Case report of a female child with right nasal chondromyxoid fibroma

نویسندگان

چکیده

Chondromyxoid fibroma; a rarely found tumor, contributing <1% of all primary bone neoplasm. We reported 4-year female child with 1-year history nasal obstruction and facial swelling. Large enhanced lesion amorphous densities spreading into the right cribriform plate floor sphenoid sinus, laterallyinto lamina papyracea, inferolaterally medial wall maxillary posteriorly nasopharynx superior aspect oropharynx was appreciated in CT scan. Mass excised by Caldwell Luc’s endoscopic maxillectomy via sublabial approach. CMF confirmed histologically post-operative biopsy. Keywords: fibroma, benign neoplasm, paprycea. Continuous...

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

Chondromyxoid fibroma of bone; report of case.

Chondromyxoid fibroma, a benign neoplasm of bone, has a histological appearance that suggests something much more malign. Indeed, this entity, named by Jaffe and Lichtenstein (1948), was recognised by them during a restudy oftheir own material filed as chondrosarcoma. Until their description and definition of this lesion, there is little doubt that many a patient suffered unnecessarily radical ...

متن کامل

Chondromyxoid Fibroma of Humerus[CMF] - A Rare Case Report

Dept. of Orthopaedics,ACPM Medical College and Hospital, Dhule. India. Address of Correspondence Dr. N. B. Goyal Asso. Proff, Dept of Orthopaedics, ACPM Medical College & Hospital, Dhule. India. Email:[email protected] Copyright © 2015 by International Journal of Surgical Cases International Journal of Surgical Cases | eISSN 2321-3817 | Available on www.surgicalcasesjournal.com/ This is a...

متن کامل

Chondromyxoid fibroma of the lateral malleolus: a case report.

Chondromyxoid fibromas account for <1% of primary bone neoplasms. We report one such case occurring in the distal fibula of a 27-year-old woman. The patient underwent curettage, followed by phenolisation, insertion of a Steinmann pin, and cementation. This treatment reduced morbidity, restored stability, and enabled rapid functional recovery. There was no recurrence after 2 years.

متن کامل

Chondromyxoid fibroma of the second metacarpal bone--a case report.

This report describes a chondromyxoid fibroma of the second metacarpal bone in a 32-year-old female patient. Chondromyxoid fibroma is a rare, benign, slow-growing bone tumor of cartilaginous origin. Tumor has a high recurrance rate. Our aim was to show successful treatment of a metacarpal chondromyxoid fibroma with wide resection and implantation of finger join endoprosthesis.

متن کامل

Chondromyxoid Fibroma: A Rare Case Report and Review of Literature

Chondromyxoid fibroma (CMF) is one of the rarest benign tumors of cartilaginous origin. It accounts for less than 0.5% of bone tumors and less than two percent of benign bone tumors. It is composed of a mixture of chondroid, myxoid, and fibrous tissues. The diagnosis of CMF depends upon its characteristic histological appearance like a lobular pattern with stellate-shaped cells in a myxoid or c...

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: Journal of Pakistan Medical Association

سال: 2021

ISSN: ['0030-9982']

DOI: https://doi.org/10.47391/jpma.720