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甲状腺乳头状癌的垂体转移:一例报告及文献复习

Pituitary metastases from papillary carcinoma of thyroid: a case report and literature review.

作者信息

Chikani Viral, Lambie Duncan, Russell Anthony

机构信息

Department of Diabetes and Endocrinology The Princess Alexandra Hospital 199 Ipswich Road, Woolloongabba, Queensland, 4102 Australia.

Department of Anatomical Pathology The Princess Alexandra Hospital 199 Ipswich Road, Woolloongabba, Queensland, 4102 Australia.

出版信息

Endocrinol Diabetes Metab Case Rep. 2013;2013:130024. doi: 10.1530/EDM-13-0024. Epub 2013 Aug 30.

Abstract

UNLABELLED

Metastases to the pituitary gland are an uncommon complication of thyroid cancer. They resemble pituitary neoplasms posing a diagnostic challenge. We present a case of an aggressive non-radioiodine avid papillary thyroid cancer with recurrent pituitary metastases and a review of the literature. A 70-year-old woman with a history of papillary thyroid cancer and bony metastases presented with symptoms of hypoadrenalism and peripheral vision loss. Magnetic resonance imaging showed a large pituitary mass impinging on the optic chiasm. She underwent transsphenoidal resection followed by (131)I ablation. Post-therapy scintigraphy showed no iodine uptake in the sellar region or bony metastases. Histology of the pituitary mass confirmed metastatic papillary thyroid cancer. Fifteen months later, she had a recurrence of pituitary metastases affecting her vision. This was resected and followed with external beam radiotherapy. Over 2 years, the pituitary metastases increased in size and required two further operations. Radioactive iodine was not considered due to poor response in the past. Progressively, she developed a left-sided III and IV cranial nerve palsy and permanent bitemporal hemianopia. There was a rapid decline in the patient's health with further imaging revealing new lung and bony metastases, and she eventually died 8 months later. To our knowledge, this is the first case of pituitary metastases from a radioiodine-resistant papillary thyroid cancer. Radioiodine-resistant metastatic thyroid cancer may exhibit rapid aggressive growth and remain poorly responsive to the currently available treatment.

LEARNING POINTS

Differentiated thyroid cancer (DTC) has an excellent prognosis with <5% of the cases presenting with distant metastases, usually to lung and bone.Metastasis to the pituitary is a rare complication of DTC.The diagnosis of pituitary insufficiency secondary to pituitary metastases from DTC may be delayed due to the non-specific systemic symptoms of underlying malignancy and TSH suppression therapy for thyroid cancer.The imaging characteristics of metastases to the pituitary may be similar to non-functioning pituitary adenoma.Radioiodine refractory metastatic thyroid cancer has significantly lower survival rates compared with radioactive iodine-avid metastases due to limited therapeutic options.

摘要

未标注

垂体转移是甲状腺癌罕见的并发症。它们与垂体肿瘤相似,给诊断带来挑战。我们报告一例侵袭性非放射性碘摄取型乳头状甲状腺癌伴复发性垂体转移的病例,并对文献进行综述。一名有乳头状甲状腺癌和骨转移病史的70岁女性,出现肾上腺功能减退和周边视力丧失症状。磁共振成像显示垂体有一个大肿块压迫视交叉。她接受了经蝶窦切除术,随后进行了碘-131消融。治疗后闪烁显像显示蝶鞍区或骨转移灶无碘摄取。垂体肿块的组织学检查证实为转移性乳头状甲状腺癌。15个月后,她垂体转移复发影响视力。再次切除后接受了外照射放疗。2年多来,垂体转移灶增大,需要再次进行两次手术。由于过去反应不佳,未考虑放射性碘治疗。逐渐地,她出现左侧动眼神经和滑车神经麻痹以及永久性双颞侧偏盲。患者健康状况迅速恶化,进一步影像学检查发现新的肺和骨转移,最终8个月后死亡。据我们所知,这是首例放射性碘抵抗型乳头状甲状腺癌发生垂体转移的病例。放射性碘抵抗型转移性甲状腺癌可能生长迅速且侵袭性强,对目前可用的治疗反应仍然不佳。

学习要点

分化型甲状腺癌(DTC)预后良好,<5%的病例出现远处转移,通常转移至肺和骨。垂体转移是DTC罕见的并发症。由于潜在恶性肿瘤的非特异性全身症状以及甲状腺癌的促甲状腺激素抑制治疗,DTC垂体转移继发垂体功能减退的诊断可能会延迟。垂体转移的影像学特征可能与无功能垂体腺瘤相似。由于治疗选择有限,放射性碘难治性转移性甲状腺癌的生存率明显低于放射性碘摄取型转移癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3555/3922192/9bead7ad235d/edmcr-2013-130024-g001.jpg

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