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由痤疮丙酸杆菌引起的罕见原发性垂体脓肿。

A Rare Primary Pituitary Abscess Caused by Cutibacterium Acnes.

作者信息

Yip Chi-Man

机构信息

Division of Neurosurgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.

出版信息

J Neurol Surg Rep. 2025 Jul 12;86(3):e136-e139. doi: 10.1055/a-2641-6415. eCollection 2025 Jul.

Abstract

INTRODUCTION

Pituitary abscess is a rare but potentially life-threatening condition with an incidence of 0.2 to 1.1% of operative pituitary lesions. Preoperative diagnosis is difficult because it shares many similarities with other pituitary lesions in terms of signs and symptoms and radiographic findings. The author would like to share a case of primary pituitary abscess due to Cutibacterium acnes infection, which is probably the first case reported in an adult patient.

CASE PRESENTATION

A 60-year-old woman with having medical history of diabetes mellitus who suffered from severe headache, fever, chillness, and vomiting in January 2024. She had been admitted to the Infectious Diseases Department; however, no definite infection source was found, but hypopituitarism was detected. Her brain magnetic resonance imaging (MRI) showed a rim-like enhanced sellar lesion with suprasellar extension. She underwent an endoscopic endonasal transsphenoidal approach with the removal of the lesion and skull base reconstruction. During the surgery, pus-like material and some solid tissue, which was yellowish white in color, were found. The culture of the pus revealed the growth of Cutibacterium acnes, and the histological report of the solid tissue proved nonneoplastic pituitary gland tissue, admixed with fibrous tissue and marked chronic inflammation. She recovered well after surgery and completed antibiotic treatment.

CONCLUSION

Preoperative diagnosis of pituitary abscess is difficult. The majority of pituitary abscesses are diagnosed during the operation or postoperatively. Prompt diagnosis and treatment of pituitary abscess yield a favorable prognosis. The mainstay of treatment is transsphenoidal surgical resection in combination with antibiotic therapy.

摘要

引言

垂体脓肿是一种罕见但可能危及生命的疾病,在手术治疗的垂体病变中发生率为0.2%至1.1%。术前诊断困难,因为其在体征、症状及影像学表现方面与其他垂体病变有许多相似之处。作者想分享一例由痤疮丙酸杆菌感染引起的原发性垂体脓肿病例,这可能是首例报道的成年患者病例。

病例介绍

一名60岁女性,有糖尿病病史,于2024年1月出现严重头痛、发热、寒战及呕吐症状。她曾入住感染科;然而,未发现明确的感染源,但检测到垂体功能减退。她的脑部磁共振成像(MRI)显示鞍区有边缘强化病变并向上延伸至鞍上。她接受了内镜下经鼻蝶窦入路手术,切除病变并进行颅底重建。手术中发现了脓性物质和一些灰白色的实性组织。脓液培养显示痤疮丙酸杆菌生长,实性组织的组织学报告证实为非肿瘤性垂体腺组织,混有纤维组织和明显的慢性炎症。她术后恢复良好并完成了抗生素治疗。

结论

垂体脓肿术前诊断困难。大多数垂体脓肿在手术中或术后被诊断出来。及时诊断和治疗垂体脓肿可取得良好预后。治疗的主要方法是经蝶窦手术切除并联合抗生素治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee83/12255486/0bef031b5684/10-1055-a-2641-6415_26418838.jpg

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