227 results match your criteria: "Imaging in Congenital Lobar Emphysema"

Introduction: Congenital thoracic disorders represent a spectrum of fetal lung bud development abnormalities, which may affect breathing capacity and quality of life. We aim to evaluate the impact of surgery in the treatment of 4 major congenital conditions.

Materials And Methods: We performed a retrospective cohort analysis of patients who underwent surgical treatment in our tertiary center, from 2007 to 2022.

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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.
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A three month old infant with severe respiratory distress.

J Pak Med Assoc

April 2024

Department of Paediatric Critical Care, The Indus Hospital, Karachi, Pakistan.

This case report discusses the diagnostic challenge of congenital lobar emphysema (CLE) in a three-month old infant with severe respiratory distress. The infant was initially misdiagnosed and managed as a case of pneumothorax. This case highlights the importance of CT scans as a diagnostic tool for early diagnosis and lifesaving management of CLE.

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There has been an increased recognition of a subset of congenital lobar emphysema (CLE), termed congenital sublobar hyperinflation (CSLH), which may affect only a segment of lung as opposed to an entire lobe. This is an uncommon variant for which there is a paucity of information in published literature. The majority of CLE are managed surgically.

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Performance: Congenital pulmonary malformations (CPM) are rare and can be associated with high morbidity. Clinical presentation, diagnostic procedures, imaging, and therapy of CPM are discussed.

Achievements: Today, most CPM can be diagnosed prenatally by ultrasound.

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Congenital lobar emphysema: A diagnostic dilemma with coexistent congenital heart defects.

Clin Case Rep

February 2024

Department of Pediatric Cardiac Surgery, Bhanubhai and Madhuben Patel Cardiac Centre Shree Krishna Hospital, Bhaikaka University Karamsad Gujarat India.

Key Clinical Message: Clinicians should think beyond pneumonia and left-to-right shunts when young children have persistent respiratory distress. Congenital lung anomalies, including congenital lobar emphysema, should be considered differential diagnoses. Chest X-ray and CT imaging should be conducted to gain insight regarding and establish diagnosis, respectively.

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Introduction: Over the years, congenital lung malformations (CLM) management remains a controversial topic in pediatric thoracic surgery. The Italian Society of Pediatric Surgery performed a national survey to study the current management variability among centers, trying to define national guidelines and a standardized approach of children with congenital lung malformations.

Methods: Following a National Society approval, an electronic survey including 35 items on post-natal management was designed, focusing on surgical, anesthesiology, radiology and pneumology aspects.

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Background: Congenital pulmonary malformations (CPMs) are rare in children. This study aimed to describe the clinical, imaging characteristics, and treatment of patients with this pathology.

Methods: We conducted a descriptive and retrospective study with data from patients with CPMs diagnosed at Instituto Nacional de Salud del Niño-Breña (Lima-Peru), from January 2010 to December 2020.

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Pulmonary sequestration (PS) is a rare congenital malformation, which mainly contains two variants involving extralobar and intralobar sequestrations. Extralobar sequestrations (ELS) are isolated from the remaining lung tissue and have their visceral pleura. Herein, we report the first case of a torsed ELS associated with congenital lobar emphysema.

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Congenital lobar emphysema: A rare cause of respiratory failure in neonates.

Pediatr Pulmonol

June 2023

Department of Pediatrics, Division of Pulmonology, West Virginia University, Morgantown, West Virginia, USA.

Congenital lobar overinflation, also known as congenital lobar emphysema (CLE), is an uncommon (1/20,000-30,000 live births) abnormality characterized by hyperinflation of one or more pulmonary lobes, usually with contralateral displacement of the mediastinum. While the etiology of most cases of CLE is poorly understood and labeled idiopathic, some cases are thought to be due to an intrinsic or extrinsic bronchial wall abnormality causing a ball valve mechanism with resultant hyperinflation of the affected lobe. CLE tends to have a predilection for males presenting insidiously in the first 6 months of life and have respiratory distress and progressive failure, with 50% of cases being asymptomatic at birth.

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Congenital lobar emphysema (CLE)/congenital alveolar overdistension/congenital lobar overinflation or infantile lobar emphysema is a rare developmental anomaly of the lower respiratory tract which is characterised by hyperinflation of one or more of the pulmonary lobes. Histopathology may be variable, which may show abnormality in the cartilage, granulation tissue, mucosal folds, etc. We report a rare underlying histopathology in a preterm neonate with CLE.

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Management of Congenital Lung Malformations.

Clin Perinatol

December 2022

Division of Pediatric, Thoracic, and Fetal Surgery, University of California-Davis Medical Center, 2335 Stockton Boulevard, Sacramento, CA 95817, USA. Electronic address:

Article Synopsis
  • - Congenital lung malformations are a range of conditions that vary in cause and require specific clinical approaches tailored to each type.
  • - The article specifically covers congenital pulmonary airway malformations, bronchopulmonary sequestration, congenital lobar emphysema, and bronchogenic cysts, analyzing each from developmental, functional, and treatment angles.
  • - It includes a review of current best practices for medical and surgical management of these conditions, along with established treatment algorithms.
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Surgery versus conservative management in congenital lobar emphysema: follow up and indicators for surgery.

Pediatr Surg Int

April 2022

Department of Pediatric Pulmonology, Ankara City Hospital, University of Health Science, Üniversiteler District, 1604, Street No: 9, Çankaya, 06800, Ankara, Turkey.

Introduction: Congenital lobar emphysema (CLE), a rare developmental lung malformation, involves the hyperaeration of one or more lung lobes caused by partial obstruction and occurs at a rate of 1/20,000-30,000 live births. Here, we aimed to retrospectively examine the clinical, radiological, and bronchoscopy findings of patients with CLE who were diagnosed and treated by surgical or non-surgical (conservative) approaches at our center and compared our results with those in the literature.

Methods: We examined the clinical, radiological, and bronchoscopy findings of 20 patients with CLE aged 0-18 years at our center between 2013 and 2020.

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[Congenital Malformations of the Lung - an Overview].

Zentralbl Chir

February 2022

Klinik für Thoraxchirurgie, Universitätsklinikum Freiburg, Medizinische Fakultät, Albert-Ludwigs-Universität Freiburg, Freiburg, Deutschland.

Article Synopsis
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Fatal congenital lobar emphysema in a puerpera: a case report and literature review.

BMC Pulm Med

December 2021

Department of Thoracic Surgery, West China Hospital, Sichuan University, No. 37 Guoxue Alley, Chengdu, 610041, Sichuan, China.

Background: Congenital lobal emphysema (CLE) is a developmental lung abnormality usually diagnosed in the neonatal period and is rarely observed in adults. Adults with CLE are usually asymptomatic and only a small fraction may present with coughing, recurrent pneumonia and respiratory distress. In imaging studies, the most frequently affected lobe of CLE is the left upper lobe, followed by the right middle lobe.

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Bronchopulmonary dysplasia in extremely premature infant with congenital lobar emphysema: a case report.

BMC Pediatr

July 2021

Department of Neonatology, Shenzhen Maternity & Child Healthcare Hospital, Cheeloo College of Medicine, Shandong University, Shenzhen, Guangdong, China.

Background: Congenital lobar emphysema (CLE) is a congenital pulmonary cystic disease, characterized by overinflation of the pulmonary lobe and compression of the surrounding areas. Most patients with symptoms need an urgent surgical intervention. Caution and alertness for CLE is required in cases of local emphysema on chest X-ray images of extremely premature infants with bronchopulmonary dysplasia (BPD).

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Narrative review of congenital lung lesions.

Transl Pediatr

May 2021

Division of General Pediatric Surgery, Johns Hopkins Children's Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

This article reviews the contemporary diagnosis and management of antenatally diagnosed congenital lung lesions. These anomalies, which include congenital pulmonary airway malformation (CPAM) (formerly congenital cystic adenomatoid malformation), bronchopulmonary sequestration (BPS), bronchogenic cyst, and congenital lobar emphysema (CLE), are relatively rare but are increasingly encountered by clinicians because of the improved resolution and enhanced sensitivity of fetal ultrasound. Serial assessment of these lesions throughout pregnancy remains the norm rather than the exception.

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Congenital Lobar Emphysema: Perioperative Evaluation and Management.

Heart Surg Forum

June 2021

Cardithoracic Surgery Department, Faculty of Medicine, Menoufia University, Almenoufia, Egypt.

Background: Congenital lobar emphysema (CLE) is a lung malformation characterized by overdistension and air trapping in the affected lobe. It is one of the causes of neonatal and infantile respiratory distress. This study aimed to evaluate our experience regarding perioperative and surgical management in children with CLE.

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Background: Lobar emphysema in dogs and cats is caused by bronchial collapse during expiration and subsequent air trapping. Congenital causes such as bronchial cartilage defects or acquired causes such as compressive neoplastic lesions have been reported. Morbidity results from hyperinflation of the affected lung lobe and compression of adjacent thoracic structures.

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