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异时性双发性甲状旁腺腺瘤,涉及两种不同细胞类型:主细胞和嗜酸性细胞。

Metachronous double parathyroid adenomas involving two different cell types: chief cell and oxyphil cell.

作者信息

Zhou Wei, Katz Matthew H, Deftos Leonard J, Snyder Cynthia S, Baird Stephen, Bouvet Michael

机构信息

Department of Surgery, University of California at San Diego and the San Diego VA Medical Center, San Diego, California 92161, USA.

出版信息

Endocr Pract. 2003 Nov-Dec;9(6):522-5. doi: 10.4158/EP.9.6.522.

Abstract

OBJECTIVE

To describe a patient with the rare occurrence of metachronous double parathyroid adenomas involving two different cell types.

METHODS

We present a case report and a summary of the related literature.

RESULTS

Double parathyroid adenomas are rare, occurring in 1.7 to 9% of patients with primary hyperparathyroidism. Most double parathyroid adenomas are synchronous lesions; few metachronous double parathyroid adenomas have previously been reported. Most parathyroid adenomas are of the chief cell variety, with oxyphil cell adenomas occurring in less than 1% of cases. In a 73-year-old man with no prior history or known family history of endocrine disease, primary hyperparathyroidism developed, and cervical ultrasonography demonstrated a mass in the right side of the neck. Subsequent parathyroidectomy revealed a right superior chief cell adenoma. Postoperatively, the patient's parathyroid hormone and serum calcium levels returned to normal and remained so for at least 9 years. Twelve years after the first operation, recurrent hyperparathyroidism prompted repeated surgical exploration of the neck, which disclosed a large left superior parathyroid mass. Surgical excision and histologic examination revealed the lesion to be an oxyphil cell adenoma.

CONCLUSION

To our knowledge, this is the first reported case of metachronous double parathyroid adenomas involving two different cell types: chief cell and oxyphil cell.

摘要

目的

描述1例罕见的异时性双发性甲状旁腺腺瘤,累及两种不同细胞类型。

方法

我们报告1例病例并总结相关文献。

结果

双发性甲状旁腺腺瘤很罕见,在原发性甲状旁腺功能亢进患者中发生率为1.7%至9%。大多数双发性甲状旁腺腺瘤是同步性病变;此前报道的异时性双发性甲状旁腺腺瘤很少。大多数甲状旁腺腺瘤是主细胞型,嗜酸细胞腺瘤发生率不到1%。在1例无内分泌疾病既往史或已知家族史的73岁男性中,发生了原发性甲状旁腺功能亢进,颈部超声检查显示颈部右侧有一肿块。随后的甲状旁腺切除术发现右侧上位主细胞腺瘤。术后,患者的甲状旁腺激素和血清钙水平恢复正常,并至少维持9年。首次手术后12年,复发性甲状旁腺功能亢进促使再次对颈部进行手术探查,发现左上位甲状旁腺有一较大肿块。手术切除及组织学检查显示该病变为嗜酸细胞腺瘤。

结论

据我们所知,这是首例报道的异时性双发性甲状旁腺腺瘤,累及主细胞和嗜酸细胞两种不同细胞类型。

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