Results 261 to 270 of about 52,061 (305)

Surgical aspects of primary splenic neoplasms

American Journal of Surgery, 1951
Abstract 1. 1. The surgical aspects and implications of primary splenic neoplasm, as based on 171 malignant and thirty-two benign lesions collected from the literature, are presented and discussed. 2. 2. A case of hemangiosarcoma of the spleen first becoming manifest by spontaneous splenic rupture is presented.
M D, PAREIRA, J G, PROBSTEIN
exaly   +3 more sources

Splenic involvement by peripheral T-cell and NK-cell neoplasms

Seminars in Diagnostic Pathology, 2003
In contrast to B-cell lymphomas, the literature on the splenic pathology of peripheral T-cell and NK-cell lymphomas is limited. Several different patterns of splenic involvement can be observed in peripheral T-cell and NK-cell lymphomas: 1) solitary or multiple fleshy nodule, which is seen predominantly in tumors rich in large cells; 2) diffuse red ...
John Chan
exaly   +3 more sources

Neoplasms, Splenic, Malignant

2008
Piero Boraschi
exaly   +2 more sources

Neoplasms, Splenic, Benign

2008
Piero Boraschi
exaly   +2 more sources

Splenic Metastases from Mucinous Neoplasms of the Appendix and Colon

Tumori Journal, 2006
Aims and Background Splenic metastases associated with mucinous intraabdominal tumors have been an enigma in the radiologic and oncology literature. These focal parenchymal defects from a non-metastasizing malignancy within an organ that rarely develops metastatic foci, even with high-grade cancer, were studied.
Jacobo Cabanas, Jesus Esquivel, Gomes da Silva Rodrigo, Luis Zappa, Carlos Cerruto, Paul H Sugarbaker, Paulo Goldstein   +6 more
openaire   +2 more sources

Splenic Marginal Zone Lymphoma

The American Journal of Surgical Pathology, 1996
The splenic marginal zone is a morphologically and perhaps immunologically distinct B-cell compartment. Lymphomas arising from cells of the splenic marginal zone are rare. Here we describe the morphologic, immunologic, and clinical features of 14 cases. Patient age ranged from 35 to 79 years (median, 68 years) with a male-to-female ratio of 1:1.8.
R D, Hammer, A D, Glick, J P, Greer, R D, Collins, J B, Cousar   +4 more
openaire   +2 more sources

Primary Splenic Angiosarcoma: Clinical and Imaging Manifestations of This Rare Aggressive Neoplasm

Current Problems in Diagnostic Radiology, 2016
Primary splenic angiosarcoma is a rare and fatal neoplasm arising from vascular endothelial cells within the spleen. With an incidence of 2 cases per 10 million people worldwide, the diagnosis and treatment of this rare entity is unfamiliar and challenging.
Ali, Batouli, Samuel W, Fairbrother, Jan F, Silverman, Maria De Los Angeles, Muniz, Kevin B, Taylor, Mark A, Welnick, Sheri A, Mancini, Matthew S, Hartman   +7 more
openaire   +2 more sources