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 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.

Accessory Scrotum with Penoscrotal Transposition and Retrocerebellar Arachnoid Cyst: A Case Report

1997 ◽  
Vol 4 (3) ◽  
pp. 327-328 ◽  
Author(s):  
Gen Kawa ◽  
Shigenari Kawakita ◽  
Takashi Ohara ◽  
Tadashi Matsuda
Keyword(s):  
Case Report ◽  
Arachnoid Cyst ◽  
Accessory Scrotum ◽  
Penoscrotal Transposition

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 Surgical correction of ectopic penis and scrotum associated with bilateral orchidopexy

2017 ◽  
Vol 15 (2) ◽  
pp. 223-225 ◽  
Author(s):  
Daniel Santos Rocha Sobral Filho ◽  
Helder Damásio da Silva ◽  
Eulálio Damázio
Keyword(s):  
Male Patient ◽  
Surgical Approach ◽  
Rare Case ◽  
Skin Flap ◽  
The Self ◽  
Surgical Correction ◽  
Self Image ◽  
Bilateral Cryptorchidism ◽  
Perineal Skin ◽  
Penoscrotal Transposition

ABSTRACT Ectopic penis is usually associated with penoscrotal transposition, and it is rarely observed in isolation. We report a surgical approach for an extremely rare case. A 10-year-old male patient with bilateral cryptorchidism and ectopic penis and scrotum in perineal area, with no penoscrotal transposition, representing an association not yet described in literature. A previous orchiopexy failed due to ectopic scrotum. By means of an inverted Y incision, the penis was mobilized and a perineal skin flap in form of a testicular sac was prepared. Finally orchiopexy was performed. The surgery was essential to treat cryptorchidism and to improve the self-image of the patient.

scholarly journals Perineal Accessory Scrotum with Congenital Lipoma: A Rare Case Report

2012 ◽  
Vol 2012 ◽  
pp. 1-2 ◽  
Author(s):  
Souvik Chatterjee ◽  
Vishal Gajbhiye ◽  
Sasanka Nath ◽  
Dipak Ghosh ◽  
Sarbani Chattopadhyay ◽  
...  
Keyword(s):  
Rare Case ◽  
Normal Development ◽  
External Genitalia ◽  
Histological Findings ◽  
Tumor Mass ◽  
Accessory Scrotum ◽  
Rare Case Report ◽  
Male External Genitalia ◽  
The Right ◽  
Urological Anomaly

A case of accessory scrotum in a 1-year-old boy is reported because of its rarity. A boy presented with a tumor mass attached with scrotum-like skin on its tip in the right side of perineum between the scrotum and anus. Both testes had descended into the scrotum. There was no other urological anomaly. Histological findings of the tumor indicated perineal lipoma, and the scrotum-like portion accessory scrotum. An overview of sequences during the normal development of male external genitalia has been provided and the deranged mechanism resulting in this anomaly has been reviewed with hypothesis regarding etiology of accessory scrotum.

Identification of Pulmonary Deposits from a Sandpaper Worker: A Study by Electron Microscopy and X-Ray Microanalysis

1982 ◽  
Vol 40 ◽  
pp. 52-53
Author(s):  
S. K. Peng ◽  
M.A. Egy ◽  
J. K. Singh ◽  
M.B. Bishop
Keyword(s):  
Electron Microscopy ◽  
Environmental Pollution ◽  
Rare Case ◽  
Interstitial Fibrosis ◽  
X Ray ◽  
Documented Case ◽  
Etiologic Agents ◽  
Pulmonary Interstitial Fibrosis ◽  
Gold Miners ◽  
Pulmonary Changes

Electron microscopy and energy dispersive x-ray microanalysis (EDXA) are found to be very useful tools for identification of etiologic agents in pneumoconiosis or interstitial pulmonary disorders. Pulmonary interstitial fibrosis and granulomatosis are frequently associated with occupational and environmental pollution. Numerous reports of pneumoconiosis in various occupations such as coal and gold miners are presented in the literature. However, there is no known documented case of pulmonary changes in workers in the sandpaper industry. This study reports a rare case of pulmonary granulomatosis containing deposits from abrasives of sandpaper diagnosed by using EDXA.

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