Division of Endocrinology, Metabolism, and Molecular Medicine, Charles R. Drew University of Medicine and Science, Los Angeles, CA, USA.
Department of Surgery, Scripps Green Hospital, La Jolla, CA, USA.
Horm Metab Res. 2021 Mar;53(3):161-168. doi: 10.1055/a-1253-2854. Epub 2020 Oct 22.
Bilateral adrenalectomy (BLA) is a treatment option for patients with Cushing's Disease (CD) if transsphenoidal pituitary surgery fails or is not a therapeutic option. For most patients, BLA eliminates endogenous glucocorticoid and mineralocorticoid production, but for a small number of patients, endogenous secretion of adrenal hormones from adrenal tissue continues or recurs, leading to signs and symptoms of hypercortisolism. If adrenal tissue is confined to the adrenal bed, it is considered , while if it is outside the adrenal bed, it is considered . We retrospectively evaluated morning serum cortisol, nighttime serum cortisol, nighttime salivary cortisol, and 24-h urine free cortisol on at least three occasions in 10 patients suspected of having endogenous cortisol production. Imaging of adrenal remnant tissue was also reviewed. Ten of 51 patients who underwent BLA during this time period had adrenal remnant/rest tissue marked by detectable endogenous glucocorticoid production; 9 of the 10 patients had signs and symptoms of hypercortisolism. Localization and treatment proved difficult. We conclude that the incidence of adrenal remnant/rest tissue in those undergoing BLA following unsuccessful pituitary surgery was 12% although there may have been a selection bias affecting this prevalence. The first indication of remnant tissue occurrence is a reduction in glucocorticoid replacement with symptoms of hypercortisolism. If this occurs, endogenous cortisol production should be tested for by cortisol measurements using a highly specific cortisol assay while the patient is taking dexamethasone or no glucocorticoid replacement. Endocrinologists need to monitor the development of both adrenal remnant tissue and Nelson's syndrome following BLA.
双侧肾上腺切除术(Bilateral adrenalectomy,BLA)是治疗经蝶窦垂体手术失败或不适合治疗的库欣病(Cushing's Disease,CD)患者的一种选择。对于大多数患者,BLA 可消除内源性糖皮质激素和盐皮质激素的产生,但对于少数患者,肾上腺组织仍会继续或重新出现内源性肾上腺激素分泌,导致皮质醇增多症的体征和症状。如果肾上腺组织局限于肾上腺床内,则被认为是,而如果位于肾上腺床外,则被认为是。我们回顾性评估了 10 例疑似存在内源性皮质醇产生的患者至少三次的清晨血清皮质醇、夜间血清皮质醇、夜间唾液皮质醇和 24 小时尿液游离皮质醇,同时还回顾了肾上腺残馀组织的影像学检查。在此期间,51 例行 BLA 的患者中有 10 例存在可检测到内源性糖皮质激素产生的肾上腺残馀/组织标记物;其中 9 例患者有皮质醇增多症的体征和症状。定位和治疗均很困难。我们的结论是,尽管可能存在影响这一流行率的选择偏倚,但在不成功的垂体手术后行 BLA 的患者中,肾上腺残馀/组织的发生率为 12%。出现残馀组织的第一个迹象是糖皮质激素替代减少伴皮质醇增多症的症状。如果发生这种情况,应在患者服用地塞米松或不进行糖皮质激素替代的情况下,使用高度特异性皮质醇检测进行皮质醇测量以检测内源性皮质醇产生。内分泌学家需要监测 BLA 后肾上腺残馀组织和纳尔逊综合征的发展。