Anatomy, embryology, and imaging of situs ambiguous with polysplenia and left IVC

Autor: Rosa Montero-Macías, MD, David Krief, MD, Vincent Villefranque, MD, Mohamed Kilani, MD, Juan Manuel Castillo-Tuñon, MD, PhD

Publikováno v: Radiology Case Reports, Vol 18, Iss 5, Pp 1727-1732 (2023)

The situs ambiguous or heterotaxy syndrome is a type of syndrome that involves multiple visceral abnormalities, vascular ones and associated with left isomerism. Malformation of gastroenterologic system includes polysplenia (segmented spleen or multi

Externí odkaz: https://doaj.org/article/6d2ca5a9189847229b4f1f4b97330210

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Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding

Autor: Sanjeev Kharel, Dinesh Prasad Koirala, Suraj Shrestha, Hari Sedai, Bibek Man Shrestha, Sushan Homagain, Suraj Kandel

Publikováno v: Clinical Case Reports, Vol 9, Iss 8, Pp n/a-n/a (2021)

Abstract Heterotaxy syndrome is associated with asplenia/polysplenia and complex congenital heart disease. Facial palsy in heterotaxy is very rare. The management is still challenging with a poor prognosis. Proper counseling to the family about the d

Externí odkaz: https://doaj.org/article/da8b7454163347ae97eb049377a02841

Situs Ambiguous Anomaly during Laparoscopic Cholecystectomy in an Adult Female

Autor: Deepak Rana, S. R. Singh, Brij Mohan Joshi, Ashok Kumar, Mandeep Singh Sandhu

Publikováno v: Nigerian Journal of Surgery : Official Publication of the Nigerian Surgical Research Society
Nigerian Journal of Surgery, Vol 26, Iss 1, Pp 72-77 (2020)
Nigerian Journal of Surgery; Vol. 26 No. 1 (2020); 72-77

Situs anomalies are rare structural defects affecting 0.01% of general population. They present with multisystem structural defects mostly involving cardiovascular, respiratory and GI systems. Situs abnormality with presence of multiple spleen is ter

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::609915375cef5a0bf348a6664bcf350d
http://europepmc.org/articles/PMC7041347

A Rare Case of Heterotaxy Syndrome Associated with Hepatolithiasis and Pre-duodenal Portal Vein

Autor: Varna Shetty, Samir Mustaffa Paruthikunnan, Sachin Gullappa Shatagar

Publikováno v: Journal of Clinical and Diagnostic Research, Vol 11, Iss 11, Pp TD04-TD06 (2017)

Polysplenia syndrome is characterised by spectrum of abnormalities which are rarely diagnosed in adults as an incidental finding. The anomalies include multiple spleens, midline liver, gall bladder and biliary tract anomalies, short pancreas, agenes

Externí odkaz: https://doaj.org/article/2d5081d17bb941be9d6f24a14cc47036