Literature DB >> 31446541

Pituitary dysfunction in granulomatosis with polyangiitis.

Arturo Vega-Beyhart1, Irene Rocío Medina-Rangel2, Andrea Hinojosa-Azaola2, Milagros Fernández-Barrio1, Ana Sofía Vargas-Castro1, Lucía García-Inciarte1, Alberto Guzmán-Pérez1, Tania Raisha Torres-Victoria1, Froylán David Martínez-Sánchez1, Mireya Citlali Pérez-Guzmán1, José Miguel Hinojosa-Amaya1, Andrés León-Suárez1, Miguel Angel Gómez-Sámano1, Francisco Javier Gómez-Pérez1, Daniel Cuevas-Ramos3.   

Abstract

Granulomatosis with polyangiitis (GPA) is a necrotizing granulomatous vasculitis of small vessels that affect the pituitary gland in less than 1% of cases being exceptionally rare. To describe the clinical, biochemical, radiological findings, treatment, and outcomes of 4 patients with GPA-related hypophysitis. A systematic review of published cases with the same diagnosis is presented as well. A cross-sectional case series of patients with hypophysitis due to GPA from 1981 to 2018 at a third level specialty center. Literature review was performed searching in seven different digital databases for terms "granulomatosis with polyangiitis" and "pituitary gland" or "hypophysitis," including in the analysis all published cases between 1950 and 2019 with a minimum follow-up of 6 months. We found 197 patients with GPA in our institution of whom 4 patients (2.0%) had pituitary involvement. Clinical characteristics and outcomes are described. We also reviewed 7 case series, and 36 case reports describing pituitary dysfunction related to GPA from 1953 to 2019, including the clinical picture of an additional 74 patients. Pituitary dysfunction due to GPA is rare. Treatment is targeted to control systemic manifestations; nevertheless, the outcome of the pituitary function is poor. Central diabetes insipidus, particularly in younger women with other systemic features, should raise suspicion of GPA.Key Points• Involvement of the pituitary gland is an uncommon manifestation in GPA patients. The presence of central diabetes insipidus in the setting of systemic symptoms should prompt its suspicion.• In patients with pituitary involvement due to GPA, affection of other endocrine glands is rare, neither concomitant nor in different times during the disease course. This may arise the hypothesis of a local or regional pathogenesis affection of the gland.• There is no consensus on the best therapy strategy for GPA hypophysitis. Although the use of glucocorticoids with CYC is the most common drug combination, no differences in the outcome of the pituitary function and GPA disease course are seen with other immunosuppressants.• Poor prognosis regarding pituitary function is expected due to possible permanent pituitary tissue damage that results in the need of permanent hormonal replacement.

Entities:  

Keywords:  Granulomatosis with polyangiitis; Hypophysitis; Pituitary; Vasculitis

Mesh:

Substances:

Year:  2019        PMID: 31446541     DOI: 10.1007/s10067-019-04735-7

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  47 in total

1.  A disease-specific activity index for Wegener's granulomatosis: modification of the Birmingham Vasculitis Activity Score. International Network for the Study of the Systemic Vasculitides (INSSYS).

Authors:  J H Stone; G S Hoffman; P A Merkel; Y I Min; M L Uhlfelder; D B Hellmann; U Specks; N B Allen; J C Davis; R F Spiera; L H Calabrese; F M Wigley; N Maiden; R M Valente; J L Niles; K H Fye; J W McCune; E W St Clair; R A Luqmani
Journal:  Arthritis Rheum       Date:  2001-04

2.  The American College of Rheumatology 1990 criteria for the classification of Wegener's granulomatosis.

Authors:  R Y Leavitt; A S Fauci; D A Bloch; B A Michel; G G Hunder; W P Arend; L H Calabrese; J F Fries; J T Lie; R W Lightfoot
Journal:  Arthritis Rheum       Date:  1990-08

3.  Pachymeningitis in granulomatosis with polyangiitis: case series with earlier onset in younger patients and literature review.

Authors:  Violeta Higuera-Ortiz; Abraham Reynoso; Natllely Ruiz; Rosa Delia Delgado-Hernández; Gilberto Gómez-Garza; Luis Felipe Flores-Suárez
Journal:  Clin Rheumatol       Date:  2016-12-23       Impact factor: 2.980

Review 4.  Wegener's granulomatosis: a review of clinical features and an update in diagnosis and treatment.

Authors:  Hanan A Almouhawis; Jair C Leao; Stefano Fedele; Stephen R Porter
Journal:  J Oral Pathol Med       Date:  2013-01-10       Impact factor: 4.253

Review 5.  Inflammatory and infectious processes involving the pituitary gland.

Authors:  Kenneth M Lury
Journal:  Top Magn Reson Imaging       Date:  2005-07

6.  Neurological involvement in Wegener's granulomatosis: an analysis of 324 consecutive patients at the Mayo Clinic.

Authors:  H Nishino; F A Rubino; R A DeRemee; J W Swanson; J E Parisi
Journal:  Ann Neurol       Date:  1993-01       Impact factor: 10.422

Review 7.  Wegener's granulomatosis.

Authors:  Peter Lamprecht; Wolfgang L Gross
Journal:  Herz       Date:  2004-02       Impact factor: 1.443

Review 8.  Granulomatous hypophysitis: two case reports and literature review.

Authors:  Jian Shi; Jian-Min Zhang; Qun Wu; Gao Chen; Hong Zhang; Wen-Liang Bo
Journal:  J Zhejiang Univ Sci B       Date:  2009-07       Impact factor: 3.066

9.  2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides.

Authors:  J C Jennette; R J Falk; P A Bacon; N Basu; M C Cid; F Ferrario; L F Flores-Suarez; W L Gross; L Guillevin; E C Hagen; G S Hoffman; D R Jayne; C G M Kallenberg; P Lamprecht; C A Langford; R A Luqmani; A D Mahr; E L Matteson; P A Merkel; S Ozen; C D Pusey; N Rasmussen; A J Rees; D G I Scott; U Specks; J H Stone; K Takahashi; R A Watts
Journal:  Arthritis Rheum       Date:  2013-01

Review 10.  Hypophysitis: Evaluation and Management.

Authors:  Alexander Faje
Journal:  Clin Diabetes Endocrinol       Date:  2016-09-06
View more
  3 in total

Review 1.  Pituitary Involvement in Granulomatosis with Polyangiitis: A Retrospective Analysis in a Single Chinese Hospital and a Literature Review.

Authors:  Shixuan Liu; Yan Xu; Naishi Li; Shi Chen; Shangzhu Zhang; Linyi Peng; Wei Bai; Jinglan Wang; Jinming Gao; Xiaofeng Zeng; Juhong Shi; Mengzhao Wang
Journal:  Int J Endocrinol       Date:  2019-11-06       Impact factor: 3.257

2.  Ectopic Relapse of Anti-neutrophil Cytoplasmic Antibody-associated Pituitary Vasculitis with No Elevation of Anti-neutrophil Cytoplasmic Antibodies after Renal Remission.

Authors:  Reiko Muto; Koji Inagaki; Naokazu Sato; Tetsuro Sameshima; Yuka Nagakura; Satoshi Baba; Noritoshi Kato; Shoichi Maruyama; Toshiyuki Akahori
Journal:  Intern Med       Date:  2020-08-12       Impact factor: 1.271

Review 3.  Hypophysitis, the Growing Spectrum of a Rare Pituitary Disease.

Authors:  Fabienne Langlois; Elena V Varlamov; Maria Fleseriu
Journal:  J Clin Endocrinol Metab       Date:  2022-01-01       Impact factor: 5.958

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.