scholarly journals Inflammatory Myofibroblastic Tumor of Nasal Septum after Septoplasty: A Case Report

2020 ◽  
Vol 27 (1) ◽  
pp. 67-71
Author(s):  
Jeonghyun Oh ◽  
Ji Yun Choi
Keyword(s):  
Case Report ◽  
Nasal Cavity ◽  
Nasal Septum ◽  
Inflammatory Myofibroblastic Tumor ◽  
Malignant Tumors ◽  
Rare Entity ◽  
Histologic Pattern ◽  
Inflammatory Infiltrates ◽  
Uncommon Tumor

Inflammatory myofibroblastic tumor is an uncommon tumor composed of myoblasts and various types of inflammatory infiltrates. Inflammatory myofibroblastic tumor is most common in the lungs but can be rarely found in the nasal cavity. Inflammatory myofibroblastic tumor is a rare entity that represents a diverse histologic pattern that can mimic malignant tumors. We report a case of inflammatory myofibroblastic tumor of the nasal septum in a 45-year-old man who presented with a tumor-like lesion of the nasal septum after two rounds of septoplasty.

scholarly journals IMFT of the sigmoid colon: a case report

2019 ◽  
Vol 2019 (11) ◽  
Author(s):  
Narendra Pandit ◽  
Tek Narayan Yadav ◽  
Deepa Shrestha ◽  
Purbesh Adhikari ◽  
Laligen Awale
Keyword(s):  
Case Report ◽  
Sigmoid Colon ◽  
Inflammatory Myofibroblastic Tumor ◽  
Stromal Tumor ◽  
Rare Entity ◽  
Radiological Findings ◽  
Bleeding Per Rectum ◽  
Uncommon Case ◽  
Inflammatory Infiltrates

Abstract Inflammatory myofibroblastic tumor (IMFT) of the colon is a very rare entity, characterized by proliferation of myofibroblast cells admixed with inflammatory infiltrates. The entity was first described in the late 1990s, and since then less than 30 cases have been described. It frequently mimics other neoplasm of the colon, such as adenocarcinoma, lymphoma and stromal tumor, and is very difficult to clinch the diagnosis preoperatively based on the clinical and radiological findings. Here, we discuss an uncommon case of sigmoid IMFT in a 35-year old male, presenting with bleeding per rectum and managed successfully by colectomy.

scholarly journals Primary nasal meningioma- a case report

2017 ◽  
Vol 7 (1) ◽  
pp. 1127-1129
Author(s):  
A Ghosh ◽  
G Ghartimagar ◽  
S Thapa ◽  
MK Shrestha ◽  
OP Talwar
Keyword(s):  
Case Report ◽  
Nasal Cavity ◽  
Nasal Septum ◽  
Clinical Presentation ◽  
Sinonasal Tract ◽  
Nasal Stuffiness ◽  
One Year

Extracranial meningiomas may be subdivided into primary and secondary types based on absence or presence of intracranial attachments respectively. Primary sinonasal tract meningiomas are rare with unknown etiopathology and non-specific clinical presentation. Of these PEMs only 11.5% are in the nasal cavity and nasal septum. To our knowledge less than 50 cases of PEM of nasal cavity have been reported in the literature. We report a case of a 22 years old male who presented with epistaxis and increasing nasal stuffiness for the last one year.

Osteoblastoma of the nasal septum

2011 ◽  
Vol 125 (10) ◽  
pp. 1062-1066 ◽  
Author(s):  
E Young ◽  
M Dabrowski ◽  
K Brelsford
Keyword(s):  
Nasal Cavity ◽  
Nasal Septum ◽  
English Language ◽  
Ethmoid Sinus ◽  
Rare Entity ◽  
Rare Tumour ◽  
English Language Literature ◽  
History Of ◽  
Benign Osteoblastoma ◽  
Language Literature

AbstractObjectives:To present a case of, and to review the literature concerning, osteoblastoma of the nasal cavity, and to demonstrate the importance of considering this rare entity when assessing patients presenting with a nasal septum lesion.Case report:Benign osteoblastoma is a rare tumour, constituting 1 per cent of all bone tumours. Most cases occur in the long bones. Osteoblastoma involving the nasal cavity is rare, with only 10 reported cases in the English-language literature. Most nasal cavity cases originate from the ethmoid sinus and spread to involve the nasal cavity. There are only four reported cases of osteoblastoma originating from the bones of the nasal cavity. We report a case of osteoblastoma originating from the bony nasal septum in a 45-year-old man with a history of recurrent, right-sided epistaxis and nasal obstruction.Conclusion:This is the second report in the English-language literature of osteoblastoma originating from the bony nasal septum.

Fungal granulomatous disease of the nasal cavity: A case report of a rare entity

2017 ◽  
Vol 38 (5) ◽  
pp. 642-644
Author(s):  
Samuel N. Helman ◽  
Peter Filip ◽  
Ameet Kamat
Keyword(s):  
Case Report ◽  
Nasal Cavity ◽  
Granulomatous Disease ◽  
Rare Entity

scholarly journals Nasal septum extramedullary plasmacytoma

2013 ◽  
Vol 70 (2) ◽  
pp. 221-224 ◽  
Author(s):  
Branislav Belic ◽  
Slobodanka Mitrovic ◽  
Snezana Arsenijevic ◽  
Ljiljana Erdevicki ◽  
Jasmina Stojanovic ◽  
...  
Keyword(s):  
Nasal Cavity ◽  
Nasal Septum ◽  
Plasma Cells ◽  
Malignant Tumors ◽  
Combined Therapy ◽  
Extramedullary Plasmacytoma ◽  
Screening Tests ◽  
The Right ◽  
Nose And Throat

Introduction. Plasmacytomas are malignant tumors characterized by abnormal monoclonal proliferation of plasma cells. They originate in either bone - solitary osseous plasmacytoma, or in soft tissue - extramedullary plasmacytoma (EMP). EMP represents less than 1% of all head and neck malignancies. Case report. We presented a case of EMP of the nasal septum in a 44-year-old male who had progressive difficulty in breathing through the nose and frequent heavy epistaxis on the right side. Nasal endoscopy showed dark red, soft, polypoid tumor in the last third of the right nasal cavity arising from the nasal septum. The biopsy showed that it was plasmacytoma. Bence Jones protein in the urine, serum electrophoresis, bone marrow biopsy, skeletal survey and other screening tests failed to detect multiple myeloma. This confirmed the diagnosis of EMP. The mass was completely removed via an endoscopic approach, and then, 4 week later, radiotherapy was conducted with a radiation dose of 50 Gray. No recurrence was noted in a 3-year follow- up period. Conclusion. EMP of the nasal cavity, being rare and having long natural history, represents a diagnostic and therapeutic challenge for any ear, nose and throat surgeon. Depending on the resectability of the lesion, a combined therapy is the accepted treatment.

Inflammatory myofibroblastic tumor in the maxillary sinus with asymptomatic course excised during endoscopic surgery - a case report and review of the literature

2019 ◽  
Vol 8 (3) ◽  
pp. 1-5
Author(s):  
Krzysztof Poślednik ◽  
Igor Anurin ◽  
Ireneusz Kantor
Keyword(s):  
Case Report ◽  
Maxillary Sinus ◽  
Endoscopic Surgery ◽  
Rare Case ◽  
Inflammatory Myofibroblastic Tumor ◽  
Malignant Tumors ◽  
Rare Condition ◽  
Sinus Surgery ◽  
Review Of The Literature ◽  
Face Pain

Inflammatory myofibroblastic tumor (IMT) is a rare condition that can mimic potentially more dangerous states such as malignant tumors. The tumor itself can also show a local malignancy as well as malignant transformation. The paranasal sinus IMT is quite a rare case in the literature. The manifestation of the disease can include a face swelling, nasal obstruction, epistaxis, vision acuity worsening, numbness of face, pain. Etiology of this type of lesion still remains uncertain but there are a few assumptions on the issue: viral and genetic among the others, as well as posttraumatic and postinflammatory. We report the case of an adult woman with IMT detected in right maxillary sinus after endoscopic sinus surgery.

Sialadenoma papilliferum of nasal cavity: case report

2008 ◽  
Vol 122 (9) ◽  
Author(s):  
H E Ozel ◽  
G Ergul ◽  
O E Gur ◽  
S Kulacoglu ◽  
C Ozdem
Keyword(s):  
Case Report ◽  
Nasal Cavity ◽  
Nasal Septum ◽  
World Literature ◽  
Rare Case ◽  
Rare Tumour ◽  
Recurrent Epistaxis ◽  
The World ◽  
Sialadenoma Papilliferum

AbstractObjective:We report a rare case of sialadenoma papilliferum.Method:A case report of sialadenoma papilliferum is presented.Results:A 67-year-old woman presented with recurrent epistaxis. She was found to have an exophytic, well circumscribed mass on the nasal septum mucosa. The lesion was completely excised. A diagnosis of sialadenoma papilliferum was made based on the characteristic histological pattern. Follow up showed no evidence of recurrence. Subsequently, the patient remained well without complaint of epistaxis.Conclusion:To our knowledge, this is the first report in the world literature of sialadenoma papilliferum of the nasal cavity. This case indicates that this rare tumour can present with epistaxis, and can be resolved by means of total excision.

scholarly journals Sinonasal Angioleiomyoma: A Rare Entity

2020 ◽  
Vol 5 (2) ◽  
pp. 1-6
Author(s):  
Rubeena Arora ◽  
Shubh Mahindru ◽  
Komal Kathuria 
Keyword(s):  
Case Report ◽  
Nasal Cavity ◽  
Outpatient Department ◽  
Differential Diagnoses ◽  
North India ◽  
Rare Entity ◽  
Nasal Mass ◽  
First Case ◽  
Nose And Throat ◽  
Area Of Origin

The present case of angioleiomyoma of the nasal cavity in a 59-year-old male is unique, being the first case from North India and also because of its unique area of origin. The patient was referred to the Ear, Nose and Throat Outpatient Department with a diagnosis of an asymptomatic nasal mass. Biopsy done on the mass in another hospital reported angiofibroma. Excision was done after all relevant investigations. Histopathology revealed diagnosis of angioleiomyoma. Immunohistochemistry revealed desmin, SMA, and H-caldesmon positivity, consistent with the diagnosis of angioleiomyoma. Our case report thus highlights the im­portance of including this diagnosis in the differential diagnoses of nasal masses.

Monomorphic Adenoma of Posterior Palate: A Rare Case Report

2021 ◽  
Author(s):  
Abhinav Sharma
Keyword(s):  
Salivary Gland ◽  
Case Report ◽  
Rare Case ◽  
Malignant Tumors ◽  
Minor Salivary Gland ◽  
Benign Tumors ◽  
Rare Entity ◽  
Present Case Report ◽  
Rare Case Report ◽  
Monomorphic Adenoma

Background: Minor salivary gland benign tumors account for a very small percentage of salivary gland tumors of which monomorphic adenomas are a rare entity. Methods and Findings: The present case report discusses a rare case report of an 18-year-old female patient diagnosed with monomorphic adenoma of the posterior palatal region. The diagnosis was reached after thorough radiographical and pathological investigations. Conclusion: Monomorphic Adenoma in a younger individual is a rare disorder and can be used as a collective term for benign or malignant tumors comprising of one type or even two types of cells.

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