Background: 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.

Aim: To explore the application value of magnetic resonance imaging (MRI) in the differential diagnosis of fetal CCAM and BPS.

Methods: 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.

Results: 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.

Conclusion: 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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852640PMC
http://dx.doi.org/10.12998/wjcc.v9.i4.822DOI Listing

Publication Analysis

Top Keywords

ccam bps
20
blood vessels
20
ccam
11
cases
11
vessels
10
magnetic resonance
8
resonance imaging
8
differential diagnosis
8
diagnosis fetal
8
congenital cystic
8

Similar Publications

Cystic cuboid adenomatous malformations (CCAM) are congenital pulmonary lesions, usually benign, that can progress into malignancy. Bronchopulmonary sequestration (BPS) is another type of malformation that consistsof an ectopic pulmonary tissue mass that doesn't participate in blood-gas exchanges, with vascularization provided by anomalous branches of the thoracic aorta. Hybrid lesions are lesions that have histological features of CCAM but with systemic vascularization, a pathognomonic sign of BPS.

View Article and Find Full Text PDF

Congenital Pulmonary Hybrid Lesions: Clinical Presentation, Surgical Management, and Outcomes.

Indian J Pediatr

January 2025

Division of General and Thoracic Surgery, Department of Surgery, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.

Objectives: Congenital pulmonary airway malformation (CPAM) lesion with an aberrant systemic blood supply is considered a "hybrid" lesion (HL). The aim of the study was to report authors' experience in the presentation, surgical management, and outcomes of HL.

Methods: A retrospective cohort study of HL patients followed from 2000 to 2022 in a single institution was done.

View Article and Find Full Text PDF
Article Synopsis
  • Congenital lung anomalies (CLA) include various rare conditions like CCAM, BPS, CLE, and BC, which are now more commonly diagnosed thanks to better fetal ultrasound technology.
  • A study of 72 patients at Taleghani Pediatric Hospital revealed that most had CCAM, with a notable percentage showing respiratory symptoms; prenatal screenings were effective in diagnosing many cases.
  • The findings suggest a link between the type of lung anomaly and the need for surgical intervention, and highlight that improving diagnostic techniques may lead to better management of these anomalies.
View Article and Find Full Text PDF
Article Synopsis
  • The case involves a prenatal diagnosis of Bronchopulmonary Sequestration (BPS) associated with Congenital Pulmonary Airway Malformation (CPAM), identified through fetal 3D ultrasound (3D-US).
  • The diagnosis revealed an unusual configuration of two abnormal arteries originating from the celiac artery.
  • The vascular images captured via fetal 3D-US were found to be comparable to those acquired through postnatal CT angiography, indicating the potential efficacy of 3D-US in prenatal vascular assessments.
View Article and Find Full Text PDF

Antenatally Detected Thoracic Lesions: Prognosis, Management and Outcome.

Afr J Paediatr Surg

April 2024

Department of Pediatric Surgery, PGIMER, Chandigarh, India.

Background: Foetal thoracic lesions are uncommon, with the incidence of 1 in 15,000 live births. Antenatal monitoring of these lesions is required to prognosticate the parents about the postnatal outcome of the lesions and about the well-being of the baby. Foetal ultrasound and magnetic resonance imaging (MRI) are the modalities to detect these lesions and follow-up during pregnancy and postnatally.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!