scholarly journals A Rare Case of Multiple Calcifications and Vascular Malformation Within the Parenchyma of the Parotid Salivary Gland Coinciding With an Intracranial Meningioma

Author(s):  
Mahmoud M. Bakr ◽  
Pak Poon ◽  
Sylvana Parkinson ◽  
Nabil Khzam
1998 ◽  
Vol 112 (8) ◽  
pp. 784-785 ◽  
Author(s):  
W. K. Kesse ◽  
Z. P. Shehab ◽  
R. Courteney-Harris

AbstractWe present a rare case of a giant intra-parotid calculus in a 64-year-old man with recurrent parotitis. The literature is also reviewed.


2018 ◽  
Vol 43 (1) ◽  
pp. 22-26
Author(s):  
Sally S. Sakr ◽  
Gehan A. Elba ◽  
Samia S. Omar ◽  
Sahar S. Karam

2021 ◽  
pp. 1-4
Author(s):  
Serhat Yarar ◽  
Ilker Uyar ◽  
Mehmet Emin Cem Yildirim ◽  
Mehmet Dadacı ◽  
Bilsev Ince

Primary intraosseous vascular malformations (PIVMs) are rare intraosseous lesions, accounting for approximately 0.5–1% of all intraosseous tumours. In this case report, we aimed to present a rare case of intraosseous vascular malformation causing a large lytic area in the parietal bone. A 25-year-old male patient was admitted to the clinic with a mass on the parietal bone. On physical examination, it was observed that the hair density on the mass was decreased, the mass had a soft consistency, and there was no pain on palpation. The patient was operated under local anaesthesia with a provisional diagnosis of a trichilemmal cyst. However, intraoperative diagnosis was a vascular malformation. There was a 3-cm full-thickness defect on the parietal bone caused by the lesion. The mass was excised completely while preserving the integrity of the dura. The resulting defect was reconstructed with bilateral rotation advancement flaps. The calvarial defect was not reconstructed due to equipment inadequacy. No complications were encountered in the postoperative period. Ninety-three PIVM cases have been reported in the skull since 1845. In very few of these cases, the mass is located in the parietal bone. The pathogenesis of PIVMs is not completely understood. The definitive diagnosis is made by histopathological examination. The therapeutic gold standard is surgery. Surgeons should keep in mind that radiological examination before the operation could prevent undesirable complications.


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.


1997 ◽  
Vol 78 (2) ◽  
pp. 133-133
Author(s):  
H. S. Khaertynov

Diagnosis of epidemic parotitis (EP) in typical cases of the disease is not difficult, which is explained by the salivary gland involvement characteristic of this infection. It is known that in the pathological process of ES, in addition to salivary glands, pancreas, testicles, etc. can be involved. At the same time, different authors assess the possibility of their isolated involvement ambiguously: either pancreatitis or orchitis are the only manifestations of mumps infection, or involvement of salivary glands in the pathological process is a mandatory component of ES and, therefore, involvement of other glands cannot be isolated.


2018 ◽  
Vol 81 (2) ◽  
pp. 182-183
Author(s):  
Harish Kumar ◽  
Amol Dilip Amonkar ◽  
Rakesh Ramesh ◽  
G. C. Raghunandan ◽  
Bharadhwaj Ravindhran ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document