Gurazada K, Ihuoma A, Galloway M, Dorward N, Wilhelm T, Khoo B, Bouloux P M G
Centre for Neuroendocrinology, University College London, Royal Free Campus, Rowland Hill Street, Hampstead, London, NW3 2PF, UK,
Pituitary. 2014 Oct;17(5):423-9. doi: 10.1007/s11102-013-0520-2.
We report the first case of an Ectopic adrenocorticotrophin (ACTH)-secreting pituitary adenoma (EAPA) located within the posterior nasal septum associated with Nelson's syndrome, which eluded diagnosis for over a decade. In this report, we explore the reasons for such diagnostic difficulty and suggest ways in which an earlier diagnosis may be made.
A 19 years old Lebanese man presented in 2000, with overt Cushing's syndrome confirmed with markedly elevated urine free cortisols and failed dexamethasone suppression tests. An unsuppressed ACTH and a possible 5 mm adenoma on MRI (Magnetic Resonance Imaging) pituitary suggested Cushing's disease. The patient underwent trans-sphenoidal surgery (TSS), but histology revealed normal pituitary tissue and Cushing's syndrome persisted. A repeat MRI pituitary showed no anomaly, and extensive investigations failed to locate an ectopic lesion. Subsequently a bilateral adrenalectomy was performed. Over the ensuing years, the patient developed Nelson's syndrome with hyperpigmentation and markedly elevated ACTH levels. Repeated high dose dexamethasone suppression tests, corticotrophin releasing hormone (CRH) tests, and CRH stimulated inferior petrosal sinus samplings (IPSS) suggested a pituitary origin of the ACTH. Two further TSS were unsuccessful. The pituitary was irradiated. Subsequent review of his previous MRIs revealed an enlarging mass within the posterior nasal septum, which was excised in 2011. The histology confirmed the diagnosis of an EAPA within the nasal septum.
Ectopic ACTH-secreting pituitary adenomas can occur not only along the developmental route of Rathke's pouch, but other aberrant locations giving a clinical and biochemical picture identical to Cushing's disease or Nelson's syndrome. Clinicians should suspect an EAPA, when a central ACTH source seems to be apparent with no obvious pituitary adenoma. A detailed MRI involving possible EAPA sites aids in locating these unusual lesions.
我们报告首例位于后鼻中隔的异位促肾上腺皮质激素(ACTH)分泌型垂体腺瘤(EAPA)病例,该病例与尼尔森综合征相关,十多年来一直未被诊断出来。在本报告中,我们探讨了诊断困难的原因,并提出了早期诊断的方法。
一名19岁的黎巴嫩男性于2000年就诊,确诊为明显的库欣综合征,尿游离皮质醇显著升高,地塞米松抑制试验未通过。MRI(磁共振成像)垂体检查显示ACTH未被抑制,可能存在一个5毫米的腺瘤,提示库欣病。患者接受了经蝶窦手术(TSS),但组织学检查显示垂体组织正常,库欣综合征持续存在。垂体的重复MRI检查未发现异常,广泛的检查也未能定位异位病变。随后进行了双侧肾上腺切除术。在随后的几年里,患者出现了尼尔森综合征,伴有色素沉着和ACTH水平显著升高。重复的高剂量地塞米松抑制试验、促肾上腺皮质激素释放激素(CRH)试验以及CRH刺激下岩窦采血(IPSS)提示ACTH起源于垂体。另外两次TSS均未成功。对垂体进行了放射治疗。随后对其先前的MRI检查进行回顾,发现后鼻中隔内有一个不断增大的肿块,于2011年将其切除。组织学检查证实鼻中隔内为EAPA。
异位ACTH分泌型垂体腺瘤不仅可发生在拉特克囊的发育路径上,还可发生在其他异常部位,其临床和生化表现与库欣病或尼尔森综合征相同。当中央ACTH来源似乎明显但无明显垂体腺瘤时,临床医生应怀疑EAPA。对可能的EAPA部位进行详细的MRI检查有助于定位这些不寻常的病变。