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| http://dx.doi.org/10.4081/cp.2018.1004 | DOI Listing |
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Heterotaxy Syndrome Diagnosed in an Adult.
Ochsner J
January 2024
Department of Internal Medicine, Sultan 2. Abdul Hamid Khan Educational and Research Hospital, Istanbul, Turkey.
Heterotaxy syndrome, a condition in which the internal organs are abnormally arranged in the thorax or abdomen, is generally diagnosed early in life, often during the neonatal period. We present the case of a 42-year-old male who was incidentally diagnosed with polysplenia syndrome and subsequently diagnosed with heterotaxy syndrome. Upon further investigation, he was determined to have a sinus venosus type atrial septal defect.
View Article and Find Full Text PDFAnalysis of associated malformations by computed tomography in adults with polysplenia syndrome: A pilot study.
PLoS One
December 2024
Department of Medical Imaging, The Affiliated Suzhou Hospital of Nanjing Medical University, Gusu School of Nanjing Medical University, Suzhou, Jiangsu, China.
Objective: To analytically depict the associated malformations of polysplenia syndrome (PS) in adults via computed tomography (CT).
Materials And Methods: The incidence of malformations associated with PS in twelve adult patients was retrospectively analyzed via CT imaging.
Results: The number of splenic nodules ranged from three to twelve; the splenic nodules were located in the left upper quadrant in nine patients and in the right upper quadrant in three patients.
Polysplenia Syndrome and the Development of Heart Failure due to Associated Congenital Heart Defect.
J Belg Soc Radiol
December 2024
Department of Radiology, Sint-Franciscusziekenhuis, Heusden-Zolder, Belgium.
Patients with polysplenia syndrome can develop pulmonary hypertension and heart failure due to underlying congenital heart disease, underscoring the need for early recognition and intervention to prevent further progression of the condition.
View Article and Find Full Text PDFTherapeutic endoscopic retrograde cholangiopancreatography in a patient with asplenia-type heterotaxy syndrome: A case report.
World J Gastrointest Surg
November 2024
Department of Gastroenterology, The Second Affiliated Hospital of Kunming Medical University, Kunming 650101, Yunnan Province, China.
Background: Asplenia-type heterotaxy syndrome (HS) is rare and refers to visceral malposition and dysmorphism. It is associated with a high infant mortality rate due to cardiac anomalies, and related digestive endoscopic interventions are poorly understood. With the improved long-term prognosis of these individuals after modern cardiac surgery, intra-abdominal anomalies have become increasingly significant.
View Article and Find Full Text PDFA case of right middle lobectomy for primary lung cancer in a patient with heterotaxy syndrome.
Gen Thorac Cardiovasc Surg Cases
November 2024
Department of Thoracic Surgery, Akita University Graduate School of Medicine, 1-1-1 Hondo, Akita, 010-8543, Japan.
Article Synopsis
- The text discusses a case of a 71-year-old man with heterotaxy syndrome, a condition causing symmetrical development of organs, who underwent surgery for non-small cell lung cancer.
- A CT scan revealed a rapidly growing tumor in his right middle lobe, alongside anatomical anomalies in the bronchi and pulmonary artery.
- The conclusion emphasizes the need for 3D-CT scans to better understand the unique anatomy in patients with heterotaxy syndrome prior to surgical procedures, as this specific anatomical variation had not been previously documented.
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