Calcific Myonecrosis of the Upper Extremity: Case Report

2012 ◽  
Vol 37 (1) ◽  
pp. 130-133 ◽  
Author(s):  
Sara D. Rynders ◽  
Yaw D. Boachie-Adjei ◽  
Cree M. Gaskin ◽  
A. Bobby Chhabra
2020 ◽  
Vol 81 ◽  
pp. 8
Author(s):  
I. Akgün ◽  
E.E. Avcı ◽  
E. Timurtaş ◽  
İ. Demirbüken ◽  
M.G. Polat

2003 ◽  
Vol 84 (3) ◽  
pp. 458-459 ◽  
Author(s):  
Mrugeshkumar K. Shah ◽  
Randie M. Black-Schaffer

2011 ◽  
Vol 64 (1) ◽  
pp. 71
Author(s):  
Hee Jung Suh ◽  
Wan Tae Kim ◽  
Min Jeong Seo ◽  
Yoon Jung Kim

2020 ◽  
Vol 12 (4) ◽  
pp. 337-340
Author(s):  
Niki Tadayon ◽  
Sina Zarrintan ◽  
Seyed Mohammad Reza Kalantar-Motamedi

We report a case of 66-year-old woman with true aneurysm of the right brachial artery. She presented with acute upper extremity ischemia. The hand was cold and parenthesized and distal pulses were absent. CT angiography (CTA) revealed a 20*25 mm true brachial artery aneurysm. The aneurysm was thrombosed without distal run-off. We excised the aneurysm and reestablished the arterial flow by a reverse saphenous interposition graft. The postoperative course was uneventful.


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.


2016 ◽  
Vol 17 ◽  
pp. 6-11 ◽  
Author(s):  
Raid A. Abutalib ◽  
Khalid I. Khoshhal

2019 ◽  
Vol 7 ◽  
pp. 2050313X1882335
Author(s):  
Dante Palumbo ◽  
Aden Miller ◽  
Elliott Smock ◽  
Scott Farner

Muscle herniation in the upper extremity is a rare but recognized phenomenon with a paucity of reports in the current literature. In the majority of cases, the herniation is secondary to trauma, with some of the cases due to muscle hypertrophy and increased intra-compartmental pressure from the forced exertion. Treatment for this condition ranges from nonsurgical, repair, or reconstruction to fasciotomy of the flexor carpi ulnaris fascia. Here, we present a case of flexor carpi ulnaris herniation after an open in situ cubital tunnel release in a 57-year-old male 6 years after initial surgery. The patient’s symptoms did not improve with conservative management, and the patient subsequently underwent endoscopic fasciotomy with resolution of his symptoms and maintenance of his wrist and grip strength. The rationale for the treatment chosen is discussed.


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