医学影像学杂志
醫學影像學雜誌
의학영상학잡지
JOURNAL OF MEDICAL IMAGING
2015年
6期
1002-1005
,共4页
孙厚长%王镇章%李喜梅%潘克华%邰云鹏%曹国全
孫厚長%王鎮章%李喜梅%潘剋華%邰雲鵬%曹國全
손후장%왕진장%리희매%반극화%태운붕%조국전
肺淋巴瘤 ,原发性%体层摄影术 ,X 线计算机
肺淋巴瘤 ,原髮性%體層攝影術 ,X 線計算機
폐림파류 ,원발성%체층섭영술 ,X 선계산궤
Pulmonary lymphoma,Primary%Tomography,X-ray computed
目的:探讨原发性肺淋巴瘤(PPL)的 CT 表现及特征。方法对经病理证实的6例 PPL 的 CT 征象进行回顾性分析,观察肿瘤的发病部位、数目、形态、密度、伴随征象及强化特点。结果6例患者中,结节肿块型2例,肺泡或肺炎型3例,混合型1例,4例可见空气支气管征,2例跨肺叶生长;增强后大多数病灶呈中度‐明显均匀强化。结论原发性肺淋巴瘤是一种少见病,CT 表现缺乏特征性,但空气支气管征、跨叶生长、中度‐明显均匀强化的出现以及没有肺门、纵隔淋巴结肿大,可提示本病的可能,应积极行穿刺活检以明确诊断。
目的:探討原髮性肺淋巴瘤(PPL)的 CT 錶現及特徵。方法對經病理證實的6例 PPL 的 CT 徵象進行迴顧性分析,觀察腫瘤的髮病部位、數目、形態、密度、伴隨徵象及彊化特點。結果6例患者中,結節腫塊型2例,肺泡或肺炎型3例,混閤型1例,4例可見空氣支氣管徵,2例跨肺葉生長;增彊後大多數病竈呈中度‐明顯均勻彊化。結論原髮性肺淋巴瘤是一種少見病,CT 錶現缺乏特徵性,但空氣支氣管徵、跨葉生長、中度‐明顯均勻彊化的齣現以及沒有肺門、縱隔淋巴結腫大,可提示本病的可能,應積極行穿刺活檢以明確診斷。
목적:탐토원발성폐림파류(PPL)적 CT 표현급특정。방법대경병리증실적6례 PPL 적 CT 정상진행회고성분석,관찰종류적발병부위、수목、형태、밀도、반수정상급강화특점。결과6례환자중,결절종괴형2례,폐포혹폐염형3례,혼합형1례,4례가견공기지기관정,2례과폐협생장;증강후대다수병조정중도‐명현균균강화。결론원발성폐림파류시일충소견병,CT 표현결핍특정성,단공기지기관정、과협생장、중도‐명현균균강화적출현이급몰유폐문、종격림파결종대,가제시본병적가능,응적겁행천자활검이명학진단。
Objective To investigate the CT characteristics of primary pulmonary lymphoma .Methods 6 patients with primary pulmonary lymphoma proved by pathology were studied retrospectively .The analysis of imaging characteristics in‐cluded the position ,number ,shape ,density ,accompanying signs and enhancement features .Results Of the 6 cases ,2 cases were nodular or mass type ,3 cases were alveolar or pneumonia type ,1 case was mixed type .Air bronchogram was present in 4 cases ,2 cases showed across the lobar grow th ;Most of the cases showed moderate‐apparently homogeneous enhancement .Conclusion Primary pulmonary lymphoma is a rare disease ,and CT does not have characteristic features . But ,air bronchogram ,across the lobar growth ,moderate‐apparently homogeneous enhancement ,no hilar and mediastinal lymphadenophathy ,may be suggestive of the disease .Biopsy is recommended to confirm the diagnosis of primary pulmo‐nary lymphoma .