نتایج جستجو برای: extramedullary plasmacytoma

تعداد نتایج: 4906  

2017
Negi Preety Kingsley Pamela Alice Jomi Chinnu Mathew Amrith George Sneha Immanuel Vivek Abraham Puliyelil Abraham

Extramedullary plasmacytoma as a mode of relapse in multiple myeloma (MM) is unusual. Current recommendations do not incorporate the routine use of 18-fluorodeoxyglucose positron emission tomography-computed tomography (FDG PET/CT) imaging prior to haematopoietic stem cell transplant (HSCT) in MM. We report a case of relapsed MM with complete remission as per IMWG criteria. In the interim perio...

Journal: :Indian Journal of Pathology and Microbiology 2019

2012
Sevil Kilciksiz Omur Karakoyun-Celik Fulya Yaman Agaoglu Ayfer Haydaroglu

Solitary plasmacytoma (SP) is characterized by a mass of neoplastic monoclonal plasma cells in either bone (SBP) or soft tissue without evidence of systemic disease attributing to myeloma. Biopsy confirmation of a monoclonal plasma cell infiltration from a single site is required for diagnosis. The common presentation of SBP is in the axial skeleton, whereas the extramedullary plasmacytoma (EMP...

2012
Sevgi Kalayoglu-Besisik Ipek Yonal Fehmi Hindilerden Mehmet Agan Deniz Sargin

The most common site for localized forms of plasma cell neoplasms (extramedullary plasmacytoma; EMP) is the upper respiratory tract, including the oropharynx, nasal cavities, sinuses and larynx. A 50-year-old woman with a history of myeloma in complete remission after autologous stem cell transplantation complained of two weeks of epiphora of the left eye with subsequent diplopia, bloody nasal ...

Journal: :World journal of gastroenterology 2009
Wei Hong Xin-Min Yu Ming-Qiang Jiang Bo Chen Xin-Bao Wang Li-Tao Yang Yi-Ping Zhang

Extramedullary plasmacytoma (EPM) is a plasma cell tumor arising outside of the bone marrow. Solitary EMP is an uncommon neoplasm and rarely occurs in the retroperitoneum and lacks distinctive clinical manifestations. We report a 26-year-old man with a solitary EMP in the retroperitoneum and discuss its clinical features, diagnosis and treatment.

Journal: :International Journal of Hematology 2010

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