中华实用儿科临床杂志
中華實用兒科臨床雜誌
중화실용인과림상잡지
Journal of Applied Clinical Pediatrics
2014年
11期
818-820
,共3页
俞钢%洪淳%王丽敏%尚宁%唐晶%朱小春%葛午平%袁晓兰%雷琼
俞鋼%洪淳%王麗敏%尚寧%唐晶%硃小春%葛午平%袁曉蘭%雷瓊
유강%홍순%왕려민%상저%당정%주소춘%갈오평%원효란%뢰경
胎儿%先天性大叶性肺气肿%肺囊腺瘤Ⅲ型%新生儿外科
胎兒%先天性大葉性肺氣腫%肺囊腺瘤Ⅲ型%新生兒外科
태인%선천성대협성폐기종%폐낭선류Ⅲ형%신생인외과
Fetal%Congenital lobar emphysema%Congenital cystic adenomatoid malformation type Ⅲ%Neonatal surgery
目的 胎儿先天性大叶性肺气肿(CLE)的产前超声很容易与肺囊腺瘤Ⅲ型(CCAMⅢ)混淆,因为二者均表现为同一血供的高回声囊性肿块,产前超声难以鉴别.由于二者的临床结局不同,为提高对CLE的认识,结合新生儿的结局探讨胎儿CLE的诊断和治疗.方法 回顾性分析广东省妇幼保健院胎儿医学科2011年3月至2013年5月产前诊断和出生后确诊为CLE的诊治经验.结果 在胎儿产前超声诊断为胸部囊性病变的基础上,52例确诊为CCAMⅢ,其中6例(11%,6/52例)于出生后CT确诊为CLE,5例于出生后早期手术,术后病理组织诊断.6例中3例出生后即出现急性呼吸道症状,2例于新生儿期急诊手术治愈,1例放弃治疗;另3例分别于出生后第7天、第19天及3个月出现呼吸道症状行手术治愈.所有受累部位以上肺叶为主(83%,5/6例).手术肺叶切除部位分别为左上肺叶2例,右上肺1例,右上肺叶和右中肺叶1例,右下肺叶1例.手术年龄3~90 d,平均20 d.手术病例均治愈.结论 产前胎儿CLE与CCAMⅢ型在超声上尚无法鉴别,但出生时或出生后较早出现呼吸道症状并导致新生儿急诊和治疗;CT可明确诊断.以往认为的CCAMⅢ预后差是否为将CLE误诊为CCAMⅢ,需要重新认识;对于CLE新生儿急性呼吸道症状者行新生儿外科治疗是积极有效的.
目的 胎兒先天性大葉性肺氣腫(CLE)的產前超聲很容易與肺囊腺瘤Ⅲ型(CCAMⅢ)混淆,因為二者均錶現為同一血供的高迴聲囊性腫塊,產前超聲難以鑒彆.由于二者的臨床結跼不同,為提高對CLE的認識,結閤新生兒的結跼探討胎兒CLE的診斷和治療.方法 迴顧性分析廣東省婦幼保健院胎兒醫學科2011年3月至2013年5月產前診斷和齣生後確診為CLE的診治經驗.結果 在胎兒產前超聲診斷為胸部囊性病變的基礎上,52例確診為CCAMⅢ,其中6例(11%,6/52例)于齣生後CT確診為CLE,5例于齣生後早期手術,術後病理組織診斷.6例中3例齣生後即齣現急性呼吸道癥狀,2例于新生兒期急診手術治愈,1例放棄治療;另3例分彆于齣生後第7天、第19天及3箇月齣現呼吸道癥狀行手術治愈.所有受纍部位以上肺葉為主(83%,5/6例).手術肺葉切除部位分彆為左上肺葉2例,右上肺1例,右上肺葉和右中肺葉1例,右下肺葉1例.手術年齡3~90 d,平均20 d.手術病例均治愈.結論 產前胎兒CLE與CCAMⅢ型在超聲上尚無法鑒彆,但齣生時或齣生後較早齣現呼吸道癥狀併導緻新生兒急診和治療;CT可明確診斷.以往認為的CCAMⅢ預後差是否為將CLE誤診為CCAMⅢ,需要重新認識;對于CLE新生兒急性呼吸道癥狀者行新生兒外科治療是積極有效的.
목적 태인선천성대협성폐기종(CLE)적산전초성흔용역여폐낭선류Ⅲ형(CCAMⅢ)혼효,인위이자균표현위동일혈공적고회성낭성종괴,산전초성난이감별.유우이자적림상결국불동,위제고대CLE적인식,결합신생인적결국탐토태인CLE적진단화치료.방법 회고성분석광동성부유보건원태인의학과2011년3월지2013년5월산전진단화출생후학진위CLE적진치경험.결과 재태인산전초성진단위흉부낭성병변적기출상,52례학진위CCAMⅢ,기중6례(11%,6/52례)우출생후CT학진위CLE,5례우출생후조기수술,술후병리조직진단.6례중3례출생후즉출현급성호흡도증상,2례우신생인기급진수술치유,1례방기치료;령3례분별우출생후제7천、제19천급3개월출현호흡도증상행수술치유.소유수루부위이상폐협위주(83%,5/6례).수술폐협절제부위분별위좌상폐협2례,우상폐1례,우상폐협화우중폐협1례,우하폐협1례.수술년령3~90 d,평균20 d.수술병례균치유.결론 산전태인CLE여CCAMⅢ형재초성상상무법감별,단출생시혹출생후교조출현호흡도증상병도치신생인급진화치료;CT가명학진단.이왕인위적CCAMⅢ예후차시부위장CLE오진위CCAMⅢ,수요중신인식;대우CLE신생인급성호흡도증상자행신생인외과치료시적겁유효적.
Objective Fetal congenital lobar emphysema (CLE) is generally confused with congenital cystic adenomatoid malformnation type Ⅲ (CCAM Ⅲ) by prenatal ultrasound as both are hyperechoic cystic mass with the same blood supply,which is difficult to differentiate through the prenatal ultrasound.As they have different clinical outcomes,and in order to improve the understanding of CLE,the diagnosis and treatment of neonatal outcome of fetal CLE were discussed.Methods A retrospective analysis was conducted of the experience in prenatal diagnosis and treatment of postnatal CLE at Department of Fetal Medicine,Guangdong Women and Children's Hospital from Mar.2011 to May 2013.Results On the basis of prenatal ultrasound for fetal chest cystic malformations,there were 52 cases of CCAM Ⅲ in which 6 cases(11%,6/52 cases) were confirmed as CLE by CT scan after birth and 5 cases had early operation.Emphysema was detected in all pathological specimens.Of 3 cases presenting symptoms of tachypnea after birth,2 had acute lobectomy and 1 gave up therapy.The other 3 cases underwent lobectomy on 7 day,19 day and 3 months respectively after birth because of tachypnea and respiratory distress.The most common affected lobe was the upper lobe (83%,5/6 cases).The lobectomy included 2 left upper lobe,1 right upper lobe,1 right upper and middle lobe,and 1 right lower lobe.The mean age of lobectomy was 20 days(from 3 to 90 days).All the cases were cured through lobectomy.Conclusions Prenatal CLE can not be differentiated from CCAM Ⅲ on ultrasound,but it exhibited early pulmonary distress at birth or after birth leading to neonatal emergency and treatment.h can be confirmed by computed tomography scan.Previously CCAM Ⅲ prognosis was thought to be poor and it remains unconfirmed whether CLE had been misdiagnosed as CCAM]Ⅲ need to know.For the CLE with neonatal acute respiratory symptoms early surgical treatment is effective.