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侵袭性胸段放线菌病并发椎体骨髓炎和硬膜外脓肿,导致脊髓受压。

Aggressive thoracic actinomycosis complicated by vertebral osteomyelitis and epidural abscess leading to spinal cord compression.

作者信息

Yung B C, Cheng J C, Chan T T, Loke T K, Lo J, Lau P Y

机构信息

Department of Radiology and Organ Imaging, United Christian Hospital, Kwun Tong, Kowloon, Hong Kong.

出版信息

Spine (Phila Pa 1976). 2000 Mar 15;25(6):745-8. doi: 10.1097/00007632-200003150-00017.

Abstract

STUDY DESIGN

Report of a successfully diagnosed and treated case of spinal cord compression due to epidural actinomycosis.

OBJECTIVE

To illustrate that proper use of imaging strategy can greatly facilitate diagnosis and management of this rare condition.

SUMMARY OF BACKGROUND DATA

Spinal actinomycosis causing epidural abscess and significant spinal cord compression is an uncommon condition. Although diagnosis is difficult, favorable results are widely reported when specific therapy is instituted.

METHODS

A 32-year-old Chinese man had extensive dorsal thoracic soft tissue swelling and lower limb weakness. Collapse of the T5 vertebral body was found on plain radiographs with mediastinal infiltrates on chest radiograph. It took magnetic resonance imaging (MRI) to fully delineate the epidural abscess and dorsal muscular abscesses, which were not depicted by computed tomographic (CT) scan. Diagnosis was made by examination of CT-guided aspirate and tissue recovered during surgery by a microbiologist. The patient received high-dose intravenous penicillin and prompt spinal decompression once diagnosis of actinomycosis was confirmed.

RESULTS

The dorsal muscular abscesses and upper thoracic epidural abscess resolved rapidly after intravenous antibiotics and surgical drainage. This was well documented by follow-up MRI and the full recovery of motor power and lower limb sensation in the patient.

CONCLUSIONS

High clinical suspicion and proper use of imaging data led to timely diagnosis of this rare case of mediastinal, epidural, and intramuscular thoracic actinomycosis. Specific antibiotic therapy and timely, well-targeted surgical intervention greatly improve the outcome of this condition.

摘要

研究设计

硬膜外放线菌病导致脊髓压迫的一例成功诊断与治疗病例报告。

目的

说明合理运用影像学策略可极大地促进对这种罕见疾病的诊断与管理。

背景资料总结

脊髓放线菌病导致硬膜外脓肿和严重脊髓压迫是一种罕见疾病。尽管诊断困难,但采用特定治疗方法后广泛报道了良好的治疗效果。

方法

一名32岁中国男性出现广泛的胸背部软组织肿胀和下肢无力。X线平片显示T5椎体塌陷,胸部X线片显示纵隔浸润。磁共振成像(MRI)才完全清晰显示出硬膜外脓肿和背部肌肉脓肿,而计算机断层扫描(CT)未显示这些情况。通过对CT引导下穿刺抽吸物以及手术中获取的组织进行微生物学检查做出诊断。一旦确诊放线菌病,患者接受了大剂量静脉注射青霉素并迅速进行了脊髓减压。

结果

静脉使用抗生素和手术引流后,背部肌肉脓肿和上胸部硬膜外脓肿迅速消退。随访MRI以及患者运动能力和下肢感觉完全恢复对此进行了充分记录。

结论

高度的临床怀疑和对影像学数据的合理运用导致了对这例罕见的纵隔、硬膜外和胸肌放线菌病的及时诊断。特异性抗生素治疗以及及时、针对性强的手术干预极大地改善了该病的治疗效果。

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