Hypopituitarism causes
Hypopituitarism Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]
Overview
Cause
Common Causes
Hypopituitarism and panhypopituitarism can be congenital or acquired. A partial list of causes and forms:[1][2][3]
- Congenital hypopituitarism
- Hypoplasia of the pituitary
- Isolated idiopathic congenital hypopituitarism
- Associated with other congenital syndromes and birth defects
- Septo-optic dysplasia
- Holoprosencephaly
- Chromosome 22 deletion syndrome
- Rapaport syndrome
- Single gene defect forms of anterior pituitary hormone deficiency
- Hypoplasia of the pituitary
- Acquired hypopituitarism (Simmonds' disease)
- Trauma (e.g., skull base fracture)
- Surgery (e.g., removal of pituitary neoplasm)
- Tumor - secretory and non-secretory (20%) pituitary or hypothalamic neoplasms, cause hypopituitarism by compressing the remaining tissue
- Inflammation (e.g. sarcoidosis or autoimmune hypophysitis)
- Radiation (e.g., after cranial irradiation for childhood leukemia)
- Shock
- (Sheehan's syndrome is hypopituitarism after heavy bleeding in childbirth)
- Hemochromatosis
- other diseases.
Causes in Alphabetical Order
- Anorexia Nervosa
- Bulimia Nervosa
- Changes in body weight
- Congestive Heart Failure
- Emotional disorders
- Empty Sella Syndrome
- Habitual exercise
- Head Trauma
- Hemochromatosis
- Infection
- Fungal
- Malaria
- Meningitis
- Syphillis
- Tuberculosis
- Ischemic nerosis of the pituitary
- Anticoagulant therapy
- Arteriosclerosis
- Arteritis temporalis
- Blood dyscrasias
- Brain Trauma
- Diabetes Mellitus
- Eclampsia
- Increased cranial pressure
- Sheehan's Syndrome
- Sickle Cell Anemia
- Tumor
- Iatrogenic
- Parasellar tumor/pituitary compression
- Craniopharyngioma
- Chromophobe adenoma
- Intracranial cartoid branch aneurysm
- Lymphoma
- Meningioma
- Metasteses
- Optic nerve neuroma
Hypopituitarism Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Hypopituitarism causes On the Web |
American Roentgen Ray Society Images of Hypopituitarism causes |
Risk calculators and risk factors for Hypopituitarism causes |
Hypothalmic | Mass lesions
|
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Radiation : CNS and nasopharyngeal malignancies | |
Infections: Tuberculous meningitis | |
Infiltrative lesions:
| |
Other :
| |
Pituitary | Mass lesions:
|
Pituitary radiation | |
Pituitary surgery | |
Infection/abscess | |
Infiltrative lesions:
2. Hemochromatosis | |
Infarction: Sheehan syndrome | |
Apoplexy | |
Empty sella | |
Genetic mutations |
Isolated
hormone abnormalities |
Gene | Inheritance | Phenotype |
---|---|---|---|
Isolated GH deficiency | |||
Isolated GH deficiency | |||
Isolated TSH deficiency | |||
Isolated TSH deficiency | |||
Isolated ACTH deficiency | |||
HH | |||
ACTH deficiency, hypoglycemia, HH, obesity | |||
ACTH deficiency, obesity, red hair | |||
Adrenal hypoplasia congenital and HH | |||
CRH deficiency | |||
Kallman syndrome, renal agenesis, synkinesia | |||
Kallman syndrome, cleft lip and palate, facial dysmorphism | |||
HH, obesity | |||
HH, obesity | |||
HH | |||
HH | |||
Primary amenorrhea, defective spermatogenesis | |||
Delayed puberty | |||
Kallman syndrome, severe sleep disorder, obesity | |||
Kallman syndrome | |||
Diabetes insipidus | |||
Combined pituitary hormone deficiency | GH, TSH and prolactin deficiencies | ||
GH, TSH, LH, FSH, prolactin, and evolving ACTH deficiencies | |||
Specific syndromes | Septo-optic dysplasia | ||
GH, TSH, LH, FSH, prolactin deficiencies, limited neck rotation | |||
GH, TSH, ACTH deficiencies with cerebellar abnormalities | |||
Hypopituitarism and mental retardation | |||
Holoprosencephaly and multiple midline defects | |||
Anophthalmia, hypopituitarism, oesophageal atresia | |||
Pallister-Hall syndrome | |||
Rieger syndrome |
References
- ↑ Schneider HJ, Aimaretti G, Kreitschmann-Andermahr I, Stalla GK, Ghigo E (2007). "Hypopituitarism". Lancet. 369 (9571): 1461–70. doi:10.1016/S0140-6736(07)60673-4. PMID 17467517.
- ↑ van Aken MO, Lamberts SW (2005). "Diagnosis and treatment of hypopituitarism: an update". Pituitary. 8 (3–4): 183–91. doi:10.1007/s11102-006-6039-z. PMID 16508719.
- ↑ Stieg MR, Renner U, Stalla GK, Kopczak A (2017). "Advances in understanding hypopituitarism". F1000Res. 6: 178. doi:10.12688/f1000research.9436.1. PMC 5325066. PMID 28299199.