Mendes Maiana Darwich, Cavallo Rafael Ruiz, Carvalhães Cecilia Helena Vieira Franco Godoy, Ferrarini Maria Aparecida Gadiani
Escola Paulista de Medicina da Universidade Federal de São Paulo (Unifesp), São Paulo, SP, Brasil.
Escola Paulista de Medicina da Universidade Federal de São Paulo (Unifesp), São Paulo, SP, Brasil.
Rev Paul Pediatr. 2016 Sep;34(3):379-83. doi: 10.1016/j.rpped.2015.12.001. Epub 2016 Feb 1.
To report a case septic arthritis with a rare pathogen in a immunosuppressed child.
Male patient, 6 years old, had liver transplant 5 and half years ago due to biliary atresia. Patient was using tacrolimus 1mg q.12hours. This patient started to have pain in left foot and ankle and had one episode of fever 3 days before hospital admission. Physical Examination showed weight 17kg, height 109cm, temperature 36,4°C, with pain, swelling and heat in the left ankle, without other clinical signs. Initial tests: hemoglobin 11,7g/dL hematocrit 36.4%, leukocyte count 17600/uL (7% banded neutrophils, 70% segmented neutrophils, 2% eosinophils, basophils 1%, 13% lymphocytes, 7% monocytes) C-reactive protein 170,88mg/L. Joint ultrasound showed moderate effusion in the site. Patient was submitted to surgical procedure and S. multivorum was isolated from the effusion. The germ was susceptible to broad spectrum cephalosporins (ceftriaxone and cefepime) and fluoroquinolones (ciprofloxacin and levofloxacin), and it was resistant to carbapenemic antibiotics and aminoglycosides. He was treated intravenously with oxacillin for 15 days and ceftriaxone for 13 days, and orally with ciprofloxacin for 15 days, with good outcome.
The Sphingobacterium multivorum is a gram negative bacillus that belongs to Flavobacteriaceae family and it is considered non-pathogenic. It has rarely been described as a cause of infections in humans, especially in hospital environment and in immunosuppressed patients. This case report is relevant for its unusual etiology and for the site affected, which may be the first case of septic arthritis described.
报告1例免疫抑制儿童感染罕见病原体的化脓性关节炎病例。
男性患者,6岁,5年半前因胆道闭锁接受肝移植。患者使用他克莫司,1毫克,每12小时1次。该患者入院前3天开始出现左脚和踝关节疼痛,并伴有1次发热。体格检查显示体重17千克,身高109厘米,体温36.4℃,左脚踝关节疼痛、肿胀且发热,无其他临床体征。初始检查:血红蛋白11.7克/分升,血细胞比容36.4%,白细胞计数17600/微升(7%杆状核中性粒细胞,70%分叶核中性粒细胞,2%嗜酸性粒细胞,1%嗜碱性粒细胞,13%淋巴细胞,7%单核细胞),C反应蛋白170.88毫克/升。关节超声显示该部位有中等量积液。患者接受了手术,从积液中分离出多食鞘氨醇杆菌。该病菌对广谱头孢菌素(头孢曲松和头孢吡肟)和氟喹诺酮类(环丙沙星和左氧氟沙星)敏感,对碳青霉烯类抗生素和氨基糖苷类耐药。患者静脉注射苯唑西林15天,头孢曲松13天,口服环丙沙星15天,治疗效果良好。
多食鞘氨醇杆菌是一种革兰氏阴性杆菌,属于黄杆菌科,被认为是非致病性的。它很少被描述为人类感染的病因,尤其是在医院环境和免疫抑制患者中。本病例报告因其不寻常的病因和受累部位而具有相关性,这可能是描述的首例化脓性关节炎病例。