Akhaddar Ali, Hall Walter, Ramraoui Mohammed, Nabil Mehdi, Elkhader Ahmed
Department of Neurosurgery, Avicenne Military Hospital of Marrakech, Mohammed V University in Rabat, Morocco.
Department of Neurosurgery, State University of New York (SUNY), Upstate Medical University, Syracuse, New York, USA.
Surg Neurol Int. 2018 Nov 28;9:239. doi: 10.4103/sni.sni_329_18. eCollection 2018.
Primary psoas abscess is an unusual clinical entity rarely encountered in the postpartum period. Only seven cases have been reported to date. Here, we present a woman with a primary psoas abscess caused by and occurred 2 months following a normal vaginal birth. We highlight the difficulties in the management of this uncommon condition in light of the relevant literature.
A 34-year-old woman who was previously healthy was presented at 2 months' postpartum with important right sciatica and low back pain without fever. Examination of the abdomen revealed tenderness in the right iliac fossa but obstetric/gynecologic and neurologic examinations were normal. The patient had an elevated C-reactive protein level and computed tomography (CT)-scan demonstrated a large psoas abscess on the right side without sacroiliac or spine abnormalities. Initial posterior lumbar percutaneous drainage was useful, but no pathogens were identified. The patient was discharged home with oral antibiotics therapy (amoxicillin/clavulanate and metronidazole). Four weeks later, the follow-up CT-scan showed a re-accumulation of the abscess cavity. Subsequently, the patient underwent a right anterolateral laparotomy with a retroperitoneal approach for abscess drainage. Again, no microorganisms were found. However, diagnosis of tuberculosis was established on histopathologic study. She was successfully treated with antituberculous drugs with a good outcome.
Most primary psoas abscesses present with a delay in diagnosis because of the rarity of this infectious disease, the lack of specific symptoms and signs, and its similarity to many differential diagnoses. When suspected, CT-scan and/or magnetic resonance imaging help in making an accurate diagnosis and facilitate percutaneous or open surgical drainage of the abscess. Correct and fast identification of the microorganisms in addition to appropriate usage of antibiotic regimen improves the outcome.
原发性腰大肌脓肿是一种不常见的临床病症,在产后时期很少见。迄今为止,仅报道过7例。在此,我们介绍一位在正常阴道分娩后2个月出现原发性腰大肌脓肿的女性患者。我们根据相关文献强调了这种罕见病症管理上的困难。
一名34岁既往健康的女性在产后2个月出现严重的右侧坐骨神经痛和腰痛,但无发热。腹部检查发现右髂窝压痛,但产科/妇科及神经系统检查均正常。患者C反应蛋白水平升高,计算机断层扫描(CT)显示右侧有一个大的腰大肌脓肿,无骶髂关节或脊柱异常。最初的后路腰椎经皮引流有效,但未发现病原体。患者出院时接受口服抗生素治疗(阿莫西林/克拉维酸和甲硝唑)。四周后,随访CT扫描显示脓肿腔再次积液。随后,患者接受了右前外侧剖腹手术,采用腹膜后途径进行脓肿引流。同样,未发现微生物。然而,组织病理学研究确诊为结核病。她接受抗结核药物治疗后成功治愈,预后良好。
由于这种传染病罕见、缺乏特异性症状和体征以及与许多鉴别诊断相似,大多数原发性腰大肌脓肿的诊断存在延迟。怀疑该病时,CT扫描和/或磁共振成像有助于准确诊断,并便于脓肿的经皮或开放手术引流。除了正确使用抗生素方案外,正确快速地识别微生物可改善预后。