Littoral Cell Angioma in a Patient with Epstein Syndrome

1997 ◽  
Vol 98 (2) ◽  
pp. 113-115 ◽  
Author(s):  
Sabah Sallah ◽  
Pablo Gonzalez ◽  
Diane M. Maia ◽  
Nïkos Kelekis ◽  
Richard Semelka
2011 ◽  
Vol 6 (3) ◽  
Author(s):  
Tarek Hanna ◽  
Deborah A. Baumgarten ◽  
Theodore M Friedman

2018 ◽  
Vol 51 (3) ◽  
pp. 222-227
Author(s):  
Yoshihiro Takahara ◽  
Yasuhiro Otsuka ◽  
Takeshi Ogasawara ◽  
Satoru Nomura ◽  
Hidehiko Uno ◽  
...  

2020 ◽  
Vol 8 ◽  
pp. 2050313X2095987
Author(s):  
Vaclav Opatrny ◽  
Vladislav Treska ◽  
Tomas Waloschek ◽  
Jiri Molacek

Spleen tumors are an uncommon disease. Littoral cell angioma belongs to the group of vascular tumors. It is believed that this tumor originates from the tissue of the red pulp sinuses, specifically from the cells that are lining the sinuses. If this rare tumor is diagnosed, it is necessary to search for synchronous or metachronous visceral neoplasia. Littoral cell angioma can also mimic metastatic lesion of the spleen. This case report wants to draw attention on this rare tumor of the spleen which is very often associated with other visceral malignancy.


Medicine ◽  
2019 ◽  
Vol 98 (11) ◽  
pp. e14825 ◽  
Author(s):  
Man-Jiang Li ◽  
Xuan Zhou ◽  
Jing-Yu Cao ◽  
Cheng-Zhan Zhu ◽  
San-Shun Zhou ◽  
...  

2011 ◽  
Vol 201 (2) ◽  
pp. e15-e17 ◽  
Author(s):  
Julia B. Pilz ◽  
Toralf Sperschneider ◽  
Thomas Lutz ◽  
Bruno Loosli ◽  
Christoph A. Maurer

2007 ◽  
Vol 188 (5) ◽  
pp. 1365-1366 ◽  
Author(s):  
Shweta Bhatt ◽  
Jiaoti Huang ◽  
Vikram Dogra

2014 ◽  
Vol 6 (02) ◽  
pp. 117-120
Author(s):  
Recep Bedir ◽  
İbrahim Şehitoğlu ◽  
Ahmet Salih Calapoğlu ◽  
Cüneyt Yurdakul

ABSTRACTLittoral cell angioma (LCA) is a rare, benign primary vascular neoplasm of the spleen. The tumor originates from the littoral cells lining the sinuses of the red pulp of the spleen. Preoperative distinction of this tumor from other benign or malign splenic lesions is difficult. Radiologically most cases present as multiple nodules. Definitive diagnosis can only be made histopathologically and immunohistochemically following splenectomy. This clinical situation can coexist with various malignancies and autoimmune disorders. Even though, it is mostly benign, since it has the potential to become malignant after splenectomy, long-term follow-up is required. We present an LCA case, which appeared as a solitary mass in the spleen of an 11-year-old girl with abdominal pain admitted to our hospital.


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