A Rare Case of Bone Marrow Metastasis of a Splenic Angiosarcoma

10.5580/1bc5 ◽  
2010 ◽  
Vol 1 (2) ◽  
2014 ◽  
Vol 31 (4) ◽  
pp. 408-410 ◽  
Author(s):  
Soumaya Anoun ◽  
Sofia Marouane ◽  
Asmae Quessar ◽  
Said Benchekroun

2021 ◽  
Vol 116 (1) ◽  
pp. S837-S837
Author(s):  
Isaac S. Cho ◽  
Adrian Lugo ◽  
Jaydip B. Patel ◽  
Ahad Waraich ◽  
Swetha Chenna ◽  
...  

2020 ◽  
Vol 45 (1) ◽  
pp. e20-e23
Author(s):  
Hiroaki Takahashi ◽  
Tadashi Hara ◽  
Hideo Suzuki ◽  
Ryosuke Hashimoto ◽  
Manabu Minami

2010 ◽  
Vol 76 (9) ◽  
pp. 160-162
Author(s):  
Jashodeep Datta ◽  
Tania Zuluaga Toro ◽  
Vicki L. Keedy ◽  
Nipun B. Merchant

2021 ◽  
Vol 14 (4) ◽  
pp. e242315
Author(s):  
Joshua Van Allen

Urachal cancer is a rare and aggressive cancer that often presents in advanced stages. Given the rarity of this malignancy, medical case studies provide one of the few sources of literature available through which clinicians can guide medical management. Surgery is widely considered to be the mainstay of therapy when disease is localised and surgically resectable, therefore most current case studies on urachal cancer focus on surgical management, occasionally with adjuvant chemotherapy. However, few case studies discuss chemotherapy alone in the treatment of metastatic disease. Most studies indicate a median overall survival between 12 and 24 months for metastatic urachal adenocarcinoma. Bone marrow metastasis of solid tumours, when considered alone, portends a poor prognosis. The patient in this case study represents a rare case of stage IV urachal adenocarcinoma metastatic to the bone marrow without progression of disease after 6 months of treatment.


2019 ◽  
Vol 14 (10) ◽  
pp. S1062-S1063
Author(s):  
T. Omori ◽  
H. Takahashi ◽  
T. Tachibana ◽  
O. Uchida ◽  
H. Hirano ◽  
...  

2013 ◽  
Vol 31 (2) ◽  
pp. 131-136 ◽  
Author(s):  
Yuko Tanaka ◽  
Sumihito Nobusawa ◽  
Hayato Ikota ◽  
Hideaki Yokoo ◽  
Junko Hirato ◽  
...  

2014 ◽  
Vol 8 (6) ◽  
pp. 2672-2674 ◽  
Author(s):  
DO HYOUNG LIM ◽  
SOON IL LEE ◽  
KEON WOO PARK

Sarcoma ◽  
2003 ◽  
Vol 7 (3-4) ◽  
pp. 183-184 ◽  
Author(s):  
Kim Vaiphei ◽  
Virinder Singh ◽  
Subhash Varma

A middle aged chronic alcoholic presented with deep jaundice, markedly enlarged and tender spleen with leukoerythroblastic blood picture and bone marrow biopsy showing mild fibrosis. He was tested negative for HIV, hepatitis B and C viruses. Besides very high serum bilirubin, alkaline phosphatase was raised four times the normal value. Contrast enhanced CT showed enlarged spleen and liver with multiple heterogenous lesions in spleen and tiny hypo-dense lesions in liver. In hospital, he developed haemolytic uraemic syndrome and succumed to his illness. At autopsy spleen weighed 5200 gms and variegated in appearance due to large areas of necrosis and whitish tumour nodules. Histology revealed morphology of an angiosarcoma. Liver was also infiltrated by the tumour mainly in and around portal tract areas.


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