scholarly journals Invasive and the largest pancreatic tumour of Rare Intraabdominal Desmoid-type fibromatosis with curative resection: case report

Author(s):  
Hanan Alghamdi

fibromatoses (Desmoid-type) tumour is rare benign fibrous tumours account approximately for 0.03% of all neoplasms. The Pancreas origin of this tumour is even more rarely reported subset with around 5% only. We aim to report the success in cure a rare and the largest pancreatic desmoid-type

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Kozue Matsuishi ◽  
Kojiro Eto ◽  
Atsushi Morito ◽  
Hirokazu Hamasaki ◽  
Keisuke Morita ◽  
...  

Abstract Background Solitary fibrous tumor (SFT) is a relatively rare mesenchymal tumor that mainly affects adults. Its prognosis is good after curative resection, but distant recurrences after 10 years or longer have been reported. Recurrent SFT usually arises as a local lesion; distant metastasis is rarely reported. Here, we report lung metastases that recurred a decade after excising a retroperitoneal primary SFT. Case presentation A 44-year-old woman had an SFT resected from her right retroperitoneum at our hospital. Ten years later, at age 54, she underwent a lung resection after CT showed three suspected metastases in her left lung. All three were histologically diagnosed as lung metastases from the retroperitoneal SFT. However, whereas the primary SFT had 1–2 mitotic cells/10 high power fields (HPF), the metastatic lesion increased malignancy, at 50/10 HPF. Conclusion Patients who have had resected SFTs should be carefully followed up, as malignancy may change in distant metastasis, as in this case.


Author(s):  
Yuki Matsui ◽  
Madoka Hamada ◽  
Yuki Matsumi ◽  
Mitsugu Sekimoto ◽  
Mitsuaki Ishida ◽  
...  

Lupus ◽  
2008 ◽  
Vol 17 (6) ◽  
pp. 586-590 ◽  
Author(s):  
S van Wissen ◽  
BAJ Bastiaansen ◽  
AK Stroobants ◽  
EJ van den Dool ◽  
MM Idu ◽  
...  

2014 ◽  
Vol 7 (1) ◽  
Author(s):  
Katsunobu Sakurai ◽  
Kazuya Muguruma ◽  
Akihiro Murata ◽  
Takahiro Toyokawa ◽  
Ryosuke Amano ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Ashraf Al-Faouri ◽  
Khaled Ajarma ◽  
Samer Alghazawi ◽  
Sura Al-Rawabdeh ◽  
Adnan Zayadeen

The rarity of glucagonoma imposes a challenge with most patients being diagnosed after a long period of treatment for their skin rash (months-years). Awareness of physicians and dermatologists of the characteristic necrolytic migratory erythema often leads to early diagnosis. Early diagnosis of glucagonoma even in the presence of resectable liver metastases may allow curative resection. Herein, we present a typical case of glucagonoma treated at our center and review the literature pertinent to its management.


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