间质性肺疾病

Physical Examination: General: well appearing Vital Signs: BP: 110/70 ,Pulse: 85 RR ,26 breaths/minute HEENT: No skin tightness around his mouth Neck: No jugular vein distention Cardiovascular System: No findings of pulmonary hypertension Respiratory System: Inspiratory crackles over lower half of chest Extremities: clubbing Musculoskeletal System: no arthritis or synovitis
Case Study

Chief Complaint: 62-year-old man with progressive shortness of breath over the past 2 years History of Present Illness: Two years before patient began having shortness of breath (SOB). The SOB had become progressively worse in the past 12 months. A month prior to presentation, he developed severe SOB requiring admission to a local hospital. The patient reported no exposures related to hypersensitivity pneumonitis including birds, mold. His only chemical exposure was to malathion he sprayed in his backyard garden.
Paroxysmal cough, usually nonproductive
Abnormal breath sounds on chest auscultation Abnormal chest x-ray or HRCT
Restrictive pulmonary physiology with reduced lung volumes and DLCO and widened AaPO2

Rare IIPs ILIP Idiopathic pleuroparenchymal fibroelastosis
Unclassifiable IIPs
ATS/ERS 2013

特发性间质性肺炎(Idiopathic
Interstitial Pneumonia,IIP)属于ILD/DPLD中的一种。而 特发性肺纤维化(Idiopathic Pulmonary Fibrosis,IPF)属于IIP中的一种,病理学上称为 寻常性间质性肺炎（usual interstitial pneumonia,UIP )。
Classification of DPLD
不同的病因所致的ILD可以出现相同的病理表
现，如RF和SLE可引起相同病理表现的ILD。 同一种疾病可以表现为不同的病理表现，如 干燥综合症可以表现为UIP，也可为NSIP。
不同的ILD在病因、发病机制、病理改变、自
然病程、治疗方法及预后方面都不完全相同。 诊断的目的不仅限于ILD，而是要尽可能的明 确病因和病理类型。
Final diagnosis
CRP

C- Clinical R- Radiologist P- Pathologist
Idiopathic Pulmonary Fibrosis (IPF)
CLASSIFICATION OF IIP
CLASSIFICATION OF IIP

Major IIPs IPF INSIP RB-ILD DIP AIP
What is the cause of IPF?
Old
idea - inflammation causes fibrosis New idea -epithelial injury with abnormal healing cause fibrosis Limitation -patients present late in course of disease
the
mean length of survival from the time of diagnosis varied between 3.2 and 5 yr In another study, the median survival was 28.2 mo from the onset of respiratory symptoms


Laboratory Workup: ANA negative, speckled pattern with a negative Sm antibody, negative Scl-70 antibody; an echocardiogram revealed an estimated mean pulmonary artery pressure of 55 mmHg.
OVERVIEW
13–20/100,000 in US (approximately 35,000-55,000 cases) Onset: Usually between 50 and 70 yr Clinical presentation
Prevalence:
Progressive dyspnea on exertion
Physical examination
crackles are detected on chest auscultation in more than 80% of patients. These are typically “dry,” end-inspiratory, and “Velcro” in quality, and are most prevalent in the lung bases. Clubbing is noted in 25 to 50% of patients . Cyanosis, cor pulmonale, an accentuated pulmonic second sound, right ventricular heave, and peripheral edema may be observed in the late phases of the disease
临床表现
呼吸困难
咳嗽、咯血 与结缔组织并相关的症状：发热、脱发、皮
疹、关节痛、眼干、口干。
体格检查
肺部听诊爆裂音或Velcro罗音
杵状指 紫绀 肺动脉高压征象
实验室检查
一般检查：免疫学指标、ANCA,SACE
肺功能 影像学 支气管镜检查（BALF,TBLB,TBNA) 肺组织活检（开胸肺活检，VATS)
Symptoms
IPF
usually presents insidiously, with the gradual onset of a nonproductive cough and dyspnea. Dyspnea is usually the most prominent and disabling symptom. It is usually progressive and in most patients it is reported to have been present for > 6 mo before presentation. paroxysmal dry cough that is refractory to antitussive agents.
（Interstitial Lung Disease,ILD)
北京医院呼吸科与危重症医学科 许小毛
什么是肺间质
肺泡间及终末气道上皮以外的支持组织，
包括血管及淋巴管组织。
肺实质指各级支气管及肺泡结构。
概述
以肺泡壁为主并包括肺泡周围组织及其相邻
支持结构病变的一组疾病群,病因近200种。 由于病变不仅局限于肺泡间质,还可累及肺泡 上皮细胞、肺毛细血管内皮细胞和细支气管, 并常伴有肺实质受累如肺泡炎、肺泡腔内蛋 白渗出等改变,故也称为弥漫性肺实质疾病 (Diffuse Parenchymal Lung Disease,DPLD)
Initial PFT Data: FVC 63% of predicted ,FEV1/FVC 85% DLCO 30% of predicted TLC 54% of predicted

HRCT FINDINGS
Slide courtesy of G Raghu, MD.
间质性肺疾病
肺功能检查主要表现为限制性通气功能障碍和弥散功能 (DLCO)下降。动脉血气分析可显示不同程度的低氧血症,而 二氧化碳潴留罕见。
属于哪一类ILD/DPLD

(1)详Байду номын сангаас的病史是基础:包括环境接触史、 职业史、个人史、治疗史、用药史、家族史 及基础疾病情况。
(2)胸部X线影像(特别是HRCT)特点可提供 线索:根据影像学的特点、病变分布、有无淋 巴结和胸膜的受累等,可对ILD/DPLD进行鉴 别诊断。
POTENTIAL RISK FACTORS
Cigarette
Smoking Exposure to Commonly Prescribed Drugs Chronic Aspiration Environmental Factors Infectious Agents Genetic Predisposition to IPF
诊断思路
病史、体格检查、胸部X线检查(特别是
HRCT)和肺功能测定来进行综合分析。 诊断步骤包括 1、明确是否是ILD/DPLD 2、明确属于哪一类ILD/DPLD 3、如何对IIP进行鉴别诊断。
是否为ILD

病史中最重要的症状是进行性气短、干咳和乏力。多数 ILD患者体格检查可在双侧肺底闻及Velcro啰音。晚期病人 缺氧严重者可见紫绀。 胸部X线对的诊断有重要作用。磨玻璃样改变, 小结节影、 线状(网状)影或二者混合的网状结节状阴影。肺泡充填性疾 病表现为弥漫性边界不清的肺泡性小结节影,有时可见含气支 气管征,晚期肺容积缩小可出现蜂窝样改变。

(3)BALF检查有确诊价值或者有助于诊断:①找到感 染原,如卡氏肺孢子虫;②找到癌细胞;③肺泡蛋白沉 积症:呈牛乳样,过碘酸-希夫染色阳性;④含铁血黄素 沉着症:呈铁锈色并找到含铁血黄素细胞;⑤石棉小 体计数超过1/ml:提示石棉接触。
(4)某些实验室检查包括:①抗中性粒细胞胞浆抗体: 见于韦格纳肉芽肿;②抗肾小球基底膜抗体:见于肺 出血肾炎综合征;③针对有机抗原测定血清沉淀抗体: 见于外源性过敏性肺泡炎;④特异性自身抗体检测: 提示相应的结缔组织疾病

Past Medical & Surgical History: unremarkable Allergies: Penicillin Medicines:Nifedipine ,Furosemide ,Statin Family History: Negative for lung disease or rheumatologic processes Social History: 30 pack-years cigarette consumption and stopped 15 years earlier Travel History: Negative
如何对IIP进行鉴别诊断

如经上述详实地检查及分析,仍不能确定为何 种ILD/DPLD,就应归为IIP。其中IPF/UIP最常 见,占所有IIP的60%以上,NSIP次之,而其余类 型的特发性间质性肺炎相对少见。IIP的最后 确诊,除了IPF可以根据病史、体征、支气管 肺泡灌洗检查及胸部HRCT作出临床诊断外, 其余确诊均需依靠病理诊断