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  • 1
    Online Resource
    Online Resource
    S. Karger AG ; 1982
    In:  International Archives of Allergy and Immunology Vol. 69, No. 2 ( 1982), p. 137-142
    In: International Archives of Allergy and Immunology, S. Karger AG, Vol. 69, No. 2 ( 1982), p. 137-142
    Abstract: Mononuclear cell infiltrates in thyroid gland tissue sections from patients with drug-treated Graves’ disease (n = 5), non-toxic nodular goiter (n = 12) and papillary carcinoma (n = 5) were characterized by immunological membrane receptors. T lymphocytes were identified using 2-aminoethylisothiouronium bromide hydrobromide (AET)-treated sheep erythrocytes (E) (E-AET). E sensitized with rabbit IgM antibodies (A) and human complement (C) (EAC) were used to detect receptors for C3b (B lymphocytes and monocytes) or C3d (B lymphocytes). E sensitized with rabbit IgG antibodies were used to detect receptors for the Fc portion of IgG (FcR; lymphocytes and monocytes). The results indicate that T and B lymphocytes infiltrate the thyroid gland in Graves’ disease as well as in nodular goiter. T lymphocytes seemed to predominate in both disorders. In thyroid papillary carcinoma the number of B and T lymphocytes was negligible. However, EA absorbed strongly to sections from 3 of the 5 tumors studied, indicating the presence of FcR on tumor cells or infiltrating host cells. The percentage of active and total T lymphocytes in peripheral blood from the patients with drug-treated Graves’ disease was markedly reduced (9 ± 5 and 28 ± 11%, controls 22 ± 9 and 68 ± 11%; p 〈 0.01 and 〈 0.001). In patients with nodular goiter the percentage of total T lymphocytes was slightly, but significantly decreased (p 〈 0.05). We suggest that the marked decrease in blood T lymphocytes observed in Graves’ disease might be caused by the drug therapy. In nodular goiter the predominance of T lymphocyte infiltration together with a slight decrease in blood T lymphocytes suggest that autoimmune mechanisms are involved in the pathogenesis.
    Type of Medium: Online Resource
    ISSN: 1018-2438 , 1423-0097
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 1982
    detail.hit.zdb_id: 1482722-0
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  • 2
    In: The Journal of Clinical Endocrinology & Metabolism, The Endocrine Society, Vol. 93, No. 8 ( 2008-08), p. 2984-2990
    Type of Medium: Online Resource
    ISSN: 0021-972X , 1945-7197
    RVK:
    Language: English
    Publisher: The Endocrine Society
    Publication Date: 2008
    detail.hit.zdb_id: 2026217-6
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  • 3
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2009
    In:  European Journal of Endocrinology Vol. 160, No. 2 ( 2009-02), p. 143-148
    In: European Journal of Endocrinology, Oxford University Press (OUP), Vol. 160, No. 2 ( 2009-02), p. 143-148
    Abstract: Gamma knife radiosurgery (GKR) can be used as primary or adjuvant therapy for the treatment of an ACTH-producing pituitary tumor after bilateral adrenalectomy, called Nelson syndrome (NS). We have examined the effect of GKR on tumor growth and ACTH-hypersecretion, and characterized the adverse events of this treatment in patients with NS. Design Cross-sectional follow-up study. First, retrospective data pre- and post-GKR were collected. Patients then underwent a predefined survey including radiological, endocrinological, ophthalmological, and neurosurgical evaluation. Subjects Ten patients treated with GKR for NS after previous bilateral adrenalectomy. The mean follow-up was 7 years. No patient was lost to follow-up. Results Tumor growth was stopped in all patients. The ACTH levels declined in eight patients, and normalized in one patient. There was a significant drop in ACTH levels, with a half-time of 2.8 years. No patient developed visual field defects or any other cranial nerve dysfunction as a result of treatment. Four patients started hormone substitution therapy during the follow-up period. The substitution therapy of three pituitary axes present at GKR treatment could be stopped during the same period. One patient developed a glioblastoma in the left parieto-occipital region 14 years after GKR, far from the field of treatment. As the radiation level was below 1Gy to this area, it is unlikely that the GKR treatment itself induced the malignant tumor. Conclusion In patients with NS, GKR is an effective adjuvant treatment, carrying relatively few adverse effects. Although the risk of developing a secondary neoplasia after GKR is present, it is probably extremely low.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 2009
    detail.hit.zdb_id: 1485160-X
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  • 4
    Online Resource
    Online Resource
    Georg Thieme Verlag KG ; 1986
    In:  Hormone and Metabolic Research Vol. 18, No. 02 ( 1986-2), p. 110-113
    In: Hormone and Metabolic Research, Georg Thieme Verlag KG, Vol. 18, No. 02 ( 1986-2), p. 110-113
    Type of Medium: Online Resource
    ISSN: 0018-5043 , 1439-4286
    RVK:
    Language: English
    Publisher: Georg Thieme Verlag KG
    Publication Date: 1986
    detail.hit.zdb_id: 2056576-8
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  • 5
    Online Resource
    Online Resource
    Wiley ; 1981
    In:  Clinical Endocrinology Vol. 15, No. 3 ( 1981-09), p. 247-252
    In: Clinical Endocrinology, Wiley, Vol. 15, No. 3 ( 1981-09), p. 247-252
    Type of Medium: Online Resource
    ISSN: 0300-0664 , 1365-2265
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 1981
    detail.hit.zdb_id: 2004597-9
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  • 6
    Online Resource
    Online Resource
    Mary Ann Liebert Inc ; 2002
    In:  Thyroid Vol. 12, No. 1 ( 2002-01), p. 77-80
    In: Thyroid, Mary Ann Liebert Inc, Vol. 12, No. 1 ( 2002-01), p. 77-80
    Type of Medium: Online Resource
    ISSN: 1050-7256 , 1557-9077
    Language: English
    Publisher: Mary Ann Liebert Inc
    Publication Date: 2002
    detail.hit.zdb_id: 2030622-2
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  • 7
    Online Resource
    Online Resource
    S. Karger AG ; 1983
    In:  International Archives of Allergy and Immunology Vol. 70, No. 1 ( 1983), p. 40-45
    In: International Archives of Allergy and Immunology, S. Karger AG, Vol. 70, No. 1 ( 1983), p. 40-45
    Abstract: The expression of FcIgG receptor (FcR) was studied during various stages of growth and subculturing of: (1) fetal rat brain cells (FBC); (2) FBC during in vitro neoplastic transformation after a transplacental pulse of the alkylating carcinogen ethylnitrosurea in vivo, and (3) an established neoplastic brain tumor cell line. Hemadsorption of antibody-coated sheep erythrocytes was used for the detection of FcR-positive cells. Such cells were not detected in cryostat sections of fetal rat brains, but in primary cultures of FBC 1 day after the explantation. FcR-positive cells were present throughout the logarithmic-growth phase. When reaching confluency after 5–7 days in culture, FcR-positive cells could not be detected. In the secondary cultures the occurrence of FcR-positive cells showed a similar variation related to growth: The growth-related receptor was also present on cells growing into arteficial defects in confluent cultures, while the resting cells in the same cultures were FcR-negative. With further subculturing the cells became epithelioid and slowly growing without FcR. Morphologically induced differentiation of such epithelioid cells by 12-O-tetra-decanoyl phorbol-13-acetate did not change the FcR expression. We did not detect any change in the receptor expression related to the malignant transformation, and the malignant cell line was FcR-negative. Expression of FcR on FBC undergoing malignant transformation therefore seems to be mainly connected to the mode of growth (log-phase versus confluence).
    Type of Medium: Online Resource
    ISSN: 1018-2438 , 1423-0097
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 1983
    detail.hit.zdb_id: 1482722-0
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  • 8
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1980
    In:  Acta Endocrinologica Vol. 95, No. 2 ( 1980-10), p. 181-184
    In: Acta Endocrinologica, Oxford University Press (OUP), Vol. 95, No. 2 ( 1980-10), p. 181-184
    Abstract: A patient with Addison's disease, who was inadequately substituted with corticosteroids for twenty-five years, developed a pituitary tumour. The diagnosis of autoimmune thryroiditis with asymptomatic hypothyroidism was also made. ACTH and TSH plasma values were abnormally elevated. The ACTH secretion was suppressed by cortisone administered perorally. It seems possible that the pituitary enlargement is due to prolonged insufficient adrenocortical replacement therapy. The differential diagnosis and possible pathogenetic factors are discussed.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 1980
    detail.hit.zdb_id: 1485160-X
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  • 9
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1982
    In:  Acta Endocrinologica Vol. 100, No. 4 ( 1982-08), p. 588-594
    In: Acta Endocrinologica, Oxford University Press (OUP), Vol. 100, No. 4 ( 1982-08), p. 588-594
    Abstract: Plasma cortisol and the corresponding ACTH concentrations were determined before, and for 6 h following a single oral dose of 25 mg cortisone acetate in 7 patients with Addison's disease, 6 patients adrenalectomized for Cushing's disease and 1 patient adrenalectomized for congenital adrenal hyperplasia. The basal plasma cortisol concentrations 12 h after an evening dose of cortisone acetate 12.5 mg were below 100 nmol/l, and the corresponding ACTH concentrations were markedly elevated in all the patients. Great interindividual variations were found in cortisol peak concentrations (C max ) and the time to peak values, but without significant differences between the two patient groups. The maximal ACTH suppression occurred within 60–330 min after the cortisol C max . and was not significantly different in the two groups. The suppressed plasma ACTH concentrations were considerably above normal in 3 of the patients with Addison's disease and in 4 of the 6 patients adrenalectomized for Cushing's disease, including 2 patients with Nelson's syndrome. A similar degree of impaired ACTH suppression in patients with Addison's disease as in adrenalectomized patients suggests the occurrence of a secondary hypothalamic-pituitary dysfunction with ACTH hypersecretion in Addison's disease. The adequacy of the commonly used adrenocortical replacement therapy and its possible relation to the impaired ACTH suppression is discussed.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 1982
    detail.hit.zdb_id: 1485160-X
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  • 10
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2007
    In:  European Journal of Endocrinology Vol. 157, No. 3 ( 2007-09), p. 255-263
    In: European Journal of Endocrinology, Oxford University Press (OUP), Vol. 157, No. 3 ( 2007-09), p. 255-263
    Abstract: Background : Gamma knife radiosurgery (GKR) is an adjuvant treatment for acromegaly if surgery fails to normalize GH hypersecretion. Objective : To examine the effect of GKR on tumor growth and hypersecretion, and to characterize the adverse effect of this treatment. Design : Cross-sectional follow-up study. First, retrospective data pre- and post-GKR were collected. Patients then underwent a predefined survey including radiological, endocrinological, ophthalmological, and neurosurgical evaluation. Setting : Norwegian National Center for gamma knife treatment. Patients : Sixty-one patients treated with GKR for acromegaly. Out of 55, 53 living patients underwent a detailed survey. The mean follow-up was 5.5 years. No patient was lost to follow-up. Results : Tumor growth was stopped in all patients. At 3, 5, and 10 years after GKR, 45, 58, and 86% of patients had normal IGF-I levels. Consecutive hormone value analysis showed that patients receiving GH-suppressive medication had a more rapid decline in hypersecretion than those who did not receive such medication. Evaluated by survey baseline values alone, non-elevated IGF-I and GH levels below 5 mIU/l were found in 38%. GH-suppressive medication was terminated in 16 out of 40 patients following GKR. Nine out of 53 surveyed patients (17%) had normal IGF-I and GH nadir below 2.6 mIU/l at glucose tolerance tests, while not on hormone-suppressive medication. Two patients developed minor visual field defects. Eight patients started hormone substitution therapy during the follow-up period. Conclusion : GKR is an effective adjuvant treatment for residual acromegaly, carrying few side effects.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 2007
    detail.hit.zdb_id: 1485160-X
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