Sandbox: foreverbones

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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]


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Differentiating Non Small Cell Lung Cancer from Other Diseases

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [3]Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [4]

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 or cartilage can be benign or malignant. These tumors may be classified as "primary 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.[1] 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. 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.[2]

Classification

According to World Health Organization, bone tumors can be divided into primary and secondary. Primitive bone tumors are classified using histo-genetic criteria and malignancy anatomic-clinical criteria. The table below summarizes the findings that differentiate bone tumors according to location, age, histological features, imaging features, and tumor origin.[3][4]

Primary tumors

  • Primary tumors of bone can be divided into benign and malignant tumors.
  • Common benign bone tumors, include:
  • Common malignant bone tumors, include:

Secondary tumors

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:


For more details about each specific type of bone tumor, click on the links in blue in the table below.

Type of tumor Age Location Histological features Imaging features Origin Bone/Cartilage
Osteoma 40-50 years Skull bones Matured lamellar bone Sclerotic Benign Bone
Osteoid osteoma 10-20 years Short and long bone diaphysis Osteiod outlined by osteoblasts, incorporated in a fibrous stroma Sclerotic Benign Bone
Osteosarcoma 11-40 years Long bones metaphysis Osteoid and bone formed of malignant osteoblasts and fibroblasts Sclerotic Malignant Bone
Chondroma 30-60 years Small tubular bones of the hands and feet Maturated hyaline cartilage (enchondroma/ecchondroma), preserving lobulation Well-defined Malignant Cartilage
Chondrosarcoma 30-60 years Long bones metaphysis, axial skeleton Immature cartilage, no preserving lobulation, cells arranged in groups of two or four, with atypia and mitosis Well-defined Malignant Cartilage
Ewing sarcoma 5-25 years Long bones diaphysis Small, round, undifferentiated cells, no stroma, a lot of capillary arrangement. Ill-defined Malignant Bone
Giant cell tumor 20-40 years Knee Multinucleated giant cells, fusiform cells, mononuclear cells. Well-defined Malignant Bone
Metastases 50-90 years No site predilection Frequently adenocarcinomas. Metastases can be blastic or lytic depending on the tumor origin Sclerotic Malignant Bone

Diagnosis

Symptoms

  • Bone tumors are generally asymptomatic.
  • The majority of patients may develop non-specific symptoms, such as:
  • Dull pain
  • Worse at nights
  • Adjacent muscle soreness

Physical Examination

Physical examination findings of bone tumors, may include:

  • Painless mass
  • Weight loss
  • Limited range of motion
  • Fever
  • Tenderness
  • Swelling

Treatment

  • The treatment of choice for bone tumors is dependent on the histological type of tumor.
  • Chemotherapy and radiotherapy are effective in certain bone tumors (such as Ewing's sarcoma).
  • Treatment for some bone tumors may involve surgery, such as:

Surgery

  • The mainstray of choice for the majority of bone tumors is surgery.
  • Common surgical procedures may include:
  • Amputations (conservative or radical)
  • Radical amputation, is called hemicorporectomy (translumbar or waist amputation) which removes the legs, the pelvis, urinary system, excretory system and the genital area (penis/testes in males and vagina/vulva in females).

Acknowledgements

The content on this page was first contributed by: Editor-In-Chief: C. Michael Gibson, M.S., M.D. [5]

References

  1. 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
  2. "Questions and Answers about Bone Cancer" (PDF). Centers for Disease Control and Prevention. Retrieved 18 April 2012.
  3. Bone tumors. https://en.wikipedia.org/wiki/Bone_tumor Accessed on February 2, 2016
  4. 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

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