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2007 ICD-9-CM Diagnosis Code 200
Lymphosarcoma and reticulosarcoma
2007 ICD-9-CM Diagnosis Code 200.0
Reticulosarcoma
  • rare type of nonHodgkin's lymphoma of intermediate to high malignancy, characterized by the presence of large tumor cells that resemble histiocytes morphologically but are considered to be of lymphoid origin.
  • (foll-IK-yew-lar large cell lim-FO-ma) A rare type of non-Hodgkin's lymphoma (cancer of the lymphatic system) with large cells that look cleaved (split) or non-cleaved under the microscope. It is an indolent (slow-growing) type of lymphoma.
2007 ICD-9-CM Diagnosis Code 200.00
Reticulosarcoma unspecified site
2007 ICD-9-CM Diagnosis Code 200.01
Reticulosarcoma involving lymph nodes of head face and neck
2007 ICD-9-CM Diagnosis Code 200.02
Reticulosarcoma involving intrathoracic lymph nodes
2007 ICD-9-CM Diagnosis Code 200.03
Reticulosarcoma involving intra-abdominal lymph nodes
2007 ICD-9-CM Diagnosis Code 200.04
Reticulosarcoma involving lymph nodes of axilla and upper limb
2007 ICD-9-CM Diagnosis Code 200.05
Reticulosarcoma involving lymph nodes of inguinal region and lower limb
2007 ICD-9-CM Diagnosis Code 200.06
Reticulosarcoma involving intrapelvic lymph nodes
2007 ICD-9-CM Diagnosis Code 200.07
Reticulosarcoma involving spleen
2007 ICD-9-CM Diagnosis Code 200.08
Reticulosarcoma involving lymph nodes of multiple sites
2007 ICD-9-CM Diagnosis Code 200.1
Lymphosarcoma
  • 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.
  • A lymphoblastic lymphoma composed of immature small to medium-sized lymphoid cells (lymphoblasts). It includes the precursor B- and T-cell lymphoblastic lymphoma.
  • A non-Hodgkin lymphoma composed of monomorphic small, round B-lymphocytes in the lymph nodes. When the lymphoid process predominantly involves the bone marrow and the peripheral blood it is called chronic lymphocytic leukemia. (WHO, 2001)
2007 ICD-9-CM Diagnosis Code 200.10
Lymphosarcoma unspecified site
2007 ICD-9-CM Diagnosis Code 200.11
Lymphosarcoma involving lymph nodes of head face and neck
2007 ICD-9-CM Diagnosis Code 200.12
Lymphosarcoma involving intrathoracic lymph nodes
2007 ICD-9-CM Diagnosis Code 200.13
Lymphosarcoma involving intra-abdominal lymph nodes
2007 ICD-9-CM Diagnosis Code 200.14
Lymphosarcoma involving lymph nodes of axilla and upper limb
2007 ICD-9-CM Diagnosis Code 200.15
Lymphosarcoma involving lymph nodes of inguinal region and lower limb
2007 ICD-9-CM Diagnosis Code 200.16
Lymphosarcoma involving intrapelvic lymph nodes
2007 ICD-9-CM Diagnosis Code 200.17
Lymphosarcoma involving spleen
2007 ICD-9-CM Diagnosis Code 200.18
Lymphosarcoma involving lymph nodes of multiple sites
2007 ICD-9-CM Diagnosis Code 200.2
Burkitt's tumor or lymphoma
  • form of undifferentiated malignant lymphoma usually found in central Africa, but also reported in other parts of the world; commonly manifested as a large osteolytic lesion in the jaw or as an abdominal mass; B-cell antigens are expressed on the immature cells that make up the tumor in virtually all cases of Burkitt lymphoma; the Epstein-Barr virus (human herpesvirus 4) has been isolated from Burkitt lymphoma cases in Africa and it is implicated as the causative agent in these cases, however, most non-African cases are EBV-negative.
  • A type of non-Hodgkin's lymphoma that most often occurs in young people aged 12-30 years. The disease usually causes a rapidly growing tumor in the abdomen.
  • A rare, fast-growing cancer of the blood. Also called B-cell acute lymphocytic leukemia or B-cell acute lymphoblastic leukemia.
  • A highly aggressive lymphoma composed of monomorphic medium-sized B-cells with basophilic cytoplasm and numerous mitotic figures. It is often associated with the presence of Epstein-Barr virus (EBV) and is commonly seen in AIDS patients. Three morphologic variants are recognized: classical Burkitt lymphoma, Burkitt lymphoma with plasmacytoid differentiation, and atypical Burkitt/Burkitt-like lymphoma. All cases express the MYC translocation [t(8;14)]. (WHO, 2001)
  • The leukemic counterpart of Burkitt's lymphoma. The characteristic Burkitt cells are seen in the bone marrow and the peripheral blood. This is an aggressive leukemia.
2007 ICD-9-CM Diagnosis Code 200.20
Burkitt's tumor or lymphoma unspecified site
2007 ICD-9-CM Diagnosis Code 200.21
Burkitt's tumor or lymphoma involving lymph nodes of head face and neck
2007 ICD-9-CM Diagnosis Code 200.22
Burkitt's tumor or lymphoma involving intrathoracic lymph nodes
2007 ICD-9-CM Diagnosis Code 200.23
Burkitt's tumor or lymphoma involving intra-abdominal lymph nodes
2007 ICD-9-CM Diagnosis Code 200.24
Burkitt's tumor or lymphoma involving lymph nodes of axilla and upper limb
2007 ICD-9-CM Diagnosis Code 200.25
Burkitt's tumor or lymphoma involving lymph nodes of inguinal region and lower limb
2007 ICD-9-CM Diagnosis Code 200.26
Burkitt's tumor or lymphoma involving intrapelvic lymph nodes
2007 ICD-9-CM Diagnosis Code 200.27
Burkitt's tumor or lymphoma involving spleen
2007 ICD-9-CM Diagnosis Code 200.28
Burkitt's tumor or lymphoma involving lymph nodes of multiple sites
2007 ICD-9-CM Diagnosis Code 200.8
Other named variants of lymphosarcoma and reticulosarcoma
  • 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.
  • An antiquated term referring to non-Hodgkin lymphomas with a mixed cellular composition. This term applies to both B- and T- cell non-Hodgkin lymphomas.
2007 ICD-9-CM Diagnosis Code 200.80
Other named variants of lymphosarcoma and reticulosarcoma unspecified site
2007 ICD-9-CM Diagnosis Code 200.81
Other named variants of lymphosarcoma and reticulosarcoma involving lymph nodes of head face and neck
2007 ICD-9-CM Diagnosis Code 200.82
Other named variants of lymphosarcoma and reticulosarcoma involving intrathoracic lymph nodes
2007 ICD-9-CM Diagnosis Code 200.83
Other named variants of lymphosarcoma and reticulosarcoma involving intra-abdominal lymph nodes
2007 ICD-9-CM Diagnosis Code 200.84
Other named variants of lymphosarcoma and reticulosarcoma involving lymph nodes of axilla and upper limb
2007 ICD-9-CM Diagnosis Code 200.85
Other named variants of lymphosarcoma and reticulosarcoma involving lymph nodes of inguinal region and lower limb
2007 ICD-9-CM Diagnosis Code 200.86
Other named variants of lymphosarcoma and reticulosarcoma involving intrapelvic lymph nodes
2007 ICD-9-CM Diagnosis Code 200.87
Other named variants of lymphosarcoma and reticulosarcoma involving spleen
2007 ICD-9-CM Diagnosis Code 200.88
Other named variants of lymphosarcoma and reticulosarcoma involving lymph nodes of multiple sites