scholarly journals Pilomatrikom kao oftalmohirurski problem

2003 ◽  
Vol 50 (4) ◽  
pp. 135-137
Author(s):  
Anica Radovanovic-Bobic ◽  
Zoran Latkovic
Keyword(s):  
Benign Tumour ◽  
Diagnosis And Treatment ◽  
Hair Matrix ◽  
Rare Benign Tumour ◽  
Extensive Surgery

Pilomatricoma, relativly rare benign tumour of the hair matrix cells, is usually misdiagnosed preoperativly. This result in unnecessary extensive surgery. In order to improve diagnosis and treatment of pilomatricoma, autors discusse their ten years experience (28 cases) with this tumour.

scholarly journals Alveolar adenoma: a rare benign tumour of the lung with a challenging diagnosis

2021 ◽  
Author(s):  
Soumaya Graja ◽  
Saadia Makni ◽  
Abdessalem Hentati ◽  
Chiraz Chaari ◽  
Tahya Sellami-boudawara ◽  
...  
Keyword(s):  
Benign Tumour ◽  
Rare Benign Tumour

Cysts of the parotid gland

1975 ◽  
Vol 89 (4) ◽  
pp. 435-444 ◽  
Author(s):  
N. A. Shaheen ◽  
G. T. Harboyan ◽  
R. I. Nassif
Keyword(s):  
Parotid Gland ◽  
Salivary Glands ◽  
Diagnosis And Treatment ◽  
Cystic Lesions ◽  
Definite Diagnosis ◽  
Radical Mastoidectomy ◽  
Major Salivary Glands ◽  
Congenital Origin ◽  
Benign Tumours ◽  
Extensive Surgery

SummaryCYSTS of the major salivary glands are most frequent in the parotid where they form a small percentage of its benign tumours. They can be congenital or acquired and of parotid or extraparotid origin. Two unusual cysts are reported: a cholesteatoma arising from the ipsilateral mastoid, twenty years after successful radical mastoidectomy, and a deeply located cyst of probable congenital origin. The literature is reviewed and the management discussed. Parotidectomy, often with extensive dissection, remains in general the treatment of choice.Cysts in the parotid gland represent a small percentage of benign parotid masses. They usually arise within the gland from salivary or non-salivary parotid tissue, and may be congenital or acquired. Some, however, may arise from surrounding structures.Unless the cyst is superficial and therefore readily amenable to proper examination, it usually escapes a definite diagnosis even with the help of sialography or more sophisticated procedures. Exploration is eventually resorted to for diagnosis and treatment. That is why the surgeon should be ready to perform extensive surgery if the findings at exploration necessitate it.The purpose of this article is to present two cystic lesions of the parotid. The first is a rarity, a cholesteatoma originating from the ipsilateral mastoid; and the second an unusually deeply located cyst. These cases illustrate well the problems met with in the management of preauricular masses.

Chondroid syringoma of the nose: report of a case

1997 ◽  
Vol 111 (9) ◽  
pp. 862-864 ◽  
Author(s):  
Deepa Bhargava ◽  
Shivayogi Bhusnurmath ◽  
A. S. Daar
Keyword(s):  
Clinical Presentation ◽  
Relevant Literature ◽  
Excisional Biopsy ◽  
Benign Tumour ◽  
Mixed Tumour ◽  
Chondroid Syringoma ◽  
The Face ◽  
Rare Benign Tumour

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.

Oropharyngeal and hypopharyngeal myxoma: case report and literature review

2007 ◽  
Vol 121 (5) ◽  
pp. 1-4 ◽  
Author(s):  
S Ayache ◽  
D Chatelain ◽  
B Tramier ◽  
V Strunski
Keyword(s):  
Case Report ◽  
Surgical Treatment ◽  
Literature Review ◽  
Head And Neck ◽  
Cardiac Involvement ◽  
Cardiac Myxoma ◽  
Benign Tumour ◽  
Review Of The Literature ◽  
Rare Tumour ◽  
Rare Benign Tumour

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.

scholarly journals Fibrolipomatous hamartoma of the median nerve

2015 ◽  
Vol 19 (2) ◽  
Author(s):  
Leon Malan ◽  
Abraham F. Bezuidenhout ◽  
Ebrahim Banderker
Keyword(s):  
Median Nerve ◽  
Benign Tumour ◽  
Motor Deficits ◽  
Fibrolipomatous Hamartoma ◽  
Macrodystrophia Lipomatosa ◽  
Imaging Appearance ◽  
Nerve Enlargement ◽  
Rare Benign Tumour

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.

scholarly journals A Case of Mucinous Cystadenofibroma of the Ovary

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Dae Hyung Lee
Keyword(s):  
Cystic Lesion ◽  
Cystic Mass ◽  
Benign Tumour ◽  
The Other ◽  
Rare Benign Tumour

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.

Elastofibroma dorsi: case series of a rare benign tumour of the back

2012 ◽  
Vol 23 (6) ◽  
pp. 643-645 ◽  
Author(s):  
S. Giannotti ◽  
V. Bottai ◽  
G. Dell’osso ◽  
G. Bugelli ◽  
N. Cazzella ◽  
...  
Keyword(s):  
Case Series ◽  
Benign Tumour ◽  
Elastofibroma Dorsi ◽  
Rare Benign Tumour

scholarly journals Adrenal myelolipoma a rare benign tumour managed laparoscopically: Report of two cases

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

Leiomioma renale gigante. Descrizione di un caso: Giant renal leiomyoma: Case report

1995 ◽  
Vol 62 (2) ◽  
pp. 260-262
Author(s):  
G. Marzorati ◽  
F. Pachera ◽  
M. Caroli Costantini
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Renal Mass ◽  
Clinical Aspect ◽  
Benign Tumour ◽  
Surgical Exploration ◽  
Histological Evidence ◽  
Rare Benign Tumour

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.

Sign in / Sign up

Export Citation Format

Share Document