uncommon tumour
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2021 ◽  
pp. 10-11
Author(s):  
K Srinivasa Reddy ◽  
K Anusha ◽  
K B Vijaya Mohan Reddy

Giant cell tumour arises from the synovium of tendon sheath, joints, or bursae,mostly affects adults between 30 and 50 years of age, and is slightly more common in females.Giant cell tumour of tendon sheath of tendoachilles is uncommon tumour. Usually it has a high rate of recurrence. In this article we report the case of a 32 year old female with Giant cell tumour of tendoachilles treated by excision with no reccurence after 7 months of follow up


2020 ◽  
Vol 102 (7) ◽  
pp. e170-e172
Author(s):  
R Birla ◽  
S Clark ◽  
A Beattie ◽  
D Agarwal

2020 ◽  
Vol 31 (2) ◽  
pp. 113-115
Author(s):  
Egemen ISITAN ◽  
Esra UÇARYILMAZ ÖZHAMAM ◽  
Aydın Talat BAYDAR ◽  
Servet GÜREÇCİ ◽  
Özhan Merzuk UÇKUN ◽  
...  
Keyword(s):  

Author(s):  
Addina Mohd Baki ◽  
Rosdi Ramli ◽  
Rosli Mohd Noor ◽  
Irfan Mohamad ◽  
Murni Jais

2019 ◽  
Vol 50 (1) ◽  
pp. 65-68
Author(s):  
Ambuj Agarwal ◽  
Lileswar Kaman ◽  
Ashish Gupta ◽  
Krishna Ramavath ◽  
Kim Vaiphei

Neuroendocrine tumours (NET) are rare. They usually arise from the gastrointestinal or bronchopulmonary systems. Most are discovered incidentally and the small bowel tumours pose special difficulty in detection and treatment. Primary mesenteric involvement is very rare. Here we report such a case with a liver metastasis. This was preoperatively diagnosed and treated by enucleation of the mesenteric tumour together with right hepatectomy in a single sitting.


2019 ◽  
Vol 114 (1) ◽  
pp. S895-S895
Author(s):  
Praneeth Bandaru ◽  
Andrew Ofosu ◽  
Febin John ◽  
Madhavi Reddy

Author(s):  
Prita Pradhan ◽  
Rudra Narayan Biswal ◽  
Khageswar Rout ◽  
Ranjita Panigrahi ◽  
Pranati Misra ◽  
...  

<p class="abstract">Though the parapharyngeal space is sites of primary involvement by neoplastic process, they can rarely house masses descending from a base of skull tumour. Chordoma is an uncommon tumour of the skull base and sacrococcyx. Originating from the notochordal remnants, they are locally aggressive causing lytic destruction of the adjacent bony structures, particularly in the base of the skull. The use of surgery and adjuvant high-dose proton RT is documented to produce best results. Here we report a diagnostic challenge posed by a chordoma occurring as a parapharyngeal mass in a 68 year old male.</p>


2019 ◽  
Vol 12 (5) ◽  
pp. e228666 ◽  
Author(s):  
Eugene Wong ◽  
Siamak Choroomi ◽  
Carsten E Palme ◽  
Narinder Pal Singh

Esthesioneuroblastoma is an uncommon tumour, and isolated primary involvement of the maxillary sinus is exceedingly rare. Esthesioneuroblastoma has infrequently been reported as a source of paraneoplastic ectopic hormone production. We report a case of isolated primary maxillary esthesioneuroblastoma, presenting as idiopathic syndrome of inappropriate antidiuretic hormone (SIADH). A 17-year-old girl presented with symptoms consistent with SIADH and no sino-nasal symptoms. MRI to exclude pituitary tumour revealed an isolated lesion of the right maxillary sinus. Biopsy demonstrated esthesioneuroblastoma. The lesion was removed endoscopically as a single en bloc specimen. Following resection, the sodium level returned to normal. This is only the third report in the literature of a primary maxillary esthesioneuroblastoma presenting as SIADH.


2018 ◽  
Vol 10 (1) ◽  
pp. 199-203 ◽  
Author(s):  
Palki Dewan ◽  
Shubha P. Bhat ◽  
H. L. Kishan Prasad ◽  
Rajesh Ballal ◽  
K. Sajitha

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