A CASE OF SPLENIC HAMARTOMA WITH RENAL CELL CARCINOMA
نویسندگان
چکیده
منابع مشابه
SPLENIC HAMARTOMA: A CASE REPORT
A rare case of splenic harmartoma in a 31 year old female is reported. She was admitted with splenomegaly, fever and chronic history of epistaxis. Routine hematological survey revealed pancytopenia and mild hypercellular marrow. Abdominal sonography showed a space-occupying lesion in the spleen which was suspected as malignant tumor. Splenectomy was performed and histologic findings were d...
متن کاملsplenic hamartoma: a case report
a rare case of splenic harmartoma in a 31 year old female is reported. she was admitted with splenomegaly, fever and chronic history of epistaxis. routine hematological survey revealed pancytopenia and mild hypercellular marrow. abdominal sonography showed a space-occupying lesion in the spleen which was suspected as malignant tumor. splenectomy was performed and histologic findings were diagno...
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The standard therapy for thyroid cancer is total or near total thyroidectomy, followed by the administration of radioactive iodine for remnant ablation or residual disease. Patients with radioiodine therapy are predisposed to second malignant neoplasms in organs such as central nervous system (CNS), breast, prostate, kidney, bone marrow, salivary gland, and digestive tract. Exposure to carcinog...
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Introduction: Metastatic lesions of the oral cavity are extremely rare, accounting for approximately 1% of all malignant oral tumors. The most common primary sources of metastatic tumors in the oral region are, from the most to the least common, the breast, lung, kidney, bone, and colon. Renal cell carcinoma accounts for nearly 3% of all adult malignancies. It usually metastasizes to the lungs,...
متن کاملSplenic hamartoma associated with thrombocytopenia: A case report
INTRODUCTION Hamartomas are rare, benign tumors of the spleen. Few cases of splenic hamartomas associated with thrombocytopenia have been reported. PRESENTATION OF CASE An asymptomatic 64-year-old man with myelodysplastic syndrome was found to have a splenic tumor. Laboratory tests were significant for thrombocytopenia, with a platelet count of 7.8×104/μL. Ultrasonography showed splenomegaly ...
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ژورنال
عنوان ژورنال: Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association)
سال: 2000
ISSN: 1882-5133,1345-2843
DOI: 10.3919/jjsa.61.1283