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Your search keyword '"Segmental Ileal Dilatation"' showing total 7 results
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7 results on '"Segmental Ileal Dilatation"'

1. Segmental ileal dilatation presenting with neonatal intestinal obstruction

Author

Sachit Anand, Anjan Kumar Dhua, Jeeva Sankar, Prasenjit Das, Prabudh Goel, Minu Bajpai, and Akash Sharma

Subjects
interstitial cells of cajal, muscularis propria, neonatal intestinal obstruction, segmental ileal dilatation, Pediatrics, RJ1-570, Surgery, RD1-811
Abstract

Segmental ileal dilatation is an uncommon cause of neonatal intestinal obstruction. This report highlights a rare combination of abnormal distribution of muscles in the muscularis propria and partial loss of interstitial cells of Cajal as causative factors for segmental intestinal dilatation.

Published
2020
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2. Case Report: Expanding the Phenotypic Spectrum of Timothy Syndrome Type 1: A Sporadic Case With a de novo CACNA1C Pathogenic Variant and Segmental Ileal Dilatation

Author

Ahmed A. Nugud, Nermeen Mahmoud ELkholy, Awad Alkarim Omar, Abid Qazi, Christos Tzivinikos, Nidheesh Chencheri, Sabina Khan, and Muhammad Eyad Ba'Ath

Subjects
CACNA1C mutation, Timothy syndrome, Segmental Ileal Dilatation, syndactyly, long QT syndrome, seizure disorder, Pediatrics, RJ1-570
Abstract

Background: Long QT syndactyly syndrome (long QT syndrome type 8), also known as Timothy Syndrome (TS) was first described in 1994 with still

Published
2021
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3. Segmental ileal dilatation presenting with neonatal intestinal obstruction.

Author

Anand, Sachit, Dhua, Anjan, Sankar, Jeeva, Das, Prasenjit, Goel, Prabudh, Bajpai, Minu, and Sharma, Akash

Subjects
*BOWEL obstructions, *CHILDREN
Abstract

Segmental ileal dilatation is an uncommon cause of neonatal intestinal obstruction. This report highlights a rare combination of abnormal distribution of muscles in the muscularis propria and partial loss of interstitial cells of Cajal as causative factors for segmental intestinal dilatation. [ABSTRACT FROM AUTHOR]

Published
2020
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4. Segmental ileal dilatation presenting with neonatal intestinal obstruction

Author

Jeeva Sankar, Sachit Anand, Prabudh Goel, Akash Sharma, Minu Bajpai, Anjan Kumar Dhua, and Prasenjit Das

Subjects
Pathology, medicine.medical_specialty, neonatal intestinal obstruction, 030232 urology & nephrology, lcsh:Surgery, Case Report, digestive system, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, 030225 pediatrics, Partial loss, Medicine, segmental ileal dilatation, business.industry, digestive, oral, and skin physiology, muscularis propria, lcsh:RJ1-570, lcsh:Pediatrics, interstitial cells of cajal, lcsh:RD1-811, Intestinal dilatation, Abnormal distribution, Interstitial cell of Cajal, Pediatrics, Perinatology and Child Health, symbols, Surgery, business
Abstract

Segmental ileal dilatation is an uncommon cause of neonatal intestinal obstruction. This report highlights a rare combination of abnormal distribution of muscles in the muscularis propria and partial loss of interstitial cells of Cajal as causative factors for segmental intestinal dilatation.

Published
2020

6. Case Report: Expanding the Phenotypic Spectrum of Timothy Syndrome Type 1: A Sporadic Case With a de novo CACNA1C Pathogenic Variant and Segmental Ileal Dilatation.

Author

Nugud AA, ELkholy NM, Omar AA, Qazi A, Tzivinikos C, Chencheri N, Khan S, and Ba'Ath ME

Abstract

Background: Long QT syndactyly syndrome (long QT syndrome type 8), also known as Timothy Syndrome (TS) was first described in 1994 with still <50 case reported in the literature. The full spectrum of the syndrome is not yet known. Results: Here we report a girl who presented with new onset refractory seizures and an undiagnosed cause of intermittent abdominal distention. She also had syndactyly of her fingers and toes and was found to have prolonged QT. Upon further investigations she was found to have a de novo pathogenic variant in CACNA1C , along with Segmental Ileal Dilatation (SID), and subsequently diagnosed with Timothy syndrome. Conclusion: To our knowledge, the association of Timothy Syndrome with Segmental Ileal Dilatation, was not described before., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2021 Nugud, ELkholy, Omar, Qazi, Tzivinikos, Chencheri, Khan and Ba'Ath.)

Published
2021
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7. Segmental ileal dilatation with supernumerary intestinal muscle coat in a neonate

Author

Feridun Cahit Tanyel, Tutku Soyer, and Beril Talim

Subjects
Coat, Pathology, medicine.medical_specialty, business.industry, Segmental ileal dilatation, Histology, Case Report, Anatomy, Gastrointestinal smooth muscle, Intestinal dilatation, Ganglion, medicine.anatomical_structure, Neonate, Intestinal muscle, Gastric mucosa, Etiology, Medicine, Supernumerary, business
Abstract

Segmental intestinal dilatation (SID) is a rare developmental anomaly of the midgut, characterized by sharply demarcated dilatation of a gastrointestinal segment with clinical findings of intestinal obstruction. Although morphologic criteria for SID are clearly delineated, etiological origin of dilated intestine is unknown. Histology of the resected segment is usually reported to have normal presence of ganglion cells in the myenteric and submucosal plexuses. Intestinal muscle is hypertrophied, and heterotopic gastric mucosa may also be encountered. A 3-day-old male infant presenting with clinical findings of intestinal obstruction was diagnosed to have SID and had supernumerary intestinal muscle coat (SIMC) in the dilated segment, without any evidence of neurological abnormality. Histopathological findings of the resected ileal segment are reported to discuss the role of architectural malformation of muscularis propria as a cause of SID.

Published
2015

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