Bucci Ines, Giuliani Cesidio, Di Dalmazi Giulia, Intraina Daniele, Zotta Donato, Ieraci Alfio, Presutti Livio, Napolitano Giorgio
Department of Medicine and Aging Sciences, Center for Advanced Studies and Technology (CAST) G. d'Annunzio University Chieti-Pescara, Chieti, Italy.
Endocrinology and Metabolism Unit, ASL Pescara, Pescara, Italy.
Endocrinol Diabetes Metab Case Rep. 2024 Sep 27;2024(3). doi: 10.1530/EDM-24-0023. Print 2024 Jul 1.
Brain metastases as the first clinical presentation of a papillary thyroid carcinoma (PTC) are exceptional, while cavernous angiomas are common cerebral malformations. We report the case of a 36-year-old male with an incidental brain lesion mimicking a cavernous angioma on MRI. Gamma knife radiosurgery was performed, but after 6 months, the patient developed neurological symptoms, and a repeat brain MRI revealed a significant increase in the mass. The patient underwent neurosurgery, and the histological examination of the lesion revealed metastatic carcinoma of thyroid origin. PET-CT and neck ultrasound, subsequently performed, were concordant for the presence of a right lobe nodule and ipsilateral lymph nodes, both with ultrasound features suspicious of malignancy. Total thyroidectomy with central and right lateral neck dissection was performed, and histology confirmed an intrathyroidal multifocal PTC with lymph node metastases. Postoperative radioiodine was administered, and focal uptake within the thyroid bed, without distant metastases or brain remnants, was found on the post-therapeutic whole-body scan. At 2 years from diagnosis, the patient is in good health and undergoes clinical and imaging follow-up.
Brain cavernous angiomas are common cerebral vascular malformations that are usually diagnosed by MRI. Despite the high accuracy of MRI, the exam is not pathognomonic, and misdiagnosis cannot be excluded. Brain metastases from PTC are very rare; however, they can mimic a cavernous angioma. Therefore, the differential diagnosis should always be considered.
脑转移瘤作为甲状腺乳头状癌(PTC)的首发临床表现极为罕见,而海绵状血管瘤是常见的脑畸形。我们报告一例36岁男性,其脑部偶然发现的病变在MRI上类似海绵状血管瘤。进行了伽玛刀放射外科治疗,但6个月后患者出现神经症状,复查脑部MRI显示肿块显著增大。患者接受了神经外科手术,病变的组织学检查显示为甲状腺来源的转移癌。随后进行的PET-CT和颈部超声检查均显示右叶结节及同侧淋巴结存在,两者超声特征均可疑恶性。进行了全甲状腺切除及中央区和右侧颈侧区清扫术,组织学证实为甲状腺内多灶性PTC伴淋巴结转移。术后给予放射性碘治疗,治疗后全身扫描发现甲状腺床有局灶性摄取,无远处转移或脑内残留病灶。自诊断以来2年,患者健康状况良好,正在接受临床和影像学随访。
脑海绵状血管瘤是常见的脑血管畸形,通常通过MRI诊断。尽管MRI准确性高,但该检查并非特异性的,不能排除误诊。PTC的脑转移瘤非常罕见;然而,它们可以模仿海绵状血管瘤。因此,应始终考虑鉴别诊断。