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Related Concept Videos

Graves Disease II: Pathophysiology01:24

Graves Disease II: Pathophysiology

Graves’ disease is an autoimmune disorder characterized by the production of thyroid-stimulating immunoglobulins (TSI) that activate TSH receptors, leading to excessive synthesis and release of thyroid hormones (T3 and T4) and resulting in hyperthyroidism.Among all causes of hyperthyroidism, Graves’ disease is the most common and can happen at any age, though it is more frequent in women. It produces a hypermetabolic state with features such as weight loss, tachycardia, tremor, and heat...
Graves' Disease I: Introduction01:28

Graves' Disease I: Introduction

Graves' disease is an autoimmune disorder that causes hyperthyroidism, or overactivity of the thyroid gland. It results from autoantibodies called thyroid-stimulating immunoglobulins (TSIs), which bind to thyroid-stimulating hormone (TSH) receptors, leading to overstimulation of hormone production and a hypermetabolic state.EtiologyAlthough considered idiopathic, Graves’ disease has well-established contributing factors. There is a strong genetic component, with increased prevalence in...
Goiter01:27

Goiter

Goiter refers to an abnormal enlargement of the thyroid gland that may appear as a diffuse goiter (uniform enlargement) or nodular (single or multiple nodules). Functionally, it is classified as nontoxic (normal/low hormone levels) or toxic (excess hormone production).PathophysiologyDiffuse thyroid enlargement typically results from prolonged stimulation by thyroid-stimulating hormone (TSH) or TSH-like agents, commonly seen in hypothyroidism or iodine deficiency. In contrast, in hyperthyroid...
Hyperthyroidism II: Pathophysiology01:27

Hyperthyroidism II: Pathophysiology

Hyperthyroidism is a hypermetabolic state caused by elevated levels of thyroid hormones, triiodothyronine (T3) and thyroxine (T4). It results from dysregulation at the thyroid, pituitary, or immune system level and affects multiple organ systems.PathophysiologyThe most common cause of hyperthyroidism is Graves’ disease, an autoimmune disorder in which antibodies, specifically thyroid-stimulating antibodies (TSAb), a subtype of TSH receptor antibodies (TRAb), bind to and activate TSH receptors...
Hyperthyroidism I: Introduction01:25

Hyperthyroidism I: Introduction

Hyperthyroidism is a type of thyrotoxicosis characterized by the thyroid gland's overproduction of the thyroid hormones triiodothyronine (T3) and thyroxine (T4). This hormone excess increases the basal metabolic rate and enhances sensitivity to catecholamines.DiagnosisDiagnosis is based on clinical features and biochemical testing. It typically shows suppressed thyroid-stimulating hormone (TSH) levels below 0.4 mIU/L, with elevated free T3 and/or T4. Additional tests, including thyroid...
Cryptococcal Meningitis01:27

Cryptococcal Meningitis

Cryptococcal meningitis is a life-threatening opportunistic infection predominantly associated with HIV/AIDS, accounting for over 100,000 deaths annually worldwide. However, it also affects individuals with other forms of immunosuppression, including those undergoing immunosuppressive therapy, organ transplant recipients, patients with innate immunodeficiencies, and individuals with hematological disorders. The infection is caused mainly by Cryptococcus neoformans and Cryptococcus gattii,...

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Related Experiment Video

Updated: Jun 4, 2026

Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas
07:43

Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas

Published on: January 17, 2018

Necrotizing granulomatous hypophysitis presenting as a sellar mass.

Sahar Al-Haddad1, Rafael Fandino, Bernd W Scheithauer

  • 1Department of Laboratory Medicine, St Michael's Hospital, University of Toronto, 30 Bond St, Toronto, ON M5B 1W8, Canada. al-haddads@smh.ca

Endocrine Pathology
|February 9, 2011
PubMed
Summary

A pituitary mass initially suspected to be a tumor was found to be granulomatous hypophysitis. Treatment with antituberculous medication resolved cranial nerve palsies, highlighting the importance of considering infectious causes.

Related Experiment Videos

Last Updated: Jun 4, 2026

Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas
07:43

Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas

Published on: January 17, 2018

Area of Science:

  • Endocrinology
  • Neurology
  • Pathology

Background:

  • Cranial nerve palsies and hypophyseal symptoms can indicate sellar masses.
  • Pituitary tumors are a common cause, but inflammatory and infectious etiologies must be considered.

Purpose of the Study:

  • To report a case of granulomatous hypophysitis mimicking a pituitary tumor.
  • To emphasize the diagnostic challenges and treatment outcomes.

Main Methods:

  • Case presentation of a 45-year-old female with headache, fatigue, and cranial nerve palsies.
  • Magnetic Resonance Imaging (MRI) revealing a sellar mass.
  • Transsphenoidal resection and histopathological examination.
  • Postoperative empiric treatment with antituberculous medication.

Main Results:

  • Histology showed necrotizing granulomas, inconsistent with a typical pituitary tumor.
  • Infectious and autoimmune granulomatous diseases were considered in the differential diagnosis.
  • Antituberculous treatment led to complete resolution of cranial nerve palsies within one month.

Conclusions:

  • Granulomatous hypophysitis can present as a sellar mass with neurological deficits.
  • Preoperative and even postoperative diagnosis can be challenging.
  • A high index of suspicion is crucial, especially in endemic regions for granulomatous infections or in patients with systemic granulomatous disease.