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2011 Casefinding List Revised 02/2011 ICD-9-CM Codes Diagnosis (New codes are in Bold) 140.0 – 199.1 199.2 200.0 – 202.98 203.0 – 208.92 209.0 – 209.30 209.31 – 209.36 209.40 – 209.69 209.7 – 209.79 225.0 – 225.9 227.3 – 227.4 228.02 228.1 Malignant neoplasms – “solid tumors” Malignant neoplasm associated with transplanted organ Malignant neoplasms of lymphoid and histiocytic tissue Multiple myeloma, immunoproliferative neoplasms, and leukemias Malignant neuroendocrine neoplasms Merkel cell carcinoma of skin and other specified sites *Benign carcinoid tumor of specified sites, other and unknown sites Secondary neuroendocrine tumors; secondary carcinoid tumors Benign neoplasm of brain and other parts of the CNS Benign neoplasm of pituitary, craniopharyngeal duct, pineal gland Hemangioma of intracranial structures Lymphangioma, any site (screen for reportable brain, CNS and endocrine) 229.9 230.0 – 234.9 Benign neoplasm of unspecified site (screen for potential 225-227 miscodes) Carcinoma in situ Exceptions; 233.4 prostatic intraepithelial neoplasia) Note: 233.1 includes CIN (non-reportable) and adenocarcinoma in situ of Cervix (REPORTABLE) Endometrial stromal neoplasia, low grade (8931/1) Stromal endometriosis (8931/3 per ICD-O-3) Stromal myosis (endolymphatic) (8931/3 per ICD-O-3) Stromatosis, endometrial (8931/3 per ICD-O-3) Neoplasm of uncertain behavior of pituitary gland, craniopharyngeal duct, pineal gland 236.0 237.0 – 237.1 237.5 – 237.72 237.9 238.4 238.6 238.71 238.72 238.73 238.74 238.75 238.76 238.77 238.79 Neoplasm of uncertain behavior of brain, spinal cord, meninges (NOS, cerebral, spinal), cranial nerve, other CNS site, acoustic neuroma, neurofibromatosis type 2 Polycythemia vera (9950/3) Solitary plasmacytoma (9731/3) Extramedullary plasmacytoma (9734/3) Essential Thrombocythemia (9962/3) Essential hemorrhagic thrombocythemia Essential thrombocytosis Idiopathic (hemorrhagic) thrombocythemia Primary thrombocytosis Refractory anemia (RA) (9980/3) Refractory anemia with ringed sideroblasts (RARS) (9982/3) Refractory cytopenia with multilineage dysplasia (RCMD) (9985/3) Refractory cytopenia with multilineage dysplasia and ringed sideroblasts (RCMD-RS) Refractory anemia with excess blasts-1 (RAEB-1) (9983/3) Refractory anemia with excess blasts-2 (RAEB-2) (9983/3) Myelodysplastic syndrome with 51 deletion (9986/3) - 51 minus syndrome NOS Chronic myeloproliferative disease (9960/3) Myelosclerosis with myeloid metaplasia (9961/3) Refractory cytopenia with multilineage dysplasia (9985/3) Therapy-related myelodysplastic syndrome (9987/3) Myelodysplastic syndrome, unspecified (9989/3) Myelofibrosis with myeloid metaplasia (9961/3) Agnogenic myeloid metaplasia Idiopathic myelofibrosis (chronic) Myelosclerosis with myeloid metaplasia Primary myelofibrosis Post-transplant lymphoproliferative disorder (9987/3) Lymphoproliferative disease (chronic)NOS (9970/1) 2011 Casefinding List ICD-9-CM Codes 239.6 – 239.7 259.2 273.2 273.3 273.9 277.88 288.3 288.4 289.6 289.83 511.81 789.51 999.81 V07.3 V07.5 – V07.59 V10.0 – V10.91 V12.41 V58.0 V58.11 – V58.12 V87.41 V87.42 62.3 – 62.42 92.20 – 92.29 92.30 – 92.39 Revised 02/2011 Diagnosis (New codes are in Bold) Megakaryocytic myelosclerosis (9961/3) Myloproliferative disease (chronic) J5511 NOS (9906/3) Panmyelosis (acute) (9931/3) Neoplasm of unspecified nature of brain, meninges, cranial nerves Carcinoid syndrome; hormone secretion by carcinoid tumors Gamma heavy chain disease; Franklin disease (9762/3) Waldenstrom macroglobulinemia (9761/3) Unspecified disorder of plasma protein metabolism (screen for potential 273.3 miscodes) Tumor lysis syndrome – spontaneous; following antineoplastic drug therapy Hypereosinophilic Syndrome (9964/3) Hemophagocytic syndrome (9751/3, 9754/3) Reportable inclusion terms: Histiocytic syndromes Familial Polycythemia (synonym for polycythemia vera) Acute myelofibrosis (9931/3) Malignant pleural effusion Malignant acites Extravasation of vesicant chemotherapy Other prophylactic chemotherapy (screen carefully for miscoded malignancies) Prophylactic use of agents affecting estrogen receptors and estrogen levels Selective estrogen receptor modulators (SERMs) Aromatase inhibitors Other agents affecting estrogen receptors and estrogen levels Personal history of malignancy (review these for recurrences, subsequent primaries and/or subsequent treatment.) Personal history of benign neoplasm of the brain Admission for radiotherapy Admission for chemotherapy Personal history of antineoplastic chemotherapy Personal history of monoclonal drug therapy Orchiectomies (Treatment for prostate malignancies) Therapeutic radioisotope administration Stereotactic radiosurgery, NOS * Carcinoid tumor NOS (8240/3) is reportable for all sites except appendix. Records coded as benign carcinoid tumors should be reviewed to verify that the tumors are actually benign. Supplementary List The following table includes ICD-9 codes that CDC-NPCR or others suggest may be included in a reportable list. MCR does not include these codes in their reportable list. MCR feels that Including these codes will result in significantly more cases to review but few cases that are reportable so should only be screened if time allows. ICD-9-CM CODES 042 079.4 079.50 – 079.59 210.0 – 229.9 DIAGNOSIS (New codes are in bold) AIDS (review cases for AIDS-related malignancies) Human papillomavirus Retrovirus (HTLV, types I, II and 2) Benign neoplasms, if non-CNS sites (Screen for incorrectly coded malignancies or reportable by agreement tumors) 2011 Casefinding List 227.9 235.0 – 236.7, 236.90 – 236.99, 237.2 - 237.4 237.73 238.0 – 239.9 253.6 258.02 – 258.03 259.8 273.0 273.1 273.8 275.42 279.00 279.02 – 279.06 279.10 279.12 279.13 284.81 284.89 284.9 285.0 285.22 285.3 288.03 289.83 289.9 323.81 379.59 528.01 630 686.01 695.89 701.2 710.3 710.4 733.10-733.16 758.0 785.6 790.93 795.06 795.16 796.76 795.8 795.81 795.82 795.89 999.31 E879.2 E930.7 Revised 02/2011 Benign neoplasm of endocrine gland, site unspecified Neoplasms of uncertain behavior (except for 236.0, which is included in the Reportable list) (Screen for incorrectly coded malignancies or reportable by agreement tumors) Schwannomatosis Neoplasms of uncertain behavior (except for 238.4, 238.6, 238.71-238.79, 239.6, 239.7, 239.81 and 239.89, which are listed in the Reportable list) (Screen for incorrectly coded malignancies or reportable by agreement tumors) Syndrome of inappropriate secretion of antidiuretic hormone (Note: Part of the paraneoplastic syndrome*) Multiple endocrine neoplasia (MEN) type IIA and IIB (rare familial cancer syndrome) Other specified endocrine disorders Polyclonal hypergammaglobulinemia (Waldenstrom) (Review for miscodes) Monoclonal gammopathy of undetermined significance (9765/1) (Screen for incorrectly coded Waldenstrom macroglobulinemia or progression) Other disorders of plasma protein metabolism Hypercalcemia (Note: Part of the paraneoplastic syndrome*) Hypogammaglobulinemia (Predisposed to lymphoma or stomach cancer) Selective IgM immunodeficiency (Associated with lymphoproliferative disorders) Immunodeficiency with predominant T-Cell defect, NOS Wiskott-Aldrich Syndrome Nezelof”s Syndrome Red cell aplasia (acquired, adult, with thymoma) Other specified aplastic anemias due to drugs (chemotherapy or immunotherapy), infection, radiation Aplastic anemia, unspecified (Review for miscodes) Sideroblastic anemia Anemia in neoplastic disease (neoplasm may be causing anemia) Antineoplastic chemotherapy induced anemia (Anemia due to antineoplastic chemotherapy) Drug induced neutropenia Myelofibrosis (NOS) (9961/3) (some associated with malignancy) Other specified diseases of blood and blood-forming organs (Review for miscodes) Encephalomyelitis; specified cause NEC (Note: Part of the paraneoplastic syndrome*) Opsoclonia (Note: Part of the paraneoplastic syndrome*) Mucositis due to antineoplastic therapy Hydatiform Mole (9100/0) a benign tumor that can become malignant, but is then coded as Choriocarcinoma (9100/3) and is coded in the 140-209 range Pyoderma gangrenosum (Note: Part of the paraneoplastic syndrome*) Sweet’s syndrome (Note: Part of the paraneoplastic syndrome*) Acanthosis nigricans (Note: Part of the paraneoplastic syndrome*) Dermatomyositis (Note: Part of the paraneoplastic syndrome*) Polymyositis (Note: Part of the paraneoplastic syndrome*) Pathologic fracture (bones weakened by process, perhaps neoplasm) Down’s Syndrome (sometimes associated with myeloid leukemia, 9898/3) Enlargement of lymph nodes Elevated prostate specific antigen [PSA] Papanicolaou smear of cervix with cytologic evidence of malignancy Papanicalaou smear of vagina with cytologic evidence of malignancy Papanicolaou smear of anus with cytologic evidence o f malignancy Abnormal tumor markers; Elevated tumor associated antigens [TAA]; Elevated tumor specific antigens [TSA]; Elevated carcinoembryonic antigen [CEA] Elevated cancer antigen 125 [CA -125] Other abnormal tumor markers Infection due to central venous catheter (porta-cath) Adverse effect of radiation therapy Adverse effect of antineoplastic therapy 2011 Casefinding List E933.1 V12.72 V42.81 – V42.82 V51.0 V84.81 V86.0 V86.1 Revised 02/2011 Adverse effect of immunosuppressive drugs Colonic polyps (history of) Organ or tissue replaced by transplant; bone marrow transplant; peripheral stem cell transplant Encounter for breast reconstruction following mastectomy Genetic susceptibility to multiple endocrine neoplasia [MEN] Estrogen receptor positive status [ER+} Estrogen receptor negative status [ER-] * These diseases are part of the paraneoplastic syndrome*. “Paraneoplastic syndrome* isn’t cancer. It’s a disease or symptom that is the consequence of cancer but is not due to the local presence of cancer cells. A paraneoplastic syndrome* may be the first sign of cancer.”