ArticleCureus2024
A Rare Case of Situs Inversus Partialis With Levocardia in a 73-Year-Old Patient.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Situs Inversus Partialis: An Incidental Discovery in a Young Patient with Obstructed Left Inguinal Hernia.Rwanda journal of medicine and health sciences · 2026Article
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Situs inversus partialis (SIP) is an extremely rare congenital disorder in which most of the visceral organs are located on the opposite side of their usual anatomical locations. The condition is usually associated with levocardia, in which the apex of the heart is directed toward the left side. In our case study, a female patient with a history of dysphagia and weight loss presented to the outpatient clinic under the urgent two-week wait pathway. She underwent a CT scan of the thorax, abdomen, and pelvis, which revealed that she has SIP in which some of the abdominal organs are reversed and others are in their normal anatomical locations. The patient was diagnosed with esophageal carcinoma. However, because of her rare condition, it was challenging to insert a nasogastric tube into her reversed stomach and to explore other feeding options, e.g., jejunostomy. This report discusses a rare case of SIP, incidentally discovered in a patient with suspected esophageal malignancy, and its associated surgical challenges in her management.
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