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无皮样窦道的感染性硬膜内皮样囊肿酷似脑脓肿:一例报告

Infected intradural dermoid cyst without dermal sinus tract mimicking brain abscess: A case report.

作者信息

Pham Anh Hoang, Le Tam Duc, Chu Hung Thanh, Le Tuan Anh, Duong Ha Dai, Van Dong He

机构信息

Neurosurgery Department I, Viet Duc University Hospital, Hanoi, Viet Nam.

Hanoi Medical University, Hanoi, Viet Nam.

出版信息

Int J Surg Case Rep. 2020;72:142-146. doi: 10.1016/j.ijscr.2020.05.052. Epub 2020 May 30.

Abstract

INTRODUCTION

Infection is a rare complication of intradural dermoid cyst. We reported an infected intradural dermoid cyst without dermal sinus tract mimicking brain abscess.

PRESENTATION OF CASE

A 4-year-old boy with no medical history complained of a palpable mass on his head. On examination, the occipital palpable mass was firm and immobile, had no redness, swelling, and pain. The preoperative MRI showed a well-defined, ring-enhancing lesion. White blood count was 12.8 × 10  cells/liter. We have sought no other infection sites. We encountered intraoperatively the pus from the infected mass invading subcutaneous layer and skull bone. We excised completely the tumor and carefully coagulated the residual capsule invading superior sagittal sinus. Histopathological examination was infected dermoid cyst. The infection agent was Staphylococcus aureus. The patient was received systemic antibiotic therapy for 21 days following oral antibiotics for 1 month. He was discharged with no complications.

DISCUSSION

The diagnosis of infected dermoid cyst was often based on MRI images and especially dermal sinus tract. However, in the absence of a dermal sinus tract, preoperative diagnosing an infected dermoid cyst might be very challenging. The ideal treatment of the dermoid cyst was total resection of the cyst with the epithelial lining. Nevertheless, due to the benign nature of dermoid cyst, adequate gross total resection with meticulous hemostasis the residual capsule firmly adhering eloquent areas and major vessels was more appropriate.

CONCLUSION

Diagnosing infected dermoid cyst with no dermal sinus might be challenging. Systemic antibiotic therapy after gross total resection was an effective treatment.

摘要

引言

感染是硬脊膜内皮样囊肿罕见的并发症。我们报告了一例无皮样窦道的感染性硬脊膜内皮样囊肿,其表现类似脑脓肿。

病例介绍

一名4岁无病史男孩主诉头部可触及肿块。检查时,枕部可触及的肿块质地坚硬、固定不动,无红肿及疼痛。术前MRI显示一个边界清晰、环形强化的病变。白细胞计数为12.8×10⁹个/升。我们未发现其他感染部位。术中我们发现感染肿块的脓液侵入皮下层和颅骨。我们完整切除了肿瘤,并仔细凝固了侵犯上矢状窦的残留包膜。组织病理学检查为感染性皮样囊肿。感染病原体为金黄色葡萄球菌。患者术后接受了1个月口服抗生素及21天全身抗生素治疗。他出院时无并发症。

讨论

感染性皮样囊肿的诊断通常基于MRI图像,尤其是皮样窦道。然而,在没有皮样窦道的情况下,术前诊断感染性皮样囊肿可能极具挑战性。皮样囊肿的理想治疗方法是完整切除囊肿及上皮内衬。然而,由于皮样囊肿的良性性质,充分的大体全切并对牢固附着于重要区域和大血管的残留包膜进行细致止血更为合适。

结论

诊断无皮样窦道的感染性皮样囊肿可能具有挑战性。大体全切术后的全身抗生素治疗是一种有效的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc23/7298525/f26a9e3cc807/gr1.jpg

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