Wang Yuanhui, Li Yuwen, Wang Qian, Zhang Lili, Li Jun, Zhu Chuanlong
Department of Infectious Disease.
Department of Pediatrics, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Medicine (Baltimore). 2019 Feb;98(8):e14537. doi: 10.1097/MD.0000000000014537.
Acute fibrinous and organizing pneumonia (AFOP) is an uncommon type of acute lung injury associated with infection, connective tissue disorders, drug exposure, and hematologic malignancies.
A 53-year-old female presented with intermittent fever, chills, and dry cough since 10 days. Chest computed tomography scan showed multiple bilateral patchy infiltrates. PPD skin test was positive but tuberculosis antibody test and T-SPOT were negative.
Histologic examination revealed massive fibrinous exudation with organization within alveolar spaces and scattered neutrophilic infiltrates, which was consistent with AFOP.
This patient was treated with prednisolone therapy.
Chest radiograph improvement and symptom improvement, including fever and respiratory symptoms, was observed after 2 week of oral prednisolone treatment. After 9-month of treatment, the patient was asymptomatic with stable disease and improved quality of life.
AFOP has unique pathologic manifestations; however, the condition is liable to be misdiagnosed as community-acquired pneumonia ortuberculosis. Antibiotics are ineffective, while some patients show good response to glucocorticoid therapy.
急性纤维蛋白性及机化性肺炎(AFOP)是一种与感染、结缔组织病、药物暴露及血液系统恶性肿瘤相关的罕见急性肺损伤类型。
一名53岁女性,自10天前起出现间断发热、寒战及干咳。胸部计算机断层扫描显示双侧多发斑片状浸润影。结核菌素皮肤试验阳性,但结核抗体试验及T-SPOT均为阴性。
组织学检查显示肺泡腔内有大量伴有机化的纤维蛋白渗出及散在的中性粒细胞浸润,符合AFOP。
该患者接受了泼尼松龙治疗。
口服泼尼松龙治疗2周后,胸部X线片及症状改善,包括发热及呼吸道症状。治疗9个月后,患者无症状,病情稳定,生活质量改善。
AFOP有独特的病理表现;然而,该病易被误诊为社区获得性肺炎或肺结核。抗生素治疗无效,而部分患者对糖皮质激素治疗反应良好。