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

机译:甲状腺乳头状癌垂体转移瘤1例并文献复习

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SummaryMetastases 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 131I 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.
机译:总结垂体转移瘤是甲状腺癌的罕见并发症。它们类似于垂体瘤,对诊断具有挑战性。我们提出了一个具有复发性垂体转移的侵略性非放射性核素类狂热乳头状甲状腺癌病例,并复习了文献。一名70岁的女性,有甲状腺乳头状癌和骨转移的病史,表现为肾上腺皮质功能减退和周围视力丧失。磁共振成像显示有大的垂体肿块撞击在视交叉上。她进行了蝶窦切除术,然后进行131I消融。治疗后闪烁显像显示在鞍区无碘吸收或骨转移。垂体肿块的组织学证实为转移性甲状腺乳头状癌。 15个月后,她发生了垂体转移瘤复发,影响了她的视力。将其切除并进行外部束放射治疗。在两年的时间里,垂体转移瘤的大小增加,需要进行两次进一步的手术。由于过去反应不佳,因此未考虑放射性碘。她逐渐发展为左侧的III和IV型颅神经麻痹和永久性的颞侧偏盲。随着进一步影像学检查发现新的肺和骨转移,患者的健康迅速下降,她最终在8个月后死亡。据我们所知,这是第一例来自耐放射性碘的乳头状甲状腺癌的垂体转移病例。耐放射性碘的转移性甲状腺癌可能表现出快速的侵袭性生长,并且对目前可用的治疗反应仍然较差。学习要点分化型甲状腺癌(DTC)的预后极佳,<5%的远处转移病例通常发生于肺和骨垂体转移是DTC的罕见并发症。由于潜在的恶性和TSH抑制疗法对甲状腺癌的非特异性全身症状,DTC继发于垂体转移的垂体功能不全的诊断可能会延迟。放射性碘难治性转移性甲状腺癌与放射性碘-avid转移相比由于治疗选择有限而具有较低的生存率。

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