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Lymphoid leukemia



Lymphoid leukemia
Classification & external resources
ICD-10 C91.
ICD-9 204
MeSH D007945

Lymphoid leukemia (or lymphocytic leukemia) is a type of leukemia affecting lymphoid tissue.

They are most commonly divided by the stage of maturation at which the clonal (neoplastic) lymphoid population stopped maturing:

However, they are sometimes divided by the cells affected:


v • d • e
Pathology: hematology (primarily C81-C96/200-208, D45-D47, D50-D77/280-289)
WBCshematological malignancy (lymphoma, leukemia, multiple myeloma), myeloproliferative disease, myelodysplastic syndrome
-cytosis (Agranulocytosis, Leukocytosis, Lymphocytosis, Monocytosis) • -penia (Lymphopenia, Neutropenia)
RBCs/anemia/
hemoglobinopathy		nutritional anemia: Iron deficiency anemia, Plummer-Vinson syndrome, Megaloblastic anemia (Pernicious anemia)
hereditary hemolytic anemia: G6PD Deficiency, Thalassemia, Sickle-cell disease/trait, Hereditary spherocytosis, Hereditary elliptocytosis, Hereditary stomatocytosis

acquired hemolytic anemia: Autoimmune (Warm), HUS, MAHA, PNH, PCH

aplastic anemia: Acquired PRCA, Diamond-Blackfan anemia, Fanconi anemia • Sideroblastic anemia • Hemochromatosis
Coagulation/plateletscoagulopathy: DIC • Hemophilia (A/VII, B/IX, C/XI, XIII) • Von Willebrand disease

Purpura: Henoch-Schönlein, ITP (Evans syndrome), TTP

primary hypercoagulable state: Protein C deficiency - Protein S deficiency - Antithrombin III deficiency - Antiphospholipid syndrome - Factor V Leiden

other hemorrhagic conditions: Bernard-Soulier syndrome - Glanzmann's thrombasthenia - Grey platelet syndrome
HistiocytosisWHO-I Langerhans cell histiocytosis - non-Langerhans-cell histiocytosis/WHO-II (Juvenile xanthogranuloma, Hemophagocytic lymphohistiocytosis) - malignant histiocytic disorders/WHO-III (Acute monocytic leukemia, Malignant histiocytosis, Erdheim-Chester disease)
OtherAsplenia/hyposplenism - Methemoglobinemia
v • d • e
Hematological malignancy histology (ICD-O 9590-9989)
Lymphomas (9590-9759)Hodgkin's lymphoma vs. Non-Hodgkin lymphoma - Diffuse lymphoma vs. Follicular lymphoma

B-cell lymphoma (Small cell, Primary effusion, Diffuse large, ,Burkitt's, Splenic marginal zone, MALT)
T-cell lymphoma (Cutaneous , Mycosis fungoides/Sézary's disease, Angioimmunoblastic, Anaplastic large cell, Hepatosplenic)
plasma cell (Plasmacytoma, Multiple myeloma)

mast cell tumor (Mast-cell sarcoma, Malignant mastocytosis, Malignant histiocytosis, Langerhans cell histiocytosis)
Immunoproliferative disorders (9760-9799)Waldenström macroglobulinemia - Lymphomatoid granulomatosis
Lymphoid leukemias (9800-9839)ALL - CLL - T-cell leukemia (Adult, Large granular lymphocyte, Prolymphocytic, Acute lymphoblastic) - B-cell leukemia (Prolymphocytic)
Myeloid leukemias (9840-9939, 9963)AML (M2, APL/M3, AMoL/M5, Erythroleukemia/M6) - CML (CMoL, CNL, Philadelphia chromosome) - Granulocytic sarcoma
Other leukemias (9940-9949)Hairy cell leukemia - Aggressive NK-cell leukemia
Myeloproliferative disease (9950-9961)Polycythemia vera - Essential thrombocytosis - Myelofibrosis
Other (9964-9989)Hypereosinophilic syndrome - Post-transplant lymphoproliferative disorder - Myelodysplastic syndrome
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Lymphoid_leukemia". A list of authors is available in Wikipedia.
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