Unusual neoplasm on the hard palate of a child: a case report

نویسندگان

  • Mathangi Kumar
  • Shruthi Acharya
  • Kanthilatha Pai
  • Vijay Kumar
  • Sundeep P Thotan
چکیده

BACKGROUND Myoepitheliomas account for less than 1% of salivary gland tumors. They mostly affect the parotid glands of adults during the third to fifth decades. CASE PRESENTATION A 10-year-old Indian boy reported a small swelling in the roof of his mouth of 10 days' duration. History revealed that the lesion was painless and not associated with bleeding or pus discharge. On examination, a purplish well-circumscribed growth was noted on his posterior hard palate. Magnetic resonance imaging was suggestive of a well-encapsulated hemangioma. An excisional biopsy was performed and histopathology along with immunohistochemistry analysis showed that the lesion was a spindle cell variant of benign myoepithelioma. CONCLUSION Palatal myoepitheliomas are rare and their occurrence in young individuals is rarer.

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

Schwannoma in the Posterior Hard Palate and Anterior Mandibular Gingiva: a report of two cases

Background: Schwannoma is a benign tumor which usually presents as a solitary slow-growing painless mass. Approximately 25–48% of all schwannomas occurs in the head and neck region and is found rarely in oral cavity, about 1% of head and neck cases. Tongue is the most common site, followed by buccal mucosa, palate, floor of the mouth, jaw, gingiva and lips. This tumor may prese...

متن کامل

A Case Report: Nager Acrofacial Dysostosis

Introduction: Nager syndrome is a malformation resulting from problems in the development of the first and second branchial arches and limb buds. The cause of the abnormal development of the pharyngeal arches in Nager syndrome is unknown. It is also unclear why affected individuals have bone abnormalities in their arms and legs. Nager syndrome is thought to have an autosomal recessive inherita...

متن کامل

Angiomyoma of the Hard Palate

Leiomyoma is a rare benign neoplasm deriving from smooth muscle. Vascular leiomyoma is its most common subtype in the oral cavity. It may appear at any age with the greatest incidence in the 4th and 5th decade of life. The common manifestation is a slow-growing, asymptomatic, submucousal mass. The diagnosis is only through microscopic examination requiring special staining...

متن کامل

A Schwannoma of the Soft Palate in a Child: Histological and Immunohistochemical Features and Surgical Method

Introduction: Schwannoma, or neurilemmoma, is a benign neoplasm of Schwann cells that is extremely rare in the soft palate. Herein we present a case of a soft palate schwannoma presenting with an ulcerated surface and purplish colour in a 12 year-old girl. This report also introduces a successful surgical technique for coverage of the defect left by surgery.

متن کامل

Plasmacytoid Myoepithelioma of the Palate with Rapid Growth: A Case Report

  Myoepitheliomas are benign tumors which account for less than 1% of all salivary gland tumors. In this article, we report the clinical, pathologic, and immunohistochemical features of plasmacytoid myoepithelioma of the hard palate in a 73-year-old man having a painless hard palate mass with progressiv...

متن کامل

A Rare Case of Epignathus Combined with Soft Cleft Palate, Bifida Tongue, and Lingual Lipoma

Congenital tumors of the oral cavity are not common.Teratoids are the most common tumors, and in rare cases are associated with cleft soft palate. In this paper a rare case of Epignathus with cleft soft palate, bifida tongue, jaw malocclusion, tongue lipoma, Hypertelorism and low-set ears has been presented. A female infant with a large mass covered with skin and hair arising from hard palate, ...

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 11  شماره 

صفحات  -

تاریخ انتشار 2017