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锝甲状腺闪烁扫描术检测Marine-Lenhart综合征的患病率及对放射性碘的反应:一项单机构回顾性研究。

Prevalence of Marine-Lenhart syndrome on Tc-thyroid scintigraphy and response to radioiodine: A single institutional retrospective study.

作者信息

Agrawal Kanhaiyalal, Patro P Sai Sradha, Meher Bikash Ranjan, Gnanasegaran Gopinath

机构信息

Department of Nuclear Medicine, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India.

Department of Pharmacology, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India.

出版信息

World J Nucl Med. 2021 Sep 22;20(4):369-373. doi: 10.4103/wjnm.wjnm_130_20. eCollection 2021 Oct-Dec.

Abstract

Marine-Lenhart Syndrome is a rare entity, described as Graves' disease with coexisting functioning thyroid nodules. It is often diagnosed on thyroid scintigraphy as a cold nodule with surrounding extranodular hyperactivity initially and postradioiodine ablation, they regain function on the follow-up thyroid scintigraphy due to endogenous thyroid-stimulating hormone (TSH) stimulation. We retrospectively reviewed all thyroid scintigraphy database performed between January 2018 and March 2020 in our institute. We searched patients with Graves' disease with the following criteria to suggest Marine-Lenhart Syndrome: (a) initial thyroid scintigraphy showing features of Graves' disease with coexistent poorly functioning nodules (b) There is normalization of uptake within the nodule on thyroid scan after radioiodine ablation suggestive of endogenous TSH stimulation (this also indirectly proves nodules are TSH dependent), (c) nodule(s) is/are benign on fine-needle aspiration cytology. Four patients (1.46%) were confirmed as Marine-Lenhart Syndrome as per the criteria. Three patients were female, and one was male. The eye signs were present in two of four patients. Two patients had two hypofunctioning nodules, whereas the remaining two had a single nodule and required re-ablation with radioiodine. Marine-Lenhart Syndrome requires special attention as these patients are relatively radioiodine resistant, require higher activity for iodine-131; however, it is curable with radioiodine treatment.

摘要

马林-伦哈特综合征是一种罕见病症,被描述为伴有共存的功能性甲状腺结节的格雷夫斯病。它在甲状腺闪烁扫描中通常最初被诊断为冷结节,周围有结节外高活性,在放射性碘消融后,由于内源性促甲状腺激素(TSH)刺激,在后续甲状腺闪烁扫描中它们恢复功能。我们回顾性分析了2018年1月至2020年3月在我院进行的所有甲状腺闪烁扫描数据库。我们按照以下标准搜索患有格雷夫斯病且提示马林-伦哈特综合征的患者:(a)初始甲状腺闪烁扫描显示格雷夫斯病特征且伴有共存的功能不良结节;(b)放射性碘消融后甲状腺扫描显示结节内摄取正常化,提示内源性TSH刺激(这也间接证明结节依赖TSH);(c)细针穿刺细胞学检查显示结节为良性。根据标准,有4例患者(1.46%)被确诊为马林-伦哈特综合征。3例为女性,1例为男性。4例患者中有2例出现眼部体征。2例患者有2个功能减退结节,而其余2例有单个结节,需要再次进行放射性碘消融。马林-伦哈特综合征需要特别关注,因为这些患者对放射性碘相对耐药,进行碘-131治疗需要更高的活度;然而,放射性碘治疗可治愈该病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9418/8686752/43417f82113f/WJNM-20-369-g001.jpg

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