類白血病反応
WordNet
- (mechanics) the equal and opposite force that is produced when any force is applied to a body; "every action has an equal and opposite reaction"
- a response that reveals a persons feelings or attitude; "he was pleased by the audiences reaction to his performance"; "John feared his mothers reaction when she saw the broken lamp"
- a bodily process occurring due to the effect of some antecedent stimulus or agent; "a bad reaction to the medicine"; "his responses have slowed with age" (同)response
- doing something in opposition to another way of doing it that you dont like; "his style of painting was a reaction against cubism"
- an idea evoked by some experience; "his reaction to the news was to start planning what to do"
- extreme conservatism in political or social matters; "the forces of reaction carried the election"
PrepTutorEJDIC
- {名}(…に対する)『反応』《+『to』+『名』》 / 〈U〉(…に対する)(政治的・社会的な)『反動』,逆コース《+『against』+『名』》 / 〈U〉〈C〉化学反応,化学変化 / 〈U〉〈C〉(物理学で)反作用
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/05/08 15:20:51」(JST)
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Leukemoid reaction |
Classification and external resources |
ICD-10 |
D72.8 |
ICD-9 |
288.62 |
DiseasesDB |
30101 |
MedlinePlus |
000575 |
MeSH |
D007955 |
The term leukemoid reaction describes an increased white blood cell count, or leukocytosis, which is a physiological response to stress or infection (as opposed to a primary blood malignancy, such as leukemia).
It may be lymphoid or myeloid.[1]
Contents
- 1 Definition and diagnosis
- 2 Causes of leukemoid reaction
- 3 References
- 4 See also
Definition and diagnosis
Conventionally, a leukocytosis exceeding 50,000 WBC/mm3 with a significant increase in early neutrophil precursors is referred to as a leukemoid reaction.[2] The peripheral blood smear may show myelocytes, metamyelocytes, promyelocytes, and rarely myeloblasts; however, there is a mix of early mature neutrophil precursors, in contrast to the immature forms typically seen in acute leukemia. Serum leukocyte alkaline phosphatase is normal or elevated in leukemoid reaction, but is depressed in chronic myelogenous leukemia. The bone marrow in a leukemoid reaction, if examined, may be hypercellular but is otherwise typically unremarkable.
Leukemoid reactions are generally benign and are not dangerous in and of themselves, although they are often a response to a significant disease state (see Causes below). However, leukemoid reactions can resemble more serious conditions such as chronic myelogenous leukemia (CML), which can present with identical findings on peripheral blood smear.
Historically, various clues including the leukocyte alkaline phosphatase score and the presence of basophilia were used to distinguish CML from a leukemoid reaction. However, at present the test of choice in adults to distinguish CML is an assay for the presence of the Philadelphia chromosome, either via cytogenetics and FISH, or via PCR for the BCR/ABL fusion gene. The LAP (Leukocyte Alkaline Phosphatase) score is high in reactive states but is low in CML. In cases where the diagnosis is uncertain, a qualified hematologist or oncologist should be consulted.
Causes of leukemoid reaction
As noted above, a leukemoid reaction is typically a response to an underlying medical issue. Causes of leukemoid reactions include:
- Hemorrhage
- Drugs
- Use of Sulfa drugs
- Use of Dapsone
- Use of glucocorticoids
- Use of G-CSF or related growth factors
- All-trans retinoic acid (ATRA)
- Infections
- Clostridium difficile
- Tuberculosis
- Pertussis
- Infectious mononucleosis (lymphocyte predominant)
- Visceral Larva Migrans (eosinophil predominant)
- Asplenia
- Diabetic ketoacidosis
- Organ necrosis
- Hepatic necrosis
- Ischemic colitis
- As a feature of Trisomy 21 in infancy (incidence of ~10%)
- As a paraneoplastic phenomenon (rare)
References
- ^ Ian M. Hann; Owen P. Smith (26 September 2006). Pediatric hematology. Wiley-Blackwell. pp. 763–. ISBN 978-1-4051-3400-2. Retrieved 5 November 2010.
- ^ Ronald Hoffman et al. (2005). Hematology: basic principles and practice. St. Louis, Mo: Elsevier Churchill Livingstone. ISBN 0-443-06628-0. p. 803.
See also
- Neutrophilia
- Leukocytosis
- Leukemid
Myeloid hematological malignancy/leukemia histology (ICD-O 9590–9989, C81–C96, 200–208)
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|
CFU-GM/
and other granulocytes |
CFU-GM |
Myelocyte |
AML: |
- Acute myeloblastic leukemia
- M0
- M1
- M2
- APL/M3
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|
MP |
- Chronic neutrophilic leukemia
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Monocyte |
AML |
- AMoL/M5
- Myeloid dendritic cell leukemia
|
|
CML |
- Philadelphia chromosome
- Accelerated phase chronic myelogenous leukemia
|
|
|
Myelomonocyte |
AML |
|
|
MD-MP |
- Juvenile myelomonocytic leukemia
- Chronic myelomonocytic leukemia
|
|
|
Other |
|
|
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CFU-Baso |
|
|
CFU-Eos |
AML |
|
|
MP |
- Chronic eosinophilic leukemia/Hypereosinophilic syndrome
|
|
|
|
MEP |
CFU-Meg |
|
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CFU-E |
AML |
|
|
MP |
|
|
MD |
- Refractory anemia
- Refractory anemia with excess of blasts
- Chromosome 5q deletion syndrome
- Sideroblastic anemia
- Paroxysmal nocturnal hemoglobinuria
- Refractory cytopenia with multilineage dysplasia
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|
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CFU-Mast |
Mastocytoma |
- Mast cell leukemia
- Mast cell sarcoma
- Systemic mastocytosis
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|
Mastocytosis: |
- Diffuse cutaneous mastocytosis
- Erythrodermic mastocytosis
- Adult type of generalized eruption of cutaneous mastocytosis
- Urticaria pigmentosa
- Mast cell sarcoma
- Solitary mastocytoma
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|
Systemic mastocytosis |
- Xanthelasmoidal mastocytosis
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|
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Multiple/unknown |
AML |
- Acute panmyelosis with myelofibrosis
- Myeloid sarcoma
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MP |
- Myelofibrosis
- Acute biphenotypic leukaemia
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Index of cells from bone marrow
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Description |
- Immune system
- Cells
- Physiology
- coagulation
- proteins
- granule contents
- colony-stimulating
- heme and porphyrin
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|
Disease |
- Red blood cell
- Monocyte and granulocyte
- Neoplasms and cancer
- Histiocytosis
- Symptoms and signs
- Blood tests
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Treatment |
- Transfusion
- Drugs
- thrombosis
- bleeding
- other
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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
|
By development/
marker |
TdT+ |
- ALL (Precursor B acute lymphoblastic leukemia/lymphoma)
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|
CD5+ |
- mantle zone (Mantle cell)
|
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CD22+ |
- Prolymphocytic
- CD11c+ (Hairy cell leukemia)
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CD79a+ |
- 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)
|
|
RS (CD15+, CD30+) |
- Classic Hodgkin's lymphoma (Nodular sclerosis)
- CD20+ (Nodular lymphocyte predominant Hodgkin's lymphoma)
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PCDs/PP
(CD38+/CD138+) |
- see immunoproliferative immunoglobulin disorders
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|
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By infection |
- KSHV (Primary effusion)
- EBV (Lymphomatoid granulomatosis
- Post-transplant lymphoproliferative disorder)
- HIV (AIDS-related lymphoma)
- Helicobacter pylori (MALT lymphoma)
|
|
Cutaneous |
- 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 |
T cell
(lymphoma,
leukemia)
(most CD3
|
By development/
marker |
- TdT+: ALL (Precursor T acute lymphoblastic leukemia/lymphoma)
- prolymphocyte (Prolymphocytic)
- CD30+ (Anaplastic large-cell lymphoma
- Lymphomatoid papulosis type A)
|
|
Cutaneous |
MF+variants |
- indolent: Mycosis fungoides
- Pagetoid reticulosis
- Granulomatous slack skin
aggressive: Sézary disease
- Adult T-cell leukemia/lymphoma
|
|
Non-MF |
- 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 |
- 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 |
- HTLV-1 (Adult T-cell leukemia/lymphoma)
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NK cell/
(most CD56) |
- Aggressive NK-cell leukemia
- Blastic NK cell lymphoma
|
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T or NK |
- EBV (Extranodal NK-T-cell lymphoma/Angiocentric lymphoma)
- Large granular lymphocytic leukemia
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Lymphoid+myeloid |
- Acute biphenotypic leukaemia
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Lymphocytosis |
- 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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Index of the immune system
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Description |
- Physiology
- cells
- autoantigens
- autoantibodies
- complement
- surface antigens
- IG receptors
|
|
Disease |
- Allergies
- Immunodeficiency
- Immunoproliferative immunoglobulin disorders
- Hypersensitivity and autoimmune disorders
- Neoplasms and cancer
|
|
Treatment |
- Procedures
- Drugs
- antihistamines
- immunostimulants
- immunosuppressants
- monoclonal antibodies
|
|
|
UpToDate Contents
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English Journal
- A leukemoid leucocytosis.
- Cherif E, Kechaou I, Hassine LB, Boukhris I, Azzabi S, Kaouech Z, Kooli C, Khalfallah N.SourceService de médecine interne B, Hôpital Charles Nicolle, Tunis, Tunisie.
- Annales de biologie clinique.Ann Biol Clin (Paris).2012 Jun 1;70(3):333-334.
- Leukemoid reaction is a rare paraneoplastic syndrome. It can occur in association with carcinomas, in particular of the lung, gastric and renal. However, its association with sarcoma is infrequent. Leukemoid reaction occuring in patients with uterine sarcoma have not been previously reported. We rep
- PMID 22565182
- Hyperleukocytosis in a premature infant with intrauterine herpes simplex encephalitis.
- Underwood MA, Wartell AE, Borghese RA.SourceDepartment of Pediatrics, University of California, Davis School of Medicine, Sacramento, CA, USA.
- Journal of perinatology : official journal of the California Perinatal Association.J Perinatol.2012 Jun;32(6):469-72. doi: 10.1038/jp.2011.138.
- Herpes encephalitis is a rare but devastating infection in premature infants. We report a 29 week gestation infant with severe intrauterine cutaneous and central nervous system herpes accompanied by hyperleukocytosis. Leukemoid reactions are not uncommon in this population, but the association of he
- PMID 22643292
Japanese Journal
- Infected Marantic Endocarditis With Leukemoid Reaction:– The Uncertain Role of Positron Emission Tomography/Computed Tomography –
- 類白血病反応を伴った granulocyte-colony stimulating factor (G-CSF) 産生尿路上皮癌の1剖検例
Related Links
- A leukemoid reaction is an increase in the white blood cell count, which can mimic leukemia. The reaction is actually due to an infection or another disease and is not a sign of cancer. Blood counts often return to normal when the ...
- leukemoid [loo-ke´moid] having blood counts and sometimes other clinical findings resembling those of leukemia but not due to uncontrolled proliferation of leukocytes. leukemoid reaction a peripheral blood picture resembling that of leukemia ...
Related Pictures
★リンクテーブル★
[★]
- 英
- leukemoid reaction
- 同
- 白血性反応 leukemic reaction、偽白血病 仮性白血病 pseudoleukemia
- 関
定義
- 末梢血中の白血球が著明に増加し(5万/μL以上)、幼若な白血球(特に骨髄芽球)が出現している病態
鑑別
- NAPスコアは正常・上昇 ← 好中球ホスファターゼが上昇傾向
国試
[★]
- 関
- react、respond、response、responsive