scholarly journals Spindle Cell Liposarcoma – A Rare Tumour Occurring at a Rare Site?

Author(s):  
Varuna Mallya
Keyword(s):  
2019 ◽  
Vol 12 (10) ◽  
pp. e231959
Author(s):  
Nishu Bhardwaj ◽  
Rajni Yadav ◽  
Venkatesan Sampath Kumar ◽  
Shah Alam Khan

Melanotic neuroectodermal tumour of infancy (MNTI) is an uncommon tumour, predominantly occurring in head and neck, mostly maxilla, but also in skull and mandible. Although a benign lesion, it is known to recur in 15%–27% of cases, and rarely, may undergo malignant transformation. We present a case of a 5-month-old female patient, who presented with a gradually progressive swelling in the right thigh. On imaging, an osteolytic lesion was seen, involving the metadiaphysis of shaft of right femur. A biopsy was performed, on which diagnosis of MNTI was made. MNTI is rarely seen in extremities. To the best of our knowledge, only six cases have been reported in femur, the present case being the seventh. The tumour showed spontaneous regression on follow-up in our patient, which has rarely been described. A knowledge of characteristic morphology and immunohistochemistry is the key to differentiate it from other tumours.


1986 ◽  
Vol 10 (4) ◽  
pp. 261-263 ◽  
Author(s):  
A. O. El-Tabbakh ◽  
K. M. Al-Arabi

2020 ◽  
Vol 4 (4) ◽  
pp. 1-7 ◽  
Author(s):  
Qianqian Wang ◽  
Xiaojie Wang ◽  
Qing Zhu ◽  
Xinghua Gu ◽  
Peng Gao ◽  
...  

Abstract Background Primary extraskeletal chondroblastic osteosarcoma has very poor prognosis, especially in the elderly. The pericardium is an extremely rare site for this tumour. Case summary A 67-year-old man presented with a large pericardial effusion and an intrapericardial mass. His past medical history of pulmonary tuberculosis led us to initially suspect tuberculous pericarditis. Primary extraskeletal chondroblastic osteosarcoma arising from the pericardium was diagnosed by the pathologist after surgery. The patient suffered severe intraoperative blood loss and surgical trauma. He went into shock and died a few hours after surgery. Discussion Extraskeletal chondroblastic osteosarcoma is a very rare tumour with a grim prognosis. Clinical manifestations frequently are not specific and can be explained by associated pathology. In this report, we describe an unusual case of primary extraskeletal chondroblastic osteosarcoma located in the pericardium and present a review of the literature.


2020 ◽  
Vol 2020 ◽  
pp. 1-4
Author(s):  
Pamathy Gnanaselvam ◽  
Malintha Lahiru ◽  
Mariathas Priatharshan ◽  
Umesh Jayarajah ◽  
Kathirvetpillai Kopinath

Primary spindle cell sarcoma is a rare tumour. The presentation of acute intra-abdominal bleeding from a metastatic spindle cell tumour has not been previously reported. We report a case of a 40-year-old woman with a history of curative resection of the medial compartment of the right thigh for spindle cell sarcoma presenting with an acute onset abdominal pain and haemorrhagic shock after 5 uneventful years. Emergency exploratory laparotomy was conducted that revealed a retropancreatic mass which had ruptured along its inferior border. Histological evaluation revealed a metastatic deposit of the spindle cell sarcoma. In cases of spontaneous abdominal haemorrhage, it is important to consider the possibility of a ruptured metastatic deposit among the differentials especially in patients with a history of malignancies. Moreover, this is the first reported case of metastatic malignant spindle cell sarcoma presenting with intra-abdominal haemorrhage.


2011 ◽  
Vol 2011 ◽  
pp. 1-4
Author(s):  
Prateek Kinra ◽  
V. Srinivas ◽  
Kavita Sinha ◽  
Vibha Dutta

Spindle cell carcinoma of the tonsillar pillar is a rare malignancy. A case of spindle cell carcinoma of the anterior tonsillar pillar in a 59-year-old man is presented. A growth on the anterior tonsillar pillar, measuring9×7×6 mm, was resected. The neoplasm occurred as a complication of radiotherapy (excessive cumulative radiation dose of 60 Gray) for carcinoma larynx with a latency period of three years. Postradiation spindle cell carcinoma is an uncommon disease manifesting as sarcoma in a previously irradiated field, usually with a latent period of 5 years or more. Literature is limited to small series. Histologically, this tonsillar growth was composed of a squamous cell carcinoma (epithelial component) and a spindle cell sarcomatous component. The two components of the tumour were confirmed using the immunohistochemical staining (cytokeratin and vimentin). Further p53 positivity of the sarcomatous elements aided in ruling out radiation-induced nonmalignant changes of mesenchymal tissue. This paper discusses this rare tumour in a common setting.


2016 ◽  
Vol 1 (3) ◽  
pp. 126
Author(s):  
SohaelM Khan ◽  
Karan Mane ◽  
Shraddha Singhania ◽  
Mahendra Gudhe ◽  
Saherish Khan ◽  
...  

Author(s):  
Jiangyuan Zhou ◽  
Kaiying Yang ◽  
Yi Ji
Keyword(s):  

Dental Update ◽  
2019 ◽  
Vol 46 (7) ◽  
pp. 684-685
Author(s):  
Amandeep Bains ◽  
Thomas Dennis ◽  
Dimtrios Doumpiotis

This case report demonstrates the management of a myoepithelioma in the minor salivary glands of the palate. Myoepitheliomas are rare, benign, salivary gland tumours which usually affect the parotid glands. The rare neoplasms only account for 1–1.5% of all salivary gland neoplasms. This case shows a minimal approach to treating this rare tumour found in a rare site. CPD/Clinical Relevance: This case demonstrates the potential for rapid epithelial recovery within the oral cavity.


2018 ◽  
Vol 69 (2) ◽  
pp. 189-194 ◽  
Author(s):  
Magro Gaetano ◽  
Angelico Giuseppe ◽  
Spadola Saveria ◽  
Ragusa Rosalia ◽  
Righi Alberto ◽  
...  

2016 ◽  
Vol 21 (2) ◽  
pp. 108
Author(s):  
K.K. Mane ◽  
S Khan ◽  
S Singhania ◽  
M Gudhe ◽  
G Mundada ◽  
...  

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