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Boxes in red color signify that an urgent management is needed. | Boxes in red color signify that an urgent management is needed. | ||
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{{Family tree | | | | | | | | | | | | | | A01 | | | | | | | | | | | | | | |A01=<div style="float: left; text-align: left; line-height: 150% ">'''Obtain patient's medical history:''' <br> ❑ [[]] <br> ❑ [[]] <br> ❑ <br> ❑ | {{Family tree | | | | | | | | | | | | | | A01 | | | | | | | | | | | | | | |A01=<div style="float: left; text-align: left; line-height: 150% ">'''Obtain patient's medical history and focus on these signs and symptoms:''' <br> ❑ [[Fatigue]] <br> ❑ [[Weight loss]] <br> ❑ [[Anorexia]] <br> ❑ [[Lymphadenopathy]] <br> ❑ [[Bone pain]] <br> ❑ [[Bleeding]] <br> ❑ [[Early satiety]] <br> ❑ History of specific and chronic exposures such as alkylating agents, benzene, radiation, or previous chemotherapy <br> [[Headache]] <br> ❑ [[History of recurrent fever]]</div>}} | ||
{{Family tree | | | | | | | | | | | | | | |!| | | | | | | | | | | | | | | |}} | {{Family tree | | | | | | | | | | | | | | |!| | | | | | | | | | | | | | | |}} | ||
{{Family tree | | | | | | | | | | | | | | F01 | | | | | | | | | | | | | | |F01=<div style="float: left; text-align: left; line-height: 150% ">'''Obtain a focused history:''' <br> ❑ Onset <br> ❑ Severity compared to previous episodes <br> ❑ Possible causes <br> ❑ <br> ❑ <br> ❑ Exacerbations in previous 1 year <br> ❑ </div> }} | {{Family tree | | | | | | | | | | | | | | F01 | | | | | | | | | | | | | | |F01=<div style="float: left; text-align: left; line-height: 150% ">'''Obtain a focused history:''' <br> ❑ Onset <br> ❑ Severity compared to previous episodes <br> ❑ Possible causes <br> ❑ <br> ❑ <br> ❑ Exacerbations in previous 1 year <br> ❑ </div> }} |
Revision as of 22:29, 9 October 2020
Acute leukemia Resident Survival Guide |
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Overview |
Causes |
FIRE |
Diagnosis |
Treatment |
Do's |
Don'ts |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];
Synonyms and keywords: Acute lymphocytic leukemia, Acute myeloid leukemia, ALL, AML
Overview
Acute Leukemia is a malignancy of bone marrow myeloid and lymphoblastic precursor cells, in which these poorly differentiated hematopoietic cells proliferate rapidly. Hence, their accumulation would disrupt the performance of bone marrow to produce normal blood cells
Causes
AML and ALL are life-threatening diseases, which would result in death if left untreated. In the majority of cases, etiology is not apparent.
Common Causes of AML
- Gene mutations:FLT3, IDHI, IDH2, KRAS, DNMT3A, NPM1
- Chromosomal translocations, deletions, and inversions
- Benzene or radiation exposure chronically[1]
Common Causes of ALL
- Radiation exposure:
- Genetic disorders; e.g., Down syndrome, ataxia-telangiectasia, Fanconi anemia
- Certain infections: e.g., HTLV-1
FIRE
A Focused Initial Rapid Evaluation (FIRE) should be performed to identify patients in need of immediate intervention.[5]
Boxes in red color signify that an urgent management is needed.
Obtain patient's medical history and focus on these signs and symptoms: ❑ Fatigue ❑ Weight loss ❑ Anorexia ❑ Lymphadenopathy ❑ Bone pain ❑ Bleeding ❑ Early satiety ❑ History of specific and chronic exposures such as alkylating agents, benzene, radiation, or previous chemotherapy Headache ❑ History of recurrent fever | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Obtain a focused history: ❑ Onset ❑ Severity compared to previous episodes ❑ Possible causes ❑ ❑ ❑ Exacerbations in previous 1 year ❑ | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Order tests: ❑ Spirometry (FEV1, Peak expiratory flow PEF)* ❑ O2 saturation (pulse oximetry) ❑ Arterial blood gas (not routine) ❑ Order additional tests if needed | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Classify the severity | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Diagnosis
Treatment
Do's
Don'ts
References
- ↑ Cancer Genome Atlas Research Network. Ley TJ, Miller C, Ding L, Raphael BJ, Mungall AJ; et al. (2013). "Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia". N Engl J Med. 368 (22): 2059–74. doi:10.1056/NEJMoa1301689. PMC 3767041. PMID 23634996.