Panhypopituitarism - NYSORA

Explore NYSORA knowledge base for free:

Table of Contents

Contributors

Panhypopituitarism

Panhypopituitarism

Learning objectives

  • Definition of panhypopituitarism
  • Management of panhypopituitarism

Definition and mechanisms

  • A rare condition in which the pituitary there’s a deficiency in all of the hormones produced by the pituitary gland
  • The anterior lobe of the pituitary gland produces:
    • Adrenocorticotropic hormone (ACTH or corticotropin)
    • Follicle-stimulating hormone (FSH)
    • Growth hormone (GH)
    • Luteinizing hormone (LH)
    • Prolactin (PRL)
    • Thyroid stimulation hormone (TSH)
  • The posterior lobe of the pituitary gland produces:
    • Antidiuretic hormone (ADH)/vasopressin
    • Oxytocin
  • Can affect anyone at any age
  • It can be life-threatening, especially if significant deficiencies of ACTH are present, and affects 4 people per 100,000 people 
  • Panhypopituitarism is a type of hypopituitarism
    • A deficiency or lack in one or multiple of the hormones produced by the pituitary gland
  • Patients with hormonal deficiencies present with the following:
    • ACTH deficiency – adrenal insufficiency
    • TSH deficiency – hypothyroidism
    • Gonadotropin deficiency – hypogonadism
    • GH deficiency – difficult to thrive and short stature in children, adults are usually asymptomatic; however, they may feel fatigued and weak
    • ADH deficiency – diabetes insipidus presenting with polydipsia and polyuria

Signs and symptoms

  • Symptoms depend on the hormones depend on which hormone is deficient
    • Growth problems (in children)
    • Obesity
    • Hair loss
    • Bradycardia
    • Hypoglycemia
    • Hypotension
    • Fatigue
    • Nausea or dizziness
    • Depression and/or anxiety
    • Frequent infections
    • Sensitivity to cold
    • Unusually dry skin
    • Unexplained weight loss or weight gain
    • Dyslipidemia
    • Tachycardia
    • Excessive thirst and urination
    • Female and male infertility
  • Additional symptoms specific to infants, children, or adolescents
    • Prolonged jaundice in newborns
    • Micropenis
    • Slowed growth
    • Delayed puberty

Causes

Pituitary-related
Hypothalamus-related
Pituitary adenoma
Infection
Injury
Pituitary gland surgery
Radiation therapy
Pituitary apoplexy
Congenital (related to midline craniofacial defects)
Kallman syndrome
Idiopathic
Traumatic brain injury
Brain surgery
Tumors such as craniopharyngiomas
Secondary metastasis
Pressure from hydrocephalus
Stroke
Tuberculous meningitis

Complications

  • Adrenal crisis (acute cortisol insufficiency) which is characterized by the following symptoms:
  • Secondary diseases:
    • Obesity
    • Increased cholesterol
    • Metabolic syndrome
    • Estradiol deficiency potentially leads to osteoporosis

Diagnosis

  • MRI
  • CT
  • Hormone level tests:
    • Blood tests
    • ACTH-stimulation test
    • Growth hormone stimulation test
    • Insulin tolerance test
    • Modern combined test

Treatment

Management

Panhypopituitarism, adrenocortical insuffiency, hydrocortisone

Panhypopituitarism, adrenergic crisis, adrenal insufficiency, cortisol, hydrocortisone

Suggested reading

  • Raut MS, Kar S, Maheshwari A, Shivnani G, Dubey S. Perioperative management in a patient with panhypopituitarism – evidence based approach: a case report. Eur Heart J Case Rep. 2019;3(3):ytz145. Published 2019 Sep 18.
  • Malhotra, Surender & Jangra, Kiran & Saini, Vikas. (2013). Pituitary Surgery and Anesthetic Management: An Update. World Journal of Endocrine Surgery. 5. 1-5. 10.5005/jp-journals-10002-1114.
  • Menon R, Murphy PG, Lidnley AM. 2011. Anaesthesia and pituitary disease. Continuing Education in Anaesthesia Critical Care & Pain. 11;4:133-137.  

We would love to hear from you. If you should detect any errors, email us customerservice@nysora.com