scholarly journals Extraosseous Intradural Chondrosarcoma of the Cervical Spine: A Case Report with Brief Review of Literature

2018 ◽  
Vol 2018 ◽  
pp. 1-7
Author(s):  
Elizabeth Presutto ◽  
Sejal Patel ◽  
Joseph Fullmer ◽  
Sajeev Ezhapilli
Keyword(s):  
Case Report ◽  
Cervical Spine ◽  
Soft Tissue ◽  
Spinal Canal ◽  
Rare Case ◽  
Soft Tissue Sarcomas ◽  
Mesenchymal Chondrosarcoma ◽  
Review Of Literature ◽  
Imaging Characteristics ◽  
Mesenchymal Chondrosarcomas

Mesenchymal chondrosarcoma (MCS) is a malignant cancer of the cartilage that accounts for less than 1% of all chondrosarcomas and typically occurs within the bone. One-third of all mesenchymal chondrosarcomas are extraosseous soft tissue sarcomas, rendering this as an uncommon entity. We report a rare case of an extraosseous chondrosarcoma with the cervical spinal canal in a 21-year-old male. The purpose of this case report is to discuss the imaging characteristics of this pathology proven diagnosis.

scholarly journals Well-Differentiated Liposarcoma of The Larynx: A Case Report and Review of Literature

2016 ◽  
Vol 9 (1) ◽  
pp. 85-89
Author(s):  
Svetlana A. Mateva ◽  
Margarita R. Nikolova ◽  
Alexandar V. Valkov ◽  
Margarita R. Nikolova
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Soft Tissue Sarcomas ◽  
World Health ◽  
Low Grade ◽  
Review Of Literature ◽  
Grade Malignancy ◽  
Well Differentiated ◽  
Health Organization ◽  
Histologic Types

Summary Liposarcoma is one of the most common soft tissue sarcomas in adults with a relative incidence amongst other sarcomas ranging from 9.8% to 16%. It usually locates in the limbs and retroperitoneum. Primary liposarcomas of the larynx and hypopharynx are rare, comprising less than 20% of all head and neck liposarcomas. According to World Health Organization, these tumors are divided into four histologic types, and well-differentiated liposarcoma is the most common one. It is a tumor of low-grade malignancy that may recur locally, but does not metastasize. We present a case of laryngopharyngeal well- differentiated liposarcoma in an old patient with two previous removals. We also discuss recently published cases with this unusual location of liposarcoma.

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 Oral focal mucinosis of gingiva - a rare case report and review of literature

2017 ◽  
Vol 5 (1) ◽  
pp. 26
Author(s):  
Chandini Dabbiru ◽  
Raghavendra Mahadev Naik ◽  
Kishore Moturi ◽  
Govind Rajkumar
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Histopathological Examination ◽  
Excisional Biopsy ◽  
Unknown Etiology ◽  
Review Of Literature ◽  
Soft Tissue Lesion ◽  
Rare Case Report ◽  
Myxoid Degeneration

Oral focal mucinosis (OFM) is a rare soft-tissue lesion of unknown etiology. Clinically it appears as asymptomatic round lesions and histologically, characterized by focal myxoid degeneration of connective tissue with presence of stellate shaped fibroblasts which were also evident in the present case. This case report stresses on the fact that diagnosis of OFM is almost impossible hence diagnosis should be confirmed by histopathological examination following incisional or excisional biopsy. Through this article we present a rare case of one such lesion on the gingiva and enumerate the most characteristic and myxomatous lesions. Thus though rare, OFM must be considered in the differential diagnosis of soft tissue overgrowths in oral cavity. Here, we describe the clinical and histopathological   presentation and subsequent management of OFM in a female patient.

scholarly journals A rare case of necrotizing fasciitis of eyelid in a young immunocompetent lady- case report and review of literature

2021 ◽  
Vol 7 (11) ◽  
pp. 1834
Author(s):  
Nithya Venkataramani ◽  
Sonali Muralidhar ◽  
Ravi Sachidananda
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Early Identification ◽  
Rare Case ◽  
Rare Condition ◽  
Necrotising Fasciitis ◽  
Aggressive Treatment ◽  
Review Of Literature ◽  
Significant Morbidity ◽  
Rapid Spread

<p class="abstract">Necrotising fasciitis of the periorbital region is a rare condition where there is destruction of the periorbital soft tissue with potential of rapid spread causing significant morbidity and mortality. It is generally seen in immuno suppressed individuals following trivial trauma. Here we present a case of periorbital necrotising fasciitis in a young immonocompetent lady with emphasis on early identification and aggressive treatment to prevent loss of vision and mortality.</p>

scholarly journals Congenital Angiosarcoma, a Case Report and Review of Literature

2020 ◽  
Vol 30 (5) ◽  
Author(s):  
Mansoureh Shokripour ◽  
Bita Geramizadeh ◽  
Babak Samizadeh ◽  
Mohammad Sadegh Masoudi
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Histological Grade ◽  
Soft Tissue Sarcomas ◽  
Tumor Location ◽  
Review Of Literature ◽  
Skull Bone ◽  
Bone Invasion ◽  
Case Presentation ◽  
Clinical Behavior

Introduction: Angiosarcoma, originating from vessels, constitutes about 0.2% to 0.3% of all pediatric soft tissue sarcomas. Prognosis of angiosarcoma is poor and depends on patient’s age, tumor location, size, histological grade and extent of tumor progression. Case Presentation: We report a rare case of a congenital angiosarcoma of scalp with dural and skull bone invasion in a one-month-old boy. His mother noticed the mass 2 days after birth as a very small insignificant nodule, but it grew rapidly afterward. Conclusions: The treatment consisted of only a wide surgical resection. After 15 months there was no sign of local recurrence or metastasis was noticeable and the tumor showed favorable outcome. This case indicates the possibility of a better clinical behavior in congenital angiosarcoma.

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