scholarly journals Huge Capillary Haemangioma of the Nasal Fossae

2019 ◽  
Vol 7 (2) ◽  
Author(s):  
Khdim M ◽  
Choukry K ◽  
Chaouki A ◽  
Abada R ◽  
Rouadi S ◽  
...  
1997 ◽  
Vol 111 (6) ◽  
pp. 588-589 ◽  
Author(s):  
R. G. M. Hughes ◽  
J. Oates

AbstractHaemangioma of the parotid gland is a well-described condition that accounts for 50 per cent of parotid tumours presenting during the first year of life. Parotid haemangiomas in adults are much rarer and until now only the cavernous variety have been reported. We report a case of a capillary haemangioma in an adult and discuss the literature.


1981 ◽  
Vol 53 (3) ◽  
pp. 277-277 ◽  
Author(s):  
S. K. SHARMA ◽  
M. J. REDDY ◽  
V. V. JOSHI ◽  
B. C. BAPNA

2009 ◽  
Vol 88 (4) ◽  
pp. e137-e138 ◽  
Author(s):  
Thomas Ach ◽  
Dorothea Thiemeyer ◽  
Alexandra Eva Hoeh ◽  
Karen Beate Schaal ◽  
Stefan Dithmar

2014 ◽  
Vol 2014 (oct10 1) ◽  
pp. bcr2014207196-bcr2014207196 ◽  
Author(s):  
D. R. Nayak ◽  
A. M. Bhandarkar ◽  
A. Shivamurthy ◽  
J. Joy

2020 ◽  
Vol 24 (3) ◽  
pp. 132
Author(s):  
U. G. Kolbik ◽  
A. V. Gorustovich ◽  
Yu. I. Linnik ◽  
M. M. Shved ◽  
V. V. Drozdovskaya ◽  
...  

<p>This publication presents the clinical observation in a paediatric patient with haemangioma of the left stomach. The effectiveness of surgical treatment of this disease is also noted. We assess the challenges in diagnosis and the choice of treatment of this pathology in children and the effectiveness of surgical treatment disease.<br />Primary cardiac tumours are rare; vascular tumours and haemangiomas are rarer. The clinical picture of heart haemangioma is non-specific and varies as per its location and size. Echocardiography is the main diagnostic method for this disease. However, in most cases of preoperative diagnostic examination, the pre-surgery diagnosis is not confirmed. The final diagnosis of capillary haemangioma is established following immunohistochemical staining of the surgical material. Thus far, owing to the rare occurrence, a generally accepted tactic for the treatment of such patients with vascular heart tumours has not been developed.<br />This clinical case describes our experience of treating a rare pathology in children with unusual localisation as well as the rapid successful surgical removal of the tumour without complications and with a favourable post-surgery recovery period.</p><p>Received 14 May 2020. Revised 15 June 2020. Accepted 26 June 2020.</p><p><strong>Funding:</strong> The study did not have sponsorship.</p><p><strong>Conflict of interest:</strong> Authors declare no conflict of interest.</p><p><strong>Author contributions</strong> <br />Literature review: U.G. Kolbik, A.V. Gorustovich, Y.I. Linnik<br />Illustrations: U.G. Kolbik, I.V. Sakharov, V.V. Drozdovskaya <br />Drafting the article: U.G. Kolbik, A.V. Gorustovich, I.V. Sakharov<br />Critical revision of the article: I.V. Sakharov, M.M. Shved, Yu.I. Linnik<br />Surgical treatment: A.V. Gorustovich, M.M. Shved, U.G. Kolbik<br />Final approval of the version to be published: U.G. Kolbik, A.V. Gorustovich, Yu.I. Linnik, M.M. Shved, V.V. Drozdovskaya, <br />I.V. Sakharov, K.V. Drozdovski</p>


2005 ◽  
Vol 21 (4) ◽  
pp. 265-271 ◽  
Author(s):  
Anne Le Bihannic ◽  
Charlotte Michot ◽  
Anne Heckly ◽  
Philip Loget ◽  
Alain Beucher ◽  
...  

1999 ◽  
Vol 41 (5) ◽  
pp. 369-375 ◽  
Author(s):  
P. Tortori-Donati ◽  
M. P. Fondelli ◽  
A. Rossi ◽  
G. L. Bava

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