scholarly journals The importance of postoperative control: adrenal insufficiency after unilateral adrenalectomy for Conn’s syndrome. A case study

2016 ◽  
Vol 20 (2) ◽  
pp. 73-74
Author(s):  
Marta Sołtysiak ◽  
Paweł Sołtysiak ◽  
Anna Brzeska ◽  
Krystyna Widecka
2014 ◽  
Vol 5 (2) ◽  
Author(s):  
Fahimeh Soheilipour ◽  
Mohammad Ahmadi ◽  
Fatemeh Jesmi

Author(s):  
Jay D. Raman ◽  
Augustyna Gogoj ◽  
Brian D. Saunders ◽  
Daniel J.Canter ◽  
Jay D. Raman ◽  
...  

Introduction: Acquired adrenal insufficiency is a known risk of unilateral adrenalectomy. However, the rates of early and prolonged adrenal insufficiency following unilateral adrenalectomy are not well defined in the literature. Patients and Methods: We reviewed a case series of 184 consecutive patients to determine the likelihood of steroid supplementation at 30 days and 1 year following adrenalectomy. 109 lesions were non-functional and 75 (41%) demonstrated functionality, including 33 pheochromocytomas, 20 cortisol-producing adenomas, 19 aldosteronomas, and 3 cases of cortisol-secreting hyperplasia. No patients with a nonfunctional lesion, pheochromocytoma, or aldosteronoma required steroid supplementation following surgery. Eleven of 23 patients (48%) with primary adrenal Cushing syndrome required cortisol supplementation at 30 days, and only 1 patient (4%) necessitated supplementation one year following surgery. Discussion: Approximately 50% of patients with cortisol-producing lesions in the adrenal gland will require supplementation 30-days following surgery. Only 4% will require persistent exogenous steroids at 1-year. Conversely, less than 1% of patients with different types of functional or non-functional tumors required supplementation after surgery. Conclusion: The incidence of adrenal insufficiency following unilateral adrenalectomy is low. A large majority of patients requiring steroid supplementation 30 days following surgery are able to wean off this requirement by 1 year. With this information, we can better counsel our patients and set clearer expectations for the potential need of cortisol supplementation following adrenalectomy


Author(s):  
Matthew D. Sjoblom ◽  
Diane Gordon ◽  
Lori A. Aronson

Hypopituitarism is a decreased secretion of pituitary hormones. It is especially concerning during surgery and anesthesia if it results in adrenal insufficiency, hypothyroidism, or diabetes insipidus. Common causes in children include pituitary tumor and/or treatment, traumatic brain injury, and empty sella syndrome. Perioperative management includes recognition of clinical symptoms, such as hypotension, fatigue, polydipsia, and increased urine output. Unrecognized adrenal insufficiency may result in significant morbidity or mortality. Intraoperative treatment may involve stress-dose corticosteroids, careful fluid management, and desmopressin. This chapter uses the case study of a 9-year-old boy who presents for bilateral removal of tibial orthopedic hardware to illustrate the concepts.


2017 ◽  
Vol 197 (4S) ◽  
Author(s):  
Jeffrey B. Walker ◽  
Brian D. Saunders ◽  
Kathleen Lehman ◽  
Jay D. Raman

2021 ◽  
pp. 249-328
Author(s):  
Jeremy Tomlinson

This chapter covers the adrenal gland. It begins with the anatomy and physiology of the adrenal gland, then continues with imaging techniques. It then covers adrenal disorders, including Conn’s syndrome, adrenal Cushing’s syndrome, Adrenal insufficiency, Addison’s disease, and multiple autoimmune disorders. The investigation, treatment, and long-term management of primary insufficiency is covered. Various adrenal tumours and associated disorders, along with their management, are described.


2015 ◽  
Vol 19 (3) ◽  
pp. 430 ◽  
Author(s):  
Bindu Kulshreshtha ◽  
Arpita Arora ◽  
Anshita Aggarwal ◽  
Minakshi Bhardwaj

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