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一名年轻女性的甲状旁腺腺瘤表现为复发性急性胰腺炎并伴有下颌骨棕色瘤——病例报告

Parathyroid adenoma in a young female presenting as recurrent acute pancreatitis with a brown tumour of the mandible-A case study.

作者信息

Kunte A R, Dube V S, Balwantkar S S, Kulkarni K K

机构信息

General Surgical residency, B. J. Medical College and Sassoon General Hospitals, Pune, India.

B. J. Medical College and Sassoon General Hospitals, Pune, India.

出版信息

Int J Surg Case Rep. 2015;7C:10-5. doi: 10.1016/j.ijscr.2014.11.048. Epub 2014 Nov 27.

Abstract

INTRODUCTION

Primary hyperparathyroidism is usually seen in females above the age of 50 years, with a prevalence of 21/1000,(1) whereas the incidence in patients aged 12-28 years is less than 5%.(2) A solitary adenoma is responsible for 80% of cases of primary hyperparathyroidism.(3) Primary hyperparathyroidism is most commonly asymptomatic.(4) The incidence of acute pancreatitis associated with hyperparathyroidism is less than 10%.(5,6) The incidence of hyperparathyroidism associated with a Brown tumour is less than 5%.(7) PRESENTATION OF CASE: A 19 year old female patient presented with recurrent acute pancreatitis and swelling over the mandible. Complete investigative workup revealed a solitary parathyroid adenoma causing hyperparathyroidism. Surgical exploration with excision of the parathyroid adenoma was performed, following which the patient recovered uneventfully.

DISCUSSION

The patient was initially managed as a case of acute pancreatitis, and although not suspected initially, a high index of suspicion for hyperparathyroidism developed after a biopsy of the mandibular swelling showed the presence of osteoclastic giant cells indicating the possibility of a Brown tumour. Further investigations then revealed the presence of a solitary parathyroid adenoma with coexistent hyperparathyroidism which was then managed surgically.

CONCLUSION

The young age of the patient, and her presentation with acute pancreatitis and a Brown tumour of the mandible make this an extremely rare presentation of parathyroid adenoma.

摘要

引言

原发性甲状旁腺功能亢进症通常见于50岁以上的女性,患病率为21/1000,(1) 而12 - 28岁患者的发病率低于5%。(2) 80%的原发性甲状旁腺功能亢进症病例由单个腺瘤引起。(3) 原发性甲状旁腺功能亢进症最常见的是无症状的。(4) 与甲状旁腺功能亢进症相关的急性胰腺炎的发病率低于10%。(5,6) 与棕色瘤相关的甲状旁腺功能亢进症的发病率低于5%。(7) 病例介绍:一名19岁女性患者出现复发性急性胰腺炎和下颌肿胀。全面的检查发现一个导致甲状旁腺功能亢进的单个甲状旁腺腺瘤。进行了手术探查并切除甲状旁腺腺瘤,随后患者顺利康复。

讨论

患者最初被当作急性胰腺炎病例处理,虽然最初未被怀疑,但在下颌肿胀活检显示存在破骨细胞巨细胞提示可能为棕色瘤后,对甲状旁腺功能亢进症的怀疑指数升高。进一步检查发现存在单个甲状旁腺腺瘤并伴有甲状旁腺功能亢进症,随后进行了手术治疗。

结论

患者年轻,且表现为急性胰腺炎和下颌棕色瘤,这使得甲状旁腺腺瘤的这种表现极为罕见。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aabc/4336398/6f59f26e5a74/gr1.jpg

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