Jiang Kun, Zhang Wenxiao, Fu Guoyong, Cui Guanghe, Li Xuna, Ren Shousong, Fu Tingliang, Geng Lei
Department of Pediatric Surgery, Binzhou Medical Unversity Hospital, Binzhou, China.
Department of Ultrasonic Medicine, Binzhou Medical Unversity Hospital, Binzhou, China.
Front Surg. 2022 Jun 27;9:871292. doi: 10.3389/fsurg.2022.871292. eCollection 2022.
Iliopsoas abscess with septicemia in the pediatric population is rare. Early diagnosis and effective management of this emergent disorder remain challenging for clinicians.
A 14-year-old girl presented with right lateral and posterior hip pain and fever for 7 days before admission. Blood culture was positive for Enhanced magnetic resonance imaging revealed abscesses located in the right iliopsoas muscle and on the surface deep to the fascia of the right sacroiliac joint that were 6.8 cm × 6.2 cm × 5.7 cm and 3.7 cm × 3.5 cm × 2.1 cm, respectively. A diagnosis of right iliopsoas abscesses with septicemia was made. The patient received intravenous antibiotics, underwent ultrasound-guided percutaneous catheter drainage, and recovered uneventfully. Medical literature regarding this issue published in the English language during the last two decades was reviewed.
Primary synchronous psoas and iliacus muscle abscesses are rare and emergent disorders in the pediatric age group. The diagnosis is generally delayed owing to the deep anatomic location and nonspecific signs and symptoms. A comprehensive medical history, meticulous physical examination, and judicious use of imaging studies could establish a timely and accurate diagnosis. Surgeons should be aware of the occurrence of multiple abscesses. Prompt and adequate antibiotic therapy accompanied by a mini-invasive approach, such as ultrasound-guided, laparoscopic, or video-retroperitoneoscopic drainage of the infectious focus, if indicated and feasible, is important to achieve a good outcome in the management of iliopsoas abscess.
小儿人群中伴有败血症的髂腰肌脓肿较为罕见。对这种紧急病症进行早期诊断和有效管理,对临床医生来说仍然具有挑战性。
一名14岁女孩入院前7天出现右髋外侧和后侧疼痛及发热症状。血培养结果为阳性。增强磁共振成像显示,右髂腰肌及右骶髂关节筋膜深层表面有脓肿,大小分别为6.8 cm×6.2 cm×5.7 cm和3.7 cm×3.5 cm×2.1 cm。诊断为右髂腰肌脓肿伴败血症。患者接受了静脉抗生素治疗,进行了超声引导下经皮导管引流,最终顺利康复。回顾了过去二十年以英文发表的关于此问题的医学文献。
原发性同步腰大肌和髂肌脓肿在儿童年龄组中是罕见的紧急病症。由于解剖位置较深以及体征和症状不具特异性,诊断通常会延迟。全面的病史、细致的体格检查以及合理使用影像学检查能够及时准确地做出诊断。外科医生应意识到可能出现多个脓肿。如果有指征且可行,及时且充分的抗生素治疗并辅以微创方法,如超声引导、腹腔镜或视频后腹腔镜下对感染灶进行引流,对于髂腰肌脓肿的治疗取得良好效果至关重要。