scholarly journals Mesenchymal chondrosarcoma in the maxillary gingiva of a Maltese dog: a case report

2021 ◽  
Vol 61 (3) ◽  
pp. e27
Author(s):  
So-Jeong Yim ◽  
Jinyong Lee ◽  
Jae-Hoon Kim ◽  
Ji-Youl Jung
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Hard Palate ◽  
Mesenchymal Cells ◽  
Mesenchymal Chondrosarcoma ◽  
Cartilage Tissue ◽  
Mesenchymal Tissue ◽  
S 100 ◽  
The Right ◽  
Histopathology Examination

A 13-year-old castrated male Maltese dog was presented to a local animal hospital with an oral hemorrhage. An intraoral examination revealed an irregular proliferated lobular mass at the right side of the maxillary gingiva and hard palate. A surgically excised mass was requested for a histopathology examination. Histopathologically, the neoplastic foci were composed of biphasic morphologic patterns, such as primitive mesenchymal tissue and mature or immature cartilage tissue. Immunohistochemically, most of the neoplastic cells forming cartilaginous islands tested positive for S-100; the surrounding mesenchymal cells tested positive for vimentin. This paper describes a rare case of mesenchymal chondrosarcoma in the maxillary gingiva of a Maltese dog.

Popliteal nodal metastasis from squamous cell cancer of the foot. Case report and literature review

2019 ◽  
pp. 1-2
Keyword(s):  
Case Report ◽  
Lymph Node ◽  
Literature Review ◽  
Squamous Cell ◽  
Rare Case ◽  
Squamous Cell Cancer ◽  
Cell Cancer ◽  
Nodal Metastasis ◽  
Regional Disease ◽  
The Right

We report a very rare case of squamous cell cancer of the right foot which had metastasize to the ipsilateral popliteal lymph node after initial diagnosis and treatment for the loco-regional disease.

scholarly journals Canalicular adenoma of the hard palate: A rare case report

2021 ◽  
Vol 18 (1) ◽  
pp. 15
Author(s):  
Sona Rafieyan ◽  
Milad Khodaei ◽  
Masoomeh Amani ◽  
Sina Mirinezhad
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Hard Palate ◽  
Rare Case Report

Orbito-cranial mesenchymal chondrosarcoma in a young female: A rare case report

2015 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
Shyam Sharma ◽  
Somnath Roy ◽  
Imraan Khan ◽  
SuparnaKanti Pal ◽  
Anup Majumdar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Young Female ◽  
Mesenchymal Chondrosarcoma ◽  
Rare Case Report

scholarly journals Retromastoid osteoma—a rare case report

2020 ◽  
Vol 2020 (1) ◽  
Author(s):  
Edmund Wooi Keat Tan ◽  
Jason Bae Barco ◽  
Mutee Ur Rehman ◽  
Choon Chieh Tan
Keyword(s):  
Case Report ◽  
Genetic Testing ◽  
Temporal Bone ◽  
Rare Case ◽  
Screening Colonoscopy ◽  
Adenomatous Polyposis ◽  
Rare Case Report ◽  
Computed Topography ◽  
The Right ◽  
Slow Growing

Abstract Osteomas are slow growing bone tumours and are often asymptomatic. Rarely, they can be present in the temporal bone—only few cases had been reported, with an incidence of 0.1–1%. We describe a case of an osteoma of the temporal bone (retromastoid) found in a 40 year old female, who presented with a slow growing swelling behind the right ear for 9 years. Diagnosis was made on non-contrast computed topography (CT) of the skull. Treatment is indicated in symptomatic cases or cosmetic reasons. Screening colonoscopy and genetic testing for familial adenomatous polyposis (FAP) and Gardner’s syndrome are advised.

scholarly journals A maxillary ameloblastic fibrosarcoma tumor: a rare case report from Syria

2020 ◽  
Vol 2020 (8) ◽  
Author(s):  
Amjad Soltany ◽  
Ghazal Asaad ◽  
Rami Daher ◽  
Mouhannad Dayoub ◽  
Ali Khalil ◽  
...  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Soft Tissue Sarcomas ◽  
Surgical Excision ◽  
Low Grade ◽  
Rare Case Report ◽  
Ameloblastic Fibrosarcoma ◽  
The Right

Abstract Ameloblastic fibrosarcoma (AFS) is a rare, aggressive malignant odontogenic tumor. AFS is seen most frequently in second and third decades of life. We are reporting a case of a low grade AFS in a 21-year-old male complaining of a painless swelling in the right side of the maxilla. The patient was treated with surgical excision followed by radiotherapy, which is considered the most effective approach for most of soft tissue sarcomas. AFS has a high-reported recurrence rate (up to 37%); therefore, long-term surveillance for recurrence is crucial.

An Unusual Unilateral Deformity of the Hand: A Case Report

HAND ◽  
1980 ◽  
Vol os-12 (2) ◽  
pp. 197-199
Author(s):  
P. I. Gigis ◽  
P. M. Kafandaris
Keyword(s):  
Case Report ◽  
Family History ◽  
Upper Extremity ◽  
Rare Case ◽  
Carpal Bones ◽  
Metacarpal Bones ◽  
The Right

A rare case of a congenital unilateral deformity of the right upper extremity is described consisting of: absence of the carpal bones except the capitate and hamate, absence of the first three metacarpal bones and phalanges and a thumb-like extension to the palm of the dislocated radius. No hereditary family history was found.

A Rare Case Report of Recurrent Basal Cell Adenoma Involving Minor Salivary Gland of Hard Palate

2019 ◽  
Vol 10 (9) ◽  
pp. 1705
Author(s):  
Harsh Mohan Pathak ◽  
Santosh Kumar Subudhi ◽  
Satya Patnaik ◽  
Swagatika Panda ◽  
Kalyan Sundar Pal
Keyword(s):  
Salivary Gland ◽  
Case Report ◽  
Basal Cell ◽  
Rare Case ◽  
Hard Palate ◽  
Minor Salivary Gland ◽  
Basal Cell Adenoma ◽  
Cell Adenoma ◽  
Rare Case Report

Congenital stapedial suprastructure fixation with normal footplate mobility: case report

2009 ◽  
Vol 124 (6) ◽  
pp. 680-683 ◽  
Author(s):  
J H Lee ◽  
S H Jung ◽  
H C Kim ◽  
C H Park ◽  
S M Hong
Keyword(s):  
Hearing Loss ◽  
Case Report ◽  
Rare Case ◽  
Conductive Hearing Loss ◽  
Branchial Arch ◽  
Fallopian Canal ◽  
Stapes Footplate ◽  
The Right ◽  
Conductive Hearing

AbstractObjective:We report a case of bilateral conductive hearing loss caused by stapedial suprastructure fixation with normal footplate mobility.Case report:A 50-year-old woman had suffered hearing loss in both ears since childhood. Exploratory tympanotomy revealed immobility of the stapes due to a bony bridge between the stapedial suprastructure and the fallopian canal. The incus was missing, while the malleus handle was minimally deformed. The mobility of the stapes footplate was normal. Post-operatively, the hearing in the right ear improved both subjectively and audiographically, while that in the left ear did not improve because of footplate subluxation during surgery.Conclusion:This is a rare case of congenital stapedial suprastructure fixation with normal footplate mobility. In this patient, development of the second branchial arch was arrested. When performing exploratory tympanotomy for stapedial fixation, one must keep in mind that normal footplate mobility is possible.

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