A low-grade chondrosarcoma presenting as an unusual cervical mass in the hyoid bone: a case report

نویسندگان

  • Hirohiko Tachino
  • Hiroaki Fushiki
  • Masayuki Ishida
  • Yukio Watanabe
چکیده

INTRODUCTION A chondrosarcoma originating from the hyoid bone is very rare. Here, we describe a case of low-grade chondrosarcoma of hyoid origin and discuss its preoperative imaging features, including those on positron emission tomography-computed tomography, and its recurrence rate. CASE PRESENTATION A 42-year-old Japanese man noticed a mass in the right submandibular region of his neck. A hard 3.0 × 2.8 cm tumor was noted on the right side of his hyoid bone. The mass was immobile and moved with deglutition. CONCLUSION Even though radiographic studies, including positron emission tomography-computed tomography, were inconclusive, the cartilaginous tumor was surgically removed en bloc, and the tumor was diagnosed based on the results of pathological investigations. Close follow-up is recommended in such cases due to the potential for recurrences, because local recurrence occurred in 50% of the reported cases of grade one chondrosarcomas.

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

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Pituitary Chondrosarcoma presenting as a sellar and suprasellar mass with parasellar extension: An Unusual presentation

Chondrosarcoma is a mesenchymal tumor composed of tumor cells producing cartilage. It is more common in older age and often affects the axial skeleton. We report a rare case of chondrosarcoma mimicking a sellar and suprasellar mass with parasellar extension. A 40 yr woman presented with decreasing visual acuity and headache. Magnetic resonance (MR) image revealed a cystic sellar and suprasellar...

متن کامل

Chondrosarcoma of cranial vault: case report and review of literature

Chondrosarcoma is a rare malignant cartilage forming tumour usually arising from long bones and rarely seen in cranium. In cranium it is seen to commonly arises from skull base with skull vault being a highly unusual site. We report a case of a 30-year female presenting with complaints of headache for 6 months found to have a large chondrosarcoma in right fronto-parietal region which is an extr...

متن کامل

A Rare Case of Pheochromocytoma Presenting as Cervical Mass

Introduction: Angiofollicular lymph node hyperplasia (ALNH) or Castleman’s disease (CD) is an unusual benign non-neoplastic lymphoproliferative disease. CD can present as a localised mass. In this paper a rare case of Castleman’s disease in a 34 years old woman with a cervical mass is presented. Case Presentation: A 34 years-old woman presented in July 2018 with a painful mass neck that was app...

متن کامل

Myeloid Sarcoma Presenting with Lateral Cervical Mass and Eosinophilia; a Diagnostic and Therapeutic Dilemma: Case Report

Myeloid sarcoma is a rare extramedullary tumor of immature myeloid cells. It has been very rarely reported as lateral cervical mass in English literature. Myeloid sarcoma has also been reported with marked eosinophilia. Here we present a 17 year old boy with lateral cervical mass and persistent eosinophilia. The mass was isointense in MRI and homogenously enhanced after contrast injection which...

متن کامل

Dedifferentiated chondrosarcoma of the cervical spine: a case report

Dedifferentiated chondrosarcoma (DDCS) is a rare and aggressive bone tumor with poor prognosis. Primary DDCS of the mobile spine is extremely rare, particularly in the cervical spine. We herein describe a first case of cervical DDCS in an 81-year-old male presenting with a slowly growing mass. Radiographs showed an expansion of the cortical contour of the C2 lamina and a soft tissue mass with p...

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

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

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2012