Feinstein Marc B, DeSouza Shilpa A, Moreira Andre L, Stover Diane E, Heelan Robert T, Iyriboz Tunç A, Taur Ying, Travis William D
Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
J Clin Pathol. 2015 Jun;68(6):441-7. doi: 10.1136/jclinpath-2014-202626. Epub 2015 Mar 5.
Cryptogenic organising pneumonia (COP) and acute fibrinous and organising pneumonia (AFOP) are recognised patterns of organising pneumonia (OP), a condition that resembles pneumonia but is not caused by infection. We have recognised granulomatous organising pneumonia (GOP) to be a similar histopathological entity where non-necrotising granulomata are intimately associated with the organising connective tissue. To what degree COP, AFOP and GOP represent distinct clinical and pathological disorders is unknown. This cross-sectional study sought to compare the pathological, clinical, and radiographical features of these OP patterns.
Surgical lung biopsy specimens were reviewed for consecutive patients referred with OP to a metropolitan cancer centre. Clinical information and CT images were acquired from the hospital electronic medical record to determine the clinical and CT characteristics of each OP pattern.
Sixty-one patients (35 men, 26 women), mean age 61.5 years (range 8-85 years), were available for analysis. Of these, 43 patients (70%) had at least one prior cancer; 27 (44%) had received chemotherapy and 18 (30%) had received radiation. Approximately, half (32 patients) had respiratory symptoms, most commonly cough, dyspnoea and/or wheezing. While symptoms and mortality rates were not different among OP groups, AFOP patients more commonly had fever (p=0.04). GOP patients less commonly had received chemotherapy (p=0.03) and were more likely to present as masses/nodules (p=0.04).
AFOP and GOP, a newly described OP form, possess clinical and pathological findings that set it apart from a COP, suggesting an emerging spectrum of OP.
隐源性机化性肺炎(COP)和急性纤维素性及机化性肺炎(AFOP)是机化性肺炎(OP)的公认类型,OP类似肺炎但并非由感染引起。我们已认识到肉芽肿性机化性肺炎(GOP)是一种类似的组织病理学实体,其中非坏死性肉芽肿与机化的结缔组织密切相关。COP、AFOP和GOP在多大程度上代表不同的临床和病理疾病尚不清楚。这项横断面研究旨在比较这些OP类型的病理、临床和影像学特征。
对转诊至一家大城市癌症中心的OP连续患者的手术肺活检标本进行回顾。从医院电子病历中获取临床信息和CT图像,以确定每种OP类型的临床和CT特征。
61例患者(35例男性,26例女性),平均年龄61.5岁(范围8 - 85岁)可供分析。其中,43例患者(70%)至少有过一种癌症;27例(44%)接受过化疗,18例(30%)接受过放疗。大约一半(32例)患者有呼吸道症状,最常见的是咳嗽、呼吸困难和/或喘息。虽然OP各亚组间症状和死亡率无差异,但AFOP患者发热更为常见(p = 0.04)。GOP患者接受化疗的比例较低(p = 0.03),且更有可能表现为肿块/结节(p = 0.04)。
AFOP和GOP(一种新描述的OP形式)具有使其有别于COP的临床和病理表现,提示存在一个新出现的OP谱系。