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表现为异位库欣综合征的转移性甲状腺髓样癌。

Metastatic medullary thyroid carcinoma presenting as ectopic Cushing's syndrome.

作者信息

Forde Hannah E, Mehigan-Farrelly Niamh, Ryan Katie, Moran Tom, Greally Megan, Duffy Austin G, Byrne Maria M

机构信息

Department of Endocrinology, Mater Misericordiae University Hospital, Dublin, Ireland.

Department of Pathology, Mater Misericordiae University Hospital, Dublin, Ireland.

出版信息

Endocrinol Diabetes Metab Case Rep. 2021 Apr 1;2021. doi: 10.1530/EDM-20-0207.

Abstract

SUMMARY

A 41-year-old male presented to the Emergency Department with a 6-month history of back and hip pain. Skeletal survey revealed bilateral pubic rami fractures and MRI of the spine demonstrated multiple thoracic and lumbar fractures. Secondary work up for osteoporosis was undertaken. There was no evidence of hyperparathyroidism and the patient was vitamin D replete. Testosterone (T) was low at 1.7 nmol/L (8.6-29.0) and gonadotrophins were undetectable. The patient failed a 1 mg dexamethasone suppression test (DST) with a morning cortisol of 570 nmol/L (<50) and subsequently a low dose DST with a cortisol post 48 h of dexamethasone of 773 nmol/L (<50) and an elevated ACTH 98 ng/L. A corticotropin-releasing factor (CRF) test suggested ectopic ACTH secretion. The patient was commenced on teriparatide for osteoporosis and metyrapone to control the hypercortisolaemia. A positron emission tomography (PET) scan to look for the source of ACTH secretion demonstrated right neck adenopathy. Biopsy and subsequent lymph node dissection were performed and histology revealed a metastatic neuroendocrine tumour. Immunostaining was positive for calcitonin and thyroid transcription factor 1 (TTF1). Serum calcitonin was also significantly elevated at 45 264 ng/L (<10). The patient proceeded to a total thyroidectomy and left neck dissection. Histology confirmed a 7 mm medullary thyroid carcinoma (MTC). Post-operatively, the patient commenced vandetanib therapy and achieved a clinical and biochemical response. After approximately 18 months of vandetanib therapy, the patient developed recurrent disease in his neck. He is currently on LOXO-292 and is doing well 36 months post-diagnosis.

LEARNING POINTS

Unexplained osteoporosis requires thorough investigation and the workup for secondary causes is not complete without excluding glucocorticoid excess. MTC should be considered when searching for sources of ectopic ACTH secretion. Resistance to tyrosine kinase inhibitors is well described with MTC and clinicians should have a low threshold for screening for recurrent disease.

摘要

摘要

一名41岁男性因背部和臀部疼痛6个月就诊于急诊科。骨骼检查发现双侧耻骨支骨折,脊柱MRI显示多个胸椎和腰椎骨折。对骨质疏松症进行了进一步检查。没有甲状旁腺功能亢进的证据,患者维生素D充足。睾酮(T)水平较低,为1.7 nmol/L(8.6 - 29.0),促性腺激素检测不到。患者1毫克地塞米松抑制试验(DST)结果异常,上午皮质醇水平为570 nmol/L(<50),随后低剂量DST结果也异常,地塞米松给药48小时后皮质醇水平为773 nmol/L(<50),促肾上腺皮质激素(ACTH)升高至98 ng/L。促肾上腺皮质激素释放因子(CRF)试验提示异位ACTH分泌。患者开始使用特立帕肽治疗骨质疏松症,并使用美替拉酮控制高皮质醇血症。正电子发射断层扫描(PET)用于寻找ACTH分泌源,显示右颈部淋巴结肿大。进行了活检及后续淋巴结清扫,组织学检查显示为转移性神经内分泌肿瘤。免疫染色降钙素和甲状腺转录因子1(TTF1)呈阳性。血清降钙素也显著升高,达45264 ng/L(<10)。患者接受了全甲状腺切除术和左颈部清扫术。组织学证实为7毫米甲状腺髓样癌(MTC)。术后,患者开始使用凡德他尼治疗,并取得了临床和生化反应。接受凡德他尼治疗约18个月后,患者颈部出现复发疾病。目前他正在使用LOXO - 292,确诊后36个月情况良好。

学习要点

不明原因的骨质疏松症需要全面检查,在未排除糖皮质激素过量的情况下,继发性病因的检查并不完整。在寻找异位ACTH分泌源时应考虑MTC。MTC对酪氨酸激酶抑制剂耐药已得到充分描述,临床医生对复发性疾病的筛查阈值应较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43bf/8115413/7b4865db275b/EDM20-0207fig1.jpg

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