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
- an abnormal or physiologically unbalanced state of the body
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
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/02/27 13:36:12」(JST)
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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]
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 |
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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
- 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
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English Journal
- Transcriptional dysregulation of the deleted in colorectal carcinoma gene in multiple myeloma and monoclonal gammopathy of undetermined significance.
- Nagoshi H1, Taki T2, Chinen Y1, Tatekawa S1, Tsukamoto T1, Maegawa S1, Yamamoto-Sugitani M1, Tsutsumi Y1,3, Kobayashi T1, Matsumoto Y1, Horiike S1, Okuno Y4, Fujiwara S4, Hata H5, Kuroda J1, Taniwaki M1,2.
- Genes, chromosomes & cancer.Genes Chromosomes Cancer.2015 Sep 22. doi: 10.1002/gcc.22290. [Epub ahead of print]
- The deleted in colorectal carcinoma (DCC) gene at 18q21 encodes a netrin-1 receptor, a tumor suppressor that prevents cell growth. While allele loss or decreased expression of DCC has been associated with the progression of solid tumors and hematologic malignancies, including leukemias and malignant
- PMID 26390996
- Prognostic value of serum heavy/light chain ratios in patients with POEMS syndrome.
- Wang C1, Su W2, Cai QQ1, Cai H1, Ji W2, Di Q2, Duan MH1, Cao XX1, Zhou DB1, Li J1.
- European journal of haematology.Eur J Haematol.2015 Sep 18. doi: 10.1111/ejh.12682. [Epub ahead of print]
- POEMS syndrome is a rare plasma cell dyscrasia. Serum concentrations of the monoclonal protein in this disorder is typically low, and inapplicable to monitor disease activity in most cases, resulting in limited practical and prognostic values. Novel immunoassays measuring isotype-specific heavy/ligh
- PMID 26383741
- Strengths and weaknesses of methods for identifying monoclonal free light chains of Ig: examples from two cases with renal disease.
- Levinson SS.
- Clinical chemistry and laboratory medicine : CCLM / FESCC.Clin Chem Lab Med.2015 Sep 12. pii: /j/cclm.ahead-of-print/cclm-2015-0482/cclm-2015-0482.xml. doi: 10.1515/cclm-2015-0482. [Epub ahead of print]
- BACKGROUND: Serum free light chain (FLC) analysis with ratio and urine immunofixation electrophoresis (IFE) are both available for routine use in helping to detect plasma cell dyscrasia and related diseases.CASES: Case reports showing one serum positive for serum FLC but that showed a hook effect an
- PMID 26368046
Japanese Journal
- Monoclonal gammopathy of undetermined significance(MGUS)に続発した口腔内アミロイドーシスの1例
Related Links
- plasma cell dyscrasia plasma cell dyscrasias plasma cell gingitivitis-pharyngitis plasma cell gingitivitis-pharyngitis plasma cell gingitivitis-pharyngitis plasma cell gingivitis Plasma Cell Growth Index plasma cell hepatitis ...
- 1. Baillieres Clin Haematol. 1995 Dec;8(4):705-19. Plasma cell dyscrasias: classification, clinical and laboratory characteristics, and differential diagnosis. Boccadoro M(1), Pileri A. Author information: (1 ...
Related Pictures
★リンクテーブル★
[★]
- 英
- plasma cell dyscrasia
- 関
- 異常蛋白血症、単クローン性γグロブリン血症
[★]
形質細胞
- 同
- plasma cells, in peripheral blood smeare
[★]
悪液質
- 関
- cachectic、cachexia
[★]
細胞