Li Zhi, Lv Yi-Dan, Fang Rong, Li Xu, Luo Zhi-Qin, Xie Ling-Hong, Zhu Ling
Department of Radiology, Huzhou Maternity & Child Health Care Hospital, Huzhou 313000, Zhejiang Province, China.
Department of Endocrinology, Huzhou Central Hospital, Affiliated Central Hospital of Huzhou University, Huzhou 313000, Zhejiang Province, China.
World J Clin Cases. 2021 Feb 6;9(4):822-829. doi: 10.12998/wjcc.v9.i4.822.
Congenital cystic adenomatoid malformation (CCAM) and bronchopulmonary sequestration (BPS) are the most common lung diseases in fetuses. There are differences in the prognosis and treatment of CCAM and BPS, and the clinical diagnosis and treatment plan is usually prepared prior to birth. Therefore, it is quite necessary to make a clear diagnosis before delivery. CCAM and BPS have similar imaging features, and the differentiation mainly relies on the difference in supply vessels. However, it is hard to distinguish them due to invisible supplying vessels on some images.
To explore the application value of magnetic resonance imaging (MRI) in the differential diagnosis of fetal CCAM and BPS.
Data analysis for 32 fetuses with CCAM and 14 with BPS diagnosed by prenatal MRI at Huzhou Maternal and Child Health Care Hospital and Anhui Provincial Children's Hospital from January 2017 to January 2020 was performed to observe the source blood vessels of lesions and their direction. Pathological confirmation was completed through CT examination and/or operations after birth.
After birth, 31 cases after birth were confirmed to be CCAM, and 15 were confirmed to be BPS. The CCAM group consisted of 21 macrocystic cases and 10 microcystic cases. In 18 cases, blood vessels were visible in lesions. Blood supply of the pulmonary artery could be traced in eight cases, and in 10 cases, only vessels running from the midline to the lateral down direction were observed. No lesions were found in four macrocystic cases and one microcystic case with CCAM through CT after birth; two were misdiagnosed by MRI, and three were misdiagnosed by prenatal ultrasonography. The BPS group consisted of 12 intralobar cases and three extralobar cases. Blood vessels were visible in lesions of nine cases, in four of which, the systemic circulation blood supply could be traced, and in five of which, only vessels running from the midline to the lateral up direction were observed. Three were misdiagnosed by MRI, and four were misdiagnosed by prenatal ultrasonography.
CCAM and BPS can be clearly diagnosed based on the origin of blood vessels, and correct diagnosis can be made according to the difference in the direction of the blood vessels, but it is hard distinguish microcystic CCAM and BPS without supplying vessels. In some CCAM cases, mainly the macrocystic ones, the lesions may disappear after birth.
先天性囊性腺瘤样畸形(CCAM)和肺隔离症(BPS)是胎儿期最常见的肺部疾病。CCAM和BPS在预后及治疗方面存在差异,临床诊断和治疗方案通常在出生前制定。因此,在分娩前明确诊断非常必要。CCAM和BPS具有相似的影像学特征,鉴别主要依靠供血血管的差异。然而,由于某些图像上供血血管不可见,难以区分它们。
探讨磁共振成像(MRI)在胎儿CCAM和BPS鉴别诊断中的应用价值。
对2017年1月至2020年1月在湖州市妇幼保健院和安徽省儿童医院经产前MRI诊断为CCAM的32例胎儿及诊断为BPS的14例胎儿进行数据分析,观察病变的供血血管及其走行方向。出生后通过CT检查和/或手术完成病理确诊。
出生后,31例确诊为CCAM,15例确诊为BPS。CCAM组中,21例为大囊型,10例为微囊型。18例病变中可见血管。8例可追溯到肺动脉供血,10例仅观察到从中线向外侧下方走行的血管。出生后4例大囊型CCAM和1例微囊型CCAM经CT检查未发现病变;2例MRI误诊,3例产前超声误诊。BPS组中,12例为叶内型,3例为叶外型。9例病变中可见血管,其中4例可追溯到体循环供血,5例仅观察到从中线向外侧上方走行的血管。3例MRI误诊,4例产前超声误诊。
根据血管起源可明确诊断CCAM和BPS,并可依据血管走行方向的差异做出正确诊断,但对于无供血血管的微囊型CCAM和BPS难以区分。部分CCAM病例,主要是大囊型,出生后病变可能消失。