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腰大肌原发性脓肿:一例免疫功能正常患者的病例报告。

Psoas primary abscess: A case report in an immunocompetent subject.

作者信息

Essobiyou Tamassi Bertrand, Labou Albert Kossi, Diendere Pegwende Rachid Cedric, Sakiye Kodjo Abossisso

机构信息

Department of Surgery and Surgical Specialties, university of Lome, Togo.

Department of Surgery and Surgical Specialties, university of Lome, Togo.

出版信息

Int J Surg Case Rep. 2023 Sep;110:108640. doi: 10.1016/j.ijscr.2023.108640. Epub 2023 Aug 12.

Abstract

INTRODUCTION

Primary psoas abscess is a rare disease characterised by a purulent collection in the thickness of the psoas muscle. Its incidence and etiopathogenesis are not well defined. It is mainly encountered in developing countries in weakened conditions. The involvement of an immunocompetent subject is exceptional. We report a case of primary psoas abscess in an immunocompetent patient in Togo.

CASE PRESENTATION

A 67-year-old retired teacher with no previous medical history was seen in the emergency room with acute and severe abdominal pain. The clinical examination revealed an infectious syndrome and a painful abdominal mass in the right iliac fossa. CT scan showed a heterogeneous fluid collection in the right psoas muscle. Surgical drainage was indicated and performed. The patient was treated postoperatively with dual antibiotics with a favourable outcome. No germs were isolated from the collection.

CLINICAL DISCUSSION

Rare infectious disease, its real incidence is unknown. The most common germ is staphylococcus aureus. Its etiopathogenesis is also poorly understood. Immune deficiency is a predisposing factor for the condition. Diagnosis of the disease is difficult due to a lack of specificity of the signs encountered. Imaging is the key to positive diagnosis with a high sensitivity of CT scan. Treatment is medical-surgical with drainage and antibiotic therapy.

CONCLUSION

Primary psoas abscess is a potentially serious disease requiring early diagnosis and management.

摘要

引言

原发性腰大肌脓肿是一种罕见疾病,其特征为腰大肌内有脓性积液。其发病率和病因尚不明确。该病主要在发展中国家的虚弱患者中出现。免疫功能正常的个体患病极为罕见。我们报告了多哥一名免疫功能正常患者的原发性腰大肌脓肿病例。

病例介绍

一名67岁无既往病史的退休教师因急性剧烈腹痛被送往急诊室。临床检查发现有感染综合征,右髂窝有压痛性腹部肿块。CT扫描显示右侧腰大肌有不均匀的液性聚集。遂行手术引流。术后患者接受双联抗生素治疗,预后良好。引流液未分离出病菌。

临床讨论

罕见的感染性疾病,实际发病率未知。最常见的病菌是金黄色葡萄球菌。其病因也了解甚少。免疫缺陷是该病的一个易感因素。由于所出现体征缺乏特异性,该病诊断困难。影像学检查是确诊的关键,CT扫描具有高敏感性。治疗采用手术联合药物治疗,包括引流和抗生素治疗。

结论

原发性腰大肌脓肿是一种潜在的严重疾病,需要早期诊断和处理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/10436164/79149261d9c0/gr1.jpg

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