scholarly journals What do we know about intravascular fasciitis affecting inferior vena cava? management and report of a case

2017 ◽  
Vol 5 (1) ◽  
pp. 325
Author(s):  
Fernando Mendoza Moreno ◽  
Javier Minguez Garcia ◽  
Maria del Rocio Diez Gago ◽  
Gabriel Olmedilla Arregui ◽  
Benjamin Tallon Iglesias ◽  
...  

Intravascular fasciitis is a rare entity characterized by the proliferation of myofibroblasts and giant cells in relation to small and medium-sized blood vessels. It characterized by a rapid growth and its morphology can simulate other malignant neoplastic processes of more aggressive behavior such as sarcomas. It belongs to a group of benign lesions that affect the subcutaneous tissue and fascia (sometimes to the muscle) sharing characteristics similar to proliferative fasciitis, nodular fasciitis and proliferative myositis. It can sometimes be confused with lesions typical of fibromatosis even. We report a case of a patient with a symptomatic retroperitoneal mass who underwent surgery. The intraoperative findings showed a tumor originating in the inferior vena cava. The histopathological study revealed an intravascular fasciitis.

CHEST Journal ◽  
2017 ◽  
Vol 152 (4) ◽  
pp. A602
Author(s):  
Praneet Iyer ◽  
Rabin Shrestha ◽  
Muhammad Zaman

2013 ◽  
Vol 95 (4) ◽  
pp. e6-e9 ◽  
Author(s):  
SZ Koh ◽  
HY Tiong ◽  
S Wang ◽  
K Madhavan

Solitary fibrous tumours are infrequent neoplasms based in the pleura that are predominantly benign with malignant pathology and behaviour described in 10–36% of cases. Extrathoracic solitary fibrous tumours (ESFTs) have been considered separately to their intrathoracic counterparts and comprise a third of all solitary fibrous tumours. The extrathoracic location was identified as an adverse prognostic factor for local recurrence but not for metastatic disease. So far, there have not been any reports of solitary fibrous tumours demonstrating caval infiltration. We present a case of a benign ESFT infiltrating into the perirenal inferior vena cava. Together with extrauterine leiomyomas, ESFTs should also be considered as a differential diagnosis for the rare benign lesions invading the inferior vena cava.


2018 ◽  
Vol 2018 ◽  
pp. 1-5
Author(s):  
Sameera Rashid ◽  
Mohammed Akhtar

Sarcomatoid variant of urothelial carcinoma (SVUC) of the renal pelvis is a rare entity. To the best of our knowledge, around 25 cases of this neoplasm have been reported in the literature to date, most of which were of high stage. The inferior vena cava tumour thrombus, which is a hallmark of renal cell carcinoma (RCC), may rarely be found in urothelial carcinoma of renal pelvis. In this report, a case of SVUC associated with tumour extension to inferior vena cava is documented. This association has been encountered in only one previously reported case. The possibility of urothelial carcinoma of the renal pelvis should therefore be included in the differential diagnosis of tumour thrombus of the inferior vena cava.


2004 ◽  
Vol 54 (4) ◽  
pp. 256-260 ◽  
Author(s):  
Takashi Nikaido ◽  
Yasuhiko Endo ◽  
Satoshi Nimura ◽  
Hiroshi Ishikura ◽  
Shinichiro Ushigome

2015 ◽  
Vol 2015 ◽  
pp. 1-4 ◽  
Author(s):  
Aasim M. Afzal ◽  
Jamil Alsahhar ◽  
Varsha Podduturi ◽  
Jeffrey M. Schussler

Primary sarcomas of the great vessels (aorta, pulmonary artery, and inferior vena cava (IVC)) are exceedingly rare. We report a rare case of an undifferentiated intimal sarcoma of the IVC with extension to the right atrium, adrenal, and renal veins. The patient underwent extensive resection, reconstruction of the IVC, and subsequent adjuvant chemotherapy. Patient has tolerated chemotherapy and, at 17 months after resection, the patient remains free of tumor recurrence. Undifferentiated intimal sarcomas remain a rare entity with only five cases of venous undifferentiated intimal sarcomas reported in the literature, two of which occurred in the IVC. Intimal sarcomas tend to carry a poor prognosis with the limited literature available on treatment approaches. Our objective is to highlight this rare entity and possible treatment approach which we utilized. Primary sarcomas of IVC need to be included as part of a complete differential diagnosis in patients with atrial masses or recurrent pulmonary emboli.


2020 ◽  
Vol 152 (7) ◽  
pp. 155
Author(s):  
Rishikesh Velhal ◽  
PankajkumarJayprakash Zanwar

2001 ◽  
Vol 45 (4) ◽  
pp. 448-451 ◽  
Author(s):  
Deshmukh Hemant ◽  
Rathod Krantikumar ◽  
Joshi Amita ◽  
Ashish Chawla ◽  
Narlawar Ranjeet

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