Results 251 to 260 of about 161,904 (296)
Splenic Vein Tumor Thrombosis in a Patient With an Oligometastatic Pancreatic Neuroendocrine Tumor: A Case Report and Literature Review. [PDF]
Francis A +5 more
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Splenic involvement by peripheral T-cell and NK-cell neoplasms
Seminars in Diagnostic Pathology, 2003In 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 ...
exaly +3 more sources
Surgical aspects of primary splenic neoplasms
The American Journal of Surgery, 1951Abstract 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
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Splenic Metastases from Mucinous Neoplasms of the Appendix and Colon
Tumori Journal, 2006Aims 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 +6 more
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Splenic Marginal Zone Lymphoma
The American Journal of Surgical Pathology, 1996The 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 +4 more
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Primary Splenic Angiosarcoma: Clinical and Imaging Manifestations of This Rare Aggressive Neoplasm
Current Problems in Diagnostic Radiology, 2016Primary 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 +7 more
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Accessory Splenic Stomach Wall Abscess Mass Simulating Neoplasm
Australian and New Zealand Journal of Surgery, 1974A case is described of the diagnostic dilemma presented by a mass in the fundus of the stomach which proved at laparotomy to be caused by a large granulation tissue mass central to accessory splenic tissue. Relevant extracts from the literature are quoted in a discussion of the problems arising from this unusual pathology.
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Surgical Endoscopy, 2005
Laparoscopic distal pancreatectomy to conserve the spleen is a beneficial operation for patients with benign and borderline malignancy in the pancreas. With this procedure, it is very desirable to preserve the splenic artery and vein as well.From May 2000 to July 2003, five laparoscopic distal pancreatectomies with preservation of the spleen and ...
H-S, Han +4 more
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Laparoscopic distal pancreatectomy to conserve the spleen is a beneficial operation for patients with benign and borderline malignancy in the pancreas. With this procedure, it is very desirable to preserve the splenic artery and vein as well.From May 2000 to July 2003, five laparoscopic distal pancreatectomies with preservation of the spleen and ...
H-S, Han +4 more
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Splenic metastasis from gastrointestinal neoplasms: a review.
Acta gastro-enterologica Belgica, 2012Spleen metastases from solid tumours are rather exceptional, especially for those located in the digestive tract. Although these lesions are usually associated with multivisceral disease at terminal stage, several cases of isolated lesions have also been described in the literature.
T, Delaunoit +3 more
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