Pediatric Human Granulocytic Anaplasmosis is Rare in Europe.

M. Pokorn, T. A. Županc, F. Strle
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引用次数: 6

Abstract

6 358 | www.pidj.com The Pediatric Infectious Disease Journal • Volume 35, Number 3, March 2016 fever up to 39.7°C accompanied by chills, headache, neck and lumbar pain and passing of dark urine. The patient lived in a rural area and reported being bitten by numerous ticks in the preceding month. He had no underlying illnesses and at the age of 12 had completed a 3-dose basic tick-borne encephalitis (TBE) vaccination. On admission, he was afebrile with jaundice and a discrete maculopapular rash on the trunk and neck. A systolic murmur was heard in the precordium, and the abdomen was tender to palpation below the right costal margin and in the right flank region. Elevated C-reactive protein (10.1 mg/dL), normal white blood cells count (4300/mm) with 19% band forms, thrombocytopenia (91,000/mm), elevated transaminases (aspartate aminotransferase, 1.96; alanine aminotransferase, 1.47; gamma-glutamyltransferase, 1.96 μkat/L; normal values, <0.58, <0.74 and <0.92 μkat/L, respectively), lactate dehydrogenase (8.67 μkat/L; normal level < 4.13) and bilirubin (total, 64 μmol/L; direct, 18 μmol/L; upper normal values, 17 and 5 μmol/L, respectively) as well as prolonged prothrombin time (0.63, international normalized ratio, 1.32) were found. Serum electrolytes, urea and creatinine were normal. The patient was given cefotaxime and flucloxacillin for suspected sepsis but remained febrile. Because blood, urine and stool cultures were negative, white blood cells (nadir 1600/mm) and platelet (53,000/mm) counts further decreased and transaminase levels increased (maximum values aspartate aminotransferase, 3.59; alanine aminotransferase, 3.05 and γ-GT, 3.80 μkat/L) and tests for A. phagocytophilum infection [demonstration of morulae in peripheral blood smear, detection of A. phagocytophilum genome in blood with polymerase chain reaction (PCR) and immunofluorescence assay for detection of A. phagocytophilum antibodies] were performed on day 3 of hospital stay. Based on a positive specific PCR result, treatment with doxycycline 100 mg/12 hours was accompanied by prompt defervescence and normalization of laboratory values. Differential diagnoses included tests for hantavirus infection (serology) and infection with Leptospira sp. (PCR in urine) that were negative, whereas serology for TBE was compatible with postvaccination levels (positive IgG and negative IgM). The patient made an uneventful recovery after 10 days of doxycycline treatment. The test results for A. phagocytophilum and Ehrlichia chaffeensis infection are shown in Table 1. HGA is rare in Europe and affects predominately adults with only 2 cases described in children. In a prospective Pediatric Human Granulocytic Anaplasmosis is Rare in Europe Letters to the editor
小儿粒细胞无形体病在欧洲很少见。
6 358 | www.pidj.com儿科传染病杂志•第35卷,第3号,2016年3月发烧高达39.7°C伴有寒战,头痛,颈部和腰椎疼痛和通过深色尿液。该患者居住在农村地区,并报告在前一个月被大量蜱虫叮咬。他没有潜在疾病,并在12岁时完成了3剂蜱传脑炎(TBE)疫苗接种。入院时,患者发热伴黄疸,躯干和颈部有离散性黄斑丘疹。心前区可听到收缩期杂音,右肋缘以下及右侧区域腹部触痛。c反应蛋白升高(10.1 mg/dL),白细胞计数正常(4300/mm),带型19%,血小板减少(91000 /mm),转氨酶升高(天冬氨酸转氨酶,1.96;丙氨酸转氨酶,1.47;γ -谷氨酰转移酶,1.96 μkat/L;正常值<0.58、<0.74、<0.92 μkat/L),乳酸脱氢酶(8.67 μkat/L;正常水平< 4.13)和胆红素(总,64 μmol/L;直接,18 μmol/L;凝血酶原时间延长,分别为0.63 μmol/L,国际标准化比值1.32 μmol/L。血清电解质、尿素、肌酐正常。患者因怀疑败血症给予头孢噻肟和氟氯西林,但仍保持发热。由于血、尿、便培养呈阴性,白细胞(最低点1600/mm)和血小板(53000 /mm)计数进一步下降,转氨酶水平升高(最大值天冬氨酸转氨酶,3.59;住院第3天进行丙氨酸转氨酶(3.05 μkat/L)和γ-GT (3.80 μkat/L)及嗜吞噬单胞菌感染检测[外周血涂片显示斑疹菌,采用聚合酶链式反应(PCR)检测血液嗜吞噬单胞菌基因组,免疫荧光法检测嗜吞噬单胞菌抗体]。基于阳性的特异性PCR结果,强力霉素100mg /12小时治疗伴有迅速退热和实验室值正常化。鉴别诊断包括汉坦病毒感染(血清学)和钩端螺旋体感染(尿液PCR)检测均为阴性,而TBE血清学检测与接种后水平(IgG阳性和IgM阴性)一致。患者接受强力霉素治疗10天后恢复正常。嗜吞噬单胞菌和沙菲埃立体感染检测结果见表1。HGA在欧洲很少见,主要影响成人,只有2例儿童。在一项前瞻性儿科研究中,人类粒细胞无形体病在欧洲很少见
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