scholarly journals Synchronous pancreatic metastasis from extraskeletal mesenchymal chondrosarcoma of the buttock

Suizo ◽  
2013 ◽  
Vol 28 (6) ◽  
pp. 792-799
Author(s):  
Chihiro KAWAGUCHI ◽  
Masayuki SHO ◽  
Takahiro AKAHORI ◽  
Shoichi KINOSHITA ◽  
Minako NAGAI ◽  
...  
2021 ◽  
Vol 7 (2) ◽  
Author(s):  
Afaque Ali ◽  
Sara Rehman ◽  
Kashif Siddique

Introduction: Extraskeletal mesenchymal chondrosarcoma (ESMC) is rare, aggressive, and high grade malignant tumors originating from soft tissues. It carries a poor prognosis with a tendency for local recurrence and distant metastasis, necessitating long-term follow-up. The most common sites for metastasis are the lungs, bones, and lymph nodes. Meanwhile, pancreatic metastases are extremely rare. Case Description: A 35-year-old female presented with a history of wide local excision for the left upper limb mass; histopathology showed ESMC. She was on surveillance with a computed tomography scan of the thorax and magnetic resonance imaging of the left upper limb at 3-months intervals until she developed vertebral and pancreatic lesions after 6 months post-surgery. No pulmonary metastases were noted. Considering the unusual site for metastasis and to exclude the possibility of any second malignancy, bone biopsy, and endoscopic ultrasound-guided fine-needle aspiration was performed that confirmed metastases. Later she developed osseous metastases in the pelvis and femora. Practical Implication: Pancreatic metastasis from ESMC is extremely rare. In case of new visceral or osseous lesions in a patient with a past medical history of ESMC, the possibility of metastatic disease should be considered. A biopsy can be performed to confirm the diagnosis.


Author(s):  
Saloni Naresh Shah ◽  
Ashok Parameswaran ◽  
Prasanna Kumar Reddy

AbstractExtraskeletal mesenchymal chondrosarcoma (ESMC) metastasizing to the pancreas in isolation is a rare occurrence. We report a 49-year-old gentleman who had undergone excision of an ESMC of the thigh in 2009 and presented with sudden onset abdominal pain and icterus in 2019. Radiological imaging revealed calcified mass of the pancreas with multiple nodules with extension into the adipose tissue. Distal pancreatectomy was performed and the pathology revealed a bimorphic tumor composed of undifferentiated round blue cells with abrupt transition to hyaline cartilage, typical of mesenchymal chondrosarcoma. To the best of our knowledge, there are only seven prior cases of metastatic ESMC of the pancreas in the English literature. Surgical intervention appears to be the preferred modality of treatment for metastatic pancreatic tumors. These patients may have long latency period before metastasizing and seem to have a good survival period post excision.


2018 ◽  
Vol 142 (11) ◽  
pp. 1421-1424 ◽  
Author(s):  
Komal Arora ◽  
Nicole D. Riddle

Extraskeletal mesenchymal chondrosarcoma is a rare soft tissue sarcoma arising from soft tissues, mainly of the lower extremities, meninges, and orbits. It usually presents during the second to third decades of life, and has a slight predominance in females. Histologically, it has a typical biphasic pattern comprising small cells and islands of hyaline cartilage. It can pose a diagnostic challenge in small biopsy specimens where 1 of the 2 components can be absent. The prognosis is extremely variable; survival varies depending on the location of the tumor.


2017 ◽  
Vol 24 (3) ◽  
pp. 181-186 ◽  
Author(s):  
Rajesh Chhabra ◽  
Manjul Tripathi ◽  
Devi Prasad Patra ◽  
Narendra Kumar ◽  
Bishan Radotra ◽  
...  

2020 ◽  
Vol 11 (02) ◽  
pp. 344-348
Author(s):  
Sandeep Bhardwaj ◽  
Ashish Sharma ◽  
Akangsha Sharma

AbstractMesenchymal chondrosarcoma of the brain is one of the rarest tumors with dismal prognosis. A 26-year-old man presented with headache, vomiting, and diplopia. On evaluation, a moderately enhancing extra-axial lesion was seen in right temporal region involving right greater wing of sphenoid, adjacent right maxillary sinus, and lateral wall of right orbit. Patient underwent magnetic resonance imaging of the spine and computed tomography (CT) of the chest for possible metastasis which showed lesion in lumbar vertebrae and left lung. Patient was planned for CT-guided lung biopsy which proved inconclusive. The patient was further planned for craniotomy and underwent craniotomy with microscopic excision of the mass. Histoimmunochemistry was suggestive of extraskeletal mesenchymal chondrosarcoma. Mesenchymal chondrosarcoma of the brain is highly aggressive tumors which are difficult to differentiate radiologically. Radical excision followed by chemoradiotherapy is optimal treatment of choice.


2017 ◽  
Vol 38 (10) ◽  
pp. 1058-1061 ◽  
Author(s):  
Hua Zhang ◽  
Shuai Wang ◽  
Zhihua Cheng ◽  
Han Liu

2006 ◽  
Vol 13 (3) ◽  
pp. 285-286 ◽  
Author(s):  
TAKUJI KANEKO ◽  
YASUSHI SUZUKI ◽  
RYO TAKATA ◽  
KOH TAKATA ◽  
TSUTOMU SAKUMA ◽  
...  

2015 ◽  
Vol 96 (9) ◽  
pp. 965-967 ◽  
Author(s):  
N. Ali ◽  
D. Vanel ◽  
A. Righi ◽  
M. Colangeli ◽  
M. Manfrini

Sign in / Sign up

Export Citation Format

Share Document