由嗜aphrophilus聚集杆菌引起的下肢大脓肿的不寻常表现:1例报告

IF 0.7 Q4 SURGERY
Takashi Higuchi , Yoshihiro Araki , Mikino Saito , Atsushi Taninaka , Satoru Demura
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引用次数: 0

摘要

aphrophilus聚集杆菌(a.a aphrophilus)是一种罕见的严重感染原因,包括牙周炎、脑脓肿和心内膜炎。虽然它通常是口腔感染,但它累及四肢软组织脓肿是罕见的,这给诊断带来了挑战,经常模仿肿瘤。本报告报告一例罕见的阿佛洛菲菌感染,表现为无外伤史的大而自发引流的下肢脓肿。一例63岁男性糖尿病患者,未经治疗后膝关节疼痛。初步MRI提示股二头肌肌腱血肿,保守治疗。因肿胀、皮肤浸润及自发引流进展,怀疑软组织肿瘤,转介至我院。MRI显示胫骨近端骨髓信号增强的小区域,周围软组织增强,大的不均匀关节外肿块。清除脓肿的穿刺活检和组织培养鉴定为aphrophila。患者用哌拉西林成功治疗,需要住院5周进行伤口处理。当非典型地出现在软组织时,本病例突出了嗜蚜杆菌感染的诊断复杂性。最初误诊为血肿和随后的肿瘤怀疑强调考虑罕见的细菌病因的持续或引流病变,特别是在免疫功能低下的患者。aphrophilus可能需要特殊的培养或分子方法来鉴定。及时诊断和靶向抗生素治疗至关重要。即使没有外伤史,在鉴别诊断大的、自发引流的下肢软组织病变时,也应考虑Aphrophilus。本病例强调微生物培养诊断非典型感染和防止延误治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An unusual presentation of a large lower extremity abscess caused by Aggregatibacter aphrophilus: A case report

Introduction

Aggregatibacter aphrophilus (A. aphrophilus) is a rare cause of severe infections, including periodontitis, brain abscess, and endocarditis. While typically oral commensals, its involvement in extremity soft tissue abscesses is uncommon, posing diagnostic challenges and often mimicking tumors. This report describes a rare A. aphrophilus infection presenting as a large, spontaneously draining lower extremity abscess without trauma history.

Presentation of case

A 63-year-old male with untreated diabetes presented with posterior knee pain. Initial MRI suggested a biceps femoris tendon hematoma, treated conservatively. Because swelling, skin infiltration, and spontaneous drainage progressed, a soft tissue tumor was suspected, leading to referral to our hospital. MRI showed a small area of increased signal intensity in the proximal tibial bone marrow, with an enhancing, large heterogeneous extrarticular mass in surrounding soft tissue. Needle biopsy and tissue culture from the debrided abscess identified A. aphrophilus. The patient was successfully treated with piperacillin, requiring five weeks of hospitalization for wound management.

Discussion

This case highlights the diagnostic complexity of A. aphrophilus infection when presenting atypically in soft tissues. Initial misdiagnosis as a hematoma and subsequent tumor suspicion underscore considering rare bacterial etiologies in persistent or draining lesions, especially in immunocompromised patients. A. aphrophilus may require specific culture or molecular methods for identification. Prompt diagnosis and targeted antibiotic therapy were crucial.

Conclusion

A. aphrophilus should be considered in the differential diagnosis of large, spontaneously draining lower extremity soft tissue lesions, even without a history of trauma. This case emphasizes microbiological culture for diagnosing atypical infections and preventing delayed treatment.
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CiteScore
1.10
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1116
审稿时长
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