Bone or cartilage mass overview: Difference between revisions
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Laboratory findings consistent with the diagnosis of bone and cartilage tumors, may include elevated LDH, alkaline phosphatase (related with prognosis), and aspartate aminotransferase (AST). | Laboratory findings consistent with the diagnosis of bone and cartilage tumors, may include: elevated LDH, elevated alkaline phosphatase (related with prognosis), and elevated aspartate aminotransferase (AST). | ||
===Imaging=== | ===Imaging=== | ||
Revision as of 14:00, 22 February 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]
Overview
Tumors of the bone (also known as "Bone and cartilage tumors") are generally defined as the neoplastic growth of tissue in the bone and cartilage. Abnormal growths found in the bone can be benign or malignant. Bone and cartilage tumors may be classified according to the WHO histological classification system into 5 sub-types: cartilage tumors, osteogenic tumors, fibrohistiocytic tumors, notochordal tumors, hematopoietic tumors, and miscellaneous tumors.[1][2] In addition, bone and cartilage tumors may be sub-classified according to tumor location into 4 subtypes: diaphysis, metaphysis, epiphysis, and ungrouped/others.[3] "Primary bone tumors", which originate in bone or from bone-derived cells and tissues, and "secondary tumors" which originate in other sites and metastasize to the skeleton, is another nomenclature to classify bone tumors.[4] Carcinomas of the prostate, breasts, lungs, thyroid, and kidneys are the carcinomas that most commonly metastasize to bone. Secondary malignant bone tumors are more common than primary bone cancers. Bone and cartilage tumors are uncommon, they represent 0.2% of all neoplasms in general population. The prevalence of bone and cartilage tumors is approximately 0.9 per 100,000 individuals. Bone and cartilage tumors have a bimodal age distribution. These tumors are more frequent in children and adolescents, and older adults.[5] Bone and cartilage tumors are slightly more common among individuals of Caucasian race.[6] The most common symptom of bone tumors is pain, which will gradually increase over time. The pain increases with the growth of the tumor. Additional symptoms may include fatigue, fever, weight loss, anemia, and/or sudden bone fractures. In some cases, bone tumors may be asymptomatic. Bone tumors may weaken the structure of the bone, causing pathologic fractures.[7]
Classification
Bone and cartilage tumors may be classified according to the WHO histological classification system into benign and malignant tumors, and categorized into 5 sub-types: cartilage tumors, osteogenic tumors, fibrohistiocytic tumors, notochordal tumors, hematopoietic tumors, and miscellaneous tumors.[1][2] In addition, bone and cartilage tumors may be sub-classified according to tumor location into 4 subtypes: diaphysis, metaphysis, epiphysis, and ungrouped/others.[3] "Primary bone tumors", which originate in bone or from bone-derived cells and tissues, and "secondary tumors" which originate in other sites and metastasize to the skeleton, is another nomenclature to classify bone tumors.[8] Carcinomas of the prostate, breasts, lungs, thyroid, and kidneys are the carcinomas that most commonly metastasize to bone. Secondary malignant bone tumors are more common than primary bone cancers. Common benign bone tumors, include: osteoma, osteoid osteoma, osteochondroma, aneurysmal bone cyst, and fibrous dysplasia. Common malignant bone tumors, include: osteosarcoma, Ewing's sarcoma, and chondrosarcoma. Secondary bone tumors include metastatic tumors which have spread from other organs (usually, adenocarcinomas). In general, metastatic tumors frequently involve the axial skeleton and the appendicular skeleton. Common secondary bone tumors, include: breast cancer, lung cancer, and prostate cancer.
Causes
Bone and cartilage tumors may be caused by precursor lesions, such as radiation injury, chronic osteomyelitis, and some genetically determined syndromes (McCune-Albright syndrome, Ollier disease, Maffucci syndrome, and Beckwith-Wiedemann syndrome).[1]
Differential Diagnosis
Bone and cartilage tumors may be differentiated according to clinical features, laboratory findings, imaging features, histological features, and genetic studies, from other diseases that cause limited range of motion, limb deformity, bone pain, local swelling, and limb deformity.[2][9] Common differential diagnosis includes: osteoma, osteosarcoma, chondroma, chondrosarcoma, Ewing sarcoma, giant cell tumor, and metastases.
Epidemiology and Demographics
Bone and cartilage tumors are uncommon, they represent 0.2% of all neoplasms in general population. The prevalence of bone and cartilage tumors is approximately 0.9 per 100,000 individuals. Bone and cartilage tumors have a bimodal age distribution. These tumors are more frequent in children and adolescents, and older adults. The average age at diagnosis is between 10-25 years old and 60-75 years old. Males are more commonly affected than females, with a 1.5:1 ratio.[5] Bone and cartilage tumors are slightly more common among individuals of Caucasian race.[6]
Screening
According to the the National Cancer Institute (NCI) there is insufficient evidence to recommend routine screening for bone or cartilage tumors.[10]
Diagnosis
Evaluation of Bone or Cartilage Mass
The evaluation of bone or cartilage mass will depend on detailed medical history, age, and morphology of the lesion.[11]
Staging
According to the Enneking system there are 6 stages of benign and malignant bone and cartilage tumors based on the grade, anatomic site, and metastasis.[12]
History and Symptoms
Bone and cartilage tumors are generally asymptomatic. The majority of patients may develop non-specific symptoms, such as: dull localized bone pain (related with locally aggressive tumors), adjacent muscle soreness, local swelling or mass, progressive pain that is not relieved with rest, night pain, and recent weight loss. Obtaining the detailed history is an important aspect of making a diagnosis of bone and cartilage tumors, specific areas of focus when obtaining the history, are personal history of cancer, and family history of bone tumors.
Physical Examination
Physical examination findings of bone or cartilage masses will depend on the location of the tumor. Common physical examination findings include skeletal deformity, swelling, increased skin temperature, increased sweating, and tenderness.[13]
Laboratory Studies
Laboratory findings consistent with the diagnosis of bone and cartilage tumors, may include: elevated LDH, elevated alkaline phosphatase (related with prognosis), and elevated aspartate aminotransferase (AST).
Imaging
Conventional radiography is the method of choice to diagnose primary bone tumors.
Other Diagnostic Studies
Other diagnostic studies may include: bone scintigraphy and bone biopsy.[14]
Acknowledgements
The content on this page was first contributed by: Editor-In-Chief: C. Michael Gibson, M.S., M.D. [3]
References
- ↑ 1.0 1.1 1.2 Bone tumors. https://en.wikipedia.org/wiki/Bone_tumor Accessed on February 2, 2016
- ↑ 2.0 2.1 2.2 Alina Maria Sisu. On the Bone Tumours: Overview, Classification, Incidence, Histopathological Issues, Behavior and Review Using Literature Data. http://www.intechopen.com/books/histopathology-reviews-and-recent-advances/on-the-bone-tumours-overview-classification-incidence-histopathological-issues-behavior-and-review Accessed on February 2, 2016
- ↑ 3.0 3.1 Miller TT (2008). "Bone tumors and tumorlike conditions: analysis with conventional radiography". Radiology. 246 (3): 662–74. doi:10.1148/radiol.2463061038. PMID 18223119.
- ↑ Henk Jan van der Woude and Robin Smithuis. Bone tumor - Systematic approach and Differential diagnosis. Radiology assistant. http://www.radiologyassistant.nl/en/p494e15cbf0d8d/bone-tumor-systematic-approach-and-differential-diagnosis.html Accessed on February 2, 2016
- ↑ 5.0 5.1 Franchi A (2012). "Epidemiology and classification of bone tumors". Clin Cases Miner Bone Metab. 9 (2): 92–5. PMC 3476517. PMID 23087718.
- ↑ 6.0 6.1 Tubiana-Hulin M (1991). "Incidence, prevalence and distribution of bone metastases". Bone. 12 Suppl 1: S9–10. PMID 1954049.
- ↑ "Questions and Answers about Bone Cancer" (PDF). Centers for Disease Control and Prevention. Retrieved 18 April 2012.
- ↑ Henk Jan van der Woude and Robin Smithuis. Bone tumor - Systematic approach and Differential diagnosis. Radiology assistant. http://www.radiologyassistant.nl/en/p494e15cbf0d8d/bone-tumor-systematic-approach-and-differential-diagnosis.html Accessed on February 2, 2016
- ↑ Bone tumors. https://en.wikipedia.org/wiki/Bone_tumor Accessed on February 2, 2016
- ↑ Bone Cancer—Health Professional Version (2016) http://www.cancer.gov/types/bone/hp Accessed on February, 8th 2016
- ↑ Balach T, Stacy GS, Peabody TD (2011). "The clinical evaluation of bone tumors". Radiol. Clin. North Am. 49 (6): 1079–93, v. doi:10.1016/j.rcl.2011.07.001. PMID 22024289.
- ↑ Enneking System for Staging of Benign and Malignant Bone and Soft Tissue Lesion. Orthopaedics One. http://www.orthopaedicsone.com/x/TwAjAQ. Accessed on February 12, 2016
- ↑ Greenspan A (1993). "Benign bone-forming lesions: osteoma, osteoid osteoma, and osteoblastoma. Clinical, imaging, pathologic, and differential considerations". Skeletal Radiol. 22 (7): 485–500. PMID 8272884.
- ↑ Focacci C, Lattanzi R, Iadeluca ML, Campioni P (1998). "Nuclear medicine in primary bone tumors". Eur J Radiol. 27 Suppl 1: S123–31. PMID 9652512.