甲状腺乳头状癌与孤立性甲状腺纤维性肿瘤同时发生1例。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Journal of Medical Case Reports Pub Date : 2024-12-04 DOI:10.1186/s13256-024-04923-3
Maissa Ben Thayer, Imen Helal, Raoueh Hedhli, Emna Rejeb, Fatma Khanchel, Ehsen Ben Brahim, Raja Jouini, Aschraf Chadli-Debbiche
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引用次数: 0

摘要

背景:孤立性纤维性肿瘤(SFT)是一种普遍存在的具有中等恶性潜能的间质肿瘤。头部和颈部的SFTs很少见,占所有SFTs的不到0.1%。孤立性甲状腺纤维性肿瘤(SFTT)更为罕见。文献中仅记录了49例SFTTs,其中仅有2例与甲状腺乳头状癌(PTC)同时发生。通过提出一个同步PTC和SFTT病例,我们的目的是回顾临床表现,诊断挑战,组织病理学特征,以及与这种不寻常的合并发生相关的治疗策略。病例介绍:一名46岁的北非女性患者,无既往病史,表现为一年的宫颈水肿。宫颈超声示右甲状腺叶2个结节,左甲状腺叶1个结节。第一个右甲状腺结节,直径50毫米,被归类为欧洲甲状腺成像和报告数据系统(EU-TIRADS) III。第2个右侧甲状腺结节,大小为15mm,第2个左侧甲状腺结节为25mm,分类为EU-TIRADS IV。行甲状腺全切除术并双侧淋巴结切除术。镜下检查显示左结节和右结节约15mm,为浸润性ptc。右脑叶的第二个结节对应于梭形细胞的增生,呈片状排列,呈波浪形或层状束,呈血管外皮细胞瘤样血管模式。梭形细胞边界不清,细胞核细长。没有有丝分裂。免疫化学染色显示梭形细胞CD34和CD99呈强烈弥漫性阳性。平滑肌肌动蛋白、S100和细胞角蛋白呈阴性。随后确认为SFTT病例。最终诊断为同步PTC和SFTT。结论:我们报告了第三例同步PTC和SFTT。这些肿瘤的同时出现可能是偶然的。然而,需要进一步的研究来评估这种关联的生理病理和分子改变。
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Synchronous occurrence of papillary thyroid carcinoma and solitary fibrous tumor of the thyroid: a case report.

Background: Solitary fibrous tumors (SFT) are ubiquitous mesenchymal neoplasms of intermediate malignant potential. SFTs of the head and neck are rare, representing less than 0.1% of all SFTs. Solitary fibrous tumors of the thyroid (SFTT) are even rarer. Only 49 cases of SFTTs have been documented in the literature, with just two cases being synchronous with papillary thyroid carcinoma (PTC). By presenting a synchronous PTC and SFTT case, we aim to review the clinical presentation, diagnostic challenges, histopathological characteristics, and management strategies associated with this unusual co-occurrence.

Case presentation: A 46-year-old North African female patient with no prior medical history presented with a year-long, indwelling cervical swelling. Cervical ultrasound revealed two nodules in the right thyroid lobe and one nodule in the left thyroid lobe. The first right thyroid nodule, measuring 50 mm, is classified as European Thyroid Imaging and Reporting Data System (EU-TIRADS) III. The second right thyroid nodule, measuring 15 mm, and the 25 mm left thyroid nodule were classified as EU-TIRADS IV. A total thyroidectomy with bilateral lymphadenectomy was performed. Microscopic examination revealed that the left nodule and right nodule measuring 15 mm corresponded to invasive PTCs. The second nodule in the right lobe corresponded to a proliferation of spindle cells arranged in sheets and wavy or storiform bundles with a hemangiopericytoma-like vascular pattern. The spindle cells had indistinct boundaries with elongated non-atypical nuclei. There was no mitosis. On immunochemistry, the spindle cells showed strong and diffuse positivity for CD34 and CD99. They are negative for smooth muscle actin, S100, and cytokeratin. It was then confirmed to be an SFTT case. The final diagnosis was of synchronous PTC and SFTT.

Conclusion: We presented the third case of synchronous PTC and SFTT. The co-occurrence of these tumors is likely incidental. However, further studies are needed to assess the physiopathology and molecular alterations of this association.

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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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