Endobronchial sclerotic neurofibroma: a very rare benign tumour

Author(s):  
Sana Iftikhar ◽  
Sofian Youssef ◽  
Daniel G Van Pittius ◽  
Shilajit Ghosh ◽  
Mohammed Haris
Author(s):  
Soumaya Graja ◽  
Saadia Makni ◽  
Abdessalem Hentati ◽  
Chiraz Chaari ◽  
Tahya Sellami-boudawara ◽  
...  

1997 ◽  
Vol 111 (9) ◽  
pp. 862-864 ◽  
Author(s):  
Deepa Bhargava ◽  
Shivayogi Bhusnurmath ◽  
A. S. Daar

AbstractChondroid syringoma or mixed tumour of the skin is a rare benign tumour which can present on the face. We present here the case of a patient who underwent an excisional biopsy of a small painless nodule in the soft triangle of the nose for cosmetic reasons. The clinical presentation, histology and treatment, with review of the relevant literature, is discussed.


2007 ◽  
Vol 121 (5) ◽  
pp. 1-4 ◽  
Author(s):  
S Ayache ◽  
D Chatelain ◽  
B Tramier ◽  
V Strunski

Objectives: To describe the features of an oropharyngeal and hypopharyngeal myxoma.Materials and methods: Case report of a 34-year-old patient operated upon for a dual-location tumour, and review of the literature.Results: The myxoma is a rare tumour. Various head and neck locations have been described, but not (to our knowledge) a tumour in both the oropharynx and the hypopharynx. Multiple synchronous locations must be searched for, particularly regarding cardiac myxoma.Conclusion: The myxoma is a rare, benign tumour, even rarer in the head and neck. Surgical treatment must be complete in order to avoid recurrences, and should be performed after assessment for cardiac involvement.


2015 ◽  
Vol 19 (2) ◽  
Author(s):  
Leon Malan ◽  
Abraham F. Bezuidenhout ◽  
Ebrahim Banderker

Fibrolipomatous hamartoma is a rare benign tumour most commonly affecting the median nerve and is characterised by fibro-fatty nerve infiltration. It results in fusiform nerve enlargement with a pathognomonic ‘spaghetti-like’ imaging appearance. Patients present with numbness and paraesthesia and later with motor deficits in the affected nerve distribution. The condition frequently coexists with macrodystrophia lipomatosa in up to two-thirds of cases.


2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Dae Hyung Lee

Ovarian adenofibroma is a rare benign tumour originating from the germinal lining and stroma of the ovary. We describe here the case of a 36-year-old woman with an ovarian mucinous cystadenofibroma that was diagnosed as a benign cystic mass of the ovary before surgery. The tumour was a cystic lesion composed of 2 regions: one filled with mucinous fluid and the other with yellowish solid components. The patient successfully underwent a left oophorectomy.


2012 ◽  
Vol 23 (6) ◽  
pp. 643-645 ◽  
Author(s):  
S. Giannotti ◽  
V. Bottai ◽  
G. Dell’osso ◽  
G. Bugelli ◽  
N. Cazzella ◽  
...  

2009 ◽  
Vol 5 (4) ◽  
pp. 118 ◽  
Author(s):  
Bandar Al Harthi ◽  
MuhammadM Riaz ◽  
AmalH Al Khalaf ◽  
Mohammad Al Zoum ◽  
Wafa Al Shakweer

1995 ◽  
Vol 62 (2) ◽  
pp. 260-262
Author(s):  
G. Marzorati ◽  
F. Pachera ◽  
M. Caroli Costantini

Giant renal leiomyoma is a rare benign tumour with a prevalently smooth muscular component; its clinical aspect and radiological and histological aspects are described. Renal leiomyoma should always be considered in differential diagnosis of a renal mass and surgical exploration is necessary to obtain the histological evidence.


2003 ◽  
Vol 23 (4) ◽  
pp. 305-308 ◽  
Author(s):  
Shah Masabat Saleem ◽  
Shabbir Hussain ◽  
Zafar Nazir

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