- Home
- ICD-10-CM Codes
- C00–D48
- C73-C75
- Malignant neoplasm of endo glands and related structures (C75)
Malignant neoplasm of endo glands and related structures (C75)
ICD-10 Index
Neoplasms (C00–D48)
Malignant neoplasms of thyroid and other endocrine glands (C73-C75)
- C75 - Malignant neoplasm of endo glands and related structures NON-BILLABLE CODE
- C75.0 - Malignant neoplasm of parathyroid gland BILLABLE CODE
- C75.1 - Malignant neoplasm of pituitary gland BILLABLE CODE
- C75.2 - Malignant neoplasm of craniopharyngeal duct BILLABLE CODE
- C75.3 - Malignant neoplasm of pineal gland BILLABLE CODE
- C75.4 - Malignant neoplasm of carotid body BILLABLE CODE
- C75.5 - Malignant neoplasm of aortic body and other paraganglia BILLABLE CODE
- C75.8 - Malignant neoplasm with pluriglandular involvement, unsp BILLABLE CODE
- C75.9 - Malignant neoplasm of endocrine gland, unspecified BILLABLE CODE
Malignant neoplasm of endo glands and related structures (C75)
Clinical Information for Malignant neoplasm of endo glands and related structures (C75)
Esthesioneuroblastoma, Olfactory - A malignant olfactory neuroblastoma arising from the olfactory epithelium of the superior nasal cavity and cribriform plate. It is uncommon (3% of nasal tumors) and rarely is associated with the production of excess hormones (e.g., SIADH, Cushing Syndrome). It has a high propensity for multiple local recurrences and bony metastases. (From Holland et al., Cancer Medicine, 3rd ed, p1245; J Laryngol Otol 1998 Jul;112(7):628-33)
Neuroblastoma - A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2099-2101; Curr Opin Oncol 1998 Jan;10(1):43-51)
Retinoblastoma - A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)
Instructional Notations
Type 1 Excludes Type 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
- malignant carcinoid tumors C7A.0
- malignant neoplasm of adrenal gland C74
- malignant neoplasm of endocrine pancreas C25.4
- malignant neoplasm of islets of Langerhans C25.4
- malignant neoplasm of ovary C56
- malignant neoplasm of testis C62
- malignant neoplasm of thymus C37
- malignant neoplasm of thyroid gland C73
- malignant neuroendocrine tumors C7A