Okamoto Mitsumasa, Tsuruno Yudai, Fukuzawa Hiroaki
Department of Pediatric Surgery, Himeji Red Cross Hospital, 1-12-1, Shimoteno, Himeji, Hyogo, 670-8540, Japan.
Surg Case Rep. 2023 Jun 14;9(1):105. doi: 10.1186/s40792-023-01690-z.
Necrotizing fasciitis in neonates is a rare and life-threatening infection involving necrosis of the skin, subcutaneous tissues, deep fascia, and sometimes underlying muscles, with a fulminant course and high mortality rate. Necrotizing fasciitis with gas gangrene related to infection of a peripherally inserted central catheter is very rare.
The patient was a full-term female neonate born by vaginal delivery. Following diagnosis of patent ductus arteriosus, indomethacin was administered from a peripherally inserted central catheter for 3 days. Four days after the termination of medical treatment for the patent ductus arteriosus, the patient developed fever and a severely elevated inflammatory response was identified from blood testing. Around the right anterior chest wall, corresponding to the site of the catheter tip, redness was increased and gas crepitus was felt under the skin. Computed tomography revealed emphysema in the anterior chest, in subcutaneous areas and between muscles. Emergency surgical debridement was performed under a diagnosis of necrotizing fasciitis with gas gangrene. With antibiotic treatment, we started to fill the wound with a dialkyl carbamoyl chloride-coated dressing and povidone-iodine sugar ointment after washing with saline once a day. The patient survived and after 3 weeks of treatment with the dressing, the wound had successfully resolved without motor impairments.
In addition to medical treatment and prompt surgical debridement, we used dialkyl carbamoyl chloride-coated dressing and povidone-iodine sugar ointment for antiseptic dressings and successfully treated neonatal necrotizing fasciitis with gas gangrene caused by peripherally inserted central catheter infection with Citrobacter koseri.
新生儿坏死性筋膜炎是一种罕见且危及生命的感染,累及皮肤、皮下组织、深筋膜,有时还包括深层肌肉坏死,病程凶险,死亡率高。与外周中心静脉导管感染相关的伴有气性坏疽的坏死性筋膜炎非常罕见。
该患者为足月顺产女婴。诊断为动脉导管未闭后,通过外周中心静脉导管给予吲哚美辛治疗3天。动脉导管未闭治疗结束4天后,患者出现发热,血液检查发现炎症反应严重升高。在右前胸壁对应导管尖端的部位,皮肤发红加重,皮下可触及捻发音。计算机断层扫描显示前胸、皮下区域及肌肉间有肺气肿。在诊断为伴有气性坏疽的坏死性筋膜炎后进行了急诊外科清创术。在抗生素治疗的同时,我们开始每天用生理盐水冲洗伤口一次后,用二烷基甲酰氯涂层敷料和聚维酮碘糖膏填充伤口。患者存活,使用该敷料治疗3周后,伤口成功愈合,无运动功能障碍。
除药物治疗和及时的外科清创术外,我们使用二烷基甲酰氯涂层敷料和聚维酮碘糖膏进行抗菌敷料,成功治疗了由克氏柠檬酸杆菌引起的外周中心静脉导管感染导致的新生儿伴有气性坏疽的坏死性筋膜炎。