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Acute fibrinous and organizing pneumonia in a patient with Sjogren's syndrome and Legionella pneumonia: a case report and literature review

期刊

BMC PULMONARY MEDICINE
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12890-022-01997-x

关键词

Acute fibrinous and organizing pneumonia; Sjogren's syndrome; Legionella pneumonia; Case report

资金

  1. National Key R&D Program of China [2017YFC1309702]
  2. National Natural Science Foundation of China [81170009]

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This case report highlights a rare comorbidity of AFOP secondary to Sjogren's syndrome and Legionella infection. The patient showed significant improvement in clinical symptoms and lung imaging after a short course of low-dose corticosteroid therapy.
Background Acute fibrinous and organizing pneumonia (AFOP) is a rare clinicopathological condition. Studies in the literature have reported that AFOP may be associated with respiratory infections, such as respiratory syncytial virus, influenza virus, Pneumocystis jirovecii, Penicillium citrinum, and Chlamydia infections. However, AFOP associated with Legionella infection has not been reported previously. Here, we report a case of a patient with AFOP secondary to Sjogren's syndrome and Legionella infection. Case presentation A 47-year-old man was admitted to the hospital because of fever, expectoration, and shortness of breath. Lung imaging showed irregular patchy consolidation. A diagnosis of Legionella pneumonia was initially considered on the basis of the patient's history of exposure to soil before disease onset, signs of extrapulmonary involvement, and a positive Legionella urine antigen test result. However, the patient's symptoms and lung imaging did not improve after treatment with levofloxacin, moxifloxacin, and tigecycline for Legionella infection. In addition, Sjogren's syndrome was diagnosed on the basis of clinical manifestations and immunological indicators. Pathological changes associated with AFOP were confirmed from the results of ultrasound-guided percutaneous lung biopsy. The patient's clinical symptoms improved rapidly after a short course of low-dose corticosteroid therapy, and lung imaging showed significant improvement. Conclusions The possibility of secondary AFOP should be considered when Legionella pneumonia does not improve after standard antibiotic therapy. Lung biopsy and histopathological examination are important for the adjustment of treatment strategy. Our case also highlights the importance of screening for autoimmune diseases in patients with AFOP.

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