Capezzone Marco, Morabito Eugenia, Bellitti Pasquale, Giannasio Paolo, de Santis Domenico, Bruno Rocco
Unit of Endocrinology, Hospital of Tinchi-Pisticci, Matera, Italy.
Endocr Pract. 2007 Jan-Feb;13(1):56-8. doi: 10.4158/EP.13.1.56.
To describe a rare case of ectopic intrathyroidal parathyroid cyst (PC) in a 29-year-old woman who had been referred to us because of a multinodular goiter.
We review the clinical, laboratory, and radiographic findings as well as the treatment in our patient and provide a brief discussion of the associated literature.
Ultrasonography of the neck showed the presence of 2 thyroid nodules in the left lobe, the larger of which was solid and the smaller of which had a cystic appearance. A small nodular area was also found in the right thyroid lobe (diameter, less than 8 mm). A thyroid scan performed with technetium showed the absence of uptake by both left lobe nodules. Fine-needle aspiration biopsy (FNAB) of the 2 major nodular lesions revealed that the larger thyroid nodule was benign and the smaller was a cyst with clear fluid. Measurement of parathyroid hormone in the FNAB fluid showed a high concentration, suggestive of the diagnosis of PC. Normal serum levels of parathyroid hormone and calcium indicated that it was a nonfunctioning intrathyroidal PC. The PC disappeared after FNAB, but the lesion recurred 3 months later. Therefore, the patient underwent near-total thyroidectomy. Histologic examination confirmed the diagnosis of intrathyroidal PC, and a papillary microcarcinoma (6 mm in diameter) was found in the right lobe of the thyroid.
Although an ectopic intrathyroidal PC is rare, the frequency of occult papillary microcarcinoma of the thyroid is high. The association we describe, however, should be considered incidental. To our knowledge, this is the first report of an association of an intrathyroidal PC with papillary microcarcinoma of the thyroid.
描述一例罕见的异位甲状腺内甲状旁腺囊肿(PC),患者为一名29岁女性,因多结节性甲状腺肿前来就诊。
我们回顾了该患者的临床、实验室及影像学检查结果以及治疗情况,并对相关文献进行简要讨论。
颈部超声检查显示左叶有2个甲状腺结节,较大的为实性,较小的呈囊性。右甲状腺叶也发现一个小结节区域(直径小于8mm)。用锝进行的甲状腺扫描显示左叶两个结节均无摄取。对两个主要结节性病变进行细针穿刺活检(FNAB),结果显示较大的甲状腺结节为良性,较小的是一个含清亮液体的囊肿。FNAB液中甲状旁腺激素测量显示浓度较高,提示PC诊断。甲状旁腺激素和钙的血清水平正常,表明这是一个无功能的甲状腺内PC。FNAB后PC消失,但3个月后病变复发。因此,患者接受了近全甲状腺切除术。组织学检查证实为甲状腺内PC诊断,且在甲状腺右叶发现一个直径6mm的乳头状微小癌。
尽管异位甲状腺内PC罕见,但甲状腺隐匿性乳头状微小癌的发生率较高。然而,我们所描述的这种关联应被视为偶然。据我们所知,这是甲状腺内PC与甲状腺乳头状微小癌关联的首例报告。