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具有非典型影像学特征的原发性垂体脓肿:一例罕见病例报告

Primary pituitary abscess with atypical imaging features: A rare case report.

作者信息

Samha Raghad, Raya Maria, Mansour Marah, Mansour Amal, Mohsen Mohammad Ayham, Alromhain Basel

机构信息

Faculty of Medicine, AlBaath University, Homs, Syrian Arab Republic.

Faculty of Medicine, University of Kalamoon, Damascus, Syria.

出版信息

Int J Surg Case Rep. 2024 Jun;119:109753. doi: 10.1016/j.ijscr.2024.109753. Epub 2024 May 15.

Abstract

INTRODUCTION AND IMPORTANCE

A pituitary abscess (PA) is an extremely rare disease. It is characterized by the presence of an infected purulent collection within the Sella turcica. PAs are categorized in two categories: primary, when the pituitary is normal before the infection, or secondary, when there is a pre-existing sellar pathology (e.g., pituitary adenoma, Rathke's cleft cysts, or craniopharyngioma), meningitis, paranasal sinusitis, or head surgery, which may be indicative of the source of infection.

CASE PRESENTATION

We presented a case of a 52-year-old male with visual disturbances. Both a computerized tomography scan and magnetic resonance imaging revealed a sellar mass lesion, initially suspected to be a pituitary tumor. During transsphenoidal surgery for excision of the pituitary mass, an amount of pus was drained, indicating a pituitary abscess, which was confirmed by positive Staphylococcus aureus colonies in the culture. After surgery, the patient received antibiotic treatment for 12 weeks. After two years of follow-up, the patient remained free of complications and did not require hormone replacement therapy.

CLINICAL DISCUSSION

In previous research, there were a total of 488 patients, of those, 318 were primary pituitary abscess. Preoperative diagnosis is still difficult due to a combination of nonspecific symptoms and imaging findings. Endonasal trans-sphenoidal pus evacuation, culture, and individualized antibiotic therapy are available treatment options.

CONCLUSION

Pituitary abscess is a rare illness, but it should always be considered when evaluating a patient with a fast visual decline. Following the diagnosis, surgery and antibiotics should be started immediately. Proper therapy usually yields a positive effect.

摘要

引言与重要性

垂体脓肿(PA)是一种极其罕见的疾病。其特征是蝶鞍内存在感染性脓性聚集物。垂体脓肿分为两类:原发性,即感染前垂体正常;继发性,即存在先前的鞍区病变(如垂体腺瘤、拉克氏囊肿或颅咽管瘤)、脑膜炎、鼻窦炎或头部手术,这些可能提示感染源。

病例介绍

我们报告了一例52岁男性视力障碍患者。计算机断层扫描和磁共振成像均显示鞍区有占位性病变,最初怀疑为垂体肿瘤。在经蝶窦手术切除垂体肿块时,引出了一定量的脓液,提示为垂体脓肿,培养结果显示金黄色葡萄球菌菌落阳性,从而确诊。术后,患者接受了12周的抗生素治疗。经过两年的随访,患者未出现并发症,也无需激素替代治疗。

临床讨论

在先前的研究中,共有488例患者,其中318例为原发性垂体脓肿。由于非特异性症状和影像学表现的综合作用,术前诊断仍然困难。经鼻蝶窦排脓、培养和个体化抗生素治疗是可行的治疗选择。

结论

垂体脓肿是一种罕见疾病,但在评估视力快速下降的患者时应始终予以考虑。确诊后,应立即开始手术和使用抗生素。恰当的治疗通常会产生积极效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a8b/11127560/db94eb688de7/gr1.jpg

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