Kim Hee Ju, Lee So Hee
Division of Endocrine Surgery, Department Surgery, Eunpyeong St. Mary's Hospital, College of Medicine, the Catholic University of Korea, Seoul, Republic of Korea.
Gland Surg. 2023 Jun 30;12(6):860-866. doi: 10.21037/gs-22-521. Epub 2023 Jun 14.
Skin pigmentation after adrenalectomy occurs due to an increase in adrenocorticotropic hormone (ACTH) following adrenal insufficiency. ACTH-induced pigmentation usually appears as generalized hyperpigmentation and is known to appear after bilateral adrenalectomy. We report a case of unusual transient hyperpigmentation that developed immediately after unilateral adrenalectomy for pheochromocytoma and spontaneously resolved without corticosteroid supplementation.
A 29-year-old woman was admitted to the hospital due to sudden-onset chest pain and headache. A 2.8-cm left adrenal mass with heterogeneous enhancement was incidentally found in chest computed tomography during the evaluation. Multiple old infarctions were observed in brain magnetic resonance imaging (MRI), and left ventricular thrombi were found by echocardiography. Biochemical evidence confirmed the diagnosis of pheochromocytoma, while serum ACTH and cortisol levels were within normal ranges. The patient underwent laparoscopic left adrenalectomy via a posterior retroperitoneal approach and recovered without immediate postoperative complications. On day 3 after surgery, a crescent-shaped café-au-lait skin pigmentation occurred on both the subcostal and the lumbar areas of the abdomen. Serial serum cortisol slightly decreased during the immediate postoperative period and recovered on day 3. Serum ACTH was elevated. Under close observation without corticosteroid supplementation, the pigmentation faded on day 8 after surgery. On day 15, the pigmentation clearly disappeared and serum ACTH decreased to within the normal range. A month later, ACTH and all adrenal hormones were within normal range.
We hypothesized that skin pigmentation appeared due to an imbalance of the hypothalamic-pituitary-adrenal (HPA) axis after resection of one adrenal gland. Skin pigmentation may be the first and early manifestation of adrenal insufficiency in patients who undergo unilateral adrenalectomy due to a non-Cushing's tumor. Therefore, a careful physical examination may allow early detection of adrenal insufficiency and optimal treatment planning.
肾上腺切除术后皮肤色素沉着是由于肾上腺功能不全后促肾上腺皮质激素(ACTH)增加所致。ACTH诱导的色素沉着通常表现为全身性色素沉着,已知在双侧肾上腺切除术后出现。我们报告一例不寻常的短暂性色素沉着病例,该病例在因嗜铬细胞瘤行单侧肾上腺切除术后立即出现,并在未补充皮质类固醇的情况下自发消退。
一名29岁女性因突发胸痛和头痛入院。在评估过程中,胸部计算机断层扫描偶然发现左肾上腺有一个2.8厘米的肿块,增强不均匀。脑磁共振成像(MRI)观察到多处陈旧性梗死,超声心动图发现左心室血栓。生化证据证实诊断为嗜铬细胞瘤,而血清ACTH和皮质醇水平在正常范围内。患者通过后腹腔镜腹膜后途径接受了腹腔镜左肾上腺切除术,术后恢复良好,无即刻并发症。术后第3天,腹部肋下和腰部区域出现新月形咖啡牛奶斑样皮肤色素沉着。术后即刻血清皮质醇水平略有下降,并在第3天恢复。血清ACTH升高。在未补充皮质类固醇的密切观察下,色素沉着在术后第8天消退。第15天,色素沉着明显消失,血清ACTH降至正常范围内。1个月后,ACTH和所有肾上腺激素均在正常范围内。
我们推测,一侧肾上腺切除术后皮肤色素沉着是由于下丘脑-垂体-肾上腺(HPA)轴失衡所致。皮肤色素沉着可能是因非库欣肿瘤行单侧肾上腺切除术患者肾上腺功能不全的首发及早期表现。因此,仔细的体格检查可能有助于早期发现肾上腺功能不全并制定最佳治疗方案。