A patient with sinonasal leiomyoma presenting with exophthalmos: Case report and review of the literature

نویسندگان

  • Tomoko HANADA
  • Hitoshi YAMAHATA
  • Ryosuke HANAYA
  • Yuichi KURONO
  • Hiromi NAGANO
  • Shinichi KITAJIMA
  • Tsubasa HIRAKI
  • Kazunori ARITA
چکیده

A 71-year-old woman presented with a 2-month history of progressive exophthalmos. Magnetic resonance imaging revealed a tumor occupying the right frontal sinus that compressed the right orbit and eye ball. The tumor was resected through a right frontal craniotomy. The pathologic diagnosis was leiomyoma and similar to the histologic diagnosis of a uterine leiomyoma resected 4 years earlier. We suggest that this rare sinonasal leiomyoma was a benign metastasizing leiomyoma from the uterus to the nasal sinus. Neurology Asia 2013; 18(3) : 327 – 330 Address correspondence to: Tomoko HANADA, M.D., Department of Neurosurgery, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima 890-8544, Japan. Tel: +81-99-275-5375, Fax: +81-99-265-4041, e-mail: [email protected] INTRODUCTION Leiomyomas are benign myogenic tumors that most commonly arise in the uterus. Other organs lacking smooth muscle are rarely involved and neck and head lesions are particularly rare. To our knowledge, only 10 sinonasal leiomyomas have been reported in English literature to date. Benign metastasizing leiomyoma (BML) was first documented in 1939. The term BML has since been used to describe multiple benign leiomyomatous lesions in patients with a previous history of leiomyoma of the uterus. We present here a patient with BML to the nasal sinus.

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

Round Ligament Leiomyoma Developing During Pregnancy: A Case Report and Literature Review

Round ligament leiomyoma of uterus is rare. It can be presented as inguinal swelling mimicking the inguinal hernia or lymph node. Surgical excision is its curative treatment. Definitive diagnosis is made by histopathological examination. A 32 year old pregnant patient having round ligament leiomyoma as diagnosed histopathologically in Recep Tayyip Erdogan University Hospital in 2014 was present...

متن کامل

Sinonasal Teratocarcinosarcoma Report of a case

Sinonasal teratocarcinosarcoma (SNTCS) is a rare tumor characterized by mixture architecture of epithelial and mesenchymal components. SNTCS is a highly malignant tumor displaying progressive and aggressive growth with poor prognosis. Only about 40% of all patients survive after five years. It seems the combination of surgery and radiotherapy currently is the most effective treatment. In this r...

متن کامل

Prolonged Hemoptysis Caused by Primary Pulmonary Epithelioid Hemangioendothelioma; A Case Report and Review of the Literature

Epithelioid hemangioendothelioma is a vascular tumor with an intermediate malignant potential. This tumor is very rare in the lung parenchyma, and most of the previously reported cases have been asymptomatic. There is no standard therapy for this tumor and prognosis in the previous reports has been variable.Herein we report our experience with a 60-year-old woman presenting with hemoptysis and ...

متن کامل

Endometriosis Presenting as Recurrent Haemorrhagic Ascites: A Case Report and Literature Review

Endometriosis is a common condition that occurs in 6-10% of all reproductive age women. This number increases to approximately 40% in women with infertility and nearly 75% in women with complaints of chronic pelvic pain. Endometriosis is characterized by the presence of endometrial glands and stroma outside the uterine cavity. The most common complaints associated with endometriosis are dysmeno...

متن کامل

Giant Esophageal Leiomyoma with Megaesophagus: A Case Report

A 48-year-old man with a giant leiomyoma of the esophagus accompanied by megaesophagus is reported in this paper. He presented with dysphagia and was treated successfully by means of an esopahgogastric resection. The literature is reviewed and the clinical and pathological aspects of this rare tumor are discussed. 

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   شماره 

صفحات  -

تاریخ انتشار 2013