Solitary fibrous tumor with intracranial invasion.

نویسندگان

  • Leonardo C Welling
  • José Carlos Lynch
  • Leandro Alcy S Ferreira
  • Juliano Baptista Correa
  • Mendel Sapunaru
  • Wladimir Cortezzi
  • Renata Schulz
چکیده

Dr. Leonardo C. Welling – Rua Sacadura Cabral 178 Hospital dos Servidores do Estado RJ / Serviço de Neurocirurgia / 7° andar 20221-161 Rio de Janeiro RJ Brasil. E-mail: [email protected] Various orbital pathological process can cause unilateral proptosis, these include a variety of neoplastic and non-neoplastic lesions. The most common cause of unilateral and bilateral proptosis is Graves’s disease. Other common causes of proptosis are lymphomas and metastatic lesions. Less common causes include inflammatory pseudotumors, hemangiopericytomas, nerve sheat tumors, fibromatosis and meningeomas. Mesenchymal tumors of the orbit account for 5–8% orbital neoplasms. These include solitary fibrous tumors (SFT) which are benign neoplasms with uncertain histogenesis. The World Health Organization includes SFT’s among mesenchymal, non-meningothelial tumors. They have been described in the pleura, skin, orbit, paranasal sinuses and other sites. Atypical or malignant SFT’s are often encountered in the thorax but extrathoracic malignant tumors are much more rare. Solitary fibrous tumors occur most commonly in adults and show a slight male predominance. We present an unusual case of paranasal SFT with orbital and intracranial invasion.

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

Solitary fibrous tumor of the paranasal sinuses: CT and MR appearance.

We describe the CT and MR appearance of a solitary fibrous tumor of the paranasal sinuses with intracranial invasion. The tumor was hypointense on T2-weighted MR images and had a large calcific component that proved to be reactive remodelling of native bone.

متن کامل

Role of Immunohistochemistry in the Diagnosis of Solitary Fibrous Tumor, a Review

Background: Solitary fibrous tumor (SFT) is a mesenchymal tumor which is most commonly seen in the pleura; however it can be seen in other organs such as the meninge, gastrointestinal tract, soft tissue, bone, and skin. SFT should be differentiated from other mesenchymal tumors in these organs. Immunohistochemistry plays a pivotal role for the histopathologic diagnosis...

متن کامل

Unusual Presentations of Intracranial Solitary Fibrous Tumor with Malignant Transformation

Background: Intracranial solitary fibrous tumor was rare. However, most intracranial solitary fibrous tumors are benign, cerebral solitary fibrous tumor with malignant transformation was even more unusual. Case present: Herein, we presented a 55 year-old-male who was diagnosed intracranial solitary fibrous tumor five years ago. Partial tumor excision was performed via the pterional craniotomy. ...

متن کامل

Solitary Fibrous Tumor of the Parotid Gland: A Case Report

Introduction: Solitary fibrous tumor is a rare, mesenchymal neoplasm that has been reported in numerous sites. Occurrence in the parotid gland is exceedingly rare.   Case Report: A 53-year-old man with a 2 cm solitary fibrous tumor of the left parotid gland, that was observed clinically and operatively and thought to be a neoplasm arising from Stensen's duct, is described. A pre-operative CT sc...

متن کامل

Giant solitary fibrous tumor of pleura

A 60-year-old male presented with dyspnea and chest pain. He was referred with massive bulky mass. A mass in the left lung was observed using chest X-ray (Figures 1).  A computed tomography scan of the chest showed a mass on the left lung with complete lung collapse Figures 2 (A, B). The needle biopsy was performed and the case was diagnosed with solitary fibro...

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:
  • Arquivos de neuro-psiquiatria

دوره 67 3A  شماره 

صفحات  -

تاریخ انتشار 2009