1. Apply and assign the correct ICD-9-CM and ICD-10-CM codes in accordance with Official Guidelines for Coding and Reporting 2. Identify major differences between ICD-9-CM and ICD-10-CM related to neoplasms 3. Identify pertinent anatomy and physiology for neoplasm 5. Identify neoplastic diseases 6. Assign the correct V/Z codes and procedure codes related to neoplasms 7. Identify common treatments, medications, laboratory values, and diagnostic tests 8. Explain the importance of documentation in relation to MS-DRGs for reimbursement Please refer to the companion Evolve website for the most current guidelines. 2. Chapter 2: Neoplasms (140-239) Chapter 2 of the ICD-9-CM contains the codes for most benign and all malignant neoplasms. Certain benign neoplasms, such as prostatic adenomas, may be found in the specific body system chapters. To properly code a neoplasm it is necessary to determine from the record if the neoplasm is benign, in-situ, malignant, or of uncertain histologic behavior. If malignant, any secondary (metastatic) sites should also be determined. a. Treatment directed at the malignancy If the treatment is directed at the malignancy, designate the malignancy as the principal diagnosis. b. Treatment of secondary site c. Coding and sequencing of complications 1) Anemia associated with malignancy 2) Anemia associated with chemotherapy, immunotherapy and radiation therapy 3) Management of dehydration due to the malignancy 4) Treatment of a complication resulting from a surgical procedure d. Primary malignancy previously excised e. Admissions/Encounters involving chemotherapy, immunotherapy and radiation therapy 1) Episode of care involves surgical removal of neoplasm. 2) Patient admission/encounter solely for administration of chemotherapy, immunotherapy and radiation therapy 3) Patient admitted for radiotherapy/chemotherapy and immunotherapy and develops complications f. Admission/encounter to determine extent of malignancy g. Symptoms, signs, and ill-defined conditions listed in Chapter 16 associated with neoplasms Symptoms, signs, and ill-defined conditions listed in Chapter 16 characteristic of, or associated with, an existing primary or secondary site malignancy cannot be used to replace the malignancy as principal or first-listed diagnosis, regardless of the number of admissions or encounters for treatment and care of the neoplasm. See section I.C.18.d.14, Encounter for prophylactic organ removal. h. Admission/encounter for pain control/management See Section I.C.6.a.5 for information on coding admission/encounter for pain control/management. i. Malignant neoplasm associated with transplanted organ 6. Chapter 6: Diseases of Nervous System and Sense Organs (320-389) Apply the General Coding Guidelines as found in Chapter 5 and the Procedural Guidelines as found in Chapter 6. Please refer to the companion Evolve website for the most current guidelines. 2. Chapter 2: Neoplasms (C00-D49) Chapter 2 of the ICD-10-CM contains the codes for most benign and all malignant neoplasms. Certain benign neoplasms, such as prostatic adenomas, may be found in the specific body system chapters. To properly code a neoplasm it is necessary to determine from the record if the neoplasm is benign, in-situ, malignant, or of uncertain histologic behavior. If malignant, any secondary (metastatic) sites should also be determined. Primary malignant neoplasms overlapping site boundaries Malignant neoplasm of ectopic tissue a. Treatment directed at the malignancy If the treatment is directed at the malignancy, designate the malignancy as the principal diagnosis. b. Treatment of secondary site c. Coding and sequencing of complications 1) Anemia associated with malignancy 2) Anemia associated with chemotherapy, immunotherapy and radiation therapy 3) Management of dehydration due to the malignancy 4) Treatment of a complication resulting from a surgical procedure d. Primary malignancy previously excised e. Admissions/Encounters involving chemotherapy, immunotherapy and radiation therapy 1) Episode of care involves surgical removal of neoplasm 2) Patient admission/encounter solely for administration of chemotherapy, immunotherapy and radiation therapy 3) Patient admitted for radiation therapy, chemotherapy or immunotherapy and develops complications f. Admission/encounter to determine extent of malignancy g. Symptoms, signs, and abnormal findings listed in Chapter 18 associated with neoplasms Symptoms, signs, and ill-defined conditions listed in Chapter 18 characteristic of, or associated with, an existing primary or secondary site malignancy cannot be used to replace the malignancy as principal or first-listed diagnosis, regardless of the number of admissions or encounters for treatment and care of the neoplasm. h. Admission/encounter for pain control/management See Section I.C.6. for information on coding admission/encounter for pain control/management. i. Malignancy in two or more noncontiguous sites j. Disseminated malignant neoplasm, unspecified k. Malignant neoplasm without specification of site l. Sequencing of neoplasm codes 1) Encounter for treatment of primary malignancy 2) Encounter for treatment of secondary malignancy 3) Malignant neoplasm in a pregnant patient When a pregnant woman has a malignant neoplasm, a code from subcategory O9A.1-, Malignant neoplasm complicating pregnancy, childbirth, and the puerperium, should be sequenced first, followed by the appropriate code from Chapter 2 to indicate the type of neoplasm. 4) Encounter for complication associated with a neoplasm 5) Complication from surgical procedure for treatment of a neoplasm 6) Pathologic fracture due to a neoplasm m. Current malignancy versus personal history of malignancy See Section I.C.21. Factors influencing health status and contact with health services, History (of) n. Leukemia, Multiple Myeloma, and Malignant Plasma Cell Neoplasms in remission versus personal history See Section I.C.21. Factors influencing health status and contact with health services, History (of) o. Aftercare following surgery for neoplasm See Section I.C.21. Factors influencing health status and contact with health services, Aftercare p. Follow-up care for completed treatment of a malignancy See Section I.C.21. Factors influencing health status and contact with health services, Follow-up q. Prophylactic organ removal for prevention of malignancy r. Malignant neoplasm associated with transplanted organ Apply the General Coding Guidelines as found in Chapter 5 and the Procedural Guidelines as found in Chapter 7. There are additional ICD-10-CM guidelines that address the following: Malignancy in two or more noncontiguous sites Unspecified disseminated malignant neoplasm Malignant neoplasm without specification of site Current malignancy versus personal history of malignancy Leukemia in remission versus personal history of leukemia Sequencing of neoplasm codes when the encounter is for treatment of: In ICD-10-CM, when an encounter is for the management of anemia associated with malignancy, the malignancy is sequenced as the principal or first-listed diagnosis because of an instructional note, and there is a guideline that addresses this situation. There is a change in terminology for neoplasm codes that could be identified with regard to remission status. The terminology in ICD-9-CM is “without mention of remission,” but in ICD-10-CM, “not in remission” is used. A neoplasm is an abnormal tissue that grows by cellular proliferation more rapidly than normal tissue. Neoplasms show partial or complete lack of structural organization and functional coordination with normal tissue, and they usually form a distinct mass of tissue that may be benign (benign tumor) or malignant (cancer) (Figure 10-1). Both benign and malignant neoplasms are classified according to the type of tissue in which they are found. Benign neoplasms are tumors that are not malignant. Malignancy is a neoplasm that has the ability to invade adjacent structures and spread to distant sites. Fibromas are benign neoplasms of fibrous connective tissue, and melanomas are malignant changes of melanin cells. Malignant tumors originating from epithelial tissue (e.g., skin, bronchi, stomach) are called carcinomas (Table 10-1). Malignancies of epithelial glandular tissue such as those found in the breast, prostate, and colon are known as adenocarcinomas. Malignant growths of connective tissue (e.g., muscle, cartilage, bone) are called sarcomas (Table 10-2). Lymphomas form in lymphatic tissue, and leukemias are malignancies that arise from white blood cells. A myeloma originates within the bone marrow. TABLE 10-1 CARCINOMA AND THE EPITHELIAL TISSUES FROM WHICH THEY DERIVE1 TABLE 10-2 SARCOMAS AND THE CONNECTIVE TISSUES FROM WHICH THEY DERIVE2 Grading involves pathologic examination of tumor cells. The degree of abnormality of cells determines the grade of cancer (Table 10-3). When the level of cell abnormality is greater, the cancer is of higher grade. Cells that are well-differentiated closely resemble mature, specialized cells. Tumor cells that are undifferentiated are highly abnormal (i.e., immature and primitive). TABLE 10-3 In situ cancers have been diagnosed at the earliest possible stage. Stage I or “local” cancers have been diagnosed early and have not spread. Stage II has spread into surrounding tissues but not beyond the location of origin. Stage III or “regional” cancer has spread to nearby lymph nodes. Stage IV or “distant” cancers have spread to other parts of the body and are the most difficult to treat. See Table 10-4 for an example of how the TNM (tumor-node-metastasis) staging system would be used to classify a lung cancer. TABLE 10-4 INTERNATIONAL TNM STAGING SYSTEMS FOR LUNG CANCER3 The coding of most neoplasms requires an extra step, which involves use of the Neoplasm Table (Figure 10-2). The main term for the type of neoplasm is located in the Alphabetic Index. All subterms must be reviewed to facilitate assignment of proper codes, including M codes if required. One must follow all instructions, such as see Neoplasm, by site, benign, or see also Neoplasm, by site, malignant. It is important to follow all steps to ensure correct code assignment. The temptation to go directly to the Neoplasm Table should be avoided.
Neoplasms
(ICD-9-CM Chapter 2, Codes 140-239, and ICD-10-CM Chapter 2, Codes C00-D49)
ICD-9-CM Official Guidelines for Coding and Reporting
ICD-10-CM Official Guidelines for Coding and Reporting
Guideline Differences between ICD-9-CM and ICD-10-CM
Major Differences between ICD-9-CM AND ICD-10-CM
Anatomy and Physiology
Types of Epithelial Tissue
Malignant Tumor (Carcinoma)
Gastrointestinal Tract
Colon
Adenocarcinoma of the colon
Esophagus
Esophageal carcinoma
Liver
Hepatocellular carcinoma (hepatoma)
Stomach
Gastric adenocarcinoma
Glandular Tissue
Adrenal glands
Carcinoma of the adrenals
Breast
Carcinoma of the breast
Pancreas
Carcinoma of the pancreas (pancreatic adenocarcinoma)
Prostate
Carcinoma of the prostate
Thyroid
Carcinoma of the thyroid
Kidney and Bladder
Renal cell carcinoma (hypernephroma)
Transitional cell carcinoma of the bladder
Lung
Adenocarcinoma (bronchioloalveolar)
Large cell carcinoma
Small (oat) cell carcinoma
Squamous cell (epidermoid)
Reproductive Organs
Adenocarcinoma of the uterus
Carcinoma of the penis
Choriocarcinoma of the uterus or testes
Cystadenocarcinoma (mucinous or serous) of the ovaries
Seminoma and embryonal cell carcinoma (testes)
Squamous cell (epidermoid) carcinoma of the vagina or cervix
Skin
Basal cell layer
Basal cell carcinoma
Melanocyte
Malignant melanoma
Squamous cell layer
Squamous cell carcinoma
Types of Connective Tissue
Malignant Tumor
Bone
Osteosarcoma (osteogenic sarcoma)
Ewing’s sarcoma
Muscle
Smooth (visceral) muscle
Leiomyosarcoma
Striated (skeletal) muscle
Rhabdomyosarcoma
Cartilage
Chondrosarcoma
Fat
Liposarcoma
Fibrous Tissue
Fibrosarcoma
Blood Vessel Tissue
Angiosarcoma
Blood-Forming Tissue
All leukocytes
Leukemias
Lymphocytes
Hodgkin’s disease
Plasma cells
Non-Hodgkin’s lymphoma
Burkitt’s lymphoma
Multiple myeloma
Nerve Tissue
Embryonic nerve tissue
Neuroblastoma
Glial tissue
Astrocytoma (tumors of glial cells, called “astrocytes”)
Glioblastoma multiforme
Grade 1
Cells slightly abnormal and well-differentiated
Grade 2
Cells more abnormal and moderately differentiated
Grade 3
Cells very abnormal and poorly differentiated
Grade 4
Cells immature and undifferentiated
Stage
TNM Description
5-Year Survival, %
I
T1-T2, N0, M0
60-80
II
T1-T2, N1, M0
25-50
IIIA
T3, N0-N1, M0
25-40
IIIB
T1-T3, N2, M0
10-30
IV
Any T4 or N3, M0
<5
Any M1
<5
Primary Tumor (T)
T1
Tumor >3 cm in diameter
T2
Tumor <3 cm in diameter or with associated atelectasis–obstructive pneumonitis extending to the hilar region
T3
Tumor with direct extension into the chest wall, diaphragm, mediastinum, pleura, or pericardium
T4
Tumor invades the mediastinum, or presence of a malignant pleural effusion
Regional Lymph Nodes (N)
N0
No node involvement
N1
Metastasis to lymph nodes in the peribronchial and ipsilateral (same side as the primary tumor) hilar regions
N2
Metastasis to ipsilateral hilar and subcarinal (under the bifurcation of the trachea into the lungs) lymph nodes
N3
Metastasis to contralateral mediastinal or hilar nodes or any nodes new to the clavicular (collar) bone
Distance Metastasis (M)
M0
No known metastasis
M1
Distant metastasis present with site specified (e.g., brain, tumor)
Neoplasm Table