Simultaneous antrochoanal and sphenochoanal polyps: a rare clinical entity

2005 ◽  
Vol 119 (2) ◽  
pp. 152-154 ◽  
Author(s):  
Muge Ozcan ◽  
Samet Ozlugedik ◽  
Aykut Ikinciogullari

Choanal polyps almost always appear as solitary growths and most commonly arise from the maxillary sinus. Sphenochoanal and ethmoidochoanal polyps are extremely rare. Co-existence of more than one choanal polyp is even more infrequent. We present a patient with an antrochoanal and an accompanying sphenochoanal polyp for the first time in the literature. We discuss the clinical presentation, pathogenesis and surgical management of this rare clinical entity.

Author(s):  
Kulwinder Singh Sandhu ◽  
Shiffali . ◽  
Jagdeepak Singh

<p class="abstract">Choanal polyp arising from the sphenoid sinus and presenting at the choana are rare. These are known as sphenochoanal polyp. We present a case of sphenochoanal polyp and its clinical features and surgical management is discussed. Our aim in this case was to properly delineate the origin of the polyp and differentiate it from other lesions such as the antrochoanal polyp and meningocele, followed by meticulous endoscopic excision of the polyp. Radiological investigations include a CT scan paranasal sinuses or a MRI diagnostic nasal endoscopy will confirm the diagnosis. Once the diagnosis is made surgical removal must be done<span lang="EN-IN">.</span></p>


2016 ◽  
Vol 07 (02) ◽  
pp. 302-304 ◽  
Author(s):  
Anil Kumar Sharma ◽  
Amey R. Savardekar ◽  
B. N. Nandeesh ◽  
A. Arivazhagan ◽  
Malla Bhaskar Rao

ABSTRACTIntraparenchymal schwannomas arising in the brainstem are very rare, and only eight cases have been reported in literature till now. We report an intraparenchymal brainstem schwannoma presenting with the classical clinical presentation of an intrinsic brainstem lesion, and discuss its clinicoradiological characteristics and histological origins. We highlight the importance of an intraoperative frozen section diagnosis in such cases. Intraoperative tissue diagnosis significantly may alter the surgical strategy, which should be aimed at near total intracapsular decompression of the schwannoma.


2013 ◽  
Vol 14 (1) ◽  
pp. 47-50 ◽  
Author(s):  
Jihène Marrakchi ◽  
Houda Chahed ◽  
Rym Zainine ◽  
Habiba Mizouni ◽  
Semia Sahtout ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Anna Scavuzzo ◽  
Zael Arturo Santana Ríos ◽  
Nancy Reynoso Noverón ◽  
Miguel Angel Jimenez Ríos

Growing teratoma syndrome (GTS) is a rare clinical entity, which presents with enlarging teratomas masses of the retroperitoneum or other locations, occurring during or after systemic chemotherapy for the treatment of nonseminomatous germ cell of the testis (NSGCT), with normalised tumour markers. Awareness of this syndrome is necessary in order to prevent unnecessary chemotherapy and allow optimal management. Prognosis is excellent after the excision of these tumors, but surgery has to be as complete as possible. Surgical resection of bulky GTS lesions is technically challenging; intraoperative complications may occur; that is, why the treatment must not be delayed. Our experience in the surgical management of these lesions is reviewed in the following work.


2001 ◽  
Vol 115 (6) ◽  
pp. 497-499 ◽  
Author(s):  
Maheshwar ◽  
Harris ◽  
Al-Mokhthar ◽  
Evans

Pott’s puffy tumour is a rare clinical entity in this era of antibiotics. It is usually seen as a complication of frontal sinusitis. This is the first report of Pott’s puffy tumour presenting as a complication of maxillary sinusitis. This is also the first reported case of Pott’s puffy tumour treated with debridement and gentamicin beads. We discuss the clinical presentation and successful treatment of this rare disease.


2020 ◽  
Vol 86 (6) ◽  
pp. 820-823 ◽  
Author(s):  
Dongwon Kim ◽  
Kyung-Un Choi ◽  
Hak-Jin Kim ◽  
Kyu-Sup Cho

2007 ◽  
Vol 59 (1) ◽  
pp. 56-57
Author(s):  
S. S. Bist ◽  
Rajesh Kumar ◽  
Saurabh Varshney ◽  
Manisha Bisht

Author(s):  
Suha Ertugrul ◽  
Serdar Ensari

Solitary, benign soft tissue masses starting at the nasal cavity and extending to the nasopharynx are termed choanal polyps. They most frequently originate in the maxillary sinus and are termed antra-choanal polyp. Cases of CP originating in the upper concha are rather rare and only one case has been reported in literature in the English language to the best of our knowledge. This paper discusses a CP case originating in the upper concha, which was treated by endoscopic surgical technique, in the light of its clinical presentation and radiological findings. 


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