1.The diagnosis of mycoplasma pneumoniae pneumonia by high density composite particles agglutinin test.
Hae Jin CHOEH ; Jung Hae PARK ; Chong Sung CHUNG ; Kyu Chul CHOEH
Journal of the Korean Pediatric Society 1991;34(8):1102-1109
No abstract available.
Diagnosis*
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Mycoplasma pneumoniae*
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Mycoplasma*
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Pneumonia*
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Pneumonia, Mycoplasma*
4.The Development of Bronchiolitis obliterans after Mycoplasma pneumoniae Pneumonia: Relationship with Antibody Titer and X-ray Pattern.
Chang Keun KIM ; Churl Young CHUNG ; Jung Suk KIM ; Gahm HUR ; Hee Eun LEE ; Young Yull KOH
Pediatric Allergy and Respiratory Disease 1998;8(1):64-71
The aims of this study were to document bronchiolitis obliterans(BO), the long term pulmonary sequelae after mycoplasma pneumonia, and to evaluate the difference of development of BO according to antibody titer and X-ray pattern. Twenty five subjects who had mycoplasma pneumonia underwent high resolution CT(HRCT) 1.3 years(1.0-2.0 years) after the initial infection. Fifteen boys and 10 girls, with mean age of 6.3 years(3-15 year) at the time of the infection, were included. The clinical diagnosis of Mycoplasma pneumoniae(M. pneumoniae) pneumonia was confirmed by a fourfold or higher rise in the antibody titers between acute and convalescent phase or a single very high titers(> or = 1:640) and abnormal chest radiographs. The subjects were divided into two groups as high titer group(antibody titer 1:5120 1:20480, n=15) and low titer group(antibody titer 1:640-1:2560, n=10). Nine of 25 subjects(36.0%) demonstrated BO findings on HRCT which included mosaic perfusion in 8 of 9 subjects(88.9%), bronchiectasis in 6(66.7%), mosaic perfusion associated with bronchiectasis in 6(66.7%), bronchial wall thickening in two(22.2%), and decreased pulmonary vascularity in one(11.1%). Those findings were more commonly seen in high titer group compared to low titer group[53.3%(8/15) vs 10.0%(1/10), P<0.05] and lobar type compared to linear type[58.0%(7/12) vs 15.4% (2/13), P<0.05]. The involved areas on HRCT exactly corresponded with initially involved area on chest radiographs in 8 of 9 subjects (88.9%). The development of BO was closely related to the M. pneumoniae pneumonia and was noted significantly in individuals with high antibody titer and lobar type x-ray pattern. We suggest that it is necessary to pay attention to the development of BO after M. pneumoniae pneumonia with high antibody titer and lobar type x-ray pattern.
Bronchiectasis
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Bronchiolitis Obliterans*
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Bronchiolitis*
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Diagnosis
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Female
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Humans
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Mycoplasma pneumoniae*
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Mycoplasma*
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Perfusion
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Pneumonia*
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Pneumonia, Mycoplasma*
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Radiography, Thoracic
5.2 Cases of Mycoplasma pneumoniae Infection with Severe Pneumonia.
Shin Tae KIM ; Shun Nyung LEE ; Seok Jeong LEE ; Pil Moon JUNG ; Hong Jun PARK ; Myung Sang SHIN ; Chong Whan KIM ; Bu Ghil LEE ; Sang Ha KIM ; Won Yeon LEE ; Kye Chul SHIN ; Suk Joong YONG
Tuberculosis and Respiratory Diseases 2007;63(6):515-520
Mycoplasma pneumoniae (M. pneumoniae) is the leading cause of pneumonia in older children and young adults. Normally, it does not progress to a condition requiring hospitalization but improves spontaneously or has a mild clinical course. We report two cases of M. pneumoniae pneumonia with different clinical manifestations from the normal course. The patients were young healthy individuals. The diagnoses were made by serology. However, it could not be determined beforehand that they had M. pneumoniae pneumonia. Based on the empirical treatment strategy of severe community acquired pneumonia, the patients were treated with broad-spectrum antibiotics including cephalosporin, quinolone and macrolide. After administering the antibiotics, they showed a gradually favorable clinical course and recovered without residual complications. A M. pneumoniae infection should be considered as a cause of severe community acquired pneumonia, and empirical treatment targeting this organism might be helpful in treating patients with the severe manifestation.
Anti-Bacterial Agents
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Child
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Diagnosis
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Hospitalization
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Humans
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Mycoplasma pneumoniae*
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Mycoplasma*
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Pneumonia*
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Pneumonia, Mycoplasma*
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Young Adult
6.2 Cases of Mycoplasma pneumoniae Infection with Severe Pneumonia.
Shin Tae KIM ; Shun Nyung LEE ; Seok Jeong LEE ; Pil Moon JUNG ; Hong Jun PARK ; Myung Sang SHIN ; Chong Whan KIM ; Bu Ghil LEE ; Sang Ha KIM ; Won Yeon LEE ; Kye Chul SHIN ; Suk Joong YONG
Tuberculosis and Respiratory Diseases 2007;63(6):515-520
Mycoplasma pneumoniae (M. pneumoniae) is the leading cause of pneumonia in older children and young adults. Normally, it does not progress to a condition requiring hospitalization but improves spontaneously or has a mild clinical course. We report two cases of M. pneumoniae pneumonia with different clinical manifestations from the normal course. The patients were young healthy individuals. The diagnoses were made by serology. However, it could not be determined beforehand that they had M. pneumoniae pneumonia. Based on the empirical treatment strategy of severe community acquired pneumonia, the patients were treated with broad-spectrum antibiotics including cephalosporin, quinolone and macrolide. After administering the antibiotics, they showed a gradually favorable clinical course and recovered without residual complications. A M. pneumoniae infection should be considered as a cause of severe community acquired pneumonia, and empirical treatment targeting this organism might be helpful in treating patients with the severe manifestation.
Anti-Bacterial Agents
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Child
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Diagnosis
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Hospitalization
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Humans
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Mycoplasma pneumoniae*
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Mycoplasma*
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Pneumonia*
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Pneumonia, Mycoplasma*
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Young Adult
7.Diagnostic Significance of Cold Agglutinin and Antimycoplasma Antibody for Mycoplasma pneumoniae Infection.
Chung Sook KIM ; Chae Hoon LEE ; Chang Ho JEON ; Eun Kyung BAE ; Seak il HONG
Yeungnam University Journal of Medicine 1987;4(1):97-103
A study to evaluate the diagnostic significance of M. pneumoniae Infection by measurements of cold agglutinin and antimycoplasma antibody titers is performed with 191 pediatric patients who have visited Yeungnam University Hospital during the period through January to July, 1987. Forty eight of 191 cases made follow up tests feasible. The results obtained are as follows: 1. It is necessary to perform routine combined measurements of cold agglutinin and antimycoplasma antibody titers for the all pediatric pneumonia caser since a large proportion of pneumonia in children is caused by M. pneumonia. 2. For the diagnosis of M. pneumoniae Infection, measurements of cold agglutinin titer alone seems to be less significant than to check both cold agglutinin and antimycoplasma antibody titers. 3. The measurement of antimycoplasma antibody titer appeared to be more specific than cold agglutinin test in the diagnosis of M. pneumoniae Infection. 4. The present study urges the necessity of follow up study of cold agglutinin and antimycoplasma antibody titer for those who initially presented with normal titers in both tests, but are clinically suspected for M. pneumoniae Infection.
Child
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Diagnosis
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Follow-Up Studies
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Humans
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Mycoplasma pneumoniae*
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Mycoplasma*
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Pneumonia
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Pneumonia, Mycoplasma*
8.Epidemic Pneumonia Caused by Mycoplasma Pneumoniae.
Tuberculosis and Respiratory Diseases 1994;41(3):289-298
BACKGROUND: Most studies of Mycoplasma pneumonia involve a group of admitted patients in hospital, usually with major medical illness. So we investigated the epidemiologic and radiologic features during the course of outbreak of pneumonia in Chunnam coastal area. METHODS: We retrospectively studied the epidemiologic and clinical feature of 105 patients with serologically proven Mycoplasma pneumonia treated at Kwang-Yang Hospital during a epidemic period of Jun. 1993 to Dec. 1993. All cases of pneumonia developed in this period were also reviewed and compared with serologically proven group. RESULTS: 1) There were 63 males and 42 females. 2) More than half(57%) of cases belonged to 5-9 years of age group, and mean age was 6.5 years old. Mean age was steadily decreased as prevalence of Mycoplasma pneumonia had been subsided. 3) A major determinant of the outbreak seemed to .to the population density rather than the population size. 4) The common radiologic features were interstitial in type, and 67 cases was restricted to one lobe. Lobar types are more common in late childhood, and interstitial or diffuse types in early childhood. CONCLUSION: These epidemiologic and radiographic characteristics would contribute to the diagnosis of Mycoplasma pneumonia.
Diagnosis
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Female
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Humans
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Male
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Mycoplasma pneumoniae*
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Mycoplasma*
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Pneumonia*
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Pneumonia, Mycoplasma*
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Population Density
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Prevalence
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Retrospective Studies
10.Diagnosis of Mycoplasma hyorhinis infection in pigs by PCR amplification of 16S-23S rRNA internal transcribed spacer region.
Sunhwa HONG ; Hyun A LEE ; Yungho CHUNG ; Okjin KIM
Journal of Biomedical Research 2015;16(3):104-108
Mycoplasma hyorhinis (M. hyorhinis) is considered an etiological agent of arthritis in suckling pigs. Recently, some M. hyorhinis strains were shown to produce pneumonia that is indistinguishable from the mycoplasmosis caused by M. hyopneumoniae. In this study, we developed a sensitive and specific PCR assay to detect M. hyorhinis and applied the developed PCR assay for detection of Mycoplasma infection in clinical piglets infected with M. hyorhinis. We developed a new PCR assay using a M. hyorhinis-specific primer pair, Mrhin-F and Mrhin-R, designed from the Mycoplasma 16S-23S rRNA internal transcribed spacer (ITS) region. The primers and probe for the assay were designed from regions in the Mycoplasma 16S-23S rRNA ITS unique to M. hyorhinis. The developed PCR assay was very specific and sensitive for the detection of M. hyorhinis. The assay could detect the equivalent of 1 pg of target template DNA, which indicates that the assay was very sensitive. In addition, M. hyorhinis PCR assay detected only M. hyorhinis and not any other Mycoplasma or bacterial spp. of other genera. The new developed PCR assay effectively detected M. hyorhinis infection in pigs. We suggest that this PCR assay using a M. hyorhinis-specific primer pair, Mrhin-F and Mrhin-R, could be useful and effective for monitoring M. hyorhinis infection in pigs.
Arthritis
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Diagnosis*
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DNA
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Mycoplasma hyorhinis*
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Mycoplasma Infections
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Mycoplasma*
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Natural Resources
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Pneumonia
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Polymerase Chain Reaction*
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Swine*