Literature DB >> 26262437

Diagnosis of Primary Hypophysitis in Germany.

Jürgen Honegger1, Sven Schlaffer1, Christa Menzel1, Michael Droste1, Sandy Werner1, Ulf Elbelt1, Christian Strasburger1, Sylvère Störmann1, Anna Küppers1, Christine Streetz-van der Werf1, Timo Deutschbein1, Mareike Stieg1, Roman Rotermund1, Monika Milian1, Stephan Petersenn1.   

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.

Entities:  

Mesh:

Year:  2015        PMID: 26262437     DOI: 10.1210/jc.2015-2152

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  31 in total

Review 1.  Visual loss in pregnancy.

Authors:  Caroline Annette Erika Bachmeier; Cameron Snell; Adam Morton
Journal:  BMJ Case Rep       Date:  2019-05-05

Review 2.  [Hypophysitis : Types and differential diagnosis].

Authors:  W Saeger
Journal:  Pathologe       Date:  2016-05       Impact factor: 1.011

Review 3.  Immunotoxicity from checkpoint inhibitor therapy: clinical features and underlying mechanisms.

Authors:  Petros Fessas; Lucia A Possamai; James Clark; Ella Daniels; Cathrin Gudd; Benjamin H Mullish; James L Alexander; David J Pinato
Journal:  Immunology       Date:  2019-11-19       Impact factor: 7.397

4.  Lymphocytic hypophysitis: modern day management with limited role for surgery.

Authors:  Angelos Kyriacou; Kanna Gnanalingham; Tara Kearney
Journal:  Pituitary       Date:  2017-04       Impact factor: 4.107

Review 5.  Primary hypophysitis and other autoimmune disorders of the sellar and suprasellar regions.

Authors:  Sriram Gubbi; Fady Hannah-Shmouni; Constantine A Stratakis; Christian A Koch
Journal:  Rev Endocr Metab Disord       Date:  2018-12       Impact factor: 6.514

6.  Neuro-radiological features can predict hypopituitarism in primary autoimmune hypophysitis.

Authors:  Tommaso Tartaglione; Sabrina Chiloiro; Maria Elena Laino; Antonella Giampietro; Simona Gaudino; Angelo Zoli; Antonio Bianchi; Alfredo Pontecorvi; Cesare Colosimo; Laura De Marinis
Journal:  Pituitary       Date:  2018-08       Impact factor: 4.107

7.  Single center study of 53 consecutive patients with pituitary stalk lesions.

Authors:  Mirjana Doknic; Dragana Miljic; Sandra Pekic; Marko Stojanovic; Dragan Savic; Emilija Manojlovic-Gacic; Tatjana Milenkovic; Vera Zdravkovic; Maja Jesic; Dusan Damjanovic; Slobodan Lavrnic; Ivan Soldatovic; Aleksandar Djukic; Milan Petakov
Journal:  Pituitary       Date:  2018-12       Impact factor: 4.107

Review 8.  Granulomatous hypophysitis causing compression of the internal carotid arteries reversible with azathioprine and rituximab treatment.

Authors:  Pauline Gendreitzig; Jürgen Honegger; Marcus Quinkler
Journal:  Pituitary       Date:  2020-04       Impact factor: 4.107

Review 9.  [Polyglandular autoimmune syndromes : An overview].

Authors:  P Komminoth
Journal:  Pathologe       Date:  2016-05       Impact factor: 1.011

10.  Granulomatous hypophysitis: a case of severe headache.

Authors:  Sharifah Faradila Wan Muhamad Hatta; M Farhan Hamdan; Siti Aishah Md Ali; Rohana Abdul Ghani
Journal:  BMJ Case Rep       Date:  2016-09-09
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