scholarly journals Primary Chordoma of the Lateral Nasal Wall: Case Report and Review

2005 ◽  
Vol 84 (9) ◽  
pp. 593-595 ◽  
Author(s):  
Alastair Lynn-Macrae ◽  
G. Kenneth Haines ◽  
Kenneth W. Altman
Keyword(s):  
Case Report ◽  
Natural History ◽  
Nasal Cavity ◽  
Paranasal Sinuses ◽  
Treatment Options ◽  
The Other ◽  
Lateral Nasal Wall ◽  
Mechanical Obstruction ◽  
Tumor Mass ◽  
Nasal Cavities

Chordomas are malignant, nonepithelial neoplasms derived from notochordal tissue. A primary chordoma of the nasal cavities and paranasal sinuses is extremely rare compared with clival chordomas, which often present as nasal masses after spreading anteriorly. Only a few cases of primary chordoma of the nasal cavities and paranasal sinuses have been reported in the literature. We report a case of a primary chordoma of the lateral nasal wall. Pathologic diagnosis was obtained using an intranasal endoscopic excision. As in our patient, a primary chordoma of the nasal cavity or paranasal sinuses may present with symptoms related to mechanical obstruction secondary to the tumor mass. We summarize our case in the context of the other reported cases, and we discuss treatment options, natural history, and prognosis.

scholarly journals Verrucous Carcinoma of the Paranasal Sinuses: A Case Report

2010 ◽  
Vol 89 (7) ◽  
pp. E21-E23 ◽  
Author(s):  
Frederick L. Durden ◽  
Charles E. Moore ◽  
Susan Muller
Keyword(s):  
Squamous Cell Carcinoma ◽  
Case Report ◽  
Nasal Cavity ◽  
Paranasal Sinuses ◽  
Verrucous Carcinoma ◽  
Neck Region ◽  
Low Grade ◽  
Management Options ◽  
Head And Neck Region ◽  
Neoplastic Lesion

Verrucous carcinoma is a low-grade variant of squamous cell carcinoma reported to occur in all anatomic sites in the head and neck region, most commonly the oral cavity. The tumor grows locally invasive but is histologically benign and metastasizes rarely. To date, 22 cases of verrucous carcinoma involving the nasal cavity and/or the paranasal sinuses have been reported. We present a case of verrucous carcinoma involving the paranasal sinuses, nasal cavity, cranium, and orbit. This case highlights the difficulty of pathologic diagnosis and management options for a rare neoplastic lesion.

Malignant melanoma arising in the frontal sinuses

1997 ◽  
Vol 111 (4) ◽  
pp. 376-378 ◽  
Author(s):  
Samuel M. Jayaraj ◽  
Jonathan D. Hern ◽  
George Mochloulis ◽  
Graham C. Porter
Keyword(s):  
Malignant Melanoma ◽  
Natural History ◽  
Nasal Cavity ◽  
Paranasal Sinuses ◽  
Frontal Sinus ◽  
Poor Prognosis ◽  
Review Of The Literature ◽  
History Of ◽  
Frontal Sinuses ◽  
Sinonasal Malignant Melanoma

AbstractSinonasal malignant melanoma is rare and usually occurs in the nasal cavity. Presentation is often varied and occurs late in the natural history of the disease, resulting in a poor prognosis. A case is reported of a patient with malignant melanoma arising from the frontal sinus who presented with a forehead swelling and progressive confusion. A review of the literature on malignant melanoma in the nasal cavity and paranasal sinuses regarding its presentation, site of origin and principles of management is discussed.

Paranasal Sinus Mucoceles in Cystic Fibrosis

1993 ◽  
Vol 7 (1) ◽  
pp. 31-35 ◽  
Author(s):  
William E. Davis ◽  
Giulio J. Barbero ◽  
William R. LaMear ◽  
Jerry W. Templer ◽  
Peter Konig
Keyword(s):  
Cystic Fibrosis ◽  
Paranasal Sinus ◽  
Computerized Tomography ◽  
Paranasal Sinuses ◽  
Endoscopic Sinus Surgery ◽  
Functional Endoscopic Sinus Surgery ◽  
The Other ◽  
Sinus Surgery ◽  
Lateral Nasal Wall ◽  
Osteomeatal Complex

Six patients between the ages of 6 and 22 years old with cystic fibrosis were found to have mucoceles of the paranasal sinuses. Four were male and two were female. They experienced nasal obstruction, purulent rhinorrhea, and anosmia, but none had fever or pain. Nasal endoscopy and coronal computerized tomography scans revealed the lateral nasal wall to be displaced medially against the septum. Functional endoscopic sinus surgery revealed large cystic spaces filled with thick yellow-green mucus. Postoperatively most patients are able to smell and breathe through their noses. The mucocele probably begins as an obstructed anterior ethmoid cell, which then enlarges and obstructs the osteomeatal complex, which further impairs drainage of the other sinuses into this area.

scholarly journals Pediatric Isolated Sinonasal Schwannoma: A New Case Report and Literature Review

2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Xiao-Hui Ma ◽  
Hai-Chun Zhou ◽  
Can Lai ◽  
Kun Zhu ◽  
Xuan Jia
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Nasal Cavity ◽  
Maxillary Sinus ◽  
Paranasal Sinuses ◽  
Pediatric Patients ◽  
Age Group ◽  
Pediatric Age ◽  
Pediatric Age Group ◽  
Group A

Schwannomas of the paranasal sinus are uncommon. Less than 4% of schwannomas involve the nasal cavity and paranasal sinuses, even less in the pediatric age group. A case of schwannoma arising in maxillary sinus in a 2.5-year-old Chinese boy is reported. The basis for discussion of this case is the exceptional rarity of sinonasal schwannoma in pediatric patients.

scholarly journals Fibromatosis of the Nasal Cavity and Paranasal Sinuses Causing Visual Disturbance; Case Report

2003 ◽  
Vol 96 (9) ◽  
pp. 791-797
Author(s):  
Junichi Ito ◽  
Hitome Kobayashi ◽  
Harumi Suzaki ◽  
Miki Kushima
Keyword(s):  
Case Report ◽  
Nasal Cavity ◽  
Paranasal Sinuses ◽  
Visual Disturbance

scholarly journals Infection with Drechslera hawaiiensis. Case report and literature review

2017 ◽  
Vol 19 (2) ◽  
Author(s):  
Jaime Álvarez
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Nasal Cavity ◽  
Key Words ◽  
Rare Disease ◽  
Paranasal Sinuses ◽  
Chronic Infection ◽  
Hard Palate ◽  
Mycotic Infection ◽  
Infection Stage

This article reports an orofacial infection caused by Drechslera hawaiiensis that normally is mortal to the patient. The case was surgically treated in Cali - Colombia in 1984 by teeth removal, and osteototomy of affected bone in the hard palate and the base of the vomer bone. Twenty years later the patient resulted infected by Dreschslera curvularia but survived both infections. A literature review (Pubmed - 2011) showed that only another case report by Drechslera hawaiiensis the patient survived. This other case was reported in the Anderson Hospital Institute in 1984. It is unknown if there is a chronic infection stage and the transmission mode of this pathogen. In patients with chronic symptoms affecting the paranasal sinuses and nasal cavity it is possible to suspect this rare disease. Key words: Oral facial infection, mycotic infection, Drechslera hawaiiensis.

scholarly journals Bilateral Total Aplasia of Paranasal Sinuses: A Rare Case Report

2015 ◽  
Vol 8 (3) ◽  
pp. 124-126
Author(s):  
Ankita Joshi ◽  
Chinmay Sundarray ◽  
Krishna Arpita Sahoo
Keyword(s):  
Case Report ◽  
Paranasal Sinus ◽  
Paranasal Sinuses ◽  
Rare Case ◽  
The Other ◽  
High Rate ◽  
Unknown Etiology ◽  
Structural Variations ◽  
The Third ◽  
Rare Case Report

ABSTRACT Paranasal sinus anatomical anomalies with unknown etiology are common. Paranasal sinus-related diseases are associated with so high rate of morbidities, it becomes essential to identify the structure and pathophysiology of the paranasal sinuses. Computed tomography (CT) is a valuable tool in displaying its anatomy, any anatomic variations and diseases. As paranasal sinus development is a complex and long-lasting process, there are great structural variations between individuals. Maxillary and/or frontal sinus aplasia or hypoplasia are more common than the other types. Several degrees and combinations of aplasias and hypoplasias have been reported; however, there is only two case of total paranasal sinus aplasia in the literature. Here, we present the third case of total paranasal sinus aplasia, and the first ever case reported from India. How to cite this article Joshi A, Sundarray C, Sahoo KA. Bilateral Total Aplasia of Paranasal Sinuses: A Rare Case Report. Clin Rhinol An Int J 2015;8(3):124-126.

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