Late Abnormal Findings on High-Resolution Computed Tomography After Mycoplasma Pneumonia

Author:

Kim Chang Keun1,Chung Churl Young1,Kim Joung Sook2,Kim Woo Sun3,Park Yang4,Koh Young Yull4

Affiliation:

1. From the Departments of Pediatrics and

2. Radiology, Inje University Sanggye Paik Hospital, and Departments of

3. Radiology and

4. Pediatrics, Clinical Research Institute, Seoul National University Hospital, Seoul, Korea.

Abstract

Background. The clinical course ofMycoplasma pneumonia is typically mild and self-limited. There are, however, several case reports of severe complication following this illness with considerable morbidity and mortality. Objectives. This study was conducted to investigate, using high-resolution computed tomography (HRCT), the long-term pulmonary structural abnormalities after Mycoplasma pneumonia and to identify risk factors (chest radiograph findings, antibody titers, and host factors) that might increase the likelihood of developing the sequelae. Methods. Thirty-eight children requiring hospitalization attributable to Mycoplasma pneumonia were recruited by the retrospective examination of hospital records. They underwent HRCT after an interval of 1.0 to 2.2 years. A control group of 17 children with the history of Mycoplasma upper respiratory infection was also studied after a similar interval. Results. Abnormal HRCT findings were present in 37% (14/38) of the pneumonia group, compared with 12% (2/17) of the control group. The abnormalities in the pneumonia group, which appeared alone or in combination, included mosaic perfusion (n =12), bronchiectasis (n = 8), bronchial wall thickening (n = 4), decreased vascularity (n = 1), and air trapping on expiratory scan (9 of 29 tested). The area affected by these abnormalities, usually involving 2 or more lobes, corresponded in all cases to the location of the infiltrate on chest radiograph at the time of pneumonia. Between subjects with abnormal HRCT (n = 14) and normal HRCT (n = 24) in the pneumonia group, significant differences were observed in age at the time of pneumonia (mean ± standard deviation: 5.3 ± 2.0 years vs 7.7 ± 3.4 years) and peak antimycoplasma antibody titer (geometric mean [range of 1 standard deviation]; 1:7943 [3126–19 953] vs 1:3093 [832–11 482]). Conclusions. We conclude that a considerable proportion of children with history of Mycoplasma pneumonia have abnormal findings on HRCT, suggestive of small airway obstruction and that younger age and higher antibody titer at the time of pneumonia may be risk factors for these sequelae.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

Reference33 articles.

1. Mycoplasma pneumoniae disease: clinical spectrum, pathophysiology, epidemiology, and control.;Denny;J Infect Dis,1971

2. Mycoplasmas as agents of human disease.;Cassell;N Engl J Med,1981

3. The protean manifestations of Mycoplasma infections in adults.;Murray;Am J Med,1975

4. Adult respiratory distress syndrome caused by Mycoplasma pneumoniae.;Fischaman;Chest,1978

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