An 8-yr-otd boy with a l-too history of culture-negative fever and anemia underwent gallium, ultrasound, and computed tomography studies as part of the evaluation of a fever of unknown origin. These studies revealed a mobile gallium-avid solid abdominal mass subsequently proven to be an inflam-matory pseudotumor of the mesentery, a rare benign mass. This report documents the gallium-avid nature of this rare lesion and discusses associated characteristic linical, path-ologic, and radiographic features. J Nucl Med 1991; 32:1614-1616 I n f lammatory pseudotumor is a rare pediatric abdominal mass with a characteristic clinical presentation (1). We discuss the pertinent clinical, pathologic, and radioiogic features of inflammatory pseudotumor an...
AbstractIntroductionInflammatory myofibroblastic tumor (IMT) is a rare benign tumor. Usually seen in...
AbstractInflammatory pseudotumor refers to a nonmalignant or low-grade neoplastic lesion characteriz...
inflammatory myofibroblastic tumors in children: report of an appendiceal case and review of th
INTRODUCTION: Inflammatory pseudotumor is a rare entity with a clinical and radiographic presentatio...
INTRODUCTION: Inflammatory pseudotumor is a rare entity with a clinical and radiographic presentatio...
Abstract. A 5-year-old boy presented with refractory microcytic anemia, growth failure, and markedly...
In this report we introduce an 8 years old boy with Transverse colon inflammatory pseudotumor.The p...
An inflammatory myofibroblastic tumor is an uncommon benign tumor located in various organs that can...
AbstractInflammatory pseudo tumor (IPT) is a rare benign lesion that can occur in any organ in the b...
Inflammatory pseudotumor is a benign, chronic, inflammatory disorder known by many names. This condi...
Background: Inflammatory pseudotumour has been used to describe an inflammatory or fibrosing tumoral...
Inflammatory pseudotumour (IPT) is a rare benign solid tumor in adults and children. The prevalence,...
Inflammatory pseudotumor is a rare benign tumor, which is histologically composed of stroma with con...
Inflammatory pseudotumor is a rare benign mesenchymal pediatric neoplasm, that can mimic tumoral res...
Inflammatory pseudotumor is an uncommon tumor with a variable natural course. We report a case of om...
AbstractIntroductionInflammatory myofibroblastic tumor (IMT) is a rare benign tumor. Usually seen in...
AbstractInflammatory pseudotumor refers to a nonmalignant or low-grade neoplastic lesion characteriz...
inflammatory myofibroblastic tumors in children: report of an appendiceal case and review of th
INTRODUCTION: Inflammatory pseudotumor is a rare entity with a clinical and radiographic presentatio...
INTRODUCTION: Inflammatory pseudotumor is a rare entity with a clinical and radiographic presentatio...
Abstract. A 5-year-old boy presented with refractory microcytic anemia, growth failure, and markedly...
In this report we introduce an 8 years old boy with Transverse colon inflammatory pseudotumor.The p...
An inflammatory myofibroblastic tumor is an uncommon benign tumor located in various organs that can...
AbstractInflammatory pseudo tumor (IPT) is a rare benign lesion that can occur in any organ in the b...
Inflammatory pseudotumor is a benign, chronic, inflammatory disorder known by many names. This condi...
Background: Inflammatory pseudotumour has been used to describe an inflammatory or fibrosing tumoral...
Inflammatory pseudotumour (IPT) is a rare benign solid tumor in adults and children. The prevalence,...
Inflammatory pseudotumor is a rare benign tumor, which is histologically composed of stroma with con...
Inflammatory pseudotumor is a rare benign mesenchymal pediatric neoplasm, that can mimic tumoral res...
Inflammatory pseudotumor is an uncommon tumor with a variable natural course. We report a case of om...
AbstractIntroductionInflammatory myofibroblastic tumor (IMT) is a rare benign tumor. Usually seen in...
AbstractInflammatory pseudotumor refers to a nonmalignant or low-grade neoplastic lesion characteriz...
inflammatory myofibroblastic tumors in children: report of an appendiceal case and review of th