scholarly journals Concomitant Anterior Shoulder Dislocation and Ipsilateral Humeral Pallet Fracture in the Athlete: Case Report and Review of the Literature

2020 ◽  
Vol 3 (2) ◽  
pp. 74-78
Author(s):  
Naoufal Elghoul ◽  
Ismail Elantri ◽  
Amine Elghazoui ◽  
Mohammed Benchakroun ◽  
Abdeloihab Jaafar

To the best of our knowledge, the case presented here is among the rare cases of simultaneous shoulder dislocation and ipsilateral pallet humeral fracture, and we discuss its mechanism and best management. We report a case of a 26-year-old male patient with a history of dislocation of the right shoulder 2 months prior to trauma, managed conservatively with a good outcome. The patient fell from a height of 2 m, which caused concomitant shoulder dislocation and ipsilateral humeral fracture, prompting him to undergo surgery. First, the shoulder dislocation was reduced, and second, a V-shaped olecranon osteotomy was performed. The fracture was then fixed using two compressing plates followed by adequate rehabilitation, which led to a good outcome. This rare combination, if it occurs, requires urgent management to save the functional prognosis of the limb.

2019 ◽  
Vol 2019 ◽  
pp. 1-4
Author(s):  
Angelo V. Vasiliadis ◽  
Christos Kalitsis ◽  
George Biniaris ◽  
Antonios Saridis

A 36-year-old woman presented with anterior shoulder dislocation as a result of breaststroke swimming training. She complained of pain and restriction of movement. A radiograph revealed the shoulder was dislocated, and the patient was treated successfully with closed reduction. The mechanism of injury seemed to be a relation between the initial pull phase of breaststroke technique and the weakest position of the shoulder in extension and external rotation. In our experience, if a patient has a history including a shoulder dislocation, this needs to be considered carefully before incorporating aquatic therapy into the rehabilitation program. Attention must also be given to the crucial timing of initiating swimming training.


2014 ◽  
Vol 2014 ◽  
pp. 1-3 ◽  
Author(s):  
K. N. Srivastava ◽  
Amit Agarwal

The term gossypiboma is used to describe a retained surgical sponge after operation. It is a rare but serious complication which is seldom reported because of the medicolegal implications. Gossypiboma usually has varied and vague presentation and is also difficult to detect on radiological investigations. It can even remain silent and present years after the operation. We report a case of a 38-year-old lady who presented with vague pain and chronic lump in the right iliac fossa region. She had a history of cesarean section 4 years ago. Radiological investigations were inconclusive in detecting the retained sponge. A working diagnosis of mesenteric cyst was made and an exploratory laparotomy was done where she was found to have a large gossypiboma densely adhered to the small bowel and surrounding structures. Though rare, gossypiboma should be kept in mind as a differential diagnosis in postoperative cases presenting as vague pain or chronic lump even years after the operation.


VASA ◽  
2011 ◽  
Vol 40 (3) ◽  
pp. 251-255 ◽  
Author(s):  
Gruber-Szydlo ◽  
Poreba ◽  
Belowska-Bien ◽  
Derkacz ◽  
Badowski ◽  
...  

Popliteal artery thrombosis may present as a complication of an osteochondroma located in the vicinity of the knee joint. This is a case report of a 26-year-old man with symptoms of the right lower extremity ischaemia without a previous history of vascular disease or trauma. Plain radiography, magnetic resonance angiography and Doppler ultrasonography documented the presence of an osteochondrous structure of the proximal tibial metaphysis, which displaced and compressed the popliteal artery, causing its occlusion due to intraluminal thrombosis..The patient was operated and histopathological examination confirmed the diagnosis of osteochondroma.


2015 ◽  
Vol 2015 ◽  
pp. 1-4 ◽  
Author(s):  
Hae Won Jung ◽  
Chong Rae Cho ◽  
Ji Yoon Ryoo ◽  
Hyun Kyo Lee ◽  
So Young Ha ◽  
...  

Actinomyces meyeriis an uncommon cause of human actinomycosis. Here, we report a rare case of empyema caused byA. meyeri. A 49-year-old male presented with a history of 10 days of dyspnea and chest pain. A large amount of loculated pleural effusion was present on the right side and multiple lung nodules were documented on radiological studies. A chest tube was inserted and purulent pleural fluid was drained.A. meyeriwas isolated in anaerobic cultures of the pleural fluid. The infection was alleviated in response to treatment with intravenous penicillin G (20 million IU daily) and oral amoxicillin (500 mg every 8 hours) for 4 months, demonstrating that short-term antibiotic treatment was effective.


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