Zobrazeno 1 - 10
of 280
pro vyhledávání: '"colonic duplication"'
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 29, Iss 4, Pp 387-389 (2024)
The association is defined as two or more malformations with unclear relationships, which do not fit the criteria of a syndrome. This case report presents a rare finding of tubular colonic duplication in association with Mayer–Rokitansky–Küster
Externí odkaz:
https://doaj.org/article/3be6d5c75a444d2d8867959348b0d61e
Autor:
Muhammad Ash-Shafhawi Adznan, Hizami Amin Tai, Aras Emre Canda, Nevra Elmas, Mustafa Cem Terzi
Publikováno v:
Annals of Coloproctology, Vol 40, Iss Suppl 1, Pp S6-S10 (2024)
One of the possible causes of chronic constipation is colonic duplication. Although seldom asymptomatic, its diagnosis is important due to the risk of malignancy that it carries. We present a case of a young female patient with long-standing constipa
Externí odkaz:
https://doaj.org/article/f3dc554a7b3b4bb09de055eaf89f50a2
Autor:
Michael A. Negussie, Leul M. Manyazewal, Fitsum A. Gemechu, Samuel Mesfin, Abebe Mekonnen, Tihitena Negussie
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 103, Iss , Pp 102791- (2024)
Introduction: Split notochord syndrome (SNS) is a rare congenital anomaly characterized by malformations in the spine, central nervous system and gastrointestinal tract. This paper presents a case of SNS accompanied by a neuroenteric fistula (NEF). C
Externí odkaz:
https://doaj.org/article/fe982727d8e14650bbc00f22a1d6374d
Publikováno v:
Zhenduanxue lilun yu shijian, Vol 22, Iss 04, Pp 385-388 (2023)
Enteric duplication is a rare malformation of the digestive tract, while colonic duplication is even rarer in adults. This paper reports one case, a 22-years old female, presented with a peritoneal cystic mass lesion measured 15 cm×10 cm. The lesion
Externí odkaz:
https://doaj.org/article/f217fd49b6e5408497f536e3602c57bd
Publikováno v:
Annals of Pediatric Surgery, Vol 19, Iss 1, Pp 1-7 (2023)
Abstract Background The occurrence of complete tubular colonic duplication is exceedingly rare. In most cases, resection of the duplicated colon may not be possible because of common blood supply with a single mesentery shared between the duplication
Externí odkaz:
https://doaj.org/article/97ed570692a54e63ae78cb270513d40d
Publikováno v:
Open Life Sciences, Vol 18, Iss 1, Pp bcr2014206638-7 (2023)
Intestinal duplication is a rare congenital malformation that can occur in any segment of the digestive tract. It is most commonly found in the ileum of infants and is rarely reported in adults, especially in the colon. Diagnosing intestinal duplicat
Externí odkaz:
https://doaj.org/article/d0a32052570e4c8c9dfb4f56fbd2edd0
Congenital colorectal tubular duplication in an infant: A tale of radiological diagnostic challenges
Autor:
Selim Ahmed, MBBS, FCPS, Mohd Syafiek Saifuddin, BSc, MB, BCh, BAO, MMED, Chiak Yot Ng, MBBS, MMED, Nik Fatimah Salwati, MBBS, MMED, Firdaus Hayati, MD, MMED, Suseela Ismail, MD, MMED
Publikováno v:
Radiology Case Reports, Vol 16, Iss 11, Pp 3289-3294 (2021)
Enteric duplications (EDs) are rare congenital anomalies that result from defect during embryonic development of the gut. Although EDs can literally occur at any part of the gastrointestinal tract, ileocecal duplication is the commonest type followed
Externí odkaz:
https://doaj.org/article/2ff1513fd44a4de197aefc32a1b209a7
Akademický článek
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Autor:
Alfredo Dominguez-Muñoz, Emilio Fernandez-Portilla, Roberto Davila-Perez, Itzel Lizarraga-Rodriguez, Ma. de Lourdes Leyva-Castellanos, Jaime Nieto-Zermeño
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 84, Iss , Pp 102374- (2022)
Introduction: Colorectal duplications (CRD) end as a blind sac, communicate to the native colon/rectum or as an external fistula. The treatment depends on duplication type and length. Case presentation: We present a case of a 2-year-old female patien
Externí odkaz:
https://doaj.org/article/59f41a6a051844d08980c7bb3615668b
Autor:
Volkan Sarper Erikci
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 11, Iss 1, Pp 108-112 (2021)
Enteric duplications are rare congenital anomalies found anywhere from mouth to anus. Colonic duplications constitute about 13% of all enteric duplications. In this report a 6-year-old boy with chronic abdominal pain for a duration of last 2 years re
Externí odkaz:
https://doaj.org/article/d96b9f91415d4e75aad9c7741e39a186