Splenic angiosarcoma: A clinicopathologic and immunophenotypic study of 28 cases

Keyphrases

• Tumor 100%
• Necrosis 100%
• Histiocytic 100%
• Immunophenotypic Profile 100%
• Splenomegaly 100%
• Clinicopathologic Study 100%
• Metastasis 50%
• Hemosiderin 50%
• Endothelial Cells 50%
• Anemia 50%
• Growth Pattern 50%
• Nodule 50%
• CD31 50%
• Neoplasms 50%
• Papillary 50%
• Abdominal Pain 50%
• Lysozyme 50%
• Immunohistochemical Study 50%
• Spleen 50%
• CD68 50%
• Fibrosarcoma 50%
• Sarcomatous 50%
• CD34 50%
• Lining Cells 50%
• Patients Included 50%
• Lymphosarcoma 50%
• Physical Findings 50%
• Vascular Differentiation 50%
• Endothelial Markers 50%
• Rare Neoplasm 50%
• Aggressive Therapy 50%
• Intracytoplasmic 50%
• Primary Angiosarcoma 50%
• Splenic Rupture 50%
• Malignant Fibrous 50%
• Cystic Spaces 50%
• Macroscopic Examination 50%

Medicine and Dentistry

• Angiosarcoma 100%
• Neoplasm 80%
• Diseases 80%
• Bleeding 40%
• Necrosis 40%
• Splenomegaly 40%
• Morphology 20%
• Endothelial Cell 20%
• Metastatic Carcinoma 20%
• Hemosiderin 20%
• Anemia 20%
• Fibrosarcoma 20%
• Abdominal Pain 20%
• Chlordane 20%
• Hyaline 20%
• Spleen Rupture 20%
• Extramedullary Hematopoiesis 20%
• Lysozyme 20%