A Rare Case of Polysplenia Syndrome Associated with Severe Cardiac Malformations and Congenital Alveolar Dysplasia in a One-Month-Old Infant: A Complete Macroscopic and Histopathologic Study

A Rare Case of Polysplenia Syndrome Associated with Severe Cardiac Malformations and Congenital Alveolar Dysplasia in a One-Month-Old Infant: A Complete Macroscopic and Histopathologic Study

Polysplenia syndrome represents a type of left atrial isomerism characterized by multiple small spleens, often associated with cardiac malformations and with <i>situs ambiguus</i> of the abdominal organs. The case presented is of a one-month-old male infant, weighing approximately 3000 g...

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Bibliographic Details
Main Authors: Cosmin Ioan Mohor, Sorin Radu Fleaca, Alexandra Oprinca Muja, George Calin Oprinca, Mihai Dan Roman, Radu Chicea, Adrian Gheorghe Boicean, Horatiu Dura, Ciprian Tanasescu, Nicolas Catalin Ionut Ion, Mihai Faur, Ciprian Ionut Bacila, Florina Batar, Calin Ilie Mohor
Format: Article
Language:English
Published: MDPI AG 2022-04-01
Series:Journal of Cardiovascular Development and Disease
Subjects:
polysplenia syndrome
left atrial isomerism
congenital alveolar dysplasia
hepatic fibrosis
infantile lactic acidosis
complete atrioventricular canal defect
Online Access:https://www.mdpi.com/2308-3425/9/5/135

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https://www.mdpi.com/2308-3425/9/5/135

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