Ambroziak Urszula, Zieliński Grzegorz, Toutounchi Sadegh, Pogorzelski Ryszard, Skórski Maciej, Cieszanowski Andrzej, Miśkiewicz Piotr, Popow Michał, Bednarczuk Tomasz
Endokrynol Pol. 2015;66(1):68-72. doi: 10.5603/EP.2015.0011.
Cushing's disease is the most common cause of endogenous hypercortisolemia, in 90% of cases due to microadenoma. Macroadenoma can lead to atypical hormonal test results and complete removal of the tumour is unlikely.
A 77-year-old woman with diabetes and hypertension was admitted because of fatigue, proximal muscles weakness, lower extremities oedema, and worsening of glycaemic and hypertension control. Physical examination revealed central obesity, 'moon'-like face, supraclavicular pads, proximal muscle atrophy, and skin hyperpigmentation. Biochemical and hormonal results were as follows: K 2.3 mmol/L (3.6-5), cortisol 8.00 86 μg/dL (6.2-19.4) 23.00 76 μg/dL, ACTH 8.00 194 pg/mL (7.2-63.3) 23.00 200 pg/mL, DHEAS 330 μg/dL (12-154). CRH stimulation test showed lack of ACTH stimulation > 35%, overnight high dose DST revealed no suppression of cortisol. Chest and abdominal CT as well as somatostatin receptor scan didn't show ectopic tumour responsible for ACTH oversecretion. MRI revealed a pituitary macroadenoma (28 × 20 × 17 mm) extending towards the left cavernous sinus. After partial transsphenoidal adenomectomy, serum cortisol of 40 μg/dL was obtained. The patient's condition was still very poor, so unilateral adrenalectomy was performed. After surgery, serum morning cortisol level dropped to 20 μg/dL and the patient's condition improved significantly. 26 months after the operations, the patient remains in remission. Because her life expectancy exceeds the prognosed duration of remission with the presence of pituitary tumour remnants and intact left adrenal gland, the patient was qualified to radiosurgery with a Gamma Knife.
In selected cases, unilateral, laparascopic adrenalectomy may serve as a life-saving procedure in a patient with ACTHdependent Cushing's syndrome.
库欣病是内源性皮质醇增多症最常见的病因,90%的病例由微腺瘤引起。大腺瘤可导致非典型的激素检测结果,且肿瘤不太可能完全切除。
一名77岁患有糖尿病和高血压的女性因疲劳、近端肌无力、下肢水肿以及血糖和血压控制恶化而入院。体格检查发现中心性肥胖、“满月”脸、锁骨上脂肪垫、近端肌肉萎缩和皮肤色素沉着。生化和激素检查结果如下:血钾2.3 mmol/L(3.6 - 5),皮质醇8.00 86 μg/dL(6.2 - 19.4)23.00 76 μg/dL,促肾上腺皮质激素8.00 194 pg/mL(7.2 - 63.3)23.00 200 pg/mL,硫酸脱氢表雄酮330 μg/dL(12 - 154)。促肾上腺皮质激素释放激素刺激试验显示促肾上腺皮质激素刺激缺乏>35%,过夜大剂量地塞米松抑制试验显示皮质醇未被抑制。胸部和腹部CT以及生长抑素受体扫描未显示导致促肾上腺皮质激素分泌过多的异位肿瘤。磁共振成像显示垂体大腺瘤(28×20×17 mm)延伸至左侧海绵窦。经蝶窦部分腺瘤切除术后,血清皮质醇降至40 μg/dL。患者病情仍很差,因此进行了单侧肾上腺切除术。术后,血清早晨皮质醇水平降至20 μg/dL,患者病情明显改善。手术后26个月,患者仍处于缓解期。由于她的预期寿命超过了存在垂体肿瘤残余和完整左肾上腺时的预计缓解期,该患者符合使用伽玛刀进行放射外科治疗的条件。
在特定病例中,单侧腹腔镜肾上腺切除术对于依赖促肾上腺皮质激素的库欣综合征患者可能是一种挽救生命的手术。