A Rare Case of Scimitar Syndrome Accompanied with an Imperforate Anus in a Newborn

2011 ◽  
Vol 18 (2) ◽  
pp. 404 ◽  
Author(s):  
Peter Chun ◽  
Hyoung Doo Lee ◽  
Young Don Kim
Keyword(s):  
Imperforate Anus ◽  
Rare Case ◽  
Scimitar Syndrome

Congenitally palliated scimitar syndrome

2014 ◽  
Vol 25 (6) ◽  
pp. 1218-1220 ◽  
Author(s):  
Massimiliano Cantinotti ◽  
Raffaele Giordano ◽  
Isabella Spadoni
Keyword(s):  
Left Atrium ◽  
Rare Case ◽  
Pulmonary Veins ◽  
Scimitar Syndrome ◽  
Caval Vein ◽  
Anatomical Variant ◽  
Inferior Caval Vein ◽  
The Right

AbstractWe present a rare case of scimitar syndrome in which the scimitar vessel, collecting all the right pulmonary veins, was stenotic at its junction, with the inferior caval vein and two anomalous vessels, connecting to the same venous collector, draining most of the flow to the left atrium.We arbitrarily defined this rare anatomical variant as a congenitally palliated scimitar syndrome.

scholarly journals A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report

2014 ◽  
Vol 12 (2) ◽  
pp. 234-236
Author(s):  
Kleiton Gabriel Ribeiro Yamaçake ◽  
Amilcar Martins Giron ◽  
Uenis Tannuri ◽  
Miguel Srougi
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Imperforate Anus ◽  
Rare Case ◽  
Coloanal Anastomosis ◽  
Histopathological Examination ◽  
Congenital Clubfoot ◽  
Anorectal Anomaly ◽  
Male Neonate ◽  
Nonpalpable Testis

A full-term male neonate with anorectal anomaly and external perineal anomalies was referred to our service. Physical examination showed an epithelized perineal mass with cutaneous orifices, which had urine fistulization, hipotrofic perineal musculature, bilateral congenital clubfoot, hipospadic urethra, criptorquidy bilateral with nonpalpable testis and imperforate anus. A colostomy was constructed immediately after birth. The child underwent excision of perineal mass, bilateral orchidopexy, Duplay neourethroplasty and coloanal anastomosis at 3 months of age. The histopathological examination of the perineal mass revealed a hamartoma.

Rectal adenocarcinoma following imperforate anus: A rare case report

2020 ◽  
pp. 252-254
Author(s):  
Sarah Khan ◽  
Hina Khan ◽  
Jan Agha ◽  
Khursheed Samo ◽  
Mujeeb Abbasi ◽  
...  
Keyword(s):  
Case Report ◽  
Imperforate Anus ◽  
Rare Case ◽  
Rectal Adenocarcinoma ◽  
Rare Case Report

A rare case of a patient with aortic root aneurysm, bicuspid aortic valve, and Scimitar syndrome with anomalous venous return to the right superior pulmonary vein

2018 ◽  
Vol 28 (4) ◽  
pp. 595-597
Author(s):  
Kamran Ahmadov ◽  
Catherine A. Beigelman ◽  
Matthias Kirsch
Keyword(s):  
Aortic Valve ◽  
Pulmonary Vein ◽  
Bicuspid Aortic Valve ◽  
Aortic Root ◽  
Rare Case ◽  
Venous Return ◽  
Scimitar Syndrome ◽  
Aortic Root Aneurysm ◽  
Superior Pulmonary Vein ◽  
The Right

AbstractA rare case of Scimitar Syndrome with an abnormal drainage of the right lower pulmonary vein into the right superior pulmonary vein associated with aortic root aneurism and bicuspid aortic valve is reported.

scholarly journals A RARE CASE OF BIFID PENIS WITH IMPERFORATE ANUS

2014 ◽  
Vol 3 (48) ◽  
pp. 11614-11616
Author(s):  
Sharan Deshmukh ◽  
Shrikant S W ◽  
Sharangouda Patil ◽  
Harilal Naik M L
Keyword(s):  
Imperforate Anus ◽  
Rare Case

scholarly journals Complete Penoscrotal Transposition with Other Extragenital Anomalies in a Neonate Delivered at Term

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
Ali Mahamudu Ayamba ◽  
Raymond Saa-Eru Maalman ◽  
Yaw Otchere Donkor ◽  
John Noah Anyorigiya
Keyword(s):  
Imperforate Anus ◽  
Rare Case ◽  
Term Neonate ◽  
Cardiac Malformation ◽  
Facial Deformity ◽  
Antenatal Services ◽  
Penoscrotal Transposition

A complete penoscrotal transposition (CPST) is a very uncommon congenital maldevelopment that is always associated with other abnormal body variations (malformations). We report a rare case of a term neonate delivered with CPST, which had a flaccid penis and an intact scrotum with unilateral limb and digital deformity, imperforate anus, cardiac malformation a facial deformity. Neonate died two hours after delivery. The foetal abnormality was not detected through routine antenatal services received by the mother.

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