ICD-9 Diagnosis Code 171.9

Mal neo soft tissue NOS

Diagnosis Code 171.9

ICD-9: 171.9
Short Description: Mal neo soft tissue NOS
Long Description: Malignant neoplasm of connective and other soft tissue, site unspecified
This is the 2014 version of the ICD-9-CM diagnosis code 171.9

Code Classification
  • Neoplasms (140–239)
    • Malignant neoplasm of bone, connective tissue, skin, and breast (170-176)
      • 171 Malignant neoplasm of connective and other soft tissue

Information for Medical Professionals

Convert to ICD-10 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

  • Adipocytic liposarcoma
  • Alveolar rhabdomyosarcoma
  • Alveolar soft part sarcoma
  • Angiosarcoma
  • Atypical fibroxanthoma of skin
  • Botryoid rhabdomyosarcoma
  • Carcinoma of bone, connective tissue, skin and breast
  • Cutaneous leiomyosarcoma with granular cell change
  • Dedifferentiated liposarcoma
  • Embryonal rhabdomyosarcoma
  • Epithelioid leiomyosarcoma of skin
  • Epithelioid malignant nerve sheath tumor
  • Ewing's sarcoma of soft tissue
  • Extraskeletal mesenchymal chondrosarcoma
  • Extraskeletal myxoid chondrosarcoma
  • Fibrosarcoma of connective tissue
  • Glandular malignant peripheral nerve sheath tumor
  • Granulocytic sarcoma affecting skin
  • Histiocytic sarcoma
  • Infantile fibrosarcoma
  • Inflammatory malignant fibrous histiocytoma of skin
  • International neuroblastoma pathology classification: Favorable histology group, patient age 1.5 years up to but less than 5 years, with differentiating neuroblastoma
  • International neuroblastoma pathology classification: Favorable histology group, patient less than 1.5 years of age, with poorly differentiated neuroblastoma
  • International neuroblastoma staging system stage 1
  • Intravascular angiosarcoma
  • Leiomyosarcoma
  • Leiomyosarcoma of connective tissue
  • Liposarcoma
  • Liposarcoma of connective tissue
  • Local recurrence of malignant tumor of soft tissue
  • Low-grade fibromyxoid sarcoma
  • Lymphangiosarcoma
  • Malignant fibromatous neoplasm
  • Malignant fibrous histiocytoma
  • Malignant fibrous histiocytoma of skin
  • Malignant granular cell tumor
  • Malignant infiltration of peripheral nerve
  • Malignant infiltration of peripheral nerve plexus
  • Malignant infiltration of soft tissue
  • Malignant lipomatous tumor
  • Malignant melanoma of soft tissues
  • Malignant neoplasm of bone, connective tissue, skin and breast
  • Malignant neoplasm of connective tissue
  • Malignant neoplasm of peripheral nerves and autonomic nervous system
  • Malignant neoplasm of soft tissue
  • Malignant neoplasm of subcutaneous fibrous tissue
  • Malignant peripheral nerve sheath tumor
  • Malignant Triton tumor
  • Malignant tumor of fibrous tissue
  • Malignant tumor of mesothelial tissue
  • Malignant tumor of muscle
  • Malignant tumor of nerve sheath origin
  • Malignant tumor of peripheral nerve
  • Malignant tumor of spinal nerve and sheath
  • Melanotic malignant nerve sheath tumor
  • Metastasis from malignant tumor of soft tissues
  • Metastatic sarcoma
  • Myxoid leiomyosarcoma of skin
  • Myxoid liposarcoma
  • Overlapping malignant neoplasm of soft tissues
  • Pleomorphic liposarcoma
  • Pleomorphic rhabdomyosarcoma
  • Primary leiomyosarcoma
  • Primary malignant neoplasm of blood vessel
  • Primary malignant neoplasm of muscle
  • Primary malignant neoplasm of peripheral nerve
  • Primary malignant neoplasm of peripheral nerves and peripheral autonomic nervous system
  • Primary malignant neoplasm of soft tissues
  • Rhabdomyosarcoma
  • Rhabdomyosarcoma of connective or soft tissue
  • Round cell liposarcoma
  • Sarcoma
  • Sarcoma of bone and connective tissue
  • Sarcoma of connective tissue
  • Sarcoma of soft tissue
  • Sarcomatous metastasis in skin
  • Sclerosing liposarcoma
  • Spindle cell liposarcoma
  • Spindle cell rhabdomyosarcoma
  • Synovial sarcoma
  • Vaccine-induced fibrosarcoma

Index of Diseases and Injuries
References found for the code 171.9 in the Index of Diseases and Injuries:

Information for Patients

Soft Tissue Sarcoma

Your soft tissues connect, support, or surround other tissues. Examples include your muscles, tendons, fat, and blood vessels. Soft tissue sarcoma is a cancer of these soft tissues. There are many kinds, based on the type of tissue they started in. They may cause a lump or swelling in the soft tissue. Sometimes they spread and can press on nerves and organs, causing problems such as pain or trouble breathing.

No one knows exactly what causes these cancers. They are not common, but you have a higher risk if you have been exposed to certain chemicals, have had radiation therapy, or have certain genetic diseases.

Doctors diagnose soft tissue sarcomas with a biopsy. Treatments include surgery to remove the tumor, radiation therapy, chemotherapy, or a combination.

NIH: National Cancer Institute

  • Adult soft tissue sarcoma
  • After chemotherapy - discharge
  • Rhabdomyosarcoma
  • Understanding Chemotherapy - NIH - Easy-to-Read (National Cancer Institute)
  • What to Know about External Beam Radiation Therapy - NIH - Easy-to-Read (National Cancer Institute)

[Read More]
Previous Code
Previous Code 171.8
Next Code
172.0 Next Code