1.Pelvic Solitary Plasmacytoma: Computed Tomography and Magnetic Resonance Imaging Findings with Histopathologic Correlation.
Ying WANG ; Xiu Liang ZHU ; Mohamad Wasil PEEROO ; Zi Hua QIAN ; Dan SHI ; Shu Mei WEI ; Ri Sheng YU
Korean Journal of Radiology 2015;16(1):146-153
OBJECTIVE: To describe the imaging features of pelvic solitary plasmacytoma and to correlate them with the pathologic grade. MATERIALS AND METHODS: A retrospective study was performed on the imaging features of 10 patients with a histological diagnosis of pelvic solitary plasmacytoma. The imaging studies were assessed for bone expansion, cortical destruction, signal intensity/density of soft tissue mass and enhancement manifestations, which were then correlated to the pathologic grade. RESULTS: The imaging features of pelvic solitary plasmacytoma revealed 3 different types: multilocular type (n = 5), unilocular type (n = 2) and complete osteolytic destruction type (n = 3) on computed tomography and MRI. Pathologically, the tumors were classified into low, intermediate and high grades. Features such as multilocular change, perilesional osteosclerosis, slight expansion, local bone cortex disruptions and masses inside bone destruction, often suggest a low-grade solitary plasmacytoma; complete osteolytic destruction, huge soft tissue mass, and osseous defects imply a higher pathologic grade. CONCLUSION: Pelvic solitary plasmacytoma has various imaging manifestations, while a slight expansile osteolytic feature with multilocular change or homogeneous enhancement highly suggests its diagnosis. The distinctive imaging features of pelvic solitary plasmacytoma are well correlated to the pathologic grade.
Adult
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Aged
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Female
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Humans
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Magnetic Resonance Imaging
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Male
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Middle Aged
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Neoplasm Grading
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Pelvic Neoplasms/*pathology/radiography
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Plasmacytoma/*pathology/radiography
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Retrospective Studies
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Tomography, X-Ray Computed
2.A Case of Primary Plasmacytoma of Lymph Nodes.
Young Hyo LIM ; Su Kyoung PARK ; Ho Suk OH ; Jung Hye CHOI ; Myung Ju AHN ; Young Yul LEE ; In Soon KIM
The Korean Journal of Internal Medicine 2005;20(2):183-186
Extramedullary plasmacytoma may originate in any organ, either as a primary tumor or as a facet of systemic multiple myeloma. These solid lesions most commonly affect the upper respiratory tract, gastrointestinal and urogenital tract, skin, and lung. Primary plasmacytoma of the lymph node is a rare hematologic neoplasm, which usually manifests as an enlargement of the cervical lymph nodes with no evidence of any other plasma cell dyscrasia. A 56-year-old man was admitted, due to the presence of multiple palpable masses in the right cervical and submandibular areas. Surgical resection revealed plasmacytoma of the lymph nodes. According to our full work-up, no evidence of the systemic involvement of plasma cell dyscrasia was discovered and thus, the diagnosis of primary plasmacytoma of the lymph node was made. Radiotherapy was administered, and the remnant mass was reduced substantially, to 1 x 2 cm in size. The patient was scheduled to be monitored by a PET CT scan, as well as by a neck CT scan.
Biopsy, Needle
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Bone Marrow/pathology
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Diagnosis, Differential
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Humans
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Lymph Node Excision
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*Lymph Nodes/pathology/radiography
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Male
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Middle Aged
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Neck
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Plasmacytoma/*diagnosis/surgery
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Tomography, X-Ray Computed
3.Extramedullary plasmacytoma in the maxillary sinus.
M A Megat SHIRAZ ; Y H JONG ; S H Primuharsa PUTRA
Singapore medical journal 2008;49(11):e310-1
Extramedullary plasmacytoma is a rare malignant plasma cell tumour. We report an extremely aggressive case of extramedullary plasmacytoma of the right maxillary sinus, which had metastasised to the brain and rib. A 56-year-old man presented with recurrent epistaxis and acute anaemia. Nasendoscopy revealed a medialised medial wall of the right maxilla and a mass occupying the whole nasopharynx. Magnetic resonance imaging revealed a right maxillary tumour with extension to the ipsilateral nasal cavity, nasopharynx, right sphenoid and ethmoidal sinuses. There was an extra-axial brain metastasis. There were metastases to the right parietal region and left eighth rib. Histopathology examination of the maxillary mass revealed abundant plasma cells with kappa-chain restriction. He was planned for four cycles of chemotherapy. Unfortunately, in view of the advanced stage of disease, he succumbed to his disease during the first cycle of chemotherapy.
Anemia
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complications
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Antineoplastic Agents
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therapeutic use
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Brain Neoplasms
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diagnosis
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pathology
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Fatal Outcome
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Humans
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Magnetic Resonance Imaging
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methods
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Male
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Maxillary Sinus
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diagnostic imaging
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pathology
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Maxillary Sinus Neoplasms
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diagnosis
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diagnostic imaging
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pathology
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Middle Aged
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Nasopharynx
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pathology
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Neoplasm Metastasis
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Plasmacytoma
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diagnosis
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diagnostic imaging
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pathology
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Radiography