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一名患有原发性甲状旁腺功能亢进症的成年女性,其甲状旁腺腺瘤与胸腺瘤相关。

Parathyroid adenoma associated with thymoma in a female adult with primary hyperparathyroidism.

作者信息

Maria Verroiotou, Saad Al Mogrampi, Ioannis Fardellas

机构信息

Surgical Clinique, Naousa General Hospital, Afoi Lanara & Pexlivanou 3, 59200 Naousa, Imathia, Greece.

出版信息

Int J Surg Case Rep. 2013;4(1):105-7. doi: 10.1016/j.ijscr.2012.09.012. Epub 2012 Oct 23.

Abstract

INTRODUCTION

Parathyroid adenoma associated with a thymoma is a rare clinical entity and few cases have been reported in the literature. This association can be explained by the common embryologic origin of the parathyroid glands and the thymus. These patients may present only with clinical signs and symptoms of primary hyperparathyroidism making it difficult to suspect the coexistence of thymoma.

PRESENTATION OF CASE

A 68-year-old female with medical history of primary hyperparathyroidism underwent surgical excision of a single parathyroid adenoma. Intra-operatively a small mass was detected in the proximity of the parathyroid adenoma and was also removed. Pathologic examination revealed parathyroid adenoma as suspected pre-operatively whereas the small mass excised was identified as a type A thymoma. The postoperative course of the patient was favourable, with normal serum calcium levels and in six months follow-up the patient is symptom-free and with no recurrence.

DISCUSSION

Objective of this study is to report the rare case of a female adult with a parathyroid adenoma and a coexisting thymoma in order to underline the importance of these two pathologies and the ideal treatment that should be followed according to the latest records.

CONCLUSION

Surgical removal of parathyroid adenoma is the treatment of choice for primary hyperparathyroidism, with complete recovery and no postoperative complications. Thymoma may be associated with primary hyperparathyoridism, with or without clinical signs and symptoms of myasthenia gravis and this is a rare clinical entity as very few cases have been described worldwide. To our knowledge this is the first case reported in Greece.

摘要

引言

甲状旁腺腺瘤合并胸腺瘤是一种罕见的临床实体,文献报道的病例较少。这种关联可以用甲状旁腺和胸腺共同的胚胎学起源来解释。这些患者可能仅表现为原发性甲状旁腺功能亢进的临床体征和症状,这使得很难怀疑胸腺瘤的共存。

病例介绍

一名68岁女性,有原发性甲状旁腺功能亢进病史,接受了单个甲状旁腺腺瘤的手术切除。术中在甲状旁腺腺瘤附近发现一个小肿块,也被切除。病理检查显示术前怀疑的甲状旁腺腺瘤,而切除的小肿块被确定为A型胸腺瘤。患者术后病程良好,血清钙水平正常,在六个月的随访中,患者无症状且无复发。

讨论

本研究的目的是报告一名成年女性甲状旁腺腺瘤合并共存胸腺瘤的罕见病例,以强调这两种疾病的重要性以及根据最新记录应遵循的理想治疗方法。

结论

手术切除甲状旁腺腺瘤是原发性甲状旁腺功能亢进的首选治疗方法,可完全康复且无术后并发症。胸腺瘤可能与原发性甲状旁腺功能亢进相关,伴有或不伴有重症肌无力的临床体征和症状,这是一种罕见的临床实体,因为全球范围内描述的病例很少。据我们所知,这是希腊报道的首例病例。

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