scholarly journals Primary peritoneal serous carcinoma, an extremely rare malignancy: A case report and review of the literature

2016 ◽  
Vol 11 (6) ◽  
pp. 4063-4065 ◽  
Author(s):  
WOO-SUNG YUN ◽  
JUNG-MIN BAE
2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
Anders Kindberg Boysen ◽  
Paw Jensen ◽  
Preben Johansen ◽  
Karen Dybkær ◽  
Mette Nyegaard

Aggressive NK-cell leukemia is a rare malignancy with neoplastic proliferation of natural killer cells. It often presents with constitutional symptoms, a rapid declining clinical course, and a poor prognosis with a median survival of a few months. The disease is usually resistant to cytotoxic agents, and no treatment has emerged as the standard of care for these patients. We report a case of an 18-year-old male who obtains complete remission following two lines of combination chemotherapy. We describe in details our regimens for induction chemotherapy and perform a review of existing literature concerning treatment of aggressive NK-cell leukemia.


2020 ◽  
Author(s):  
Ankang Wang ◽  
Peng Cong ◽  
Zhenxing He ◽  
Yueyu Qu ◽  
Tao Hu ◽  
...  

Abstract BackgroundMetastasis of the pancreas to myxoid liposarcoma is very rare.Case presentationWe report a 43-year-old woman who underwent radical surgery for myxoid liposarcoma (MLPS) of the sigmoid colon 9 years earlier and for liposarcoma of the neck 7 years earlier. The lesion later metastasized to the pancreas, and we performed pancreaticoduodenectomy, which was pathologically confirmed as myxoid liposarcoma. Unfortunately, the patient died a year later from unexplained gastrointestinal bleeding.ConclusionsMyxoid liposarcoma is a very rare malignancy that carries a risk of invasion to the pancreas, and complete surgical resection is the best chance for clinical treatment.


1996 ◽  
Vol 105 (4) ◽  
pp. 289-294 ◽  
Author(s):  
M. Cristina Da Mosto ◽  
Alessandra Rinaldo ◽  
Carlo Marchiori ◽  
Alfio Ferlito

A case report of pleomorphic rhabdomyosarcoma of the larynx is presented. It is the first case in which the diagnosis is supported by immunohistochemical investigation. A critical review of the literature follows, evaluating the clinicopathologic features of this rare malignancy.


2006 ◽  
Vol 24 (4) ◽  
pp. 307-312 ◽  
Author(s):  
Lorenzo Leggio ◽  
Giovanni Addolorato ◽  
Ludovico Abenavoli ◽  
Anna Ferrulli ◽  
Christina D’Angelo ◽  
...  

2021 ◽  
Vol 91 (1) ◽  
Author(s):  
Guido Levi ◽  
Nicla Orzes ◽  
Silvia Uccelli ◽  
Francesca Cettolo ◽  
Marianna Arici ◽  
...  

Angiosarcoma is a rare malignancy of vascular origin, mostly originating from skin, soft tissues, and breast, but rarely also from the pleura. We present the case of a 55-year-old man who referred to our hospital for a spontaneous bilateral hemothorax. The CT angiography did not show any source of active bleeding; plus, no pleural or lung masses were observable. Cytological and microbiological analyses made on a sample of pleural fluid resulted negative. Despite numerous blood transfusions and thoracenteses, the patient deceased from hemorrhagic shock ten days later and the diagnosis of primary pleural epithelioid angiosarcoma was obtained only by autopsy. Additionally, we present a review of the literature about primary pleural angiosarcomas.


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