scholarly journals Intra bronchial mucoepidermoid carcinoma in an 8 year old girl: A case report of rare tumor with review of literature

2016 ◽  
Vol 13 ◽  
pp. 41-44
Author(s):  
Natasha L. Vageriya ◽  
Rasik S. Shah ◽  
Suhas Prabhu ◽  
Deepak Naphade ◽  
Hemangi R. Athawale
Keyword(s):  
Case Report ◽  
Mucoepidermoid Carcinoma ◽  
Rare Tumor ◽  
Review Of Literature

scholarly journals Hybrid nerve sheath tumor in the orbit: A case report and review of literature

2019 ◽  
Vol 10 ◽  
pp. 250 ◽  
Author(s):  
Sukwoo Hong ◽  
Takayuki Hara
Keyword(s):  
Case Report ◽  
Nerve Sheath Tumor ◽  
Modified Rankin Scale ◽  
Case Description ◽  
Rare Tumor ◽  
Review Of Literature ◽  
Tumor Mass ◽  
First Report ◽  
Nerve Sheath Tumors ◽  
Nerve Sheath

Background: In neurosurgical practice, we rarely encounter hybrid nerve sheath tumors (HNST) in the orbit. We recently had a patient of this rare tumor. We believe that this is the first report where we resected the tumor transcranially. Case Description: A 54-year-old male presented with the left proptosis and intraconal tumor of 43 mm. We performed fronto-orbital craniotomy to resect the tumor mass. His proptosis completely improved and discharged home with a modified Rankin Scale of 1. Conclusion: Transcranial resection of orbital HNST was a safe and effective way to treat. Since we do not have much data regarding this rare tumor, we need to accumulate more cases.

Intraosseous mucoepidermoid carcinoma of the maxilla in a teenager: A case report and review of literature

2005 ◽  
Vol 100 (6) ◽  
pp. e93-e96 ◽  
Author(s):  
Abbas Khodayari Namin ◽  
Mohammad Moshref ◽  
Hossein Shahoon ◽  
Atefeh Mashhadi ◽  
Arash Khojasteh
Keyword(s):  
Case Report ◽  
Mucoepidermoid Carcinoma ◽  
Review Of Literature

scholarly journals Malignant Phyllodes Tumor of the Breast with Metastasis to the Pancreas: A Case Report and Review of Literature

2018 ◽  
Vol 2018 ◽  
pp. 1-5 ◽  
Author(s):  
R. A. Amir ◽  
Rola S. Rabah ◽  
S. S. Sheikh
Keyword(s):  
Case Report ◽  
Breast Neoplasms ◽  
Distant Metastasis ◽  
Case Reports ◽  
Phyllodes Tumor ◽  
Pancreatic Metastasis ◽  
Rare Tumor ◽  
Review Of Literature ◽  
Malignant Phyllodes Tumor ◽  
Phyllodes Tumors

Phyllodes tumor (PT) is a rare tumor of the breast accounting for approximately 1% of all breast neoplasms. In 1838, J. Muller coined the term “cystosarcoma phyllodes” based on the leaf-like projections of the tumor extending into the cystic spaces and sarcomatous stromal growth. However, seeing as up to 70% of phyllodes tumors are benign, “cystosarcoma” was removed, and the tumor is now recognized simply as phyllodes tumor. It is mainly seen in females between the ages of 35 and 55. Although most phyllodes tumors are benign, malignant cases do uncommonly occur, 22% of which have distant metastasis typically to the lungs and bones. Rarely, this tumor metastasizes to other locations. Herein, we report a case of malignant phyllodes tumor with metastasis to the pancreas. According to our knowledge, only 3 case reports of pancreatic metastasis from malignant phyllodes tumor have been reported in literature thus far. We aim to increase awareness among physicians of this rare metastasic potential of the uncommonly encountered malignant phyllodes tumor.

scholarly journals Sinonasal Undifferentiated Carcinoma: A Case Report and Review of Literature

2015 ◽  
Vol 8 (2) ◽  
pp. 60-63
Author(s):  
Chandala Chitguppi
Keyword(s):  
Case Report ◽  
Adjuvant Treatment ◽  
Undifferentiated Carcinoma ◽  
High Rate ◽  
Rare Tumor ◽  
Review Of Literature ◽  
Sinonasal Undifferentiated Carcinoma ◽  
Ultrastructural Characteristics ◽  
Other Neoplasms ◽  
The Ideal

ABSTRACT Sinonasal undifferentiated carcinoma (SNUC) is a rare tumor of the nasal cavity and paranasal sinuses. It can be differentiated from other neoplasms by correlating clinical, light microscopic, immunohistochemical and ultrastructural characteristics. Due to the small number of reported cases, the ideal treatment regimen has not been systematically evaluated. The treatment of SNUC includes aggressive multimodality therapy, including surgical resection and adjuvant treatment (i.e. radiotherapy, chemotherapy) because of high rate of both loco-regional recurrence and distant metastasis. How to cite this article Rajan S, Raj A, Chauhan A, Rathore PK, Wadhwa V, Khurana N, Chitguppi C. Sinonasal Undifferentiated Carcinoma: A Case Report and Review of Literature. Clin Rhinol An Int J 2015;8(2):60-63.

scholarly journals Sinonasal Paraganglioma: A Case Report and Review of Literature

2014 ◽  
Vol 7 (2) ◽  
pp. 87-89 ◽  
Author(s):  
Neelam Wadhwa ◽  
PP Singh ◽  
Vipin Arora ◽  
Pankaj Verma ◽  
Khyati Bhatia
Keyword(s):  
Case Report ◽  
Ct Scan ◽  
Nasal Cavity ◽  
Rare Case ◽  
Surgical Excision ◽  
Histopathological Diagnosis ◽  
Rare Tumor ◽  
Review Of Literature ◽  
Diagnostic Challenge ◽  
History Of

ABSTRACT A rare case of sinonasal paraganglioma is described. A 40-year-old female patient presented with 2 years history of unilateral nasal obstruction and bleeding. CT scan demonstrated an expansile enhancing mass involving bilateral ethmoids, right nasal cavity and right maxillary sinus. Histopathological diagnosis was neuroendocrine tumor with possibility of paraganglioma. A subtotal maxillectomy with excision of mass performed. Primary nonchromaffin paraganglioma of nose and paranasal sinus is a very rare tumor, these lesion pose diagnostic challenge to clinicians and pathologist. Only twenty five cases are reported in review of literature. Surgical excision is the mainstay of treatment. How to cite this article Arora V, Verma P, Singh PP, Wadhwa N, Bhatia K. Sinonasal Paraganglioma: A Case Report and Review of Literature. Clin Rhinol An Int J 2014;7(2):87-89.

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