Ing Steven W, Pelliteri Phillip K
Division of Endocrinology, Diabetes, and Metabolism, Ohio State University, Columbus, Ohio 43210, USA.
Endocr Pract. 2008 Jan-Feb;14(1):80-6. doi: 10.4158/EP.14.1.80.
To present the clinical course of a patient with persistent primary hyperparathyroidism (PHPT) whose intrathyroidal parathyroid gland was diagnosed by ultrasound-guided fine-needle aspiration biopsy (FNAB).
We describe the clinical course and laboratory, radiographic, and microscopic findings of a patient with persistent PHPT due to an intrathyroidal cystic parathyroid gland and review the relevant literature.
A 74-year-old man with PHPT (presenting serum calcium concentration, 16.2 mg/dL; intact parathyroid hormone [PTH] concentration, 341 pg/mL) had surgical excision of the right superior, right inferior, and left inferior parathyroid glands, but the left superior parathyroid gland remained unidentified. Microscopic examination revealed parathyroid hyperplasia. Technetium Tc 99m sestamibi single-photon emission computed tomography imaging showed uptake in 2 foci, 1 on each side of midline in the neck. Reoperation with attention to the left neck failed to locate another parathyroid gland. Neck ultrasonography demonstrated a complex nodule within the right lower lobe of the thyroid. Results from FNAB of the solid component were consistent with parathyroid cells, and cystic fluid PTH concentration was greater than 1800 pg/mL. Nine months later, neck ultrasonography showed a hypoechoic area located posterior to the inferior pole of the right thyroid. The patient remained eucalcemic 16 months postprocedure.
Autoinfarction of the parathyroid gland and aspiration of cystic fluid may explain resolution of hypercalcemia. Although PHPT due to functioning parathyroid cysts is rare, and PHPT due to cystic parathyroid hyperplasia has been described, this is the first case report of a patient with persistent PHPT due to a functional parathyroid cyst whose diagnosis by FNAB was followed by eucalcemia.
介绍一例持续性原发性甲状旁腺功能亢进症(PHPT)患者的临床病程,该患者的甲状腺内甲状旁腺经超声引导下细针穿刺活检(FNAB)得以确诊。
我们描述了一名因甲状腺内囊性甲状旁腺导致持续性PHPT患者的临床病程、实验室检查、影像学检查及显微镜检查结果,并复习相关文献。
一名患有PHPT的74岁男性(血清钙浓度为16.2mg/dL;完整甲状旁腺激素[PTH]浓度为341pg/mL)接受了右上、右下及左下甲状旁腺的手术切除,但左上甲状旁腺仍未找到。显微镜检查显示甲状旁腺增生。锝Tc 99m甲氧基异丁基异腈单光子发射计算机断层扫描成像显示在颈部中线两侧各有1个病灶摄取。再次手术时对左颈部进行仔细探查,但仍未找到另一个甲状旁腺。颈部超声检查显示甲状腺右叶下极内有一个复杂结节。实性成分的FNAB结果与甲状旁腺细胞一致,囊液PTH浓度大于1800pg/mL。9个月后,颈部超声检查显示右甲状腺下极后方有一个低回声区。术后16个月患者血钙保持正常。
甲状旁腺自梗死和囊液抽吸可能解释了高钙血症的缓解。虽然功能性甲状旁腺囊肿导致的PHPT罕见,且囊性甲状旁腺增生导致的PHPT已有报道,但这是首例因功能性甲状旁腺囊肿导致持续性PHPT且经FNAB确诊后血钙恢复正常的病例报告。