Ossifying lipoma

1989 ◽  
Vol 103 (4) ◽  
pp. 429-431 ◽  
Author(s):  
J. D. Blanshard ◽  
D. Veitch

AbstractLipomata are the most common benign tumour of the head and neck. They may undergo a variety of changes, one of which is ossification which, although rarely seen, has a characteristic radiographic appearance. We present a case of a retropharyngeal lipoma which demonstrates ossification and discuss the features which differentiate this from an osseous lipoma. Current theories on the aetiology of lipomata and their ossification are reviewed.

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.


2001 ◽  
Vol 115 (2) ◽  
pp. 136-139 ◽  
Author(s):  
P. Hazarika ◽  
Kailesh Pujary ◽  
Harish G. Kundaje ◽  
P. Lakshmi Rao

Although lipomas are the most common benign tumours of the head and neck, the involvement of the skull base is rare and it is also very rare for a lipoma to undergo osseous metaplasia to become an ossifying lipoma or osteolipoma. We present a case of a solitary osteolipoma involving the skull base in a 17-year-old girl. A few cases of osteolipoma involving the head and neck have been reported, but this may be the first reported case of a solitary osteolipoma involving the skull base with extension to the infratemporal fossa and parapharyngeal space. The computed tomography (CT) scan helped to clinch the diagnosis and the histopathology confirmed it. The clinical presentation, role of CT scan, surgical approach used, histological features and the review of literature are discussed.


1989 ◽  
Vol 103 (2) ◽  
pp. 216-218 ◽  
Author(s):  
M. B. Jordan ◽  
J. V. Soames

AbstractFibrous histiocytoma is uncommon in the head and neck region and rare in the larynx. Its behaviour is unpredictable.A case is reported in a 54-year-old male which was treated conservatively initially and which recurred several times over a seven year period. During that time the appearances of the lesion changed from those of a densely collagenous, cytologically benign tumour to those of a richly cellular and potentially malignant neoplasm. Laryngectomy was eventually undertaken.


2000 ◽  
Vol 114 (6) ◽  
pp. 465-466 ◽  
Author(s):  
A. Kalan ◽  
A. Ahmed-Shuaib ◽  
M. Tariq

We report the first case of a lipoma originating in the fossa of Rosenmu¨ ller. Although lipomas are a common benign tumour in the body, lipomas of the nasopharynx are rare.


2005 ◽  
Vol 119 (7) ◽  
pp. 570-572 ◽  
Author(s):  
H T Anil ◽  
B V Chandre Gowda ◽  
S Lakshmi ◽  
S R Niveditha

Schwannoma is a solitary, benign tumour arising from the neural sheath Schwann cells of the peripheral, cranial or autonomic nerves. In the head and neck region, it occurs most commonly in association with the acoustic nerve within the skull and is rarely found in oral structures. When it is found in oral structures, the tongue is reported to be the favoured site. Schwannoma of the tonsil is extremely rare, with only two cases reported in the literature. We report what is, to our knowledge, the third case of schwannoma of the tonsil, diagnosed by histopathology.


2020 ◽  
Vol 27 (04) ◽  
pp. 870-872
Author(s):  
Afra Samad ◽  
Namra Mahmood ◽  
Arbaz Samad

We are reporting a case of tuberculosis within warthin tumour of left parotid area in a 72 years old male with findings of benign tumour with acute and chronic inflammation on FNA (Fine Needle Aspiration). Warthin tumour is a benign tumours of the salivary gland particularly parotid region. It is the second most common benign tumour. In addition the tuberculosis in a parotid gland is very rare. Further having tuberculosis within warthin tumour is quite rare.1 To best of our knowledge there is the only few cases which are being reported.


2019 ◽  
Vol 49 (3) ◽  
pp. 246-248
Author(s):  
RJ Jefferson ◽  
GD Hildebrand

Infantile haemangioma is a relatively common benign tumour which often does not require treatment. We present a case of a segmental infantile haemangioma with periocular involvement impacting on early visual development which was successfully treated with topical timolol maleate 0.5% drops in the developing world.


2021 ◽  
Vol 9 ◽  
pp. 2050313X2110355
Author(s):  
Chiara Eberspacher ◽  
Francesco Nardi ◽  
Lisa Fralleone ◽  
Domenico Mascagni

Breast fibroadenomas are a common benign tumour in women that may need to be surgically excised. A mammary-like fibroadenoma can exceptionally be found in the pathological report after an anal polyp removal. A 60-year-old woman presented with huge anal polyp of 25 mm. It was surgically removed transanally. Histologic examination revealed a breast fibroadenoma pattern with glandular structures. Proctologist specialists must be aware that mammary-like tumours are a possible differential diagnosis for anal masses despite their rarity in the literature.


2002 ◽  
Vol 111 (8) ◽  
pp. 754-758 ◽  
Author(s):  
John S. Rhee ◽  
Phillip A. Wackym ◽  
David Wolfe ◽  
Karin Hague ◽  
Wesley A. King

Although granular cell tumors are relatively common in the head and neck, symptomatic granular cell tumors of the neurohypophysis are extremely rare. Ophthalmologic symptoms are most common, followed by endocrinologic manifestations. We report a case of a granular cell tumor of the pituitary fossa that was surgically treated. The clinical manifestations, radiographic appearance, and surgical management of granular cell tumors of the pituitary fossa are reviewed, as well as the unique histopathology and electron microscopy of this uncommon neoplasm.


HAND ◽  
1978 ◽  
Vol os-10 (3) ◽  
pp. 306-308 ◽  
Author(s):  
James G. Hoehn ◽  
Daniel T. Davis

Fibrous xanthomas* of the digital tendon sheath system are a common benign tumour. The varying recurrence rates cited in the literature have usually been attributed to inadequate surgical excision. However, Boyes (1964) has suggested “seeding” as a possible mechanism to explain persistence of the tumour. Our case of multiple fibrous xanthomas at different levels in a single digital sheath system is presented as an example of “seeding” along the tendon sheath.


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