A Case of Choledocholithiasis and Intestinal Malrotation in an Adolescent with Repaired Gastroschisis

Kim, Byung Chul; Kim, Ki Bae; Kim, Eui Joong; Park, Soonyoung; Lee, Dong Hwa; Kim, Eun Bee; Chae, Hee Bok; Park, Seon Mee

doi:10.5946/ce.2014.47.2.201

Cited by 2 publications

(1 citation statement)

References 12 publications

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“…Signs of associated congenital anomalies such as gut malrotation, diaphragmatic hernia, and so on should be ruled out. 3 Keywords: Malrotation of Left Liver; Bariatric Surgery; Choledocholithiasis.…”

Section: Answer To: Image 1 (Page 1660): Isolated Malrotation Of the mentioning

confidence: 99%

Unusual Aspect of a Choledocholithiasis

Weber¹,

Wildi

2020

Gastroenterology

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Section: Answer To: Image 1 (Page 1660): Isolated Malrotation Of the mentioning

confidence: 99%

Unusual Aspect of a Choledocholithiasis

Weber¹,

Wildi

2020

Gastroenterology

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Delayed Presentation of Malrotation after Infancy: A Systematic Review Based on Clinical Presentations, Associated Anomalies, Diagnosis, and Management

Sharma,

Borkar,

Ashwin

et al. 2024

Journal of Indian Association of Pediatric Surgeons

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Need and Purpose of Review: Approximately 75% of patients with classic malrotation and midgut volvulus present in neonatal age-group; another 15% may present up to one year. In these, the diagnosis is made because of typical presentation. However, there are many cases in which malrotation has been detected after infancy. In-spite of the variable case reports and studies in literature, there is no specific data on the incidence of malrotation after infancy, its presentation and management guidelines. With this systematic review, we aim to coalesce these findings from various individual case reports and studies. Methods Used for Collecting and Analysing Data: This systematic review was performed as per the PRISMA (preferred reporting items for systematic review and meta-analyses) guidelines. The authors conducted thorough searches in databases like PubMed/MEDLINE, SCOPUS, Google Scholar and Web of Science for relevant articles. Studies were reviewed for clinical presentation and outcome for malrotation diagnosed beyond infancy. Main Conclusions: Clinical presentation of malrotation after infancy can be acute as well as chronic; acute presentation being common under 2 years of age and chronic symptoms present as age increases. Sudden onset of abdominal pain and bilious vomiting are commonest acute symptoms and intermittent episodes of recurring vague abdominal pain associated with vomiting and diarrhoea are the commonest chronic symptoms. The diagnostic modalities vary from UGI Contrast series to USG with colour Doppler and CECT scan. Management is operative open as well as laparoscopic Ladd’s procedure is being favoured. Key Messages Presentation of malrotation beyond infancy is infact more than that reported in literature. Timely and appropriate diagnosis of malrotation is essential to avoid gangrene and subsequent gut loss and morbidity.

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A Case of Choledocholithiasis and Intestinal Malrotation in an Adolescent with Repaired Gastroschisis

Cited by 2 publications

References 12 publications

Unusual Aspect of a Choledocholithiasis

Unusual Aspect of a Choledocholithiasis

Delayed Presentation of Malrotation after Infancy: A Systematic Review Based on Clinical Presentations, Associated Anomalies, Diagnosis, and Management

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