scholarly journals An unusual presentation of an aggressive spindle cell skin cancer

2014 ◽  
Vol 12 (4) ◽  
pp. 149-152
Author(s):  
Samuel Srour ◽  
Meredith Workman ◽  
Jian Yang ◽  
Sakher Abdullah ◽  
Mohamad Cherry
2013 ◽  
Vol 6 (3) ◽  
pp. 149-151
Author(s):  
RS Mudhol ◽  
Vijayalaxmi Suranagi ◽  
Anil S Harugop ◽  
Hema B Bannur ◽  
Ganga S Pilli

ABSTRACT Vascular tumors as such are rare in the nasal cavity. Few cases of lobular capillary hemangioma, cavernous hemangioma and epitheloid hemangioendothelioma have been reported in the nasal cavity. But, there are no reports of spindle cell hemangioma occurring within the nasal cavity. They usually present as subcutaneous nodules in the extremities. A case of recurrent bleeding polypoid lesion in the left nasal cavity, arising from the middle turbinate which showed features of spindle cell hemangioma is reported for its rarity and unusual presentation. The tumor was excised by minimally invasive transnasal endoscopic approach. How to cite this article Suranagi V, Harugop AS, Bannur HB, Pilli GS, Mudhol RS. Spindle Cell Hemangioma of the Nasal Cavity: A Rare Tumor with Unusual Presentation. Clin Rhinol An Int J 2013;6(3):149-151.


2019 ◽  
Vol 32 (6) ◽  
Author(s):  
Bengu Nisa Akay ◽  
Mehmet Fatih Atak ◽  
Aylin Okcu Heper ◽  
Banu Farabi

2010 ◽  
Vol 32 (3) ◽  
pp. 240-242 ◽  
Author(s):  
Margreet A. Veening ◽  
Jonathan I. Verbeke ◽  
Melinda M. Witbreuk ◽  
Gert-Jan L. Kaspers

2015 ◽  
Vol 6 (2) ◽  
pp. 99-102
Author(s):  
Nishat Afroz ◽  
Shagufta Qadri ◽  
Divya Rabindranath ◽  
Shakeba Qadri

ABSTRACT Primary sarcomas of the salivary glands occur rarely with few cases having been reported. Fibrosarcoma is a rare type of primary sarcoma with a poor prognosis and low life expectancy. Microscopically, these tumors resemble their counterparts encountered in other areas. They can be easily confused with spindle cell (sarcomatoid) carcinomas, myoepithelial carcinomas or malignant melanomas. We present an unusual case of a primary fibrosarcoma that arose in the right parotid gland of a 50 years male, who presented with a large nodular mass in the right preauricular region. Computed tomography (CT) scan revealed a tumor arising from the right parotid gland. A near total parotidectomy was performed and the histopathology report showed neoplastic spindle cells predominantly arranged in a ‘herring bone’ pattern. On immunohistochemistry, the tumor was positive for vimentin and was negative for pancytokeratin and S-100, which lead to a firm diagnosis of fibrosarcoma. How to cite this article Qadri S, Afroz N, Rabindranath D, Qadri S. Fibrosarcoma developing in the Parotid Gland: An Unusual Presentation. Int J Head Neck surg 2015;6(2):99-102.


2015 ◽  
pp. bcr2015212317 ◽  
Author(s):  
Carla Natalie Harris ◽  
Ruth Green ◽  
Irfan Khan

2015 ◽  
Vol 19 (3) ◽  
pp. 406 ◽  
Author(s):  
OlalereOmoyosola Gbolahan ◽  
Oluyemi Fasina ◽  
AkinyeleOlumuyiwa Adisa ◽  
OlubayoA Fasola

Author(s):  
Irving Dardick

With the extensive industrial use of asbestos in this century and the long latent period (20-50 years) between exposure and tumor presentation, the incidence of malignant mesothelioma is now increasing. Thus, surgical pathologists are more frequently faced with the dilemma of differentiating mesothelioma from metastatic adenocarcinoma and spindle-cell sarcoma involving serosal surfaces. Electron microscopy is amodality useful in clarifying this problem.In utilizing ultrastructural features in the diagnosis of mesothelioma, it is essential to appreciate that the classification of this tumor reflects a variety of morphologic forms of differing biologic behavior (Table 1). Furthermore, with the variable histology and degree of differentiation in mesotheliomas it might be expected that the ultrastructure of such tumors also reflects a range of cytological features. Such is the case.


2000 ◽  
Vol 39 (5) ◽  
pp. 372-374 ◽  
Author(s):  
Joy Y. Chen ◽  
Rhea Phillips ◽  
Alan T. Lewis ◽  
Long T. Quan ◽  
Sylvia Hsu ◽  
...  

1971 ◽  
Vol 104 (2) ◽  
pp. 124-127 ◽  
Author(s):  
M. M. Schreiber
Keyword(s):  

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