scholarly journals Infantile parotid haemangioma: a report of three cases

2021 ◽  
Vol 17 (3) ◽  
pp. 279-283
Author(s):  
Nur Izzaty Nadia Mohd Ariffin ◽  
◽  
Jeyasakthy Saniasiaya ◽  
Shamina Sara Moses ◽  
Norhaslinda Abdul Gani ◽  
...  

Aim of this case: To highlight the presentation of rapidly enlarging parotid haemangioma in three children who were all successfully managed with oral propranolol. Case report: Parotid haemangioma in infancy, albeit rare, has been vastly reported due to it being the most common tumour of the salivary gland in infants. Despite that, the presence of a rapidly enlarging tumour in “the little ones” may be daunting, leading to countless unwarranted procedures by attending physicians. Herein, we present three cases of infantile rapidly tumefying parotid lesions which were diagnosed clinically with the support of imaging, and successfully managed by promptly initiating oral propranolol. Conclusion: Although several recent reports have been reviewed, the challenges in diagnosis and management of the condition need to be individualised.

2019 ◽  
Vol 2 ◽  
pp. 5
Author(s):  
Kevin Kapcio ◽  
Kamila Skalski ◽  
Vikram Dogra

Birt-Hogg-Dubé (BHD) syndrome is a rare hereditary disorder associated with autosomal dominant hereditary epithelial carcinomas, in which patients have an increased incidence of renal cell carcinomas, scattered hamartomas, pulmonary cysts, and spontaneous pneumothoraces. Other less common findings include lipomas, parathyroid adenomas, salivary gland tumors, and colonic polyps/tumors. Early diagnosis of BHD can help establish renal screening and reduce mortality by early detection and more effective treatment of renal cell carcinoma. This case report describes the sonographic features of salivary gland oncocytomas found in a patient with BHD.


2017 ◽  
Vol 4 (2) ◽  
pp. 42-45
Author(s):  
Saravana Karthikeyan Balasubramanian ◽  
◽  
Divya Vinayachandran ◽  
Sankara Aravind Warrier ◽  
Ananthi Sankar ◽  
...  

Author(s):  
B. Ouafidi ◽  
H. Kiram ◽  
H. Benaguida ◽  
A. Lamrissi ◽  
K. Fichtali ◽  
...  

2014 ◽  
Vol 9 (2) ◽  
pp. 681-684 ◽  
Author(s):  
YONGCHENG CAO ◽  
MING ZHU ◽  
RUIQI MAO ◽  
RUIXUE CAO ◽  
GUOLI YU ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-5
Author(s):  
N. Srikant ◽  
Shweta Yellapurkar ◽  
Karen Boaz ◽  
Mohan Baliga ◽  
Nidhi Manaktala ◽  
...  

Polycystic (dysgenetic) disease of the salivary glands is a rare entity that has only recently been described in the literature. The disease is more commonly seen in females and majority of the cases have presented as bilateral parotid gland swellings. This case presenting in a 21-year-old male is the first of this unusual entity involving solely the minor salivary gland on the lower lip. This case report highlights the importance for the clinician to be aware of this differential diagnosis, when treating an innocuous lesion like a mucocele.


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