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2008 ICD-9-CM Diagnosis Code 202
Other malignant neoplasms of lymphoid and histiocytic tissue
2008 ICD-9-CM Diagnosis Code 202.0
Nodular lymphoma
  • A neoplasm of follicle centre B cells which has at least a partial follicular pattern. Follicular lymphomas comprise about 35% of adult non-Hodgkin lymphomas in the U.S. and 22% worldwide. Most patients have widespread disease at diagnosis. Morphologically, follicular lymphomas are classified as Grade 1, Grade 2, and Grade 3, depending on the percentage of the large lymphocytes present. The vast majority of cases (70-95%) express the BCL-2 rearrangement [t(14;18)]. Histological grade correlates with prognosis. Grades 1 and 2 follicular lymphomas are indolent and grade 3 is more aggressive (adapted from WHO, 2001).
2008 ICD-9-CM Diagnosis Code 202.00
Nodular lymphoma unspecified site
2008 ICD-9-CM Diagnosis Code 202.01
Nodular lymphoma involving lymph nodes of head face and neck
2008 ICD-9-CM Diagnosis Code 202.02
Nodular lymphoma involving intrathoracic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.03
Nodular lymphoma involving intra-abdominal lymph nodes
2008 ICD-9-CM Diagnosis Code 202.04
Nodular lymphoma involving lymph nodes of axilla and upper limb
2008 ICD-9-CM Diagnosis Code 202.05
Nodular lymphoma involving lymph nodes of inguinal region and lower limb
2008 ICD-9-CM Diagnosis Code 202.06
Nodular lymphoma involving intrapelvic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.07
Nodular lymphoma involving spleen
2008 ICD-9-CM Diagnosis Code 202.08
Nodular lymphoma involving lymph nodes of multiple sites
2008 ICD-9-CM Diagnosis Code 202.1
Mycosis fungoides
  • (mye-KO-sis fun-GOY-deez) A type of non-Hodgkin's lymphoma that first appears on the skin and can spread to the lymph nodes or other organs such as the spleen, liver, or lungs.
  • chronic malignant T-cell lymphoma of the skin; in the late stages the lymph nodes and viscera are affected.
  • A peripheral (mature) T-cell lymphoma presenting in the skin with patches/plaques. It is characterized by epidermal and dermal infiltration of small to medium-sized T-cells with cerebriform nuclei. Patients with limited disease generally have an excellent prognosis. In the more advanced stages, the prognosis is poor. (WHO, 2001)
2008 ICD-9-CM Diagnosis Code 202.10
Mycosis fungoides unspecified site
2008 ICD-9-CM Diagnosis Code 202.11
Mycosis fungoides involving lymph nodes of head face and neck
2008 ICD-9-CM Diagnosis Code 202.12
Mycosis fungoides involving intrathoracic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.13
Mycosis fungoides involving intra-abdominal lymph nodes
2008 ICD-9-CM Diagnosis Code 202.14
Mycosis fungoides involving lymph nodes of axilla and upper limb
2008 ICD-9-CM Diagnosis Code 202.15
Mycosis fungoides involving lymph nodes of inguinal region and lower limb
2008 ICD-9-CM Diagnosis Code 202.16
Mycosis fungoides involving intrapelvic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.17
Mycosis fungoides involving spleen
2008 ICD-9-CM Diagnosis Code 202.18
Mycosis fungoides involving lymph nodes of multiple sites
2008 ICD-9-CM Diagnosis Code 202.2
Sezary's disease
  • A form of cutaneous T-cell lymphoma, a cancerous disease that affects the skin.
  • A generalized peripheral (mature) T-cell neoplasm characterized by the presence of erythroderma, lymphadenopathy, and neoplastic, cerebriform T-lymphocytes in the blood. Sezary syndrome is an aggressive disease. (WHO, 2001)
2008 ICD-9-CM Diagnosis Code 202.20
Sezary's disease unspecified site
2008 ICD-9-CM Diagnosis Code 202.21
Sezary's disease involving lymph nodes of head face and neck
2008 ICD-9-CM Diagnosis Code 202.22
Sezary's disease involving intrathoracic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.23
Sezary's disease involving intra-abdominal lymph nodes
2008 ICD-9-CM Diagnosis Code 202.24
Sezary's disease involving lymph nodes of axilla and upper limb
2008 ICD-9-CM Diagnosis Code 202.25
Sezary's disease involving lymph nodes of inguinal region and lower limb
2008 ICD-9-CM Diagnosis Code 202.26
Sezary's disease involving intrapelvic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.27
Sezary's disease involving spleen
2008 ICD-9-CM Diagnosis Code 202.28
Sezary's disease involving lymph nodes of multiple sites
2008 ICD-9-CM Diagnosis Code 202.3
Malignant histiocytosis
  • An antiquated term referring to cases of systemic non-Hodgkin lymphomas which are composed of large, atypical neoplastic lymphoid cells and cases of hemophagocytic syndromes. In the past, cases of anaplastic large cells lymphoma were called malignant histiocytosis.
2008 ICD-9-CM Diagnosis Code 202.30
Malignant histiocytosis unspecified site
2008 ICD-9-CM Diagnosis Code 202.31
Malignant histiocytosis involving lymph nodes of head face and neck
2008 ICD-9-CM Diagnosis Code 202.32
Malignant histiocytosis involving intrathoracic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.33
Malignant histiocytosis involving intra-abdominal lymph nodes
2008 ICD-9-CM Diagnosis Code 202.34
Malignant histiocytosis involving lymph nodes of axilla and upper limb
2008 ICD-9-CM Diagnosis Code 202.35
Malignant histiocytosis involving lymph nodes of inguinal region and lower limb
2008 ICD-9-CM Diagnosis Code 202.36
Malignant histiocytosis involving intrapelvic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.37
Malignant histiocytosis involving spleen
2008 ICD-9-CM Diagnosis Code 202.38
Malignant histiocytosis involving lymph nodes of multiple sites
2008 ICD-9-CM Diagnosis Code 202.4
Leukemic reticuloendotheliosis
  • neoplastic disease of the lymphoreticular cells which is considered to be a rare type of chronic leukemia; it is characterized by an insidious onset, splenomegaly, anemia, granulocytopenia, thrombocytopenia, little or no lymphadenopathy, and the presence of hairy or flagellated cells in the blood and bone marrow.
  • A type of chronic leukemia in which the abnormal white blood cells appear to be covered with tiny hairs when viewed under a microscope.
  • A rare neoplasm of small B-lymphocytes with "hairy" projections in bone marrow, spleen, and peripheral blood. Most patients are middle-aged to elderly adults and present with splenomegaly and pancytopenia. (WHO, 2001)
2008 ICD-9-CM Diagnosis Code 202.40
Leukemic reticuloendotheliosis unspecified site
2008 ICD-9-CM Diagnosis Code 202.41
Leukemic reticuloendotheliosis involving lymph nodes of head face and neck
2008 ICD-9-CM Diagnosis Code 202.42
Leukemic reticuloendotheliosis involving intrathoracic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.43
Leukemic reticuloendotheliosis involving intra-abdominal lymph nodes
2008 ICD-9-CM Diagnosis Code 202.44
Leukemic reticuloendotheliosis involving lymph nodes of axilla and upper arm
2008 ICD-9-CM Diagnosis Code 202.45
Leukemic reticuloendotheliosis involving lymph nodes of inguinal region and lower limb
2008 ICD-9-CM Diagnosis Code 202.46
Leukemic reticuloendotheliosis involving intrapelvic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.47
Leukemic reticuloendotheliosis involving spleen
2008 ICD-9-CM Diagnosis Code 202.48
Leukemic reticuloendotheliosis involving lymph nodes of multiple sites
2008 ICD-9-CM Diagnosis Code 202.5
Letterer-siwe disease
  • A multifocal, multisystem form of Langerhans-cell histiocytosis. There is involvement of multiple organ systems including the bones, skin, liver, spleen, and lymph nodes. Patients are usually infants presenting with fever, hepatosplenomegaly, lymphadenopathy, bone and skin lesions, and pancytopenia.
2008 ICD-9-CM Diagnosis Code 202.50
Letterer-siwe disease unspecified site
2008 ICD-9-CM Diagnosis Code 202.51
Letterer-siwe disease involving lymph nodes of head face and neck
2008 ICD-9-CM Diagnosis Code 202.52
Letterer-siwe disease involving intrathoracic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.53
Letterer-siwe disease involving intra-abdominal lymph nodes
2008 ICD-9-CM Diagnosis Code 202.54
Letterer-siwe disease involving lymph nodes of axilla and upper limb
2008 ICD-9-CM Diagnosis Code 202.55
Letterer-siwe disease involving lymph nodes of inguinal region and lower limb
2008 ICD-9-CM Diagnosis Code 202.56
Letterer-siwe disease involving intrapelvic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.57
Letterer-siwe disease involving spleen
2008 ICD-9-CM Diagnosis Code 202.58
Letterer-siwe disease involving lymph nodes of multiple sites
2008 ICD-9-CM Diagnosis Code 202.6
Malignant mast cell tumors
  • A rare entity characterized by localized but destructive growth of a tumor consisting of highly atypical, immature mast cells.(WHO, 2001)
  • A variant of mastocytosis characterized by multifocal, dense infiltrates of mast cells (15 or more mast cells in aggregates) detected in the bone marrow and/or other extracutaneous sites. (WHO, 2001) -- 2003
  • Malignant neoplasm originating from mast cells.
2008 ICD-9-CM Diagnosis Code 202.60
Malignant mast cell tumors unspecified site
2008 ICD-9-CM Diagnosis Code 202.61
Malignant mast cell tumors involving lymph nodes of head face and neck
2008 ICD-9-CM Diagnosis Code 202.62
Malignant mast cell tumors involving intrathoracic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.63
Malignant mast cell tumors involving intra-abdominal lymph nodes
2008 ICD-9-CM Diagnosis Code 202.64
Malignant mast cell tumors involving lymph nodes of axilla and upper limb
2008 ICD-9-CM Diagnosis Code 202.65
Malignant mast cell tumors involving lymph nodes of inguinal region and lower limb
2008 ICD-9-CM Diagnosis Code 202.66
Malignant mast cell tumors involving intrapelvic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.67
Malignant mast cell tumors involving spleen
2008 ICD-9-CM Diagnosis Code 202.68
Malignant mast cell tumors involving lymph nodes of multiple sites
2008 ICD-9-CM Diagnosis Code 202.7
Peripheral t-cell lymphoma
  • This type of lymphoma is not frequently seen in the western hemisphere. Clinically, with the exception of anaplastic large cell lymphoma, mature T- and NK-cell lymphomas are among the most aggressive of all hematopoietic neoplasms. Representative disease entities include mycosis fungoides, angioimmunoblastic T-cell lymphoma, hepatosplenic T-cell lymphoma, and anaplastic large cell lymphoma.
2008 ICD-9-CM Diagnosis Code 202.8
Other malignant lymphomas
  • malignant (clonal) proliferation of B- or T- lymphocytes which involves the lymph nodes, bone marrow and/or extranodal sites; general term for various neoplastic diseases of the lymphoid tissue.
  • (lim-FO-ma) Cancer that arises in cells of the lymphatic system.
  • A malignant (clonal) proliferation of B- lymphocytes or T- lymphocytes which involves the lymph nodes, bone marrow and/or extranodal sites. This category includes Non-Hodgkin lymphomas and Hodgkin lymphomas.
  • malignant lymphoma in which neoplastic cells diffusely infiltrate the entire lymph node without any definite organized pattern; patients whose lymphomas present a diffuse pattern generally have a more unfavorable survival outlook than those presenting with a follicular or nodular pattern.
  • An obsolete term for a malignant tumor of lymphatic tissue.
2008 ICD-9-CM Diagnosis Code 202.80
Other malignant lymphomas unspecified site
2008 ICD-9-CM Diagnosis Code 202.81
Other malignant lymphomas involving lymph nodes of head face and neck
2008 ICD-9-CM Diagnosis Code 202.82
Other malignant lymphomas involving intrathoracic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.83
Other malignant lymphomas involving intra-abdominal lymph nodes
2008 ICD-9-CM Diagnosis Code 202.84
Other malignant lymphomas involving lymph nodes of axilla and upper limb
2008 ICD-9-CM Diagnosis Code 202.85
Other malignant lymphomas involving lymph nodes of inguinal region and lower limb
2008 ICD-9-CM Diagnosis Code 202.86
Other malignant lymphomas involving intrapelvic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.87
Other malignant lymphomas involving spleen
2008 ICD-9-CM Diagnosis Code 202.88
Other malignant lymphomas involving lymph nodes of multiple sites
2008 ICD-9-CM Diagnosis Code 202.9
Other and unspecified malignant neoplasms of lymphoid and histiocytic tissue
  • Malignant neoplasms that either originate from the bone marrow (e.g. myeloid leukemias) or involve the bone marrow as secondary-metastatic tumors (e.g. metastatic carcinomas to the bone marrow). --2003
  • A neoplastic proliferation of Langerhans cells with overtly malignant cytologic features. It can be considered a higher grade variant of Langerhans cell histiocytosis (LCH) and it can present de novo or progress from antecedent LCH. (WHO, 2001)
2008 ICD-9-CM Diagnosis Code 202.90
Other and unspecified malignant neoplasms of lymphoid and histiocytic tissue unspecified site
2008 ICD-9-CM Diagnosis Code 202.91
Other and unspecified malignant neoplasms of lymphoid and histiocytic tissue involving lymph nodes of head face and neck
2008 ICD-9-CM Diagnosis Code 202.92
Other and unspecified malignant neoplasms of lymphoid and histiocytic tissue involving intrathoracic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.93
Other and unspecified malignant neoplasms of lymphoid and histiocytic tissue involving intra-abdominal lymph nodes
2008 ICD-9-CM Diagnosis Code 202.94
Other and unspecified malignant neoplasms of lymphoid and histiocytic tissue involving lymph nodes of axilla and upper limb
2008 ICD-9-CM Diagnosis Code 202.95
Other and unspecified malignant neoplasms of lymphoid and histiocytic tissue involving lymph nodes of inguinal region and lower limb
2008 ICD-9-CM Diagnosis Code 202.96
Other and unspecified malignant neoplasms of lymphoid and histiocytic tissue involving intrapelvic lymph nodes
2008 ICD-9-CM Diagnosis Code 202.97
Other and unspecified malignant neoplasms of lymphoid and histiocytic tissue involving spleen
2008 ICD-9-CM Diagnosis Code 202.98
Other and unspecified malignant neoplasms of lymphoid and histiocytic tissue involving lymph nodes of multiple sites