1.Plain chest film findings of staphylococcal pneumonia in children.
Sook Young KIM ; Seong Sook CHA ; Jong Deok KIM ; Duck Hwan CHUNG
Journal of the Korean Radiological Society 1991;27(3):409-414
No abstract available.
Child*
;
Humans
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Pneumonia, Staphylococcal*
;
Thorax*
2.A case of hyperimmunoglobuline E syndrome.
Dae Hyun LIM ; Jeong Hee KIM ; Yun Jeong CHANG ; Soon Ki KIM ; Byong Kwan SON
Journal of the Korean Pediatric Society 1993;36(1):119-125
The hyperimmunoglobulin E syndrome is a primary immunodificiency disorder characterized by recurrent staphylococcal infections and markedly elevated serum IgE level. Clinical features are coarse face and severe infections of the skin-furunculosis or chronically pruritic dermatitis and sinopulmonary tract infection from infancy by coagulase positive Staphylococcus aureus, or Candida albicans etc. The patients's serum IgE level is elevated but the basic immunologic pathogenesis not fully understood. We have experienced a case of hyperimmunoglobulin E syndrome in a 26/12-year-old who had suffered from recurrent staphylococcal pneumonias and abscesses and chronically pruritic dermatitis from 1 month of age with elevated serum IgE level. A brief review of the related literature is presented.
Abscess
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Candida albicans
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Coagulase
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Dermatitis
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Immunoglobulin E
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Pneumonia, Staphylococcal
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Staphylococcal Infections
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Staphylococcus aureus
3.A Case of Job's Syndrome.
Sung Joo LEE ; Jeung LEE ; Jeong Hun PARK ; Joo Heung LEE ; Sang Wahn KOO ; Gwang Seong CHOI ; Young Keun KIM
Korean Journal of Dermatology 2000;38(10):1382-1384
The Job's syndrome is a relatively rare primary immunodeficiency disorder characterized by recurrent staphylococcal infection and abscess formation, defective neutrophil chemotaxis, and markedly elevated serum IgE level. Clinical features are atopiclike dermatitis, furunculosis, paronychia, pulmonary bacterial pneumonia etc. We reported a case of Job's syndrome in a 12-year-old girl who had recurrent pneumonia, scaly pruritic dermatitis, fissured tongue, and nail dystrophy with elevated serum IgE level.
Abscess
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Chemotaxis
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Child
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Dermatitis
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Female
;
Furunculosis
;
Humans
;
Immunoglobulin E
;
Job Syndrome*
;
Neutrophils
;
Paronychia
;
Pneumonia
;
Pneumonia, Bacterial
;
Staphylococcal Infections
;
Tongue, Fissured
4.A Case of Job Syndrome-Experience with Thymopentin.
Myung Hyun SOHN ; Kyung Hwa PARK ; Byung Ju JEONG ; Kyu Earn KIM ; Ki Young LEE
Pediatric Allergy and Respiratory Disease 1997;7(1):122-129
The Job syndrome is a primary immunodeficiency disorder characterized by markedly elevated serum IgE levels, recurrent severe infections of the skin and sinoplmonary tract, including staphylococcal pneumonias, chronic eczematoid dermatitis, coarse facial features, and mild eosinophilia. In 1966, Davis et al discribed two patients with severe eczema, chroic sinopulmonary infections, and recurrent staphylococcal abscesses originally. The reason for immunocompromise in the Job syndrome remains unclear, but a chemotactic defect in neutrophils has been described. We have experienced a case of Job syndrome in a 9-year-old girl who had suffered from severe recurrent multiple infections since 2 month of age. After treatment with thymopentin, she was improved clinically. A brief review of related literature is presented.
Abscess
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Child
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Dermatitis
;
Eczema
;
Eosinophilia
;
Female
;
Humans
;
Immunoglobulin E
;
Job Syndrome
;
Neutrophils
;
Pneumonia, Staphylococcal
;
Skin
;
Thymopentin*
5.Detection of group B streptococcus in the cases died of neonatal pneumonia.
Jiang-hong DENG ; Kai-hu YAO ; Hui-li HU ; Sang-jie YU ; Wei GAO ; Li-bing FU ; Le-jian HE ; Alexander DMITRIEV ; Yong-hong YANG
Chinese Journal of Pediatrics 2006;44(11):850-854
OBJECTIVEFrom the 1970s, group B streptococci (GBS) have been widely recognized as an important pathogen in neonatal infectious disease, and it emerged as the leading cause of neonatal morbidity and mortality in the Western world. However, there are few data on the prevalence of neonatal GBS infections in China. The aim of this retrospective study was to estimate whether GBS is an important pathogen in severe neonatal pneumonia, and to develop a method for detection of GBS infections in fatal neonatal pneumonia.
METHODSA total of 234 neonatal cases (0 - 28 days) died in Beijing Children's Hospital from 1953 to 2004 were enrolled in this study. They were divided into two groups. Two hundred cases diagnosed as neonatal pneumonia were assigned to study group and the remaining 34 cases died of neonatal hemolysis or surgical operation without any confirmed infectious diseases were designated as control group. Formalin-fixed, paraffin-embedded lung tissues were used as source for total genomic DNA extraction. PCR and Southern blot analyses were applied to detect GBS specific cfb gene target sequence. And the clinical data of these cases were reviewed as well.
RESULTSIn the study group, 52 cases were detected positive for GBS DNA by PCR (26%), 130 cases were positive by Southern blot (65%). In the control group, 1 case was detected positive GBS DNA by PCR (3%), and 6 cases were positive by Southern blot (18%). The positive rate was significantly lower in the control group than that in the study group (PCR, chi(2) = 8.82, P < 0.01; Southern blot, chi(2) = 26.77, P < 0.01). The positive rate in the neonates younger than 7 days (early-onset) was significantly higher than that in neonates older than 7 days (late-onset) (PCR: 37% vs. 13%, chi(2) = 15.537, P < 0.01; Southern blot: 72% vs. 52%, chi(2) = 4.37, P < 0.05). In the positive early-onset cases, 39% of whom were born prematurely (29/74). Out of the 200 cases, 75 had complete clinical data. Neither blood nor lung culture for GBS was performed in any of these cases. But risk factors were identified for 35 cases, such as premature delivery, low birth weight, premature rupture of the membrane and abnormal amniotic fluid. GBS was positive in all these cases. Severe apnea appeared to be a common symptom and was present in most of the early-onset GBS-positive cases, while cough and wheezing were found in most of the late-onset GBS-positive cases. In the control group, one PCR positive case was suffered from malignant teratoma. The other 5 positive cases confirmed by Southern blot were diagnosed as kernicterus, hepatoma, aproctia complicating with cysti-urethral fistula, neonatal physio logical bleeding and aproctia complicated with archo-perineal fistula.
CONCLUSIONGroup B Streptococcus is an important pathogen in fatal neonatal pneumonia, especially in early-onset cases. southern blot may be a sensitive method to detect GBS infection in archival tissues. In the clinical work, more attention should be paid to the neonates with GBS risk factors. And GBS detection and prevention in neonates should be put into clinical practice.
China ; epidemiology ; Humans ; Infant, Newborn ; Pneumonia, Staphylococcal ; epidemiology ; Prevalence ; Retrospective Studies ; Streptococcus agalactiae ; isolation & purification
6.Post-influenza Pneumonia Caused by the USA300 Community-Associated Methicillin-Resistant Staphylococcus aureus in Korea.
Kyung Mok SOHN ; Doo Ryeon CHUNG ; Jin Yang BAEK ; So Hyun KIM ; Eun Jeong JOO ; Young Eun HA ; Kwan Soo KO ; Cheol In KANG ; Kyong Ran PECK ; Jae Hoon SONG
Journal of Korean Medical Science 2012;27(3):313-316
Panton-Valentine leukocidin (PVL)-positive USA300 clone has been the most successful community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) clone spreading in North America. In contrast, PVL-negative ST72-CA-MRSA has been predominant in Korea, and there has been no report of infections by the USA300 strain except only one case report of perianal infection. Here, we describe the first case of pneumonia caused by the USA300 strain following pandemic influenza A (H1N1) in Korea. A 50-year-old man was admitted with fever and cough and chest radiograph showed pneumonic consolidation at the right lower lung zone. He received a ventilator support because of respiratory failure. PCR for pandemic influenza A (H1N1) in nasopharyngeal swab was positive, and culture of sputum and endotracheal aspirate grew MRSA. Typing of the isolate revealed that it was PVL-positive, ST 8-MRSA-SCCmec type IV. The analysis of the PFGE patterns showed that this isolate was the same pulsotype as the USA300 strain.
Community-Acquired Infections/*etiology/microbiology
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Humans
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Influenza A Virus, H1N1 Subtype
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Influenza, Human/*complications
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Male
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*Methicillin-Resistant Staphylococcus aureus/classification/isolation & purification
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Middle Aged
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Pneumonia, Staphylococcal/*etiology/microbiology
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Republic of Korea
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Staphylococcal Infections/*etiology/microbiology
8.Analysis of serum vancomycin concentration after administration of different doses in children with Staphylococcus aureus pneumonia.
Guang-Li ZHANG ; Hui ZHAMG ; Ru LIU ; Si-Ying ZHANG ; Jun-Qi LI ; Ying LI ; Dong-Wei ZHANG ; Zheng-Xiu LUO
Chinese Journal of Contemporary Pediatrics 2014;16(10):984-987
OBJECTIVETo analyze serum vancomycin concentration after administration of different therapeutic doses in children with Staphylococcus aureus pneumonia (SAP) in order to determine the appropriate dose of vancomycin in clinical administration.
METHODSThe clinical data of 35 children who were diagnosed with SAP and treated with vancomycin from January 2008 to December 2013 were retrospectively analyzed.
RESULTSAmong the 35 SAP cases with vancomycin therapy, 22 cases (63%) had serum vancomycin trough concentration monitored. The numbers of cases with vancomycin at 10, 12.5, and 15 mg/(kg·dose) × every 6 hours (q6h) were 11, 4 and 7, respectively. The mean serum trough concentration of vancomycin in the 15 mg/(kg·dose) group was 14.98 mg/L, which was significantly higher than in the 10 mg/(kg·dose) and 12.5 mg/(kg·dose) groups (4.97 and 8.00 mg/L respectively; P<0.05). The percentage of cases that reached the expected trough concentration in the 15 mg/(kg·dose) group (71%) was significantly higher than that in the 10 mg/(kg·dose) group (9%), but there was no significant difference in this percentage between the 15 mg/(kg·dose) and 12.5 mg/(kg·dose) groups (71% vs 25%).
CONCLUSIONSThe reasonable dosage of vancomycin for the treatment of pediatric SAP is 15 mg/(kg·dose) × q6h or 60 mg/(kg·d).
Adolescent ; Anti-Bacterial Agents ; blood ; Child ; Child, Preschool ; Female ; Humans ; Infant ; Male ; Pneumonia, Staphylococcal ; blood ; drug therapy ; Vancomycin ; adverse effects ; blood
9.Clinical features of inhaled and blood-borne Staphylococcus aureus pneumonia and analysis of antibiotic resistance of the pathogen in children.
Guang-Li ZHANG ; Ru LIU ; Hui ZHANG ; Ying LI ; Dong-Wei ZHANG ; Jun-Qi LI ; Si-Ying ZHANG ; Jun ZHU ; Zheng-Xiu LUO
Chinese Journal of Contemporary Pediatrics 2014;16(10):979-983
OBJECTIVETo compare the clinical manifestations between inhaled and blood-borne Staphylococcus aureus pneumonia (SAP) and the antibiotic resistance between the isolates of inhaled and blood-borne Staphylococcus aureus.
METHODSThe clinical data of 44 pediatric SAP cases in the Children′s Hospital, Chongqing Medical University from January 2008 to December 2013 were retrospectively analyzed. Twenty-four cases were identified as inhaled SAP, and 20 cases as blood-borne SAP.
RESULTSInhaled SAP was more common in children younger than 3 years of age, while blood-borne SAP was more prevalent in children older than 6 years of age. Patients with inhaled SAP had significantly higher incidence rates of cough, wheeze, moist rales, dyspnea and empyema than those with blood-borne SAP (P<0.05). The patients with blood-borne SAP were more vulnerable to severe fever, unconsciousness, dysfunction of liver and kidney, pyogenic osteomyelitis, septic arthritis, sepsis, and abscess of skin and soft tissues (P<0.05). Inhaled SAP isolates had significantly higher rates of resistance to amoxicillin/clavulanic acid, oxacillin, and cefoxitin than blood-borne SAP isolates (P<0.05), while the latter had a higher rate of resistance to cotrimoxazole (P<0.05).
CONCLUSIONSInhaled SAP often occurs in children younger than 3 years of age, and the respiratory manifestations are commonly seen. Blood-borne SAP often occurs in children older than 6 years of age, with the infectious-toxic symptoms that result in multiple organ infection and dysfunction. The isolates of inhaled and blood-borne SAP have different antibiograms.
Adolescent ; Age Factors ; Blood-Borne Pathogens ; isolation & purification ; Child ; Child, Preschool ; Drug Resistance, Bacterial ; Female ; Humans ; Infant ; Male ; Pneumonia, Staphylococcal ; drug therapy ; microbiology ; Retrospective Studies
10.A Case of Acute Cerebral Aspergillosis Complicating Influenza A/H1N1pdm 2009.
Min Jae KIM ; Min Kyung KIM ; Chang Kyung KANG ; Kang Il JUN ; Ji Hwan BANG ; Sang Won PARK ; Myoung Don OH
Infection and Chemotherapy 2013;45(2):225-229
Invasive aspergillosis is a rare complication in patients with influenza infection. Several cases of invasive pulmonary aspergillosis accompanying influenza infections were reported during the influenza A/H1N1pdm 2009. We encountered a case of acute cerebral aspergillosis in a patient with influenza A/H1N1pdm 2009 infection. A 24-year-old man with uncontrolled diabetes was diagnosed with influenza A/H1N1pdm 2009 infection. Initial evaluation indicated methicillin-sensitive Staphylococcus aureus pneumonia and diabetic ketoacidosis along with influenza. During his hospital course, multiple new rim-enhancing mass lesions not evident in the initial evaluation developed in the fronto-parietal cortical and subcortical white matter and right cerebellum. Pathology and culture results confirmed the presence of Aspergillus fumigatus. Surgical drainage combined with a total of 18 weeks of antifungal therapy resulted in complete resolution of the infection. This case demonstrates that cerebral aspergillosis can present alongside influenza in patients with diabetes or those under intensive care. Clinical suspicion of invasive aspergillosis is required for a definite diagnosis and better prognosis in such cases.
Aspergillosis
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Aspergillus fumigatus
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Brain Abscess
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Central Nervous System
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Cerebellum
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Critical Care
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Diabetes Mellitus
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Diabetic Ketoacidosis
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Drainage
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Humans
;
Influenza, Human
;
Invasive Pulmonary Aspergillosis
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Pneumonia, Staphylococcal
;
Prognosis