Valid for Submission
C69.20 is a billable diagnosis code used to specify a medical diagnosis of malignant neoplasm of unspecified retina. The code C69.20 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions.
The ICD-10-CM code C69.20 might also be used to specify conditions or terms like malignant tumor of retina, melanoma-associated retinopathy, paraneoplastic retinopathy, pm1a: distant metastasis to bone marrow , pm1b: distant metastasis to sites other than bone marrow , primary malignant neoplasm of retina , etc.
Unspecified diagnosis codes like C69.20 are acceptable when clinical information is unknown or not available about a particular condition. Although a more specific code is preferable, unspecified codes should be used when such codes most accurately reflect what is known about a patient's condition. Specific diagnosis codes should not be used if not supported by the patient's medical record.
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Malignant tumor of retina
- Melanoma-associated retinopathy
- Paraneoplastic retinopathy
- pM1a: Distant metastasis to bone marrow
- pM1b: Distant metastasis to sites other than bone marrow
- Primary malignant neoplasm of retina
- Primary malignant neuroepithelial neoplasm of retina
- pT1: Tumor confined to the retina, vitreous, or subretinal space. No optic nerve or choroidal invasion
- pT2: Minimal invasion of the optic nerve and/or optic coats
- pT2a: Tumor invades optic nerve up to, but not through, the level of the lamina cribrosa
- pT2b: Tumor invades choroid focally
- pT2c category
- pT2c: Tumor invades optic nerve up to, but not through, the level of the lamina cribrosa and invades the choroid focally
- pT3: Significant invasion of the optic nerve and/or optic coats
- pT3a: Tumor invades optic nerve through the level of the lamina cribrosa but not to the line of resection
- pT3b: Tumor massively invades the choroid
- pT3c category
- pT3c: Tumor invades the optic nerve through the level of the lamina cribrosa but not to the line of resection and massively invades the choroid
- pT4: Extraocular tumor extension which includes sites as per AJCC 6th Edition definition
- Retinal pigment epithelial adenocarcinoma
Diagnostic Related Groups - MS-DRG Mapping
Convert C69.20 to ICD-9 Code
The General Equivalency Mapping (GEM) crosswalk indicates an approximate mapping between the ICD-10 code C69.20 its ICD-9 equivalent. The approximate mapping means there is not an exact match between the ICD-10 code and the ICD-9 code and the mapped code is not a precise representation of the original code.
Information for Patients
Cancer of the eye is uncommon. It can affect the outer parts of the eye, such as the eyelid, which are made up of muscles, skin and nerves. If the cancer starts inside the eyeball it's called intraocular cancer. The most common intraocular cancers in adults are melanoma and lymphoma. The most common eye cancer in children is retinoblastoma, which starts in the cells of the retina. Cancer can also spread to the eye from other parts of the body.
Treatment for eye cancer varies by the type and by how advanced it is. It may include surgery, radiation therapy, freezing or heat therapy, or laser therapy.
- After chemotherapy - discharge (Medical Encyclopedia)
- Lacrimal gland tumor (Medical Encyclopedia)
- Melanoma of the eye (Medical Encyclopedia)
- Retinoblastoma (Medical Encyclopedia)
[Learn More in MedlinePlus]
Retinoblastoma Retinoblastoma is a rare type of eye cancer that usually develops in early childhood, typically before the age of 5. This form of cancer develops in the retina, which is the specialized light-sensitive tissue at the back of the eye that detects light and color.In children with retinoblastoma, the disease often affects only one eye. However, one out of three children with retinoblastoma develops cancer in both eyes. The most common first sign of retinoblastoma is a visible whiteness in the pupil called "cat's eye reflex" or leukocoria. This unusual whiteness is particularly noticeable in dim light or in photographs taken with a flash. Other signs and symptoms of retinoblastoma include crossed eyes or eyes that do not point in the same direction (strabismus), which can cause squinting; a change in the color of the colored part of the eye (iris); redness, soreness, or swelling of the eyelids; and blindness or poor vision in the affected eye or eyes.Retinoblastoma is often curable when it is diagnosed early. However, if it is not treated promptly, this cancer can spread beyond the eye to other parts of the body. This advanced form of retinoblastoma can be life-threatening.When retinoblastoma is associated with a genetic change (mutation) that occurs in all of the body's cells, it is known as hereditary (or germinal) retinoblastoma. People with this form of retinoblastoma typically develop cancer in both eyes and also have an increased risk of developing several other cancers outside the eye. Specifically, they are more likely to develop a cancer of the pineal gland in the brain (pineoblastoma), a type of bone cancer known as osteosarcoma, cancers of soft tissues (such as muscle) called soft tissue sarcomas, and an aggressive form of skin cancer called melanoma.
[Learn More in MedlinePlus]