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首页> 外文期刊>BMC Endocrine Disorders >Primary hyperparathyroidism caused by enormous unilateral water-clear cell parathyroid hyperplasia
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Primary hyperparathyroidism caused by enormous unilateral water-clear cell parathyroid hyperplasia

机译:由巨大的单侧水透明细胞甲状旁腺增生引起的原发性甲状旁腺功能亢进

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Background Parathyroid water-clear cell hyperplasia (WCCH) and water-clear cell adenoma (WCCA) are rare causes of primary hyperparathyroidism. The frequency of WCCH seems to be less than 1% of all primary hyperplasia. Case presentation We report a 53-year-old woman with a large unilateral water clear cell parathyroid hyperplasia associated with primary hyperparathyroidism and severe osteoporosis. Ultrasonography showed a 5.4?cm multilobulated hypoechoic well defined mass localized in the lower half of the left thyroid lobe. Technetium sestamibi scanning showed a persistent very large area of increased activity possibly corresponding to a left inferior double parathyroid adenoma. At surgery, two large merged lobulated parathyroid glands were removed from the left superior and inferior aspects of the adjacent thyroid extending to the sub-clavicular area. Histopathology showed polygonal hyperplastic vacuolated cells with abundant water clear cytoplasm. The lesion had lack of capsule or rim of parathyroid tissue and immunohistochemistry was positive for PTH staining. These findings were consistent with diffused water clear cell hyperplasia. After parathyroidectomy, iPTH and calcium levels dropped immediately. Conclusion The clinical presentation of the patients with water clear cells parathyroid content and hyperparathyroidism is indistinguishable from that of the more common causes of primary hyperparathyroidism of adenoma or hyperplasia and the diagnosis is made only on pathological examination. In conclusion , the distinction of water clear cell hyperplasia from water clear cell adenoma can be challenging in many cases, although clinically significant as far as treatment and follow-up.
机译:背景技术甲状旁腺水透明细胞增生(WCCH)和水透明细胞腺瘤(WCCA)是原发性甲状旁腺功能亢进的罕见原因。 WCCH的频率似乎小于所有原发性增生的1%。案例介绍我们报告了一名53岁的女性,具有与原发性甲状旁腺功能亢进和严重骨质疏松症相关的大单侧水清澈的细胞甲状旁腺增生。超声检查显示5.4厘米的多伏的乳化机良好定义的质量,位于左甲状腺叶的下半部分。 SESTAMIBI扫描技术扫描显示出持续的非常大的面积增加的活动,可能对应于左下双甲状旁腺腺瘤。在手术方面,从延伸到亚锁定区域的相邻甲状腺的左上方和下几个方面中除去两个大合并的脱甲状旁腺。组织病理学表现出多边形的过增殖性真空细胞,具有丰富的水透明细胞质。病变缺乏胶囊或甲状旁腺组织的边缘,免疫组织化学对于PTH染色是阳性的。这些发现与扩散的水透明细胞增生一致。甲状旁腺切除术后,IPTH和钙水平立即掉落。结论患有水透明细胞患者甲状旁腺含量和甲状旁腺功能亢进患者的临床介绍与腺瘤或增生的原发性甲状腺功能亢进症的原因中难以区分,并且诊断只对病理检查进行了诊断。总之,在许多情况下,水透明细胞腺瘤的不同水分细胞增生的区别可能是挑战性的,尽管临床上很重要,但临床显着才能治疗和随访。

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