scholarly journals Rectal Duplication Cyst Mimicking Rectal Prolapse

2021 ◽  
Vol 11 (01) ◽  
pp. 44-45
Author(s):  
Asrar Ahmad ◽  
Eelaf Karar ◽  
Irum Saleem ◽  
Nisar Ahmad
Keyword(s):  
Gastrointestinal Tract ◽  
Rectal Prolapse ◽  
Congenital Malformations ◽  
Duplication Cyst ◽  
Distal Ileum ◽  
Posterior Sagittal Approach ◽  
Presacral Cyst ◽  
Rectal Duplication

Gastrointestinal tract duplications are rare congenital malformations that are benign, presenting usually in childhood. Most common sites include the distal ileum and oesophagus. Rectal presentation is quite uncommon and is usually cystic. This is a case of a three year old boy who came with rectal prolapse. On further examination and imaging investigations a presacral cyst was located and a diagnosis of rectal duplication was made. The cyst was completely excised by a posterior sagittal approach.

scholarly journals Rectal duplication cyst mimicking rectal prolapse: A case report

2021 ◽  
Vol 1 (2) ◽  
Author(s):  
Asrar Ahmad ◽  
Eelaf Karar ◽  
Irum Saleem ◽  
Nisar Ahmad
Keyword(s):  
Case Report ◽  
Gastrointestinal Tract ◽  
Rectal Prolapse ◽  
Congenital Malformations ◽  
Duplication Cyst ◽  
Rare Entity ◽  
Case Presentation ◽  
Posterior Sagittal Approach ◽  
Presacral Cyst ◽  
Rectal Duplication

Background: Gastrointestinal tract duplications are rare congenital malformations that are benign, presenting usually in childhood. Most common sites include the distal ileum and esophagus. Rectal presentation is quite uncommon and is usually cystic. Case Presentation: This is a case of a 3-year-old boy who came with rectal prolapse. On further examination and imaging investigations, a presacral cyst was located and a diagnosis of rectal duplication was made. The cyst was completely excised by a posterior sagittal approach. Conclusion: Rectal duplication is a rare entity that may simulate a rectal prolapse.

scholarly journals A Late Adolescent Girl with Rectal Duplication Cyst in Bangladesh: Case Report

2019 ◽  
Vol 21 (1) ◽  
pp. 45-46
Author(s):  
Mohammad Ibrahim Khalil ◽  
Andalib Amin ◽  
ATM Asaduzzaman ◽  
AZM Mahfuzur Rahaman ◽  
AZM Mostaque Hossain
Keyword(s):  
Case Report ◽  
Gastrointestinal Tract ◽  
Adolescent Girl ◽  
Duplication Cyst ◽  
Cystic Mass ◽  
Cystic Lesions ◽  
Late Adolescent ◽  
Complete Cure ◽  
High Index Of Suspicion ◽  
Rectal Duplication

Intestinal duplications, originally described in 1941, are congenital cystic lesions resemblingand associated with part of the gastrointestinal tract. Rectal duplication is the rarest of the allduplications and adolescence presentation of rectal duplication cyst is quite unusual whichis reported here. A 17 year female presented with right gluteal lump. She underwent surgeryand was found to have a smooth cystic mass, which was later found to be a Rectal Duplicationcyst in histopathology. High index of suspicion with other differentials can lead to earlydiagnosis and complete cure of the condition. Journal of Surgical Sciences (2017) Vol. 21 (1) :45-46

scholarly journals Infradiaphragmatic extralobar pulmonary sequestration asossiated with duplication cyst of the gaster in newborn

2020 ◽  
Vol 10 (1) ◽  
pp. 95-102
Author(s):  
Nikolai V. Krivosheenko ◽  
Alexey V. Gramzin ◽  
Pavel M. Pavlushin ◽  
Yana L. Manakova ◽  
Larisa M. Shpak ◽  
...  
Keyword(s):  
Surgical Treatment ◽  
Congenital Malformations ◽  
Pulmonary Sequestration ◽  
Duplication Cyst ◽  
Cystic Mass ◽  
Minimal Invasive ◽  
Retroperitoneal Mass ◽  
Extralobar Pulmonary Sequestration ◽  
Neoplastic Process ◽  
Ultrasound Investigation

Introduction. The biggest difficulties of pulmonary sequestration treatment appear when they are combined with other congenital malformations. Materials and methods. This article describes a rare case of combination of infradiaphragmatic extralobar sequestration of the lung and duplication cyst of the gaster. The antenatal ultrasound investigation at 21 week of gestation visualized a retroperitoneal mass that had a cystic-solid structure and a vessel that departed directly from the aorta. CT-scan that was performed after the birth, confirmed an existence of infradiaphragmatic cystic mass that had a vessel that departed directly from the aorta. We couldnt exclude the neoplastic process because of structure and topography of mass. Tumor markers were without pathology. Surgical treatment was performed: laparotomy and removal of the cyst and extrapulmonary sequestration. The histological investigation confirmed a pulmonary sequestrum and duplication cyst of the gaster. Conclusion. A nowadays method of visualization allows to find congenital malformation in earliest stages of gestation. The tradition surgical treatment and also minimal invasive surgical treatment are the main option of cure such congenital malformations. Also literature review of rare clinical forms of pulmonary sequestration presented in this article.

scholarly journals Posterior urethral valve and anterior rectal duplication: a new combination

2019 ◽  
Vol 12 (7) ◽  
pp. e229648
Author(s):  
Kailas P Bhandarkar ◽  
Nordeen Bouhadiba ◽  
Massimo Garriboli
Keyword(s):  
Rare Case ◽  
Posterior Urethral Valve ◽  
Duplication Cyst ◽  
New Combination ◽  
Acute Renal Injury ◽  
Urinary Stream ◽  
Urethral Valve ◽  
Rectal Duplication ◽  
Laparoscopic Assisted

We present a rare case of association of anterior rectal duplication and posterior urethral valve (PUV). A term neonate with no antenatal concerns was admitted with urosepsis and acute renal injury at 18 days of age. History revealed a poor urinary stream and dribbling. After resuscitation and stabilisation, renal tract ultrasound and micturating cysto-urethrogram were performed. Cystourethroscopy showed PUV and a mass indenting the bladder posteriorly. MRI confirmed the presence of a cystic lesion anterior to the rectum suspicious of rectal duplication. Laparoscopic-assisted excision of the anterior rectal duplication cyst was then performed. The infant recovered uneventfully. Creatinine normalised postoperatively and has been stable at follow-up.

scholarly journals RECTAL DUPLICATION CYST IN PREVIOUS ANORECTAL MALFORMATION AND DOWN SYNDROME

2012 ◽  
Vol 4 (1) ◽  
pp. 57
Author(s):  
A. Burgio ◽  
F. Ferrara ◽  
E. Cerchia ◽  
E. Brandigi ◽  
R. Angotti ◽  
...  
Keyword(s):  
Down Syndrome ◽  
Anorectal Malformation ◽  
Duplication Cyst ◽  
Rectal Duplication

scholarly journals P636 An unusual cause of gluteal swelling.....congenital rectal duplication cyst

2019 ◽  
Author(s):  
Qasim Mahmood ◽  
Uzair Shabbir ◽  
Brian Sweeney ◽  
Maureen O’Sullivan ◽  
Taha Yousif
Keyword(s):  
Duplication Cyst ◽  
Rectal Duplication

scholarly journals Gastric and esophageal duplications in children

2020 ◽  
Vol 15 (4) ◽  
pp. 110-113
Author(s):  
M.A. Aksel'rov ◽  
◽  
V.N. Evdokimov ◽  
V.V. Svazyan ◽  
T.V. Sergienko ◽  
...  
Keyword(s):  
Small Intestine ◽  
Case Report ◽  
Gastrointestinal Tract ◽  
Anal Canal ◽  
Congenital Anomalies ◽  
Congenital Malformations ◽  
Clinical Manifestations ◽  
Clear Understanding ◽  
Gastric Duplication ◽  
Esophageal Duplication

Considerable attention is currently being paid to the diagnosis and treatment of gastric malformations complicated by its obstruction. This can be attributed to stable incidence of these disorders among other congenital anomalies of the gastrointestinal tract and no clear understanding of the causes and mechanisms underlying the development of this pathology. Gastrointestinal duplications are rare congenital malformations that differ significantly in their appearance, location, size, and clinical manifestations. Their incidence is 1 case per 4,500 autopsies. Duplications can be cystic and diverticular (tubular) and can be located in any part of the gastrointestinal tract from the root of the tongue to the anal canal. The small intestine is affected most frequently, while duplications of the rectum, duodenum, and esophagus are exceedingly rare. In this article, we report two cases of gastrointestinal duplications in children treated using surgery. Key words: neonate, obstruction, developmental malformations, gastric duplication, esophageal duplication, case report

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