Diagnosis of Primary Hypophysitis in Germany

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Diagnosis of Primary Hypophysitis in Germany. / Honegger, Jürgen; Schlaffer, Sven; Menzel, Christa; Droste, Michael; Werner, Sandy; Elbelt, Ulf; Strasburger, Christian; Störmann, Sylvère; Küppers, Anna; Streetz-van der Werf, Christine; Deutschbein, Timo; Stieg, Mareike; Rotermund, Roman; Milian, Monika; Petersenn, Stephan; Pituitary Working Group of the German Society of Endocrinology.

In: J CLIN ENDOCR METAB, Vol. 100, No. 10, 10.2015, p. 3841-9.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Honegger, J, Schlaffer, S, Menzel, C, Droste, M, Werner, S, Elbelt, U, Strasburger, C, Störmann, S, Küppers, A, Streetz-van der Werf, C, Deutschbein, T, Stieg, M, Rotermund, R, Milian, M, Petersenn, S & Pituitary Working Group of the German Society of Endocrinology 2015, 'Diagnosis of Primary Hypophysitis in Germany', J CLIN ENDOCR METAB, vol. 100, no. 10, pp. 3841-9. https://doi.org/10.1210/jc.2015-2152

APA

Honegger, J., Schlaffer, S., Menzel, C., Droste, M., Werner, S., Elbelt, U., Strasburger, C., Störmann, S., Küppers, A., Streetz-van der Werf, C., Deutschbein, T., Stieg, M., Rotermund, R., Milian, M., Petersenn, S., & Pituitary Working Group of the German Society of Endocrinology (2015). Diagnosis of Primary Hypophysitis in Germany. J CLIN ENDOCR METAB, 100(10), 3841-9. https://doi.org/10.1210/jc.2015-2152

Vancouver

Honegger J, Schlaffer S, Menzel C, Droste M, Werner S, Elbelt U et al. Diagnosis of Primary Hypophysitis in Germany. J CLIN ENDOCR METAB. 2015 Oct;100(10):3841-9. https://doi.org/10.1210/jc.2015-2152

Bibtex

@article{f5dc11a54e92469db7a63f314e9c92fe,
title = "Diagnosis of Primary Hypophysitis in Germany",
abstract = "CONTEXT: Representative data on diagnostic findings in primary hypophysitis (PrHy) are scarce.OBJECTIVE: The objective of the study was to collate consistent data on clinical features in a large series of patients with PrHy. Another objective was to gain information on current practice in a diagnostic work-up.DESIGN: The Pituitary Working Group of the German Society of Endocrinology conducted a nationwide retrospective cross-sectional cohort study in Germany.PATIENTS: Seventy-six patients with PrHy were identified.MAIN OUTCOME MEASURES: Clinical and endocrinological features were assessed.RESULTS: Headache (50%) and increase in body mass (18%) were the most frequent nonendocrine symptoms. Hypophysitis was associated with pregnancy in only 11% of the female patients. Diabetes insipidus was found in 54% of the patients at presentation. Hypogonadotropic hypogonadism was the most frequent endocrine failure (62%), whereas GH deficiency was the least frequent (37%). With 86%, thickening of the pituitary stalk was the prevailing neuroradiological sign. Compared with surgical cases, the cases without histological confirmation presented more often with suprasellar lesions and had less severe nonendocrine symptoms. Granulomatous hypophysitis was associated with more severe clinical symptoms than lymphocytic hypophysitis. Examination of cerebrospinal fluid was predominantly performed in participating neurosurgical centers, whereas thyroid antibodies were almost exclusively assessed in endocrinological centers.CONCLUSION: In contrast to the literature, hypogonadism was found to be the most frequent endocrine failure in PrHy. Weight gain was identified as a clinical sign of PrHy. In the majority of patients, PrHy can be reliably identified by characteristic clinical signs and symptoms, obviating histological confirmation. The diagnostic approach should be standardized in PrHy.",
author = "J{\"u}rgen Honegger and Sven Schlaffer and Christa Menzel and Michael Droste and Sandy Werner and Ulf Elbelt and Christian Strasburger and Sylv{\`e}re St{\"o}rmann and Anna K{\"u}ppers and {Streetz-van der Werf}, Christine and Timo Deutschbein and Mareike Stieg and Roman Rotermund and Monika Milian and Stephan Petersenn and {Pituitary Working Group of the German Society of Endocrinology}",
year = "2015",
month = oct,
doi = "10.1210/jc.2015-2152",
language = "English",
volume = "100",
pages = "3841--9",
journal = "J CLIN ENDOCR METAB",
issn = "0021-972X",
publisher = "The Endocrine Society",
number = "10",

}

RIS

TY - JOUR

T1 - Diagnosis of Primary Hypophysitis in Germany

AU - Honegger, Jürgen

AU - Schlaffer, Sven

AU - Menzel, Christa

AU - Droste, Michael

AU - Werner, Sandy

AU - Elbelt, Ulf

AU - Strasburger, Christian

AU - Störmann, Sylvère

AU - Küppers, Anna

AU - Streetz-van der Werf, Christine

AU - Deutschbein, Timo

AU - Stieg, Mareike

AU - Rotermund, Roman

AU - Milian, Monika

AU - Petersenn, Stephan

AU - Pituitary Working Group of the German Society of Endocrinology

PY - 2015/10

Y1 - 2015/10

N2 - CONTEXT: Representative data on diagnostic findings in primary hypophysitis (PrHy) are scarce.OBJECTIVE: The objective of the study was to collate consistent data on clinical features in a large series of patients with PrHy. Another objective was to gain information on current practice in a diagnostic work-up.DESIGN: The Pituitary Working Group of the German Society of Endocrinology conducted a nationwide retrospective cross-sectional cohort study in Germany.PATIENTS: Seventy-six patients with PrHy were identified.MAIN OUTCOME MEASURES: Clinical and endocrinological features were assessed.RESULTS: Headache (50%) and increase in body mass (18%) were the most frequent nonendocrine symptoms. Hypophysitis was associated with pregnancy in only 11% of the female patients. Diabetes insipidus was found in 54% of the patients at presentation. Hypogonadotropic hypogonadism was the most frequent endocrine failure (62%), whereas GH deficiency was the least frequent (37%). With 86%, thickening of the pituitary stalk was the prevailing neuroradiological sign. Compared with surgical cases, the cases without histological confirmation presented more often with suprasellar lesions and had less severe nonendocrine symptoms. Granulomatous hypophysitis was associated with more severe clinical symptoms than lymphocytic hypophysitis. Examination of cerebrospinal fluid was predominantly performed in participating neurosurgical centers, whereas thyroid antibodies were almost exclusively assessed in endocrinological centers.CONCLUSION: In contrast to the literature, hypogonadism was found to be the most frequent endocrine failure in PrHy. Weight gain was identified as a clinical sign of PrHy. In the majority of patients, PrHy can be reliably identified by characteristic clinical signs and symptoms, obviating histological confirmation. The diagnostic approach should be standardized in PrHy.

AB - CONTEXT: Representative data on diagnostic findings in primary hypophysitis (PrHy) are scarce.OBJECTIVE: The objective of the study was to collate consistent data on clinical features in a large series of patients with PrHy. Another objective was to gain information on current practice in a diagnostic work-up.DESIGN: The Pituitary Working Group of the German Society of Endocrinology conducted a nationwide retrospective cross-sectional cohort study in Germany.PATIENTS: Seventy-six patients with PrHy were identified.MAIN OUTCOME MEASURES: Clinical and endocrinological features were assessed.RESULTS: Headache (50%) and increase in body mass (18%) were the most frequent nonendocrine symptoms. Hypophysitis was associated with pregnancy in only 11% of the female patients. Diabetes insipidus was found in 54% of the patients at presentation. Hypogonadotropic hypogonadism was the most frequent endocrine failure (62%), whereas GH deficiency was the least frequent (37%). With 86%, thickening of the pituitary stalk was the prevailing neuroradiological sign. Compared with surgical cases, the cases without histological confirmation presented more often with suprasellar lesions and had less severe nonendocrine symptoms. Granulomatous hypophysitis was associated with more severe clinical symptoms than lymphocytic hypophysitis. Examination of cerebrospinal fluid was predominantly performed in participating neurosurgical centers, whereas thyroid antibodies were almost exclusively assessed in endocrinological centers.CONCLUSION: In contrast to the literature, hypogonadism was found to be the most frequent endocrine failure in PrHy. Weight gain was identified as a clinical sign of PrHy. In the majority of patients, PrHy can be reliably identified by characteristic clinical signs and symptoms, obviating histological confirmation. The diagnostic approach should be standardized in PrHy.

U2 - 10.1210/jc.2015-2152

DO - 10.1210/jc.2015-2152

M3 - SCORING: Journal article

C2 - 26262437

VL - 100

SP - 3841

EP - 3849

JO - J CLIN ENDOCR METAB

JF - J CLIN ENDOCR METAB

SN - 0021-972X

IS - 10

ER -