Solitary fibrous tumour of the face: a rare case report

2002 ◽  
Vol 55 (1) ◽  
pp. 75-77 ◽  
Author(s):  
Joon Pio Hong ◽  
Yoon Kyu Chung ◽  
Sug-Won Kim ◽  
Tae-Hun Kim ◽  
Kwang-Gil Lee
2010 ◽  
Vol 63 (1) ◽  
pp. e13-e15 ◽  
Author(s):  
Christos Profyris ◽  
Elizabeth Soilleux ◽  
Rufus Corkill ◽  
Jeremy Birch

2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
Author(s):  
P Singh ◽  
S Singh

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841


2015 ◽  
Vol 6 (3) ◽  
pp. 115-117
Author(s):  
Sachin Lal Shilpakar ◽  
Bivek Aryal ◽  
Shyam Thapa Chettri ◽  
Apar Pokharel ◽  
Deepak Paudel

ABSTRACT The trichoepithelioma is a benign cutaneous neoplasm which is derived from hair follicles. It is common in the face, but there are only three reports of the solitary occurrence on the nose. It is often not recognized because of its rarity, controversial classification, origin and biological potential. The objective of this paper is to present a case of solitary trichoepithelioma on the nose, histopathological examination and treatment. It should be considered as a differential diagnosis of a solitary lesion of nose which is confused with basal cell carcinoma. The confirmation by histopathological examination is essential. How to cite this article Sah BP, Shilpakar SL, Aryal B, Chettri ST, Pokharel A, Mishra S, Paudel D. Solitary Trichoepithelioma of Nose: A Rare Case Report and Review of Literature. Int J Head Neck Surg 2015;6(3):115-117.


Author(s):  
N. R. Vignesh ◽  
Shreya Srinivasan ◽  
G. Sukanya ◽  
S. Arun Karthikeyan

Mycosis fungoides is represented as the most common epidermotropic cutaneous T-cell lymphoma, which is mainly characterized by the proliferation of atypical cells within the epidermis. We report a rare presentation of mycosis fungoides in a 60-year-old male presenting with chronic psoriasiform plaque involving the face. Punch biopsy of the lesion from the forehead was taken for routine histological examination and immunohistochemical stains. Results of biopsy and immunohistochemical findings were consistent with mycosis fungoides and diagnosed as psoriasiform presentation of mycosis fungoides involving the face.


2015 ◽  
Vol 4 (52) ◽  
pp. 9129-9133
Author(s):  
Sinha A ◽  
Navin Shankar K R ◽  
Singh R N ◽  
Ray N K

Author(s):  
Scott Arockia Singh M. ◽  
Paul Raphel ◽  
Sneha Devadas ◽  
Siny Vellukara Sasidharan

Nevus Sebaceous of Jadassohn is rare hamartomatous skin lesion. We report an interesting case of an Adolescent Arab male 18yr old, who presented to us with a velvety plaque of 7cm length in his left preauricular area. Excision biopsy revealed Nevus sebaceous of Jadassohn with infundibular and keratinous cyst. The lesion is present since birth started as a tiny lesion and grown to the current size. No such large sized lesion on the face has ever been reported in the medical literature till date. We advise an early excision as they have strong potential for malignant change.


2012 ◽  
Vol 26 (6) ◽  
pp. 619-621 ◽  
Author(s):  
Yuksel Kurban ◽  
Izzet Sahin ◽  
Ibrahim Uyar ◽  
Salih Deveci ◽  
Davut Gul

2020 ◽  
Vol 8 (7) ◽  
pp. 298-301
Author(s):  
Abira Chattopadhyay ◽  
◽  
Aritra Chatterjee ◽  
Mohsina Hussain ◽  
Tarun Kanti Santra ◽  
...  

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