Literature DB >> 26091204

Treatment of Primary Hypophysitis in Germany.

Jürgen Honegger1, Michael Buchfelder1, Sven Schlaffer1, Michael Droste1, Sandy Werner1, Christian Strasburger1, Sylvère Störmann1, Jochen Schopohl1, Stella Kacheva1, Timo Deutschbein1, Günter Stalla1, Jörg Flitsch1, Monika Milian1, Stephan Petersenn1, Ulf Elbelt2.   

Abstract

CONTEXT: The best treatment of primary hypophysitis (PrHy) is a matter of debate.
OBJECTIVE: Our main objective was to analyze the treatment practice for PrHy in Germany and to compare the outcome of the main treatment options.
DESIGN: The Pituitary Working Group of the German Society of Endocrinology conducted a nationwide retrospective cross-sectional cohort study. PATIENTS: Seventy-six patients with PrHy were eligible for the study. MAIN OUTCOME MEASURES: Clinical and endocrinological outcomes, side effects and complications of therapy, initial response, and recurrence rates were assessed. Outcome depending on the treatment modality was evaluated.
RESULTS: For mere observation, regression of space-occupying lesions was observed in 46%, unchanged size in 27%, and progression reported in 27%. Pituitary function improved in 27% of patients during observation. Deterioration of pituitary function was only found in patients with progressive lesions. The initial response to glucocorticoid pulse therapy was most favorable, with early failure in only 3%. However, the overall failure and recurrence rate was 41%. Recurrence rate was not related to duration of steroid administration. Side effects of steroids occurred in 63%. The surgical approach was transsphenoidal in 94%. The histological subtype was lymphocytic hypophysitis in 70% and granulomatous hypophysitis in 30%. Progression or recurrence was observed in 25% after surgical treatment.
CONCLUSION: Glucocorticoid pulse therapy is associated with a high recurrence rate. Evidence suggests that surgery is not able to prevent recurrence. Considering the favorable results of observation, conservative management is recommended in PrHy unless symptoms are severe or progressive.

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Year:  2015        PMID: 26091204     DOI: 10.1210/jc.2015-2146

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


  26 in total

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2.  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 3.  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

4.  Outcomes of Initial Management Strategies in Patients With Autoimmune Lymphocytic Hypophysitis: A Systematic Review and Meta-analysis.

Authors:  Diane Donegan; Zeb Saeed; Danae A Delivanis; Mohammad Hassan Murad; Juergen Honegger; Felix Amereller; Seda Hanife Oguz; Dana Erickson; Irina Bancos
Journal:  J Clin Endocrinol Metab       Date:  2022-03-24       Impact factor: 5.958

5.  Preoperative differentiation of hypophysitis and pituitary adenomas using a novel clinicoradiologic scoring system.

Authors:  Kyla Wright; Hyon Kim; Travis Hill; Matthew Lee; Cordelia Orillac; Nikita Mogar; Donato Pacione; Nidhi Agrawal
Journal:  Pituitary       Date:  2022-05-27       Impact factor: 3.599

Review 6.  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 7.  Hypophysitis: An update on the novel forms, diagnosis and management of disorders of pituitary inflammation.

Authors:  Sriram Gubbi; Fady Hannah-Shmouni; Joseph G Verbalis; Christian A Koch
Journal:  Best Pract Res Clin Endocrinol Metab       Date:  2019-12-12       Impact factor: 4.690

8.  Xanthomatous Hypophysitis Presenting in an Adolescent Girl: A Long-Term Follow-Up of a Rare Case and Review of the Literature.

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Journal:  AACE Clin Case Rep       Date:  2021-02-01

9.  A case report of lymphocytic hypophysitis.

Authors:  Stephen Yu; Ramakrishna Bethanabatla; Ahmed Taha
Journal:  Surg Neurol Int       Date:  2021-06-07

10.  Deterioration of pituitary function without relapse after steroid therapy for IgG4-related hypophysitis.

Authors:  Nobuyuki Nishi; Ken Takeshima; Shuhei Morita; Hiroshi Iwakura; Masahiro Nishi; Takaaki Matsuoka
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2021-07-01
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