» Articles » PMID: 22710101

Cushing's Disease

Overview
Publisher Biomed Central
Specialty General Medicine
Date 2012 Jun 20
PMID 22710101
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Cushing's disease, or pituitary ACTH dependent Cushing's syndrome, is a rare disease responsible for increased morbidity and mortality. Signs and symptoms of hypercortisolism are usually non specific: obesity, signs of protein wasting, increased blood pressure, variable levels of hirsutism. Diagnosis is frequently difficult, and requires a strict algorithm. First-line treatment is based on transsphenoidal surgery, which cures 80% of ACTH-secreting microadenomas. The rate of remission is lower in macroadenomas. Other therapeutic modalities including anticortisolic drugs, radiation techniques or bilateral adrenalectomy will thus be necessary to avoid long-term risks (metabolic syndrome, osteoporosis, cardiovascular disease) of hypercortisolism. This review summarizes potential pathophysiological mechanisms, diagnostic approaches, and therapies.

Citing Articles

Pasireotide-induced hyperglycemia in Cushing's disease and Acromegaly: A clinical perspective and algorithms proposal.

Witek P, Bolanowski M, Kretowski A, Glowinska A Front Endocrinol (Lausanne). 2024; 15:1455465.

PMID: 39735646 PMC: 11672337. DOI: 10.3389/fendo.2024.1455465.


PitNETs and the gut microbiota: potential connections, future directions.

Nie D, Li C, Zhang Y Front Endocrinol (Lausanne). 2023; 14:1255911.

PMID: 38027221 PMC: 10657991. DOI: 10.3389/fendo.2023.1255911.


Glymphatic transport is reduced in rats with spontaneous pituitary tumor.

Li L, Ding G, Zhang L, Luo H, Davoodi-Bojd E, Li Q Front Med (Lausanne). 2023; 10:1189614.

PMID: 37601793 PMC: 10436560. DOI: 10.3389/fmed.2023.1189614.


Neurosurgical aspects and clinical outcomes on the treatment of Cushing disease in pediatric patients: Case series and literature review.

Castillo-Huerta N, Carassa de la Cruz J, Quispe-Garate L, Levano-Martinez M, Cabrera B, Sheen E Surg Neurol Int. 2023; 14:123.

PMID: 37151460 PMC: 10159280. DOI: 10.25259/SNI_64_2023.


Pituitary adenomas and cerebrovascular disease: A review on pathophysiology, prevalence, and treatment.

Osorio R, Oh J, Choudhary N, Lad M, Savastano L, Aghi M Front Endocrinol (Lausanne). 2022; 13:1064216.

PMID: 36578965 PMC: 9791098. DOI: 10.3389/fendo.2022.1064216.


References
1.
Biller B, Grossman A, Stewart P, Melmed S, Bertagna X, Bertherat J . Treatment of adrenocorticotropin-dependent Cushing's syndrome: a consensus statement. J Clin Endocrinol Metab. 2008; 93(7):2454-62. PMC: 3214276. DOI: 10.1210/jc.2007-2734. View

2.
Boscaro M, Arnaldi G . Approach to the patient with possible Cushing's syndrome. J Clin Endocrinol Metab. 2009; 94(9):3121-31. DOI: 10.1210/jc.2009-0612. View

3.
Hofmann B, Hlavac M, Martinez R, Buchfelder M, Muller O, Fahlbusch R . Long-term results after microsurgery for Cushing disease: experience with 426 primary operations over 35 years. J Neurosurg. 2008; 108(1):9-18. DOI: 10.3171/JNS/2008/108/01/0009. View

4.
Findling J, Raff H . Screening and diagnosis of Cushing's syndrome. Endocrinol Metab Clin North Am. 2005; 34(2):385-402, ix-x. DOI: 10.1016/j.ecl.2005.02.001. View

5.
Sonino N, Fallo F, Fava G . Psychosomatic aspects of Cushing's syndrome. Rev Endocr Metab Disord. 2009; 11(2):95-104. DOI: 10.1007/s11154-009-9123-7. View