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.

scholarly journals A Rare Case of Omphalocele, Exstrophy of Bladder, Imperforate Anus and Spinal Defect Complex with Genital Anomalies in a Term Neonate

2021 ◽  
Vol 18 (3) ◽  
Author(s):  
Deepali Ambike ◽  
Abhijeet Byale ◽  
Rijwana Sayyad ◽  
Vinit Rathod ◽  
Komal Bijarniya
Keyword(s):  
Imperforate Anus ◽  
Rare Case ◽  
Term Neonate ◽  
Defect Complex

scholarly journals A Case of del(13)(q22) with Multiple Major Congenital Anomalies, Imperforate Anus and Penoscrotal Transposition

2001 ◽  
Vol 42 (5) ◽  
pp. 558 ◽  
Author(s):  
Jae Lim Chung ◽  
Jong Rak Choi ◽  
Min Soo Park ◽  
Seung Hun Choi
Keyword(s):  
Imperforate Anus ◽  
Congenital Anomalies ◽  
Penoscrotal Transposition

scholarly journals Uremic lion face syndrome

2019 ◽  
Vol 41 (2) ◽  
pp. 304-305
Author(s):  
Joana Gameiro ◽  
Inês Duarte ◽  
Cristina Outerelo ◽  
José António Lopes
Keyword(s):  
End Stage Renal Disease ◽  
Rare Case ◽  
Bone Fractures ◽  
Early Recognition ◽  
Rare Complication ◽  
Facial Deformity ◽  
Mineral Bone Disorder ◽  
Bone Disorder ◽  
Stage Renal Disease ◽  
End Stage

Abstract Mineral bone disorder is a common feature of chronic kidney disease. Lion face syndrome is rare complication of severe hyperparathyroidism in end-stage renal disease patients, which has been less commonly reported due to dialysis and medical treatment advances in the last decade. The early recognition of the characteristic facial deformity is crucial to prompt management and prevent severe disfigurement. The authors present a rare case of severe hyperparathyroidism presenting with lion face syndrome and bone fractures.

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.

Co-occurence of perineal accessory scrotum and penoscrotal transposition with anal atresia

2020 ◽  
Vol 1 (3) ◽  
pp. 100-102
Author(s):  
Gunay Ekberli ◽  
Ufuk Ates ◽  
Firat Sertturk ◽  
Anar Jafarov ◽  
Ahmet Murat Cakmak
Keyword(s):  
Rare Case ◽  
Anal Atresia ◽  
Anorectal Anomaly ◽  
Accessory Scrotum ◽  
Penoscrotal Transposition

A rare case of accessory scrotum and penoscrotal transposition with co-occuring anal atresia is reported because of it’s infrequency. Diagnosis, management and result of one-day-old newborn with high anorectal anomaly and perineal lipoma bearing accessory scrotum aimed to  be  presented in the light of literature screening.

scholarly journals Surgical Management of a Rare Case of Congenital DoubleUpper Lip

2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
Adit Srivastava ◽  
Ajit Parihar ◽  
Romesh Soni ◽  
M. C. Shashikanth ◽  
T. P. Chaturvedi
Keyword(s):  
Surgical Management ◽  
Rare Case ◽  
Developmental Anomaly ◽  
Upper Lip ◽  
Facial Deformity ◽  
Cosmetic Reason

Congenital double lip is a rare developmental anomaly which usually involves the upper lip. It may occur in isolation or as a part of Ascher's syndrome. The occurrence of double lip may result in facial deformity especially when patient attempts to talk, smile, or even try to show the teeth. It affects esthetics and also interferes with speech and mastication. Although surgery may be undertaken to facilitate speech and mastication, majority of cases are operated for cosmetic reasons. A case of congenital double upper lip which was surgically treated for cosmetic reason is reported.

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