Ben Thayer Maissa, Helal Imen, Hedhli Raoueh, Rejeb Emna, Khanchel Fatma, Ben Brahim Ehsen, Jouini Raja, Chadli-Debbiche Aschraf
Faculty of Medicine of Tunis, Tunis El Manar University, 1007, Tunis, Tunisia.
Department of Pathology, Habib Thameur Hospital, Tunis, Tunisia.
J Med Case Rep. 2024 Dec 4;18(1):595. doi: 10.1186/s13256-024-04923-3.
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.
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.
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.
孤立性纤维瘤(SFT)是一种普遍存在的具有中等恶性潜能的间叶性肿瘤。头颈部的SFT较为罕见,占所有SFT的比例不到0.1%。甲状腺孤立性纤维瘤(SFTT)则更为罕见。文献中仅记录了49例SFTT病例,其中仅有2例与甲状腺乳头状癌(PTC)同时发生。通过呈现一例PTC与SFTT同时发生的病例,我们旨在回顾与这种不寻常的同时出现相关的临床表现、诊断挑战、组织病理学特征及治疗策略。
一名46岁的北非女性患者,既往无病史,出现颈部肿物长达一年。颈部超声显示右侧甲状腺叶有两个结节,左侧甲状腺叶有一个结节。右侧甲状腺的第一个结节,大小为50毫米,分类为欧洲甲状腺影像和报告数据系统(EU-TIRADS)III类。右侧甲状腺的第二个结节,大小为15毫米,左侧甲状腺25毫米的结节分类为EU-TIRADS IV类。进行了全甲状腺切除术及双侧淋巴结清扫术。显微镜检查显示,左侧结节及右侧15毫米的结节为浸润性PTC。右侧叶的第二个结节为梭形细胞增生呈片状排列,并呈波浪状或席纹状束状,具有血管外皮细胞瘤样血管模式。梭形细胞边界不清,核细长、无明显异型性。未见有丝分裂。免疫组化显示,梭形细胞对CD34和CD99呈强阳性且弥漫性阳性。对平滑肌肌动蛋白、S100和细胞角蛋白呈阴性。随后确诊为SFTT病例。最终诊断为PTC与SFTT同时发生。
我们报告了第三例PTC与SFTT同时发生的病例。这些肿瘤同时出现可能是偶然的。然而,需要进一步研究来评估这种关联的生理病理学及分子改变情况。