Aim: Trisomy 21, also known as Down syndrome, is the most common chromosomal abnormality seen in live births and is associated with congenital abnormalities involving multiple organ systems. While the congenital cardiac and gastrointestinal associations of trisomy 21 are well known, the associated pulmonary radiological findings are less widely described. Our objective is to assess the presence, categories, and prevalence of pulmonary radiological findings in patients with trisomy 21, and to describe and provide reference images of these findings.
Materials And Methods: A database of patients with a confirmed diagnosis of trisomy 21 was provided by the congenital cardiac disease clinic. One hundred thirty-four patients who had undergone computed tomography (CT) imaging of the chest were then identified from this database, all of whom had a diagnosis of congenital cardiac disease. A retrospective review of imaging findings of these 134 patients was then conducted by two specialist consultant paediatric radiologists and a paediatric radiology fellow.
Results: The CTs of 62 patients demonstrated no abnormality. The CTs of the remaining 72 patients were abnormal. Air trapping (present in 35% of patients), subpleural cysts (17%), bronchiectasis (4%), findings suggestive of bronchopulmonary dysplasia (3%), and abnormalities of the tracheobronchial tree (4%) were among the abnormalities demonstrated.
Conclusion: This retrospective review describes the spectrum of thoracic radiological findings seen in patients with trisomy 21. This is of increasing value to practicing radiologists due to the rising life expectancy in this population.
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http://dx.doi.org/10.1016/j.crad.2025.106857 | DOI Listing |
Clin Radiol
February 2025
Department of Radiology, Children's Health Ireland, Dublin, Ireland.
Aim: Trisomy 21, also known as Down syndrome, is the most common chromosomal abnormality seen in live births and is associated with congenital abnormalities involving multiple organ systems. While the congenital cardiac and gastrointestinal associations of trisomy 21 are well known, the associated pulmonary radiological findings are less widely described. Our objective is to assess the presence, categories, and prevalence of pulmonary radiological findings in patients with trisomy 21, and to describe and provide reference images of these findings.
View Article and Find Full Text PDFJ Cell Mol Med
March 2025
Faculty of Medicine, Division of Laboratory Medicine, Medical University of Gdansk, Gdansk, Poland.
We present a case of acute clonal bone marrow 98% infiltration of atypical myeloid cells with borderline hypogranular/agranular promyelocytes/myelocytes and occasional blast cells maturity, which also formed extramedullary tumours in the chest wall, with isolated trisomy of chromosome 6 and pathogenic variant U2AF1 (S34F) that escapes established acute myeloid leukaemia (AML) diagnostic criteria according to the World Health Organization (WHO) classification. Following standard daunorubicin and cytarabine induction therapy, the disease progressed with the appearance of a previously undetected clone of leukaemic cells with a distinct immunophenotype demonstrating monocytoid differentiation and clonal evolution to a hypo-tetraploid karyotype with an average number of 84 chromosomes and new pathogenic NRAS and ZRSR2 mutations. The patient reactivated refractory disseminated intravascular coagulation (DIC) leading to a progressive supratentorial hematoma and finally cardiac arrest.
View Article and Find Full Text PDFTaiwan J Obstet Gynecol
March 2025
Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan.
Objective: We present a rare case of trisomy 18 of maternal origin in a pregnancy with omphalocele, craniorachischisis, and ectopia cordis.
Case Report: A 38-year-old woman, G3P1A1, was diagnosed with fetal anencephaly, an extrathoracic heart (ectopic cordis), deformity of spine and a stomach-and-intestine-containing omphalocele by prenatal ultrasound at 12 weeks of gestation. The patient's husband was 39 years old and healthy.
J Transl Med
February 2025
Center for Reproductive Medicine, Henan Key Laboratory of Reproduction and Genetics, The First Affliated Hospital of Zhengzhou University, Zhengzhou, China.
Background: Preimplantation genetic testing for aneuploidy and for chromosomal structural rearrangement (PGT-A/-SR) can improve clinical pregnancy rates and live birth rates, and shorten the time to pregnancy. The large-scale statistics on their efficacy and accuracy across different centres, as well as the frequency of abnormalities for each chromosome, will provide a valuable supplement to previous research.
Methods: Patients who had PGT-A or -SR procedures at five reproductive centres from 2018 to 2022 were recruited based on PGT-A/-SR indications.
J Pediatr Surg
February 2025
Section of Pediatric Surgery, Department of Surgery, Indiana University School of Medicine, 705 Riley Hospital Drive, Suite 2500, Indianapolis, IN, 46202, USA. Electronic address:
Purpose: Trisomy 13 (T13) and trisomy 18 (T18) are chromosomal abnormalities which portend high rates of feeding dysfunction and infant mortality risk. Although gastrostomy tube (GT) placement is commonly performed in this population, there is limited data assessing outcomes associated with this procedure. Our aim was to determine survival outcomes among GT and non-GT patients with T13/18.
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