Plasmacytoma of the Skull-base: A Rare Tumor
نویسندگان
چکیده
منابع مشابه
Plasmacytoma of the Skull-base: A Rare Tumor
Plasmacytoma of the skull-base is a rare entity. Differential diagnosis includes chordoma, osteosarcoma, carcinoma nasopharynx, meningioma, metastatic carcinoma, lymphoma, and multiple myeloma. Accurate and precise diagnosis is extremely important for plasmacytoma of the skull-base as its treatment and prognosis is different from other skull-base lesions. A 41-year-old man presented with concer...
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Solitary Plasmacytoma of the Skull (SPS) is very rare and only 35 cases have been reported in the English literature. It remains controversial whether a solitary plasmacytoma of the skull is essentially identical with a Solitary Plasmacytoma of Bone (SPB) or not. A solitary plasmacytoma of bone, which includes a solitary plasmacytoma of the skull, is characterized by a radiologically solitary b...
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Solitary bone plasmacytoma belongs to a group of lymphoproliferative clinical disorders typified by clonal proliferation of plasma cells. Solitary plasmacytoma typically involves a single bone or extramedullary site. It commonly occurs in the vertebrae or thorax, and rarely involves the mandible. The aim of this report is to present a rare case of solitary plasmacytoma of the jaws mimicking per...
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INTRODUCTION Special entities like solitary bone plasmocytoma (SBP) or extramedullary plasmacytoma (EMP) can be found in a less than 5% of patients with plasma cell disorders. EMP of the tongue represents very rare localization of the head and neck plasmacytoma. CASE REPORT We report a case of 78-years-old woman who developed EMP of the tongue base detected by the magnetic resonance imaging (...
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Solitary bone plasmacytomas are part of a wide range of monoclonal neoplasms that share a common progenitor in the B lymphocyte lineage. In their particular case, a single bone lesion is found, most frequently on the axial skeleton, having evidence of no other osteolytic lesions or systemic involvement. Diagnosis can sometimes prove to be difficult as they are rare tumors, occurring in 3 to 5% ...
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ژورنال
عنوان ژورنال: Cureus
سال: 2018
ISSN: 2168-8184
DOI: 10.7759/cureus.2073