Literature DB >> 25940577

Risk of catecholaminergic crisis following glucocorticoid administration in patients with an adrenal mass: a literature review.

Catherine Barrett1, Stan H M van Uum1, Jacques W M Lenders2,3.   

Abstract

BACKGROUND: Glucocorticoids as diagnostic or therapeutic agents have been reported to carry an increased risk of catecholaminergic crisis (CC) in patients with pheochromocytoma or paraganglioma (PPGL).
METHODS: We searched literature databases using the following terms: pheochromocytoma, paraganglioma, adrenal incidentaloma, steroids, glucocorticoids, dexamethasone suppression test (DST), hypertensive crisis, cosyntropin and CRH. From all published case reports (1962-2013), we reviewed medical history, presenting symptoms, dose and route of steroid administration, location and size of adrenal mass, biochemical phenotype and outcome.
RESULTS: Twenty-five case reports describing a CC were identified. Three patients with an adrenal incidentaloma suffered a CC following high-dose DST, and in one case, this was fatal. In two of these patients, biochemical testing missed the diagnosis, and in the third, a DST was done despite elevated urinary metanephrines. No CC has been reported for patients undergoing a low-dose DST. Three of 16 patients who received therapeutic glucocorticoids and four of six patients following cosyntropin testing died. No specific biochemical phenotype was related to adverse events.
CONCLUSIONS: Although a causal relationship cannot be established from this review, it seems prudent to exclude a PPGL in patients with a large incidentaloma or when high-dose DST is considered in a patient with an incidentaloma of any size. Our literature review does not support the need for biochemical testing for PPGL prior to a low-dose (1 mg) DST. Finally, before starting therapeutic glucocorticoids, any clinical signs or symptoms of a potential PPGL should prompt reliable biochemical testing to rule out a PPGL.
© 2015 John Wiley & Sons Ltd.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 25940577     DOI: 10.1111/cen.12813

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  7 in total

1.  A pheochromocytoma on steroids.

Authors:  Christopher John Warren; David Lewis Jardine; Thomas James Cawood
Journal:  Clin Auton Res       Date:  2019-11-20       Impact factor: 4.435

2.  Pheochromocytoma with Synchronous Ipsilateral Adrenal Cortical Adenoma.

Authors:  M Earth Hasassri; T K Pandian; Aleh A Bobr; Irina Bancos; William F Young; Melanie L Richards; David R Farley; Geoffrey B Thompson; Travis J McKenzie
Journal:  World J Surg       Date:  2017-12       Impact factor: 3.352

3.  Adrenal insufficiency in a child following unilateral excision of a dual-hormone secreting phaeochromocytoma.

Authors:  Annika Sjoeholm; Cassandra Li; Chaey Leem; Aiden Lee; Maria P Stack; Paul L Hofman; Benjamin J Wheeler
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2015-06-01

Review 4.  Catecholamine physiology and its implications in patients with COVID-19.

Authors:  Sriram Gubbi; Matthew A Nazari; David Taieb; Joanna Klubo-Gwiezdzinska; Karel Pacak
Journal:  Lancet Diabetes Endocrinol       Date:  2020-10-28       Impact factor: 32.069

5.  Ectopic Cushing's syndrome from an ACTH-producing pheochromocytoma with a non-functioning pituitary adenoma.

Authors:  David Kishlyansky; Gregory Kline; Amita Mahajan; Konstantin Koro; Janice L Pasieka; Patrick Champagne
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2022-03-01

6.  Primary malignant lymphoma combined with clinically "silent" pheochromocytoma in the same adrenal gland.

Authors:  Anna Babinska; Rafał Peksa; Krzysztof Sworczak
Journal:  World J Surg Oncol       Date:  2015-09-30       Impact factor: 2.754

7.  Catastrophic catecholamine-induced cardiomyopathy rescued by extracorporeal membrane oxygenation in recurrent malignant pheochromocytoma.

Authors:  Daniel Min
Journal:  Yeungnam Univ J Med       Date:  2019-05-22
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.