Pituitary Abscess Causing Panhypopituitarism in a Patient With Neurobrucellosis: Case Report

Q3 Medicine
Gustavo De la Peña-Sosa MD, Abraham I. Cabello-Hernández MD, Roxana P. Gómez-Ruíz MD, Miguel A. Gómez-Sámano MD, Francisco J. Gómez-Pérez MD
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引用次数: 0

Abstract

Background/Objective

Pituitary abscess is an uncommon life-threatening disease that could lead to panhypopituitarism. It is important to suspect its prevalence in regions with endemic infectious diseases.

Case Report

A 55-year-old man, a farmer, with a background of consumption of unpasteurized dairy products, presented with headache, impaired consciousness, and fever that started in February 2023. Initial test results were consistent with neuroinfection. Brain MRI showed ventriculitis; the pituitary gland was heterogeneous with the presence of an 8 × 8 mm abscess. The pituitary hormone axis was evaluated, and it showed results compatible with the results of panhypopituitarism with central hypothyroidism, central hypocortisolism, central hypogonadism, and growth hormone deficiency. Hormone replacement treatment with hydrocortisone and levothyroxine was started. The Rose Bengal test for Brucella spp. and 2-mercaptoethanol Brucella agglutination test showed positive results. After neurobrucellosis (NB) was diagnosed, antibiotic treatment was commenced. The patient was discharged 6 weeks later and treatment with prednisone, levothyroxine, recombinant somatropin, testosterone, as well as doxycycline, and rifampin was continued for another 4 months.

Discussion

NB and pituitary abscess are rare manifestations of brucellosis and are challenging to diagnose due to their nonspecific clinical presentation and cerebrospinal fluid (CSF) findings. NB diagnosis relies on neurologic symptoms and serological evidence of Brucella infection. Magnetic resonance imaging is the preferred diagnostic tool for pituitary abscesses. Medical management may be sufficient, while transsphenoidal drainage is not always necessary. Hormonal deficits typically remain permanent.

Conclusion

Pituitary abscess could be suspected in patients presenting with symptoms of neuroinfection, panhypopituitarism, and heterogenous image in the magnetic resonance imaging differential diagnosis. Opportune management can lead to reduced mortality and improved recovery of the pituitary hormone function.

神经布鲁氏菌病患者垂体脓肿导致垂体功能亢进:病例报告
背景/目的垂体脓肿是一种不常见的危及生命的疾病,可导致泛垂体功能障碍。病例报告一名 55 岁的男子是农民,曾食用未经消毒的乳制品,2023 年 2 月开始出现头痛、意识障碍和发热。初步检测结果与神经感染相符。脑部核磁共振成像显示为脑室炎;垂体呈异型,存在一个 8 × 8 毫米的脓肿。对垂体激素轴进行了评估,结果显示与泛垂体功能减退症、中枢性甲状腺功能减退症、中枢性皮质醇功能减退症、中枢性性腺功能减退症和生长激素缺乏症的结果相符。开始使用氢化可的松和左旋甲状腺素进行激素替代治疗。布鲁氏菌属玫瑰红试验和 2-巯基乙醇布鲁氏菌凝集试验均显示阳性结果。确诊为神经布鲁氏菌病(NB)后,患者开始接受抗生素治疗。讨论神经布鲁氏菌病和垂体脓肿是布鲁氏菌病的罕见表现,由于其临床表现和脑脊液(CSF)检查结果均无特异性,因此诊断难度很大。NB的诊断依赖于神经系统症状和布鲁氏菌感染的血清学证据。磁共振成像是垂体脓肿的首选诊断工具。药物治疗可能就足够了,经蝶窦引流并非总是必要的。结论:在磁共振成像鉴别诊断中,如果患者出现神经感染症状、泛垂体功能减退和异质影像,则应怀疑垂体脓肿。及时处理可降低死亡率,改善垂体激素功能的恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
AACE Clinical Case Reports
AACE Clinical Case Reports Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.30
自引率
0.00%
发文量
61
审稿时长
55 days
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