scholarly journals Bilateral Primary Aneurysmal Bone Cyst of Proximal Femur: A Rare Case Report

2021 ◽  
pp. 217-223
Author(s):  
Sudhir Shyam Kushwaha ◽  
Kumar Shantanu ◽  
Garima Maurya ◽  
Abhishek Pandey
Keyword(s):  
Case Report ◽  
Proximal Femur ◽  
Rare Case ◽  
Pathological Fracture ◽  
English Literature ◽  
Bone Cyst ◽  
Open Biopsy ◽  
Rare Case Report ◽  
Aneurysmal Bone Cysts ◽  
The Right

Aneurysmal bone cysts (ABC) are blood-filled, locally destructive, expansile lesions of the bone. ABC of the proximal femur is usually unilateral in presentation. As far as the English literature is concerned, there is no case report of bilateral involvement of the proximal femur by primary ABC. We hereby present a rare case of bilateral primary ABC of the proximal femur with pathological fracture of the right femoral neck. The patient underwent right hip hemiarthroplasty and open biopsy and curettage of the left proximal femur. ABC is usually unilateral in location. Whenever there is a bilateral lesion in the proximal femur usually ABC is not suspected as a differential diagnosis, but ABC may have a bilateral presentation.

scholarly journals Osteoblastoma with secondary aneurysmal bone cyst in the proximal femur of a 6-year-old boy: a rare case report

2018 ◽  
Vol 5 (5) ◽  
pp. 2026
Author(s):  
Umasankar P. ◽  
Lakshmi Priya U. ◽  
Fadiya Zainudeen
Keyword(s):  
Case Report ◽  
Proximal Femur ◽  
Aneurysmal Bone Cyst ◽  
Rare Case ◽  
Bone Cyst ◽  
Rare Case Report ◽  
Secondary Aneurysmal Bone Cyst

Osteoblastoma is a rare bone forming neoplasm. It is extremely rare for osteoblastoma to present with secondary aneurysmal bone cyst. Authors present a case of a 6-year-old boy with osteoblastoma of the femur with secondary aneurysmal bone cyst. To the best of the knowledge, this is the first such case report of the lesion presenting in proximal femur.

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.

Aneurysmal Bone Cyst of C2, C3 Cervical Spine: A Rare Case Report and Review of Literature

2015 ◽  
Vol 2 (2) ◽  
pp. 52-54
Author(s):  
Vikas Naik ◽  
GC Keshav ◽  
SA Santhosh Kumar ◽  
Sanjeev Balaji Pai
Keyword(s):  
Case Report ◽  
Cervical Spine ◽  
Aneurysmal Bone Cyst ◽  
Rare Case ◽  
Bone Cyst ◽  
Review Of Literature ◽  
Rare Case Report

scholarly journals Aneurysmal Bone Cyst of Medial End of Clavicle in a Child, a Rare Case Report

2014 ◽  
Vol 5 (2) ◽  
pp. 158-160 ◽  
Author(s):  
Kumar C. Yashavntha ◽  
K. B. Nalini ◽  
Jagdish Menon ◽  
D. K. Patro
Keyword(s):  
Case Report ◽  
Aneurysmal Bone Cyst ◽  
Rare Case ◽  
Bone Cyst ◽  
Rare Case Report

scholarly journals Triple Synchronous Primary Neoplasms of the Cervix, Endometrium, and Ovary: A Rare Case Report and Summary of All the English PubMed-Indexed Literature

2017 ◽  
Vol 2017 ◽  
pp. 1-6 ◽  
Author(s):  
Ahmed Abu-Zaid ◽  
Mohannad Alsabban ◽  
Mohammed Abuzaid ◽  
Osama Alomar ◽  
Hany Salem ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Single Case ◽  
English Literature ◽  
Genital System ◽  
Summary Table ◽  
Female Genital System ◽  
Rare Case Report ◽  
Primary Neoplasms ◽  
Female Genital

The incidence rate of triple or more synchronous primary neoplasms of the female genital system is exceedingly uncommon. To the best of our knowledge, only 13 such cases have been reported in the PubMed-indexed English literature. Herein, we report a single case of triple synchronous primary neoplasms of the cervix, endometrium, and left ovary with three distinct histological patterns that were not reported previously. Moreover, we briefly present a summary table of all the English PubMed-indexed cases of triple or more synchronous primary neoplasms of the female genital system (n=13).

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