Name
Myeloid leukemia associated with Down Syndrome
ICD-O-3 Morphology
9898/3: Myeloid leukemia associated with Down Syndrome
Effective
2010 and later
Reportable
for cases diagnosed
2010 and later
Primary Site(s)
C421
Primary site must be bone marrow (C421)
Coding Manual:
Hematopoietic Coding Manual (PDF)
Abstractor Notes
(This code is effective for cases diagnosed 2010 and later. For cases diagnosed prior to 2010 see code 9860/3.)
This disease is unique to children with Down's Syndrome (DS). Blood and bone marrow are the principle sites of involvement. Extramedullary involvement, mainly of spleen and liver, is almost always present.
If the leukemia occurs before or simultaneously with Myeloid Sarcoma, see M3 and Module 5: PH10
This disease is unique to children with Down's Syndrome (DS). Blood and bone marrow are the principle sites of involvement. Extramedullary involvement, mainly of spleen and liver, is almost always present.
If the leukemia occurs before or simultaneously with Myeloid Sarcoma, see M3 and Module 5: PH10
Diagnostic Confirmation
This histology can be determined by positive histology (including peripheral blood) with or without genetics and/or immunophenotyping. Review the Definitive Diagnostic Methods, Immunophenotyping and Genetics Data sections below, and the instructions in the Hematopoietic Manual for further guidance on assigning Diagnostic confirmation.
Grade
Not Applicable
Module Rule
See abstractor notes
Alternate Names
Acute myeloid leukemia associated with Down syndrome
AML associated with DS
Definition
Among individuals with Down syndrome, the incidence rate of acute leukemia during the first 5 years of life is 50 times the rate among individuals without down syndrome. In Down syndrome, most cases of acute myeloid leukemia (AML) are acute megakaryoblastic leukemia, which accounts for greater than or equal to 50% of all cases of acute leukemia in Down syndrome beyond the natal period.
AML often follows a prolonged myelodysplastic syndrome(MDS)-like phase. In individuals with Down syndrome, there are no biological differences between MDS and overt AML.
Because this type of disease is unique to children with Down syndrome, the term "myeloid leukemia associated with Down syndrome" encompasses both MDS and AML.
AML often follows a prolonged myelodysplastic syndrome(MDS)-like phase. In individuals with Down syndrome, there are no biological differences between MDS and overt AML.
Because this type of disease is unique to children with Down syndrome, the term "myeloid leukemia associated with Down syndrome" encompasses both MDS and AML.
Definitive Diagnostic Methods
Bone marrow biopsy
Genetic testing
Immunophenotyping
Peripheral blood smear
Genetics Data
Immunophenotyping
CD4+ (expression/positive)
CD7+ (expression/positive)
CD11b+ (expression/positive)
CD13+ (expression/positive)
CD14- (no expression/negative)
CD15- (no expression/negative)
CD33+ (expression/positive)
CD34- (no expression/negative)
CD36+ (expression/positive)
CD41+ (expression/positive)
CD42+ (expression/positive)
CD61+ (expression/positive)
CD71+ (expression/positive)
CD110 (TPOR)+ (expression/positive)
Glycophorin- (no expression/negative)
IL3R+ (expression/positive)
KIT (CD117)+ (expression/positive)
MPO- (no expression/negative)
Treatments
Chemotherapy
Hematologic Transplant and/or Endocrine Procedures
Transformations to
There are no known transformations
Transformations from
There are no known transformations
Same Primaries
Corresponding ICD-9 Codes
205.0 Acute myeloid leukemia
Corresponding ICD-10 Codes
C92.0 Acute myeloid leukemia
Corresponding ICD-10-CM Codes (U.S. only)
C92.Z Other myeloid leukemia (effective October 01, 2015)
Signs and Symptoms
Easy bruising or bleeding
Fatigue
Fever
Petechiae
Shortness of breath
Thrombocytopenia
Weakness
Weight loss or loss of appetite
Diagnostic Exams
CT (CAT) scan
Cytogenetic analysis
Immunophenotyping
Lumbar puncture
Peripheral blood smear
Reverse transcription-polymerase chain reaction test (RT-PCR)
Progression and Transformation
High rate of spontaneous remission
Non-transient AML develops 1 to 3 years in 20-30% of patients
Epidemiology and Mortality
Age: predominantly in first 3 years of life
Incidence: 1-2% of children with Down Syndrome and 20% of all pediatric patients with AML/MDS
Sources
Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J (Eds):
WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues (Revised 4th edition)
IARC: Lyon 2017
Section: Acute myeloid leukemia and related precursor neoplasms
Pages: 170-171
WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues (Revised 4th edition)
IARC: Lyon 2017
Section: Acute myeloid leukemia and related precursor neoplasms
Pages: 170-171
International Classification of Diseases for Oncology, Third Edition, Second Revision. Geneva: World Health Organization, 2020.
Section: ICD-O-3.2 (2020) Morphological Codes
Pages: http://www.iacr.com.fr/index.php?option=com_content&view=category&layout=blog&id=100&Itemid=577
Section: ICD-O-3.2 (2020) Morphological Codes
Pages: http://www.iacr.com.fr/index.php?option=com_content&view=category&layout=blog&id=100&Itemid=577
National Cancer Institute
Section: General Information About Acute Myeloid Leukemia
Pages: https://www.cancer.gov/types/leukemia/hp/adult-aml-treatment-pdq
Section: General Information About Acute Myeloid Leukemia
Pages: https://www.cancer.gov/types/leukemia/hp/adult-aml-treatment-pdq