scholarly journals Bilateral cystic lesions of the chest wall: Presentation of scapulothoracic bursitis

2019 ◽  
Vol 54 ◽  
pp. 116-119
Author(s):  
Anton Dzian ◽  
Michaela Skaličanová ◽  
Ivan Fučela ◽  
Marek Malík ◽  
Jozef Mičák
2010 ◽  
Vol 17 (S3) ◽  
pp. 321-324 ◽  
Author(s):  
Cristiano Boneti ◽  
Candy Arentz ◽  
V. Suzanne Klimberg

2001 ◽  
Vol 8 (3) ◽  
pp. 187-190 ◽  
Author(s):  
Tomas Pulido-Zamudio ◽  
William Orr ◽  
Morley Lertzman

A rare case of cystic angiomatosis of the bone (CAB) manifesting as bilateral intrathoracic masses is described. In 1996, a 47-year-old woman was referred to the chest clinic at St Boniface Hospital for evaluation of chronic cough, and her chest radiograph showed large, bilateral pleural-based intrathoracic masses. Ten years before, she had been diagnosed with CAB following bone biopsies of her hip and knee. Computed tomography revealed two chest wall masses with internal septations of bone. CAB is a rare, multicentric disease characterized by involvement of the vascular and lymphatic systems, producing diffuse cystic lesions in the skeleton. Although the ribs are frequently involved, the presentation with intrathoracic masses is uncommon.


Author(s):  
KR Chatura ◽  
CN Aarthy

Scapulothoracic bursitis is a rare disease which is caused from the inflammation of the bursa secondary to trauma or its overuse, owing to sports activities or work. It usually presents with pain, swelling without redness at the scapulothoracic interface. A 22-year-old male presented to the surgeon with the swelling in the left scapular region following a history of trauma. Ultrasound (USG) showed a large loculated fluid collection with internal debris outside the muscular plane. With the clinical diagnosis of haematoma surgical resection was done. It showed a cystic swelling containing haemorrhagic fluid attached to the chest wall. The specimen was sent for histopathological correlation. The thickened cystic structure had numerous rice grain like loose bodies on the inner surface. Microscopy showed fibrocollageneous wall with congested blood vessels, granulation tissue, fibrinoid bodies and macrophages. This case report describes a cystic lesion in left scapular region diagnosed as a case of scapulothoracic bursitis based on pathological correlation. Surgery was an effective treatment for this case with no complication and recurrence on follow-up.


2005 ◽  
Vol 24 (10) ◽  
pp. 1437-1440 ◽  
Author(s):  
Chung-Cheng Huang ◽  
Sheung-Fat Ko ◽  
Shu-Hang Ng ◽  
Chih-Che Lin ◽  
Hsuan-Ying Huang ◽  
...  

2021 ◽  
pp. 101537
Author(s):  
Norichika Iga ◽  
Yasuko Fuchimoto ◽  
Taisaku Koyanagi ◽  
Daisuke Mizuno ◽  
Hideyuki Nishi

2001 ◽  
Vol 120 (5) ◽  
pp. A764-A764
Author(s):  
M DELHAYE ◽  
C WINANT ◽  
D DEGRE ◽  
B GULBIS ◽  
C GERVY ◽  
...  

2014 ◽  
Vol 62 (S 01) ◽  
Author(s):  
L. Tewarie ◽  
A.K. Moza ◽  
A. Goetzenich ◽  
R. Zayat ◽  
R. Autschbach

Author(s):  
YRE Chean ◽  
NA Gazali ◽  
SA Uppaluri
Keyword(s):  

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