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  2. ICD-10-CM Codes
  3. C00–D48
  4. C73-C75
  5. Malignant neoplasm of adrenal gland (C74)

Malignant neoplasm of adrenal gland (C74)

    • ICD-10 Index

      • Neoplasms (C00–D48)

        • Malignant neoplasms of thyroid and other endocrine glands (C73-C75)

            • Malignant neoplasm of adrenal gland (C74)
            • C74 - Malignant neoplasm of adrenal gland NON-BILLABLE CODE
            • C74.0 - Malignant neoplasm of cortex of adrenal gland NON-BILLABLE CODE
            • C74.00 - Malignant neoplasm of cortex of unspecified adrenal gland BILLABLE CODE
            • C74.01 - Malignant neoplasm of cortex of right adrenal gland BILLABLE CODE
            • C74.02 - Malignant neoplasm of cortex of left adrenal gland BILLABLE CODE
            • C74.1 - Malignant neoplasm of medulla of adrenal gland NON-BILLABLE CODE
            • C74.10 - Malignant neoplasm of medulla of unspecified adrenal gland BILLABLE CODE
            • C74.11 - Malignant neoplasm of medulla of right adrenal gland BILLABLE CODE
            • C74.12 - Malignant neoplasm of medulla of left adrenal gland BILLABLE CODE
            • C74.9 - Malignant neoplasm of unspecified part of adrenal gland NON-BILLABLE CODE
            • C74.90 - Malignant neoplasm of unsp part of unspecified adrenal gland BILLABLE CODE
            • C74.91 - Malignant neoplasm of unsp part of right adrenal gland BILLABLE CODE
            • C74.92 - Malignant neoplasm of unspecified part of left adrenal gland BILLABLE CODE

Clinical Information for Malignant neoplasm of adrenal gland (C74)

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)