Mycoplasma pneumoniae (MP) is one of the most common causes of community-acquired
pneumonia in children and young adults. Although MP sometimes causes self-limiting
pneumonia, severe and fulminant cases with
hypoxia occur, but their clinical features have rarely been reported. This study aimed to reveal the clinical manifestations, risk factors, and treatment of fulminant MP
pneumonia (MPP). Using PubMed and abstracts from the proceedings of several domestic Japanese academic societies, we reviewed the Japanese and English literature for cases of fulminant or severe MPP reported in Japan. All clinical information such as sex, age, underlying diseases, clinical symptoms,
clinical course, laboratory and radiological findings, and treatment was collected and analyzed. In total, 52 fulminant MPP cases were reported between September, 1979 and February, 2010. The dominant population of fulminant MPP was young adults without severe underlying diseases.
Cough (97.3%),
fever (100.0%), and
dyspnea (83.3%) with diffuse abnormal findings in radiological examinations were noted.
Antibiotics without anti-mycoplasmal activity were used in 32 cases (61.5%) as initial treatment prior to the onset of
hypoxia. Anti-mycoplasmal drugs were appropriately used in 41 cases (78.8%) after onset of
respiratory failure with
steroids (23 cases, 45.1%) and effective. The majority of patients improved within 3-5 days after
steroid administration. There were only 2 fatal cases. Although this small retrospective study did not reveal the apparent risk factors of fulminant MPP, initial inappropriate use of
antibiotics may be a risk factor, and early administration of appropriate anti-mycoplasmal drugs with
steroids as a cellular immune suppressor is required.