Birlutiu Victoria, Birlutiu Rares Mircea, Baicu Marius, Iancu Gabriela Mariana
Lucian Blaga University of Sibiu, Faculty of Medicine Sibiu, Academic Emergency Hospital Sibiu, Infectious Diseases Clinic.
Lucian Blaga University of Sibiu, Faculty of Medicine Sibiu; Spitalul Clinic de Ortopedie-Traumatologie si TBC osteoarticular "Foisor" Bucuresti.
Medicine (Baltimore). 2019 May;98(20):e15651. doi: 10.1097/MD.0000000000015651.
Ecthyma gangrenosum is a cutaneous infection, most commonly occurring during sepsis evolution with Pseudomonas aeruginosa on an immunocompromised background. There have been rare case reports in previously healthy children and rarer are the cases with double etiology.
We present the case of a female Caucasian patient, aged 1 year and 8 months, who developed severe sepsis during flu evolution with predominant respiratory and cerebral manifestations. On admission, at skin level, there was noticed a necrotic coccygeal ulceration (with rapid increasing dimensions 0.5/0.5 cm in 24 hours), and with the transformation from a dry necrosis in a sphacelus at the periphery and progression of necrosis in depth.
The patient was diagnosed with ecthyma gangrenosum from which Pseudomonsa aeruginosa and Enterococcus faecalis were isolated from the samples that were harvested intraoperatively, decision that was taken considering the appearance of CT scan and the extremely rapid expansion of necrosis. Excisional debridement with necrectomy, lavage, and dressing being performed. The invasion of the fascia was excluded intraoperatively.
Treatment with Meropenem for 14 days was initiated, as well as amikacin and linezolid, the latter being replaced with teicoplanin for 14 days. Red blood cells transfusion, intravenous immunoglobulins, anticonvulsants were also administered.
Under treatment the evolution was favorable.
This case brings into discussion a double etiology of ecthyma gangrenosum, in a previously healthy child that occurred in the evolution of influenza. The evolution was favorable under broad-spectrum antibiotic treatment and surgical excision.
坏疽性脓皮病是一种皮肤感染,最常见于脓毒症进展期,在免疫功能低下的背景下由铜绿假单胞菌引起。此前健康儿童中出现坏疽性脓皮病的病例报告罕见,病因双重的病例更为罕见。
我们报告一例1岁8个月大的白种女性患者,在流感病程中出现严重脓毒症,主要表现为呼吸和脑部症状。入院时,在皮肤层面发现尾骨坏死性溃疡(24小时内迅速增大至0.5/0.5厘米),且从干性坏死转变为周边湿性坏疽,并向深部发展。
患者被诊断为坏疽性脓皮病,术中采集的样本分离出铜绿假单胞菌和粪肠球菌,根据CT扫描表现及坏死迅速扩展做出该诊断。进行了坏死组织切除、清创、冲洗和换药。术中排除了筋膜侵犯。
开始用美罗培南治疗14天,同时使用阿米卡星和利奈唑胺,后者在14天后换为替考拉宁。还进行了红细胞输血、静脉注射免疫球蛋白和抗惊厥治疗。
治疗过程中病情好转。
该病例讨论了坏疽性脓皮病的双重病因,发生在一名此前健康的儿童流感病程中。在广谱抗生素治疗和手术切除下病情好转。