中华放射学杂志
中華放射學雜誌
중화방사학잡지
Chinese Journal of Radiology
2010年
4期
374-378
,共5页
关春爽%马大庆%关砚生%陈步东%张岩松
關春爽%馬大慶%關硯生%陳步東%張巖鬆
관춘상%마대경%관연생%진보동%장암송
尘肺%体层摄影术,X线计算机%病理学
塵肺%體層攝影術,X線計算機%病理學
진폐%체층섭영술,X선계산궤%병이학
Pneumoconiosis%Tomography,X-ray computed%Pathology
目的 探讨HRCT上肺细网状影的形态学表现及病理基础.方法 搜集本院2004年8月至2007年2月107例在HRCT上有细网状影患者临床病例资料进行细网状影形态学及动态变化分析研究.搜集24例病理证实充气标本进行影像与病理的对照研究.用X~2检验进行统计学分析.结果 细网状影网间隙直径一般≤3 mm,为圆形或不规则形,网间隙内为肺实质密度.网壁光滑或粗糙,厚度约≤1 mm.107例临床患者细网状影的伴随征象有磨玻璃密度影(GGO)(68.2%,73例)、铺路石征(23.4%,25例)、小叶间隔增厚(84.1%,90例)、肺气肿(32.7%,35例)、界面征(58.9%,63例)、牵拉性支气管扩张(41.1%,44例)及蜂窝征(26.2%,28例).纤维化患者与肺炎患者在蜂窝、牵拉性支气管扩张、小叶间隔增厚、界面征及铺路石征方面差异有统计学意义(P均<0.01).肺炎大片状GGO合并细网状影形成铺路石征;癌性淋巴管炎细网状影合并小叶间隔增厚,并见串珠样结节影;特发性肺纤维化(IPF)细网状影多镶嵌在蜂窝之间;结缔组织病(CTD)并肺间质纤维化早期以细网状影为主,蜂窝影少见,及时治疗后可完全或部分吸收;慢性支气管炎细网状影合并肺气肿.58例随访患者中26例网状影增加,22例网状影减少或消失,10例无变化.24例肺标本细网状影病理基础主要为小叶内间质纤维增生、炎性细胞及肿瘤细胞浸润、渗出液充填、煤尘沉积等.结论 细网状影是由小叶内间质增厚形成,可由炎症、间质增生、肺纤维化和肿瘤引起,有助于提示这些疾病的存在,诊断价值需结合其他CT表现及动态变化.
目的 探討HRCT上肺細網狀影的形態學錶現及病理基礎.方法 搜集本院2004年8月至2007年2月107例在HRCT上有細網狀影患者臨床病例資料進行細網狀影形態學及動態變化分析研究.搜集24例病理證實充氣標本進行影像與病理的對照研究.用X~2檢驗進行統計學分析.結果 細網狀影網間隙直徑一般≤3 mm,為圓形或不規則形,網間隙內為肺實質密度.網壁光滑或粗糙,厚度約≤1 mm.107例臨床患者細網狀影的伴隨徵象有磨玻璃密度影(GGO)(68.2%,73例)、鋪路石徵(23.4%,25例)、小葉間隔增厚(84.1%,90例)、肺氣腫(32.7%,35例)、界麵徵(58.9%,63例)、牽拉性支氣管擴張(41.1%,44例)及蜂窩徵(26.2%,28例).纖維化患者與肺炎患者在蜂窩、牽拉性支氣管擴張、小葉間隔增厚、界麵徵及鋪路石徵方麵差異有統計學意義(P均<0.01).肺炎大片狀GGO閤併細網狀影形成鋪路石徵;癌性淋巴管炎細網狀影閤併小葉間隔增厚,併見串珠樣結節影;特髮性肺纖維化(IPF)細網狀影多鑲嵌在蜂窩之間;結締組織病(CTD)併肺間質纖維化早期以細網狀影為主,蜂窩影少見,及時治療後可完全或部分吸收;慢性支氣管炎細網狀影閤併肺氣腫.58例隨訪患者中26例網狀影增加,22例網狀影減少或消失,10例無變化.24例肺標本細網狀影病理基礎主要為小葉內間質纖維增生、炎性細胞及腫瘤細胞浸潤、滲齣液充填、煤塵沉積等.結論 細網狀影是由小葉內間質增厚形成,可由炎癥、間質增生、肺纖維化和腫瘤引起,有助于提示這些疾病的存在,診斷價值需結閤其他CT錶現及動態變化.
목적 탐토HRCT상폐세망상영적형태학표현급병리기출.방법 수집본원2004년8월지2007년2월107례재HRCT상유세망상영환자림상병례자료진행세망상영형태학급동태변화분석연구.수집24례병리증실충기표본진행영상여병리적대조연구.용X~2검험진행통계학분석.결과 세망상영망간극직경일반≤3 mm,위원형혹불규칙형,망간극내위폐실질밀도.망벽광활혹조조,후도약≤1 mm.107례림상환자세망상영적반수정상유마파리밀도영(GGO)(68.2%,73례)、포로석정(23.4%,25례)、소협간격증후(84.1%,90례)、폐기종(32.7%,35례)、계면정(58.9%,63례)、견랍성지기관확장(41.1%,44례)급봉와정(26.2%,28례).섬유화환자여폐염환자재봉와、견랍성지기관확장、소협간격증후、계면정급포로석정방면차이유통계학의의(P균<0.01).폐염대편상GGO합병세망상영형성포로석정;암성림파관염세망상영합병소협간격증후,병견천주양결절영;특발성폐섬유화(IPF)세망상영다양감재봉와지간;결체조직병(CTD)병폐간질섬유화조기이세망상영위주,봉와영소견,급시치료후가완전혹부분흡수;만성지기관염세망상영합병폐기종.58례수방환자중26례망상영증가,22례망상영감소혹소실,10례무변화.24례폐표본세망상영병리기출주요위소협내간질섬유증생、염성세포급종류세포침윤、삼출액충전、매진침적등.결론 세망상영시유소협내간질증후형성,가유염증、간질증생、폐섬유화화종류인기,유조우제시저사질병적존재,진단개치수결합기타CT표현급동태변화.
Objective To study the morphological appearance and pathological basis of the fine pulmonary reticulation at HRCT.Methods One hundred and seven patients were analyzed about the morphology findings and dynamic changes on pulmonary HRCT.Twenty-four coal worker's pneumoconiosis(CWP)specimens were examined to make comparison between CT and pathology.The data was analyzed by using the Chi-square test.Results The reticular gap was less than 3 mm in diameter.The morphology of reticulation was round or irregular.Pulmonary parenchyma was seen between the gaps.The reticular wall was smooth or coarse.The thickness was less than 1 mm.One hundred and seven patients had accompanying signs including ground-glass opacity(68.2%,73 patients),crazy paving(23.4%,25 patients),interlobular septal thickening(84.1%,90 patients),emphysema(32.7%,35 patients),interface sign(58.9%,63 patients),traction bronchiolectasis(41.1%,44 patients)and honeycombing(26.2%,28 patients).The differences of the honeycomb,traction bronchiolectosis,interbobular septal thickening,interface sign and paving were statistically significant between the fibrotic group and pneunonia(P<0.01).Pneumonia showed extensive area of ground-glass opacity(GGO)with fine reticulation.Fine reticulation with both interlobular septal thickening and small nodules were observed more frequently in lmphangitic carcinomatosis.Idiopathic pulmonary fibrosis(IPF)showed fine reticulation among the honeycombing.Connective tissue disease (CTD)showed fine reticulation with rarely honeycombing and it could be partly absorbed.Fine reticulation with emphysema was seen in chronic bronchitis.In the 58 follow-up patients,the fine reticulation increased in 26 patients,decreased or disappeared in 22 patients and showed no change in 10 patients.The major pathological basis of the fine reticulation was intralobular interstitial thickening,including fibrosis hyperplasia,inflammatory cells and tumor cells infiltration,effusion filling,smut deposition and so on.Conclusions The fine reticulation was caused by intralobular interstitial thickening including inflammation,interstitial hyperplasia,pulmonary fibrosis and tumor.The fine reticulation is helpful to prompt the diagnosis of these diseases,but the diagnosis need its combination with the other CT findings and dynamic changes.