A rare case of retropharyngeal fibromatosis presenting with stridor

نویسندگان

چکیده

Stridor is one of the common emergencies in otolaryngology clinics, usual causes being malignancies glottis and hypopharynx. We present a rare case stridor caused by retropharyngeal fibromatosis an elderly patient. A 62-year-old male patient presented with complaints breathing difficulty associated dysphagia for one-month duration. On evaluation, he was found to have moderate smooth mucosa-covered bulge posterior pharyngeal wall obscuring endolarynx. With working diagnosis mass causing stridor, underwent emergency tracheostomy. Initial punch biopsies from lesion were non-diagnostic. further evaluation imaging histopathological examination incisional biopsy, we arrived at giant extending skull base C6. The en-bloc trans-cervical excision tumor. Fibromatoses retropharynx group tumor entity, which benign, locally aggressive recurrent. Dysphagia presentation though large tumors can due upper airway obstruction. Imaging preoperative surgical planning play crucial role individualizing management these their inaccessible location proximity major vasculature nerves head neck. Complete, meticulous pre-operative followed paramount importance treatment thereby prevent its recurrence.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Aggressive Fibromatosis of Parapharyngeal Space: a rare case report

Aggressive fibromatosis also known as extra abdominal desmoid tumor is an uncommon benign tumor of soft tissue origin with fibroblastic proliferationSince the tumor is locally aggressive, the lesion may be misdiagnosed as low -grade fibrosarcoms. It accounts for 0.03% - 0.1% of all body tumors and 3% of all soft tissue tumors. Only 10% to 15% of these lesions occur in head and neck, usually in ...

متن کامل

Aggressive Fibromatosis of Parapharyngeal Space: a rare case report

Aggressive fibromatosis also known as extra abdominal desmoid tumor is an uncommon benign tumor of soft tissue origin with fibroblastic proliferationSince the tumor is locally aggressive, the lesion may be misdiagnosed as low -grade fibrosarcoms. It accounts for 0.03% - 0.1% of all body tumors and 3% of all soft tissue tumors. Only 10% to 15% of these lesions occur in head and neck, usually ...

متن کامل

Reviewing the Entity: Retropharyngeal Fibrolipoma and a Rare Case Report

Introduction: Fibrolipoma, a subtype of lipoma is painless, well-circumscribed, slow-growing, submucosal benign adipocyte tumour. It is uncommon in the oral cavity and oropharyngeal region, with rare incidence in the retropharynx even rarest in pediatric age group.   Case Report: A very unusual case of fibrolipoma is presented in a pediatric patient, who had a huge retropharyngeal fibrolipoma a...

متن کامل

A Rare Case of Eosinophilic Cholecystitis Presenting in a Patient with Thalassemia Intermedia; a Case Report

Eosinophilic cholecystitis is a rare inflammatory condition encountered in surgical cholecystectomy specimens. In terms of histopathology, it is defined by transmural infiltration of eosinophils composing more than 90% of leukocytes. We here report a case of 19-year-old male admitted with thalassemia intermedia and with severe left upper quadrant pain. The patient underwent open splenectomy and...

متن کامل

A Rare Case of Retropharyngeal Hibernoma.

Hibernoma is a slow growing, rare benign tumour, which derived from brown adipose tissue. This tumour is usually found in the area where foetal fat persists such as back, axilla, retro peritoneum and thorax. Hibernoma rarely occurs in the retro pharynx. We report a case of retropharyngeal hibernoma in a 44-year-old male. He presented with obstructive symptoms for six months and a retropharyngea...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: International Journal of Otorhinolaryngology and Head and Neck Surgery

سال: 2023

ISSN: ['2454-5929', '2454-5937']

DOI: https://doi.org/10.18203/issn.2454-5929.ijohns20232476