Parathyroid Carcinoma in a Patient With Secondary Hyperparathyroidism and Thyroid Hemiagenesis: A Case Report and Review of the Literature

被引:7
作者
Kada, Shinpei [1 ,2 ]
Tanaka, Miho [2 ]
Yasoda, Akihiro [3 ]
机构
[1] Natl Hosp Org Kyoto Med Ctr, Dept Otolaryngol Head & Neck Surg, Kyoto, Japan
[2] Otsu Red Cross Hosp, Dept Otolaryngol Head & Neck Surg, Otsu, Shiga, Japan
[3] Natl Hosp Org Kyoto Med Ctr, Clin Res Inst, Div Endocrinol Metab & Hypertens Res, Kyoto, Japan
关键词
parathyroid carcinoma; secondary hyperparathyroidism; tertiary hyperparathyroidism; thyroid hemiagenesis; parathyroidectomy; renal failure; CHRONIC-RENAL-FAILURE; KIDNEY-DISEASE PATIENT; HEMODIALYSIS-PATIENT; TERTIARY HYPERPARATHYROIDISM; GOITER;
D O I
10.1177/01455613211036240
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Parathyroid carcinoma is a rare endocrine tumor. Parathyroid carcinoma in patients with secondary hyperparathyroidism due to chronic kidney disease is also rare. In addition, thyroid hemiagenesis is a rare congenital anomaly. We report an extremely rare case of parathyroid carcinoma in a patient with secondary hyperparathyroidism and thyroid hemiagenesis. We also present a review of the literature of this rare entity. We also discuss the surgical procedure performed for this patient. Our review of the literature found 34 case reports of parathyroid carcinoma in patients undergoing dialysis due to chronic renal failure; 14 reports of thyroid hemiagenesis with parathyroid disease; and no previous reports of thyroid hemiagenesis with secondary hyperparathyroidism and parathyroid carcinoma. Although surgical treatment of parathyroid carcinoma requires combined resection with the thyroid, peritracheal dissection with total parathyroidectomy, and monitoring intact parathyroid hormone as a tumor marker, our procedure preserved the patient's thyroid function. There has been no evidence of recurrence for over 8 years.
引用
收藏
页码:NP25 / NP30
页数:6
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