• A 15-year-old adolescent with a rare pituitary lesion
• A case of idiopathic granulomatous hypophysitis
• A case of idiopathic granulomatous hypophysitis
• A case of pituitary gland abscess associated with granulomatous hypophysitis
• A rare cause of hypophysitis: tuberculosis
• A Remarkable Response of Granulomatous Hypophysitis to Infliximab in a Patient With a Background of Crohn's Disease-A Case Report
• A Trial of Oral Glucocorticoids in the Resolution of Recurrent Granulomatous Hypophysitis: A Case Report
• A unique coexistence of a plurihormonal pituitary adenoma with granulomatous hypophysitis
• A woman with visual loss, amenorrhoea and polyuria: the first reported case of nodular lymphocyte-predominant Hodgkin lymphoma presenting with hypopituitarism
• Acute onset of polyarthralgia and high anti-cyclic citrullinated peptide antibodies in a case of idiopathic granulomatous hypophysitis
• An intrasellar germinoma with normal tumor marker concentrations mimicking primary lymphocytic hypophysitis
• Autoimmune Granulomatous Inflammation of Lacrimal Glands and Axonal Neuritis Following Treatment With Ipilimumab and Radiation Therapy
• Autoimmune phenomena involving the pituitary gland in children: New developing data about diagnosis and treatment
• AVP deficiency (central diabetes insipidus) following immunization with anti-COVID-19 BNT162b2 Comirnaty vaccine in adolescents: A case report
• Cerebral MR imaging of malignant melanoma
• Characteristics of inflammatory and infectious diseases of the pituitary gland in patients undergoing transsphenoidal surgery
• Clinical and hormonal characteristics of patients with different types of hypophysitis: a single-center experience
• Clinical Interrogation for Unveiling an Isolated Hypophysitis Mimicking Pituitary Adenoma
• Clinical practice guideline for the diagnosis and treatment of hypophysitis
• Combined granulomatous and lymphocytic hypophysitis presenting as pituitary incidentaloma in a middle-aged woman
• Diabetes insipidus induced by suspected eosinophilic granulomatous with polyangiitis
• Diagnosis and management of tumor-like hypophysitis: A retrospective case series
• Diagnosis of Primary Hypophysitis in Germany
• Diffuse Basisphenoid Enhancement: Possible Differentiating Feature for Granulomatous Hypophysitis
• Executive summary of the consensus document on hypophysitis of the Neuroendocrinology Area of Knowledge of the Spanish Society of Endocrinology and Nutrition
• Fatal juvenile xanthogranuloma presenting as a sellar lesion: case report and literature review
• Granulomatous adenohypophysitis after interferon and ribavirin therapy
• Granulomatous and lymphocytic hypophysitis - are they immunologically distinct?
• Granulomatous hypophysistis associated with rathke's cleft cyst: a case report
• Granulomatous Hypophysitis - A Case Report
• Granulomatous hypophysitis - A rare pathology: Review of three cases
• Granulomatous hypophysitis by Mycobacterium gordonae in a non HIV-infected patient
• Granulomatous hypophysitis caused by Rathke's cleft cyst mimicking a growth hormone-secreting pituitary adenoma
• Granulomatous hypophysitis causing compression of the internal carotid arteries reversible with azathioprine and rituximab treatment
• Granulomatous hypophysitis--an interesting and rare cause mimicking pituitary mass
• Granulomatous hypophysitis: a case of severe headache
• Granulomatous hypophysitis: rare disease with challenging diagnosis
• Granulomatous hypophysitis: two case reports and literature review
• Histopathological findings in the landscape of IgG4-related pathology in patients with pituitary dysfunction: Review of six cases
• Hypercalcaemia secondary to hypophysitis and cortisol deficiency: another immunotherapy-related adverse event
• Hypophysitis
• Hypophysitis : Types and differential diagnosis
• Hypophysitis (Including IgG4 and Immunotherapy)
• Hypophysitis in granulomatosis with polyangiitis: rare presentation of a multisystem disease
• Hypophysitis in the era of immune checkpoint inhibitors and immunoglobulin G4-related disease
• Hypophysitis presenting with atypical rapid deterioration: with special reference to immunoglobulin G4-related disease-case report-
• Hypophysitis: a single-center case series
• Hypophysitis: increasingly complex clinicopathological spectrum!
• Idiopathic granulomatous hypophysitis mimicking adenoma
• Idiopathic Granulomatous Hypophysitis Mimicking Pituitary Abscess
• Idiopathic granulomatous hypophysitis presenting as pituitary apoplexy
• Idiopathic granulomatous hypophysitis presenting with galactorrhea, headache, and nausea in a woman: a case report and review of the literature
• Idiopathic Granulomatous Hypophysitis with Rapid Onset: A Case Report
• Idiopathic granulomatous hypophysitis: a rare cystic lesion of the pituitary
• Idiopathic granulomatous hypophysitis: A report of an uncommon disorder
• Idiopathic granulomatous hypophysitis: a systematic review of 82 cases in the literature
• Idiopathic granulomatous hypophysitis: comments and a disease registry
• IgG4-related hypophysitis is highly prevalent among cases of histologically confirmed hypophysitis
• IgG4-related hypophysitis: a new addition to the hypophysitis spectrum
• IgG4-related intracranial disease
• IgG4-related uveitis. A French cohort and literature review
• Imaging findings in hypophysitis: a review
• Immunohistochemical study for IgG4-positive plasmacytes in pituitary inflammatory lesions
• Intracranial Germinoma Masquerading as Secondary Granulomatous Hypophysitis: A Case Report and Review of Literature
• Intratumoral granulomatous reaction in recurrent pituitary adenoma: A unique presentation
• Lactotroph PitNET/adenoma associated to granulomatous hypophysitis in a patient with Crohn's disease: A case report
• Lymphocytic hypophysitis masquerading as pituitary adenoma
• Manifestation of idiopathic granulomatous hypophysitis as hormone-active pituitary adenoma
• MECHANISMS IN ENDOCRINOLOGY: Hypophysitis: diagnosis and treatment
• Necrotizing granulomatous hypophysitis presenting as a sellar mass
• Neuroimaging of hypophysitis: etiologies and imaging mimics
• Neurosarcoidosis-Induced Hypophysitis Mimicking Pituitary Macroadenoma
• Pituitary Adenoma with Granulomatous Hypophysitis: A Rare Coexistence
• Pituitary autoimmune disease: nuances in clinical presentation
• Pituitary Autoimmunity
• Pituitary cryptococcoma: a strange case of secondary granulomatous hypophysitis
• Pituitary dysfunction in granulomatosis with polyangiitis
• Pituitary function and the response to GH therapy in patients with Langerhans cell histiocytosis: analysis of the KIMS database
• Pituitary tuberculosis mimicking idiopathic granulomatous hypophysitis
• Pituitary tumours: inflammatory and granulomatous expansive lesions of the pituitary
• Postpartum granulomatous hypophysitis with sphenoid sinus involvement: a case study
• Postpartum Granulomatous Hypophysitis: A Case Study, Review of the Literature, and Discussion of Pathogenesis
• Primary central nervous system vasculitis preceded by granulomatous hypophysitis: Case report with a review of the literature
• Primary granulomatous hypophysitis: a case report and literature review
• Primary granulomatous hypophysitis: an interesting entity
• Primary hypophysitis: Experience of a Single Tertiary Center
• Primary non-necrotizing granulomatous hypophysitis mimicking pituitary adenomas
• Pulmocrinology: Interplay of pulmonary and endocrine diseases
• Secondary xanthogranulomatous hypophysitis mimicking a pituitary macroadenoma: a case report
• Sellar inflammatory mass with inflammatory bowel disease
• Sellar lesion: not always a pituitary adenoma
• Severe Acute Kidney Injury Due to Nivolumab/Ipilimumab-induced Granulomatosis and Fibrinoid Vascular Necrosis
• Silent ACTH cell adenoma in coincidence with granulomatous hypophysitis--a case report
• The co-occurrence of SAT, hypophysitis, and Schnitzler syndrome after COVID-19 vaccination: the first described case
• The prevalence of IgG4-positive plasma cells in hypophysitis: a possible relationship to IgG4-related disease
• Transient thickening of the pituitary stalk followed by a supra-pituitary Langerhansian histiocytosis : consequence or mere coincidence ?
• Treatment of Primary Hypophysitis in Germany
• Trigemino-autonomic headache and Horner syndrome as a first sign of granulomatous hypophysitis
• Typing of inflammatory lesions of the pituitary
• Xanthogranulomatous hypophysitis: a rare and often mistaken pituitary lesion