Myofibroma of the oral cavity. A rare spindle cell neoplasm.

نویسندگان

  • Bernardo-Ferreira Brasileiro
  • Paulo-Ricardo-Saquete Martins-Filho
  • Marta-Rabello Piva
  • Luiz-Carlos-Ferreira da Silva
  • Cassiano-Francisco-Weege Nonaka
  • Márcia-Cristina-da Costa Miguel
چکیده

Myofibroma is an uncommon spindle cell neoplasm rarely found in oral cavity. Typically, this lesion is seen in neonates and infants with few cases reported in adults patients. In the oral cavity, myofibroma occurs within the submucosal or intramuscular tissue and has a predilection by the tongue, buccal mucosa and lips. Microscopically, a typical biphasic pattern can be observed. Misdiagnosis included benign and malignant spindle cell lesions of nerve tissue or smooth muscle origin, such as neurofibroma, leiomyoma and sarcomas. Thus, immunohistochemical staining is a useful tool to identify the nature of neoplastic cells and to reach an accurate diagnosis. An immunohistochemical panel consisting of antibodies to vimentin, SMA, HHF-35, S-100p and desmin must be achieved. In most cases, positivity for vimentin, SMA and HHF-25 can be observed. Our report describes a solitary myofibroma of the tongue of a 23-year-old man with emphasis in clinical, histopathological and immunohistochemical features of this lesion.

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

Aggressive Myofibroma of Gingiva: A Case Report

Myofibroma is an uncommon spindle cell neoplasmof rare incidence in oral cavity. Typically, this lesion is seen in neonates and infants with few cases reported in adults. In the oral cavity, myofibroma occurs within the submucosal or intramuscular tissue and has a predilection for the tongue, buccal mucosa and lips. Microscopically, a typical biphasic pattern can be observed. Misdiagnosis inclu...

متن کامل

Myofibroma of the Gingiva: A Rare Case Report and Literature Review

Myofibromas are benign uncommon fibroblastic tumors of the soft tissue, bone, or internal organs affecting all ages. These lesions histopathologically may mimic many other soft tissue tumors of the oral cavity such as spindle cell tumors of neurogenic and smooth muscle cell origin, thus leading to misdiagnosis and mistreatment. This case report describes a rare benign tumor, which presented as ...

متن کامل

Juvenile Myofibromatosis of Mandible- A Case Report

Myofibroma is a solitary benign tumor of myofibroblasts. Myofibromatosis describes multiple, simultaneous myofibromas at different sites in various organs. Myofibromatosis is a rare but well recognized entity which was originally thought to affect only neonates and infants. It is now apparent however that adults may also be affected. Solitary cases affecting the oral cavity appear to be rare. T...

متن کامل

Solitary fibrous tumor of buccal mucosa: A rare entity

BACKGROUND AND AIM: Solitary fibrous tumor (SFT) is a quite uncommon tumor that commonly occurs in the pleura but occasionally involves an oral cavity. We are reporting this rare case in the oral cavity. The diagnosis depends on microscopic and immunohistochemical features. Patients with these tumors can be carefully treated with local excision, but tumors with...

متن کامل

The Spindle Cell Neoplasms of the Oral Cavity

Spindle cell neoplasms are defined as neoplasms that consist of spindle-shaped cells in the histopathology. Spindle cell neoplasms can affect the oral cavity. In the oral cavity, the origin of the spindle cell neoplasms may be traced to epithelial, mesenchymal and odontogenic components. This article aims to review the spindle cell neoplasms of the oral cavity with emphasis on histopathology. ...

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:
  • Medicina oral, patologia oral y cirugia bucal

دوره 15 4  شماره 

صفحات  -

تاریخ انتشار 2010