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chemically induced
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metabolism
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pathology
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Antibodies, Antineutrophil Cytoplasmic
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metabolism
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Bone Marrow Diseases
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chemically induced
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metabolism
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pathology
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Female
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Graves Disease
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drug therapy
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Humans
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Plasma Cells
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pathology
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Propylthiouracil
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adverse effects
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therapeutic use
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Vasculitis
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chemically induced
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immunology
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pathology
5.A Case of Autoimmune Hepatitis Combined with Graves' Disease.
Jong Hyun JHEE ; Hyun Ju KIM ; Wonseok KANG ; Sewha KIM ; Do Young KIM
The Korean Journal of Gastroenterology 2015;65(1):48-51
A 25-year-old woman presented with jaundice, palpitation, and weight loss of 5 kg during a period of 2 weeks. Laboratory tests showed elevated levels of liver enzymes (AST 1,282 IU/L, ALT 1,119 IU/L) and total bilirubin (6.4 mg/dL); negative for hepatitis virus infection; elevated serum levels of triiodothyronine (T3, 3.60 ng/dL), free thyroxine (fT4, 3.82 ng/dL), and lowered serum level of thyroid stimulating hormone (TSH, <0.025 microIU/mL); and positive for thyroid stimulating antibody and anti-mitochondrial antibody (AMA). The liver biopsy findings were consistent with autoimmune hepatitis (AIH). Accordingly, oral steroid therapy was started with 60 mg of prednisolone under the impression of AIH associated with Graves' disease. After a week of steroid therapy, the clinical manifestation showed significant improvement, with normalization of both liver and thyroid functions. Diagnosis of the liver condition of patients who present with hyperthyroidism and liver dysfunction is important, so that appropriate therapy can be promptly initiated.
Adult
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Alanine Transaminase/analysis
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Antibodies, Antinuclear/blood
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Aspartate Aminotransferases/analysis
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Bilirubin/blood
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Female
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Graves Disease/complications/*diagnosis/drug therapy
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Hepatitis, Autoimmune/complications/*diagnosis/drug therapy
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Humans
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Immunoglobulins, Thyroid-Stimulating/blood
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Liver/enzymology/metabolism/pathology
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Prednisolone/therapeutic use
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Steroids/therapeutic use
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Thyrotropin/blood