Cargando…

IgG4-related hypophysitis: a retrospective cohort study

PURPOSE: IgG4-related hypophysitis (IgG4-RH) is a rare chronic inflammatory condition of the pituitary gland. This study reports the presentation, management and outcomes for patients with histologically proven IgG4-related hypophysitis. METHODS: A prospectively maintained electronic database was se...

Descripción completa

Detalles Bibliográficos
Autores principales:	Bhargava, R., Hussein, Z., Dorward, N. L., Grieve, J. P., Jaunmuktane, Z., Marcus, H. J., Proctor, I., Baldeweg, S. E.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Vienna 2022
Materias:	Original Article - Pituitaries
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338115/ https://www.ncbi.nlm.nih.gov/pubmed/35532784 http://dx.doi.org/10.1007/s00701-022-05231-9

Ejemplares similares

PMON100 IgG4 hypophysitis with granulomatous histopathology
por: Gultekin, Sakir, et al.
Publicado: (2022)

SUN-273 A Rare Case of IgG4-Related Hypophysitis
por: Ravindra, Sindhura, et al.
Publicado: (2020)

ODP295 An Unusual Case of Isolated IgG4 Related Hypophysitis
por: Shah, Aashka, et al.
Publicado: (2022)

MON-264 Pleotropic Clinical Presentation in Two Brazilians Patients with Confirmed IgG4-Related Hypophysitis
por: de Oliveira, Rafael, et al.
Publicado: (2020)

Rathke’s cleft cysts following transsphenoidal surgery: long-term outcomes and development of an optimal follow-up strategy
por: Marcus, Hani J., et al.
Publicado: (2020)

IgG4-related hypothalamo-hypophysitis
por: Urushida, Yuki, et al.
Publicado: (2021)

Prednisolone-responsive Postpartum IgG4-related Hypophysitis
por: Koide, Hisashi, et al.
Publicado: (2017)

Idiopathic Hypophysitis
por: Amjed, Hafsa, et al.
Publicado: (2021)

Outcome of Petrosal Venous Sampling in Consecutive 68 Patients From a Major Neurosurgical Center in the United Kingdom
por: Hussein, Ziad, et al.
Publicado: (2021)

LBMON134 Igg4 Related Hypophysitis And Skull Base Lesion: Retrospective Analysis Of 10 Years’ Experience Of A Tertiary Care Hospital Of Northern India.
por: Chakraborty, Ananda Mohan, et al.
Publicado: (2022)

Clinical course of IgG4-related hypophysitis presenting with focal seizure and relapsing lymphocytic hypophysitis
por: Ngaosuwan, Kanchana, et al.
Publicado: (2015)

IgG4-Related Hypophysitis: Case Report and Literature Review
por: Decker, Lauren, et al.
Publicado: (2016)

IgG4-Related Disease with Hypophysitis and Cholangitis as the Main Manifestations
por: Huang, Yan, et al.
Publicado: (2022)

Pituitary function at presentation and following therapy in patients with non-functional pituitary macroadenomas: a single centre retrospective cohort study
por: Hussein, Ziad, et al.
Publicado: (2023)

Pituitary metastasis of breast cancer mimicking IgG4-related hypophysitis
por: Nose, Kanako, et al.
Publicado: (2018)

IgG4-Related Disease Manifesting as Interstitial Nephritis Accompanied by Hypophysitis
por: Matsuda, Ken, et al.
Publicado: (2017)

Clinical course of pituitary function and image in IgG4-related hypophysitis
por: Anno, Takatoshi, et al.
Publicado: (2017)

A rare case of isolated IgG4-related hypophysitis with Rathke’s cleft cyst presenting as panhypopituitarism
por: Hashmi, Hiba Z, et al.
Publicado: (2023)

A Case of IgG4-Related Hypophysitis Presented with Hypopituitarism and Diabetes Insipidus
por: Harano, Yumi, et al.
Publicado: (2015)

Rituximab treatment for isolated IgG4-related hypophysitis in a teenage female
por: Bullock, Danielle R, et al.
Publicado: (2018)

Sellar germinoma mimicking IgG4-related hypophysitis: a case report
por: Chen, Kang, et al.
Publicado: (2022)

IgG4-related hypophysitis: A monocentric experience from North India
por: Chakraborty, Ananda Mohan, et al.
Publicado: (2022)

SUN-416 Ipilimumab Associated Hypophysitis and Thyroiditis
por: Kazi, Fatima, et al.
Publicado: (2019)

Rituximab as an Alternative Treatment for Refractory Granulomatous Hypophysitis
por: Nokhbehzaeim, Mahrokh, et al.
Publicado: (2021)

FRI342 Hypophysitis Mimicking As Pituitary Adenoma
por: Chao, Alex, et al.
Publicado: (2023)

Two cases of immunoglobulin G4 (IgG4)-related hypophysitis diagnosed without pituitary biopsy
por: Ma, Wanlu, et al.
Publicado: (2020)

LBODP074 Autoimmune Hypophysitis: Diagnosis Beyond Imaging
por: Gonzalez, Juanita, et al.
Publicado: (2022)

FRI326 Hypophysitis: A Formidable Diagnostic Challenge
por: Pandey, Shanta, et al.
Publicado: (2023)

FRI328 Granulomatous Hypophysitis With Magnificent Response To Glucocorticoids
por: Rodriguez Caballero, Maria Galiana, et al.
Publicado: (2023)

FRI329 COVID-19: An Uncommon Cause Of Hypophysitis
por: Medina-Torres, Wilnelia, et al.
Publicado: (2023)

OR32-02 Immune Checkpoint Inhibitor-Induced Hypophysitis Is Associated with Improved Overall Survival in Cancer Patients
por: Kotwal, Anupam, et al.
Publicado: (2020)

A Case Series of Patients with Isolated IgG4-related Hypophysitis Treated with Rituximab
por: Boharoon, Hessa, et al.
Publicado: (2020)

Concurrent IgG4-related hypophysitis and clinically nonfunctioning gonadotroph pituitary neuroendocrine tumor
por: Tahara, Shigeyuki, et al.
Publicado: (2023)

SUN-298 Spectrum of Imaging in Immune Checkpoint Inhibitor Induced Hypophysitis
por: Quandt, Zoe, et al.
Publicado: (2020)

SUN-286 Lymphocytic Hypophysitis Mimicking Tolosa Hunt Syndrome
por: Del Castillo, Ma Dolores, et al.
Publicado: (2020)

MON-251 Xanthogranulomatous Hypophysitis: A Rare Case of Hypopoituitarism
por: Romero, Fabiola, et al.
Publicado: (2020)

Stuck at the Checkpoint: Pembrolizumab Induced Hypophysitis With ‘Normal’ Cosyntropin Response
por: Kasiri, Elnaz, et al.
Publicado: (2021)

Headache, Pituitary Apoplexy and Diabetes insipidus: Suspect Necrotizing Hypophysitis
por: Panthi, Sujata, et al.
Publicado: (2021)

Characterizing Immune Checkpoint Inhibitor-Induced Hypophysitis and Obstacles in Diagnosis
por: Johnson, Jake, et al.
Publicado: (2021)

LBODP076 Hypophysitis Misdiagnosed As Pituitary Macroadenoma During Pregnancy
por: Meftali, Sabrina, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_df2b9944d0u13cl3jf2g62va0q