形質細胞腫瘍
- 関
- plasma cell tumor
WordNet
- small room in which a monk or nun lives (同)cubicle
- a device that delivers an electric current as the result of a chemical reaction (同)electric cell
- a room where a prisoner is kept (同)jail cell, prison cell
- (biology) the basic structural and functional unit of all organisms; they may exist as independent units of life (as in monads) or may form colonies or tissues as in higher plants and animals
- any small compartment; "the cells of a honeycomb"
- a small unit serving as part of or as the nucleus of a larger political movement (同)cadre
- (physical chemistry) a fourth state of matter distinct from solid or liquid or gas and present in stars and fusion reactors; a gas becomes a plasma when it is heated until the atoms lose all their electrons, leaving a highly electrified collection of nuclei and free electrons; "particles in space exist in the form of a plasma"
- a green slightly translucent variety of chalcedony used as a gemstone
- the colorless watery fluid of the blood and lymph that contains no cells, but in which the blood cells (erythrocytes, leukocytes, and thrombocytes) are suspended (同)plasm, blood_plasma
PrepTutorEJDIC
- (刑務所の)『独房』;(修道院の)小さい独居室 / (ミツバチの)みつ房,巣穴 / 小さい部屋 / 『細胞』 / 電池 / 花粉室 / (共産党などの)細胞
- (また『blood plasma』)血漿,リンパ漿 / 原形質
- (体内にできる)新生物;腫瘍(しゅよう)
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/06/12 19:25:09」(JST)
[Wiki en表示]
Plasma cell dyscrasia |
Classification and external resources |
ICD-10 |
C90 |
ICD-O: |
9730-9739 |
MeSH |
D054219 |
Plasma cell dyscrasias are cancers of the plasma cells. Plasma cell dyscrasias are produced as a result of malignant proliferation of a monoclonal population of plasma cells that may or may not secrete detectable levels of a monoclonal immunoglobulin or paraprotein commonly referred to as M protein. Although the most common plasma cell dyscrasia is monoclonal gammopathy of undetermined significance (MGUS); closely related disorders include multiple myeloma, solitary plasmacytoma of bone, extramedullary plasmacytoma, Waldenström's macroglobulinemia (WM), primary amyloidosis, light chain deposition disease and heavy-chain disease. The spectrum of MGUS, solitary plasmacytoma of bone, and asymptomatic and symptomatic multiple myeloma may actually represent a natural progression of the same disease.[1]
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This article needs additional citations for verification. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. (February 2013) |
See paraproteinemia
Classification[edit]
- Cryoglobulinemia
- Heavy chain disease
- Monoclonal gammopathy of undetermined significance
- Multiple myeloma
- Plasmacytoma
- Plasma cell leukemia
- POEMS syndrome
- Primary amyloidosis (Immunoglobulin light chain amyloidosis)
- Waldenström's macroglobulinemia
References[edit]
- ^ http://www.accessmedicine.com/content.aspx?aid=2794254 DEAD URL DEC 2012
External links[edit]
- Multiple Myeloma and Other Plasma Cell Dyscrasias. 2011
Immune disorders, Immunoproliferative immunoglobulin disorders (D89, 273)
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PCDs/PP |
Plasmacytoma · Multiple myeloma (Plasma cell leukemia) · MGUS · IgM (Macroglobulinemia/Waldenström's macroglobulinemia) · heavy chain (Heavy chain disease) · light chain (Primary amyloidosis)
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Other hypergammaglobulinemia |
Cryoglobulinemia
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cell/phys/auag/auab/comp, igrc
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Hematological malignancy/leukemia histology (ICD-O 9590–9989, C81–C96, 200–208)
Lymphoid/Lymphoproliferative, Lymphomas/Lymphoid leukemias (9590–9739, 9800–9839)
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B cell
(lymphoma,
leukemia)
(most CD19
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By development/
marker
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TdT+
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- ALL (Precursor B acute lymphoblastic leukemia/lymphoma)
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CD5+
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mantle zone (Mantle cell)
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CD22+
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- Prolymphocytic
- CD11c+ (Hairy cell leukemia)
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CD79a+
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- germinal center/follicular B cell (Follicular
- Burkitt's
- GCB DLBCL
- Primary cutaneous follicular lymphoma)
marginal zone/marginal-zone B cell (Splenic marginal zone
- MALT
- Nodal marginal zone
- Primary cutaneous marginal zone lymphoma)
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RS (CD15+, CD30+)
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- Classic Hodgkin's lymphoma (Nodular sclerosis)
- CD20+ (Nodular lymphocyte predominant Hodgkin's lymphoma)
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PCDs/PP
(CD38+/CD138+)
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- see immunoproliferative immunoglobulin disorders
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By infection
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- KSHV (Primary effusion)
- EBV (Lymphomatoid granulomatosis
- Post-transplant lymphoproliferative disorder)
- HIV (AIDS-related lymphoma)
- Helicobacter pylori (MALT lymphoma)
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Cutaneous
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- Diffuse large B-cell lymphoma
- Intravascular large B-cell lymphoma
- Primary cutaneous marginal zone lymphoma
- Primary cutaneous immunocytoma
- Plasmacytoma
- Plasmacytosis
- Primary cutaneous follicular lymphoma
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T/NK
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T cell
(lymphoma,
leukemia)
(most CD3
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By development/
marker
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- TdT+: ALL (Precursor T acute lymphoblastic leukemia/lymphoma)
- prolymphocyte (Prolymphocytic)
- CD30+ (Anaplastic large-cell lymphoma
- Lymphomatoid papulosis type A)
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Cutaneous
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MF+variants
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- indolent: Mycosis fungoides
- Pagetoid reticulosis
- Granulomatous slack skin
aggressive: Sézary's disease
- Adult T-cell leukemia/lymphoma
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Non-MF
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- CD30-: Non-mycosis fungoides CD30− cutaneous large T-cell lymphoma
- Pleomorphic T-cell lymphoma
- Lymphomatoid papulosis type B
CD30+: CD30+ cutaneous T-cell lymphoma
- Secondary cutaneous CD30+ large cell lymphoma
- Lymphomatoid papulosis type A
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Other peripheral
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- Hepatosplenic
- Angioimmunoblastic
- Enteropathy-associated T-cell lymphoma
- Peripheral T-cell lymphoma-Not-Otherwise-Specified (Lennert lymphoma)
- Subcutaneous T-cell lymphoma
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By infection
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- HTLV-1 (Adult T-cell leukemia/lymphoma)
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NK cell/
(most CD56)
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- Aggressive NK-cell leukemia
- Blastic NK cell lymphoma
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T or NK
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- EBV (Extranodal NK-T-cell lymphoma/Angiocentric lymphoma)
- Large granular lymphocytic leukemia
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Lymphoid+myeloid
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- Acute biphenotypic leukaemia
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Lymphocytosis
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- Lymphoproliferative disorders (X-linked lymphoproliferative disease
- Autoimmune lymphoproliferative syndrome)
- Leukemoid reaction
- Diffuse infiltrative lymphocytosis syndrome
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Cutaneous lymphoid hyperplasia |
- Cutaneous lymphoid hyperplasia with bandlike and perivascular patterns
- Cutaneous lymphoid hyperplasia with nodular pattern
- Jessner lymphocytic infiltrate of the skin
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cell/phys/auag/auab/comp, igrc
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UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- TAK-228 (formerly MLN0128), an investigational oral dual TORC1/2 inhibitor: A phase I dose escalation study in patients with relapsed or refractory multiple myeloma, non-Hodgkin lymphoma, or Waldenström's macroglobulinemia.
- Ghobrial IM1, Siegel DS2, Vij R3, Berdeja JG4, Richardson PG1, Neuwirth R5, Patel CG6, Zohren F7, Wolf JL8.
- American journal of hematology.Am J Hematol.2016 Jun;91(4):400-5. doi: 10.1002/ajh.24300.
- The PI3K/AKT/mTOR signaling pathways are frequently dysregulated in multiple human cancers, including multiple myeloma (MM), non-Hodgkin lymphoma (NHL), and Waldenström's macroglobulinemia (WM). This was the first clinical study to evaluate the safety, tolerability, maximal-tolerated dose (MTD), do
- PMID 26800393
- Bone marrow infiltration by multiple myeloma causes anemia by reversible disruption of erythropoiesis.
- Bouchnita A1, Eymard N1, Moyo TK2, Koury MJ2, Volpert V1,3.
- American journal of hematology.Am J Hematol.2016 Jun;91(4):371-8. doi: 10.1002/ajh.24291. Epub 2016 Feb 9.
- Multiple myeloma (MM) infiltrates bone marrow and causes anemia by disrupting erythropoiesis, but the effects of marrow infiltration on anemia are difficult to quantify. Marrow biopsies of newly diagnosed MM patients were analyzed before and after four 28-day cycles of nonerythrotoxic remission indu
- PMID 26749142
- Low immunoglobulin A levels detected via the tissue transglutaminase assay can reveal previously undetected monoclonal proteins.
- Wallage M1, Dutton D2, Lock RJ3.
- Annals of clinical biochemistry.Ann Clin Biochem.2016 May;53(Pt 3):409-11. doi: 10.1177/0004563215625692. Epub 2015 Dec 17.
- Increased awareness of coeliac disease and the 2009 NICE guidance has led to an increase in patients being screened for Immunoglobulin A deficiency. We have shown previously that this provides an opportunity for the early identification of other underlying primary immunodeficiency, e.g. common varia
- PMID 26684021
Japanese Journal
- Osteopontin-integrin interaction as a novel molecular target for antibody-mediated immunotherapy in adult T-cell leukemia
- Successful Treatment of Bing-Neel Syndrome Accompanying Waldenström's Macroglobulinemia with R-MPV: A Case Report
- Journal of Clinical and Experimental Hematopathology 55(2), 113-119, 2015
- NAID 130005104663
- Histopathological Characteristics of Lymphomas in the Upper Aerodigestive Tract::A Single-Institute Study in Japan
- Journal of Clinical and Experimental Hematopathology 55(1), 7-11, 2015
- NAID 130005083789
Related Links
- Information about multiple myeloma and other plasma cell neoplasms: treatment, clinical trials, research, and statistics from the National Cancer Institute. ... General Cancer Resources Coping with Cancer: Supportive and Palliative ...
- 形質細胞腫瘍:世界の治験レビュー Plasma Cell Neoplasm Global Clinical Trials Review, H1, 2012 出版日: 2012年01月27日 ページ情報: 英文 Pages: 130 概要 関連レポート 当レポートでは、世界の形質細胞腫瘍治療薬の臨床試験 ...
★リンクテーブル★
[★]
形質細胞腫、形質細胞腫瘍
- 関
- plasma cell neoplasm、plasmacytoma、plasmocytoma
[★]
- 英
- plasma cell tumor、plasma cell neoplasm
- 関
- 形質細胞腫
[★]
- 関
- benign neoplasm、cancer、neoplasia、neoplastic、onco、oncologic、tumor、tumour
[★]
形質細胞
- 同
- plasma cells, in peripheral blood smeare
[★]
細胞