Bone tumor

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Bone cancer
)
Bone tumor
biopsy[1]
PrognosisVaries with type[4]
FrequencyCommon[4]

A bone tumor is an

fatigue, fever, weight loss, anemia and nausea.[2][3] Sometimes there are no symptoms and the tumour is found when investigating another problem.[2][3]

Diagnosis is generally by

liver function.[1] Urine may be tested for Bence Jones protein.[1] For confirmation of diagnosis, a biopsy for histological evaluation might be required.[1]

The most common bone tumor is a

five-year survival in the United States after being diagnosed with bone and joint cancer is 67%.[5] The earliest known bone tumor was an osteosarcoma in a foot bone discovered in South Africa, between 1.6 and 1.8 million years ago.[6]

Classification

giant cell bone tumor
in the head of the 4th metacarpal of the left hand.
An arm bone tumor

Bone tumors are traditionally classified as

cartilage tumors, osteogenic tumors, fibrogenic tumors, vascular tumors of bone, osteoclastic giant cell-rich tumors, notochordal tumors, other mesenchymal tumors of bone, and hematopoietic neoplasms of bone.[4][7]

Bone tumors may be classified as "

secondary tumors" which originate in other sites and spread (metastasize) to the skeleton. Carcinomas of the prostate, breasts, lungs, thyroid, and kidneys are the carcinomas that most commonly metastasize to bone. Secondary malignant bone tumors are estimated to be 50 to 100 times as common as primary bone cancers.[citation needed
]

Primary bone tumors

Primary tumors of bone can be divided into

]

Malignant primary bone tumors, known as

pleomorphic undifferentiated sarcoma" - primary in bone is known to occur occasionally,[9] current paradigms tend to consider MFH a wastebasket diagnosis, and the current trend is toward using specialized studies (i.e. genetic and immunohistochemical tests) to classify these undifferentiated tumors into other tumor classes. Multiple myeloma is a hematologic cancer, originating in the bone marrow, which also frequently presents as one or more bone lesions.[10]

Germ cell tumors, including teratoma, often present and originate in the midline of the sacrum, coccyx, or both. These sacrococcygeal teratomas are often relatively amenable to treatment.[11]

Secondary bone tumors

Secondary bone tumors are metastatic lesions which have spread from other organs, most commonly carcinomas of the breast, lung, and prostate. Rarely, primary bone malignancies such as osteosarcoma may also spread to other bones.[12] Reliable and valid statistics on the incidence, prevalence, and mortality of malignant bone tumours are difficult to come by, particularly in older adults (those over 75 years of age) - because

carcinomas that are widely metastatic to bone are rarely ever curable. Biopsies to determine the origin of the tumour in cases like this are rarely done.[citation needed
]

Signs and symptoms

Clinical features of a bone tumor depend on the type of tumor and which part of which bone is affected.[2][13] Symptoms and signs usually result from the pressure effect of the tumor.[1]

There may be a lump, with or without pain.

fatigue, fever, weight loss, anemia and nausea.[2][3] If the tumor presses a nerve, neurological signs may be present.[1] Sometimes there are no symptoms and the tumour is found when investigating another problem.[2][3]

Diagnosis

A bone tumour may be felt on examination, following which a

Other tests that might be requested include a
MRI, PET scan and bone scintigraphy. For confirmation of diagnosis, a biopsy for histological evaluation might be required, using either a needle or by incision (open biopsy).[1][2]

Staging

  • Stage 1A bone cancer
    Stage 1A bone cancer
  • Stage 1B bone cancer
    Stage 1B bone cancer
  • Stage 2A bone cancer
    Stage 2A bone cancer
  • Stage 2B bone cancer
    Stage 2B bone cancer
  • Stage 3 bone cancer
    Stage 3 bone cancer

Treatment

Treatment of bone tumors is dependent on the type of tumor.[2] Where available, people with bone tumors are treated at a specialist centre which have surgeons, radiologists, pathologists, oncologists and other support staff.[1] Generally, noncancerous bone tumors may be observed for changes and surgery offered if there is pain or pressure effects on neighbouring body parts. Surgical resection with or without cytotoxic drugs may be considered.[1]

Chemotherapy and radiotherapy

Ewing's sarcoma) but less so in others (such as chondrosarcoma).[15]
There is a variety of chemotherapy treatment protocols for bone tumors. The protocol with the best-reported survival in children and adults is an intra-arterial protocol where tumor response is tracked by serial arteriogram. When tumor response has reached >90% necrosis surgical intervention is planned.[16][17]

Medication

One of the major concerns is bone density and bone loss. Non-hormonal bisphosphonates increase bone strength and are available as once-a-week prescription pills. Strontium-89 chloride is an intravenous medication given to help with the pain and can be given in three-month intervals.

Surgical treatment

Treatment for some bone cancers may involve

bone graft, in which bone is taken from elsewhere on the body or (b) artificial bone is put in. In upper leg surgeries, limb salvage prostheses are available.[citation needed
]

There are other joint preservation surgical reconstruction options, including allograft, tumor-devitalized autograft, vascularized fibula graft, distraction osteogenesis, and custom-made implants.[18] An analysis of massive knee replacements after resection of primary bone tumours showed patients did not score as highly on the Musculoskeletal Tumour Society Score and Knee Society Score as patients who had undergone intra-articular resection.[19]

Thermal ablation techniques

Over the past two decades, CT guided radiofrequency ablation has emerged as a less invasive alternative to surgical resection in the care of benign bone tumors, most notably osteoid osteomas. In this technique, which can be performed under conscious sedation, a RF probe is introduced into the tumor nidus through a cannulated needle under CT guidance and heat is applied locally to destroy tumor cells. Since the procedure was first introduced for the treatment of osteoid osteomas in the early 1990s,[20] it has been shown in numerous studies to be less invasive and expensive, to result in less bone destruction and to have equivalent safety and efficacy to surgical techniques, with 66 to 96% of patients reporting freedom from symptoms.[21][22][23] While initial success rates with RFA are high, symptom recurrence after RFA treatment has been reported, with some studies demonstrating a recurrence rate similar to that of surgical treatment.[24]

Thermal ablation techniques are also increasingly being used in the palliative treatment of painful metastatic bone disease. Currently, external beam radiation therapy is the standard of care for patients with localized bone pain due to metastatic disease. Although the majority of patients experience complete or partial relief of pain following radiation therapy, the effect is not immediate and has been shown in some studies to be transient in more than half of patients.[25] For patients who are not eligible or do not respond to traditional therapies ( i.e. radiation therapy, chemotherapy, palliative surgery, bisphosphonates or analgesic medications), thermal ablation techniques have been explored as alternatives for pain reduction. Several multi-center clinical trials studying the efficacy of RFA in the treatment of moderate to severe pain in patients with metastatic bone disease have shown significant decreases in patient reported pain after treatment.[26][27] These studies are limited however to patients with one or two metastatic sites; pain from multiple tumors can be difficult to localize for directed therapy. More recently, cryoablation has also been explored as a potentially effective alternative as the area of destruction created by this technique can be monitored more effectively by CT than RFA, a potential advantage when treating tumors adjacent to critical structures.[28]

Prognosis

The outlook depends on the type of tumor. The outcome is expected to be good for people with noncancerous (benign) tumors, although some types of benign tumors may eventually become cancerous (malignant). With malignant bone tumors that have not spread, most patients achieve a cure, but the cure rate depends on the type of cancer, location, size, and other factors.[citation needed]

Epidemiology

Bone tumors that originate from bone are very rare and account for around 0.2% of all tumors.

five-year survival in the United States after being diagnosed with bone and joint cancer is 67%.[5]

History

The earliest known bone tumor was an osteosarcoma in a foot bone belonging to a person who died in Swartkrans Cave, South Africa, between 1.6 and 1.8 million years ago.[6]

Other animals

Bones are a common site for tumors in cats and dogs.[29]

References

  1. ^ .
  2. ^ a b c d e f g h i j k "Bone Tumor - Types and Treatments - OrthoInfo - AAOS". www.orthoinfo.org. Retrieved 27 June 2021.
  3. ^ a b c d e f g "Questions and Answers about Bone Cancer" (PDF). Centers for Disease Control and Prevention. Retrieved 27 June 2021.
  4. ^ .
  5. ^ a b "SEER Stat Fact Sheets: Bone and Joint Cancer". NCI. Retrieved 18 June 2014.
  6. ^ a b Strauss, Mark (28 July 2016). "Earliest Human Cancer Found in 1.7-Million-Year-Old Bone". Culture. Archived from the original on March 10, 2021. Retrieved 27 June 2021.
  7. ^
    S2CID 231679037
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  9. ^ Jeon DG, Song WS, Kong CB, Kim JR, Lee SY. MFH of Bone and Osteosarcoma Show Similar Survival and Chemosensitivity. Clin Orthop Rel Res 469;584-90.
  10. ^ "Multiple Myeloma". The Lecturio Medical Concept Library. Retrieved 26 August 2021.
  11. PMID 32485873
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  12. ^ "Osteosarcoma". The Lecturio Medical Concept Library. Retrieved 26 August 2021.
  13. .
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  15. Mount Sinai Hospital, New York
  16. ^ 10 year survival in Pediatric Osteosarcoma[permanent dead link]
  17. ^ Survival in Adult Osteosarcoma and MFH of Bone[permanent dead link]
  18. S2CID 208650189
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  24. S2CID 10709128. Archived from the original
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