نتایج جستجو برای: mesenchymal neoplasm

تعداد نتایج: 238623  

Journal: :The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2010
Rim Limaiem Faten Limaiem Nadia Kourda Issam Zairi Afif Chaabouni Leila El Matri

numerous orbital neoplastic and non neoplastic processes. Various mesenchymal tumours of both fibrohistiocytic and vascular origin are well-described causes. Hemangiopericytomas (HPC) are rare vascular tumours which can infrequently involve the orbit and their incidence is estimated to be 0.8% to 3% of primary orbital tumours1,2. We herein report a new case of orbital HPC revealed by unilateral...

Journal: :Tumori 2007
Guido Bellezza Tiziana Lombardi Paola Panzarola Angelo Sidoni Antonio Cavaliere Michele Giansanti

Schwannoma arising within breast parenchyma is very rare. This report describes such a case in a 58-year-old woman. The tumor, which measured 4.4 x 3.5 x 2.1 cm, was painless, mobile and elastic-soft. Mammography showed a well-circumscribed, oval-shaped nodule without microcalcifications. At ultrasonography it appeared as a hypoechoic solid mass. Fine-needle cytology revealed several clusters o...

2015

Ossifying fibromyxoid tumor (OFMT) is a rare soft tissue tumor of unknown histogenesis. OFMT is a recently described, mesenchymal neoplasm originally defined as a borderline or low-grade malignant lesion. It consists of chains and trabeculae of ovoid cells swimming in a fibromyxoid stroma [1,2]. OFMT combines the clinical course of both peripheral and central ossifying fibromas. Like POF, it is...

Journal: :International Seminars in Surgical Oncology 2006
Corrine Wong Chris Wright Angela Colclough Simon Marsh

Metaplastic breast carcinoma (MBC) is a rare neoplasm containing a mixture of epithelial and mesenchymal elements. The epithelial component is usually ductal carcinoma but may include other variants of breast carcinomas including squamous carcinoma and osteogenic sarcoma. There is a relative paucity of data regarding such tumours. Metaplastic carcinoma carries a prognosis not dissimilar to that...

2017
James T. Boothe G. Thomas Budd Matthew B. Smolkin Patrick C. Ma

Solitary fibrous tumor of the pleura is a rare and usually benign primary neoplasm arising from mesenchymal cells of the submesothelial tissue. We present here the case of a patient diagnosed with CD34-positive advanced malignant solitary fibrous tumor of the pleura whose disease failed to respond to combination cytotoxic chemotherapy agents, but demonstrated a prompt near-complete response to ...

2011
John E. Riffle Andrea H. Prosser Jeffery R. Lee Julie J. Lynn

Nodular fasciitis is a benign, reactive, fibroblastic proliferation in which nodules most commonly develop in the subcutaneous or superficial fascia of the extremities. The occurrence of these growths in the orbital region is relatively rare. Our intent is to report another orbital case of this benign fibroproliferative tumor and to provide a brief review of the pertinent medical literature. Th...

Journal: :Journal of pediatric surgery 2008
Nona Zabolinejad Mehran Hiradfar Kazem Anvari Alale Shojae Razavi

Ameloblastic fibrosarcoma (AFS) or ameloblastic sarcoma is an extremely rare odontogenic neoplasm. The authors report AFS in the maxillary sinus of a 4-month-old boy. The tumor was composed of odontogenic epithelium, resembling that of ameloblastoma, and a mesenchymal part exhibiting features of fibrosarcoma. We also found some areas with deposition of dentinoid material closely adjacent to the...

2014
Fabiana Allevi Dimitri Rabbiosi Marco Mandalà Giacomo Colletti

To cite: Allevi F, Rabbiosi D, Mandalà M, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013202827 SUMMARY The case of a recurrent phosphaturic mesenchymal tumour of the maxillary sinus 10 years after the first surgical excision is reported. The neoplasm first presented with paraneoplastic osteomalacia causing a pathological femur fracture. A right maxill...

2016
Giovanna Giordano Roberto Berretta Enrico Silini

BACKGROUND In the ovary, sarcomatoid carcinoma has been reported only as mural nodules in epithelial malignant or borderline serous or mucinous cystic neoplasms, and in teratomas. In this paper we report a rare case of a solid sarcomatoid carcinoma of the ovary, without accompanying component of giant cells, pleomorphic cells, or glandular and other epithelial structures. CASE PRESENTATION Th...

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