scholarly journals Myxoid Chondrosarcoma of the Hyoid Bone

2018 ◽  
Vol 26 (3) ◽  
pp. 230-233
Author(s):  
Kinjal Majumdar ◽  
Nirmalya Samanta ◽  
Devjani Ghosh Shrestha ◽  
Kasturi Mondal ◽  
Utpal Jana

Introduction Chondrosarcoma of hyoid bone is very rare with only 19 cases still reported. We, therefore, present this case report for the interest of medical literature to make clinicians aware of the disease. Case Report They usually present as a slow growing upper neck mass. Computed tomography (CT) and magnetic resonance imaging (MRI) are useful radiologic investigations. The tumour was resected through a trans-cervical approach. Definite diagnosis was made by postoperative histopathology and immunohistochemistry. Discussion Surgical excision is the treatment of choice for local control. Incomplete removal is a risk factor for recurrence and possible dedifferentiation. Long term follow up is necessary.

2016 ◽  
Vol 24 (4) ◽  
pp. 365-368
Author(s):  
Hakan KORKMAZ ◽  
Meltem TULĞAR ◽  
Güleser SAYLAM ◽  
Engin DURSUN ◽  
Adil ERYILMAZ

2019 ◽  
Vol 29 (04) ◽  
pp. 267-271
Author(s):  
Muhammad Salman Khan ◽  
Amir Humza Sohail ◽  
Kiran Hilal ◽  
Muhammad Hassaan Arif Maan

The cells in glomus body regulate blood flow to the skin and play a role in temperature regulation. Glomuvenous malformations (GVMs), previously reported in literature as glomus tumors or glomangiomas, are usually present in the nail bed. In 1972, Carroll and Berman described the triad of paroxysmal stabbing pain, point tenderness, and cold hypersensitivity associated with these malformations.We present an unusual case of GVM in the neck of a 17-year-old female presenting with a painful right-sided neck mass. Physical examination revealed an approximately 2.5 × 2 cm right-sided tender neck mass; pain was exacerbated by probing with a pinhead. Computed tomography identified multiple rounded masses in the neck, with the delayed contrast filling. The patient underwent excisional biopsy of the lesion and samples were sent for histopathological examination.The histopathology report, along with the radiological findings and the clinical presentation, confirmed the diagnosis of GVM. The patient remained symptom-free on long-term follow-up.Despite absence of previous reports, GVM can occur in neck. Surgical excision can lead to complete resolution of symptoms.


Author(s):  
Eduardo Anitua ◽  
Beatriz Anitua ◽  
Mohammad Hamdan Alkhraisat ◽  
Laura Piñas ◽  
Asier Eguia

2015 ◽  
Vol 10 (4) ◽  
pp. 2465-2467 ◽  
Author(s):  
YU-BAO GONG ◽  
LI-MEI QU ◽  
XIN QI ◽  
JIAN-GUO LIU

2017 ◽  
Vol 23 (4) ◽  
pp. e9-e13
Author(s):  
S.A. Lalé ◽  
E.B. Burger ◽  
J.H.J.M. Bessems ◽  
V. Pollet ◽  
C.A. van Nieuwenhoven

2014 ◽  
Vol 44 (6) ◽  
pp. 863-868 ◽  
Author(s):  
Vlajković Marina ◽  
Rajić Milena ◽  
Petronijević Vesna ◽  
Petrović Slađana ◽  
Artiko Vera

FACE ◽  
2021 ◽  
pp. 273250162110536
Author(s):  
Joshua Harrison ◽  
Samantha Marley ◽  
Shawhin Shahriari ◽  
Christian Bowers ◽  
Anil Shetty

We report a rare case of an extramedullary plasmacytoma (EMP) in the frontal sinus with an indolent clinical presentation. Although a history of trauma was absent, the initial diagnosis was a mucocele, based on the radiological findings. Upon surgical excision, the patient was found to have an EMP. EMP, a form of solitary plasmacytoma, has a significantly high rate of conversion to multiple myeloma. This mandates long-term follow-up, even after successful radiotherapy and/or resection. While radiation therapy is generally considered a first line treatment for EMP, surgical intervention may provide optimal treatment in complicated cases. This case presentation highlights the prognosis of patients diagnosed with EMP.


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