Surgical Extirpation of Glomus Tumor from Rare Localization on the Upper Extremity

نویسندگان

  • Jan Hrubý
  • Robert Novotný
  • Miroslav Špaček
  • Petr Mitáš
  • Jaroslav Hlubocký
  • David Janák
  • Ctibor Povýšil
  • Jaroslav Lindner
چکیده

Objective. To report on a very rare case of a glomus tumor manifested on the upper arm in a healthy young male patient. Case Presentation and Intervention. A 22-year-old male patient presented with bluish multifocal venous malformation on the left upper arm and was admitted for venous malformation excision. Pain, discomfort, and upper arm paraesthesia had been present for almost 6 years. Ultrasonography revealed septet tumor without blood flow in the subcutaneous region of anterior aspect of the upper arm. A multifocal venous malformation approximately 5-10 mm in diameter was excised. Histological examination showed dilated vascular area with proliferated glomus cells with round nucleus in the wall of dilated vascular structures. Based on histological examination, the final diagnosis was made as "glomangioma." Conclusion. Histological examination is the only method that can establish final diagnosis. Currently, the only available treatment for this type of tumor is surgical excision.

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

گلوموس تومور در اندام فوقانی؛ گزارش بیست مورد در طی بیست و یک سال تجربه با این تومور

Introduction & Objective: Glomus tumor is a rare benign lesion of the skin and subcutaneous tissue arising from glomus apparatus and accounts for 1.6% of soft tissue tumors that is mainly located in upper extremities and especially in finger and thumb tips. The tumor is clinically characterized by a triad of pain, point tenderness and cold sensitivity. The aim of this study was the evaluatio...

متن کامل

Glomus tumor presenting as complex regional pain syndrome of the left upper limb: a case report

BACKGROUND Glomus tumors of the hand are rare, benign but debilitating neoplasms arising from the neuromyoarterial glomus body. They may present a diagnostic dilemma, and take years with multiple consultations and investigations before an appropriate diagnosis is made, but once a diagnosis is made, surgical excision is curative. CASE PRESENTATION This is a case presentation of a 35-year-old A...

متن کامل

Factors Associated with Requesting Magnetic Resonance Imaging during the Management of Glomus Tumors

Background: The characteristic clinical presentation of glomus tumors and the low negative predictive value of themagnetic resonance imaging (MRI) raise the question whether MRI improves their management. Therefore, this studyaimed to investigate whether MRI improved the management of glomus tumors.Methods: In total, 87 patients with a histologically confirmed glomus tumor wer...

متن کامل

[Key diagnostic features and treatment of subungual glomus tumor].

Glomus tumor was first described by Wood in 1812 and named as such by Masson in 1924. It is a rare benign vascular tumor of the neuromyoarterial glomus. The triad of cold intolerance, intense paroxysmal pain, and well-defined site of pain is characteristic of the tumor. Approximately 80 % of lesions are found on the upper limbs, mostly under the nails. Between 2005 and 2008, 7 patients with thi...

متن کامل

Surgical management of the glomus tumors of the fingers: a single center experience.

INTRODUCTION Glomus tumors are rare neoplasms arising from the subcutaneous glomus apparatus. They account for 1 - 5% of the soft tissue tumors of the upper extremity, occurring in most cases in the nail bed. The typical clinical presentation includes paroxysmal pain and hypersensitivity to cold which limit the use of the affected hand causing practical, professional and often emotional discomf...

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 2013  شماره 

صفحات  -

تاریخ انتشار 2013