نتایج جستجو برای: myxofibroma

تعداد نتایج: 128  

2008
Nabeel Al-Brahim Mustafa A. Dashti

Objective: To report a rare case of ossifying fibromyxoid tumor of soft tissue in Kuwait. Clinical Presentation and Intervention: A 60-year-old woman presented with a painless tumor, increasing in size and located in the left buttock, which had been present for an uncertain duration. The patient underwent an excisional biopsy. Pathological examination revealed a 7.5-cm well-circumscribed mass w...

2013
So-Min Hwang Ka-Hyung Cho Kwang-Ryeol Lim Yong-Hui Jung Jennifer Kim Song

477 nodular lesion with a well-defined margin, but had no erosion, eschar, or bleeding. In addition, it did not invade the periungual or subungual region. Furthermore, it had a soft surface with soft tissue adhesion. There were no notable findings on radiography nor a family history. However, the patient did have a severalyear history of tinea pedis. The patient scratched the itching area, resu...

2013
Chin-Chun Chen Tsung-Ming Tsai Tzu-Hsuan Liu Hui-Ju Yang Tzu-Cheng Su Pei-Yi Chu

Ossifying fibromyxoid tumor (OFMT) is a rare soft tissue tumor of uncertain histogenesis, occurring predominantly in deep soft tissues of the extremities. Typically, OFMT presents in adults on the extremities or trunk, as a deep soft tissue mass. Less appreciated is the fact that OFMT may also present as a mass in the superficial subcutis or dermis. We herein report a female who presented with ...

Journal: :Acta dermatovenerologica Croatica : ADC 2012
Yusuke Wakabayashi Noriaki Nakai Hideya Takenaka Norito Katoh

Superficial acral fibromyxoma (SAF) is a rare, distinctive, benign soft tissue tumor with a predilection for the hands and feet, first described by Fetsch et al. in 2001. Histologically, SAF tumors are unencapsulated, mostly located in the dermis or subcutis, and composed of spindled and stellate-shaped cells with random, loose storiform and fascicular growth patterns. The stromal component of ...

Journal: :Orthopedics 2012
Andreas F Mavrogenis Roberto Casadei Marco Gambarotti Pietro Ruggieri

Fibromyxoma of bone is a rare benign tumor of fibrous tissue origin. The typical location is the jaws. Sporadic extragnathic cases have been reported, but fibromyxoma of the spine has not been reported. The histological appearance of fibromyxoma is benign and includes abundant extracellular fibrous and myxoid stroma with varying amounts of calcification and ossification. Myxoid changes are usua...

2017
Nihed Abdessayed Sarra Mestiri Houssem Ammar Ahlem Bdioui Amine Chhaidar Omar Toumi Nozha Mhamdi Rahul Gupta Marwa Guerfela Moncef Mokni

INTRODUCTION Ossifying fibromyxoid tumor (OFMT) is a rare lesion that generally occurs in the soft tissues of proximal limbs, head or neck and presents as a slowly growing mass. Abdominal or trunk locations are extremely rare. PRESENTATION OF CASE We report a case of 50-year-old man who presented with a painless, slow growing epigastric mass for 5 years. Radiologic assessment revealed a well ...

2013
Paul Klimo Tushar Jha Asim F. Choudhri Royce Joyner L. Madison Michael

Purpose Fibromyxomas and myxomas are benign tumors of mesenchymal origin usually found outside the nervous system, most commonly in the atrium of the heart. They can also arise in the mandible or maxilla, but it is exceedingly rare to find them within the skull base. The history, histologic features, and the literature, with emphasis on other pediatric cases, are reviewed for this uncommon skul...

2018
Ignacio A. Velasco Ran Zhang Tiejun Li Diancan Wang

BACKGROUND Ossifying fibromyxoid tumor of soft parts (OFMT), is a rare but morphologically distinctive neoplasm of uncertain histogenesis that most frequently affects middle-aged male adults. Clinically, it usually presents as a slowly enlarging, small, circumscribed mass, which in most cases is painless. OFMT is most frequently found within the subcutaneous tissues of extremities or trunk, and...

Journal: :The Journal of bone and joint surgery. British volume 1971
F Schajowicz H Gallardo

Chondromyxoid fibroma is the least common benign tumour of cartilage derivation. In 1948 it was described by Jaffe and Lichtenstein as a distinctive entity; formerly it was classified as myxoma (Bloodgood 1924) or a myxomatous variant ofgiant-cell tumour, or mistaken for a malignant lesion, especially chondrosarcoma, chondromyxosarcoma or myxosarcoma. The few cases reported recently in the lite...

2017
Fumiaki Kawara Shinwa Tanaka Takashi Yamasaki Yoshinori Morita Yoshiko Ohara Yoshihiro Okabe Namiko Hoshi Takashi Toyonaga Eiji Umegaki Hiroshi Yokozaki Takanori Hirose Takeshi Azuma

A 66-year-old man was diagnosed with a gastric submucosal tumor. Endoscopic ultrasound (EUS) revealed an iso/hypoechoic mass in the third layer. No malignant cells were detected in a histological examination. Yearly follow-up endoscopy and EUS showed the slow growth of the tumor. Endoscopic submucosal dissection (ESD) was performed and a glistening tumor was resected. The lesion showed a multin...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید