scholarly journals Pneumobilia: A case report and literature review on its surgical approaches

2013 ◽  
Vol 5 (1) ◽  
pp. 27 ◽  
Author(s):  
CheeSiong Wong ◽  
JamesMaurice Crotty ◽  
SyedAltaf Naqvi
2014 ◽  
Vol 7 (3) ◽  
pp. 621-624
Author(s):  
Jennifer Garland ◽  
Elizabeth O'Leary ◽  
Joseph Haggerty ◽  
Thomas G. Zorc

Hand Surgery ◽  
2013 ◽  
Vol 18 (02) ◽  
pp. 267-272 ◽  
Author(s):  
Steven B. Albright ◽  
Erik M. Wolfswinkel ◽  
Kevin J. Caceres ◽  
William M. Weathers ◽  
Larry H. Hollier

Macrodystrophia lipomatosa is a rare, non-hereditary form of congenital local gigantism characterised by enlargement and hypertrophy of all mesenchymal tissue components with a disproportionate increase in adipose tissue. This form of macrodactyly has been reported in association with other anomalies including polydactyly, brachydactyly, syndactyly, and symphalangism. We describe a previously unreported case of bilateral upper extremity macrodystrophia lipomatosa with syndactyly in a 23-month-old boy. In this report, we emphasise the importance of establishing a diagnosis with imaging and review the described surgical approaches to treating this difficult condition.


2019 ◽  
Vol 2019 (11) ◽  
Author(s):  
Amaar Aamery ◽  
Ojas Pujji ◽  
Muhammad Mirza

Abstract We present a patient who was managed surgically for cholecystogastric fistula. The patient was presented with nonspecific symptoms (upper abdominal pain, belching) and, after being investigated, was proceeded for laparoscopic cholecystectomy for gallbladder stones. Unexpectedly, intraoperative, she was found to have cholecystogastric fistula, which was operated with open single-stage approach. We highlight the incidence of these cases, the difficult preoperative clinical presentation and possible diagnostic imaging; explain further about the different surgical approaches to manage these cases and finally review the literature regarding the presentation and the management of bilioenteric fistulas.


2009 ◽  
Author(s):  
C. L. Khoo ◽  
L. Regina ◽  
S. R. K. Naik ◽  
S. Kang

2017 ◽  
Author(s):  
T Stopp ◽  
M Feichtinger ◽  
W Eppel ◽  
T Stulnig ◽  
P Husslein ◽  
...  

1998 ◽  
Vol 37 (04) ◽  
pp. 141-145
Author(s):  
F. J. C. Pallarés ◽  
A. R. Bartual ◽  
Susana Tenes Rodrigo ◽  
F. J. Ampudia-Blasco ◽  
C. R. de Ávila y Ávalos ◽  
...  

SummaryA case of a 49-year-old man suffering from bilateral adrenocortical carcinoma with local and secondary rapid progression is reported. The results of adrenocortical scintigraphy (NP 59) and histological findings allowed the diagnosis. This case report and a literature review showed the importance of using adrenocortical scintigraphy as a complementary imaging procedure of CT or MR images.


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