Study Notes on Bone Tumors from Thai Red Cross Society
Thai Red Cross Society
The document originates from the Thai Red Cross Society.
Bone Tumors Overview
Focus on bone tumors, particularly the Queen Savang Vadhana Memorial Department at the QSMH Hospital, represented by Dr. Komkrich Wattanapaiboon, MD. in the Oncology and Spine Unit.
Types of Bone Tumors
Carcinoma:
Definition: "Malignant neoplasm of epithelial cell origin, derived from ectoderm or endoderm."
Sarcoma:
Definition: "Malignant neoplasm of the mesenchymal tissue" (mostly derived from mesoderm).
Classification of Bone Tumors
Primary Bone Tumor:
Types: Benign, Malignant, Tumor-like lesion, Metastatic bone disease.
Incidence of Bone Sarcoma
Average Incidence:
Represents approximately 0.2% of all neoplasms.
0.8 new cases per 100,000 population annually.
Specific Types Incidence:
Osteosarcoma: 35.1%
Chondrosarcoma: 25.8%
Ewing’s Sarcoma: 16.0%
Chordoma: 8.4%
Pleomorphic Sarcoma and Fibrosarcoma: 5.6%
Age Correlation:
Less than 20 years old: More likely to have osteosarcoma and Ewing’s sarcoma.
Over 50 years: More likely to develop chondrosarcoma.
Etiology of Bone Tumors
Possible causes include:
Unknown factors.
Chemical Exposure.
Radiation.
Viruses.
Trauma.
Genetic Abnormalities:
Tumor Suppressor Genes:
Examples include RB (Retinoblastoma), p53 (Li-Fraumeni syndrome), p16INK4a (Familial melanoma), NF1 (Neurofibromatosis), EXT1 and EXT2 (Hereditary multiple exostosis).
Clinical Evaluation of Bone Tumors
Initial Evaluation:
Plain Film Imaging
History and Physical Examination
CT Scan and Bone Scan for probably malignant cases.
Biopsy for determining tumor type and staging.
MRI for advanced imaging and evaluation.
Gender Differences in Bone Tumors
Male Predominance: generally seen in most tumors.
Female Predominance: observed in cases such as:
Fibrous Dysplasia
Giant Cell Tumor
Hemangioma of Bone
Aneurysmal Bone Cyst
Parosteal Osteosarcoma
Clinical Presentation of Bone Tumors
Common Symptoms Include:
Pain
Mass or Swelling
Pathological Fracture
Deformity
Incidental Findings through imaging.
Detailed History for Clinical Evaluation
Duration of Symptoms:
Pain: Assessment for rest pain, night pain, progressive increase in pain.
Mass: Noting progression over time.
Pathological Fracture: Mechanism of injury and pre-fracture pain evaluation.
Initial Findings: Encouraging assessment of past medical and surgical history, and chemical or radiation exposure.
Precursor of Malignancy in Bone
High-Risk Conditions:
Ollier Disease (Enchondromatosis)
Maffucci Syndrome
Familial Retinoblastoma
Rothmund-Thompson Syndrome (RTS)
Moderate Risk Conditions:
Multiple Osteochondromas
Paget's Disease
Radiation Exposure
Osteitis
Low-Risk Precursor Conditions
Low-Risk Examples:
Fibrous Dysplasia
Bone Infarcts
Chronic Osteomyelitis
Metallic and Polyethylene Implants
Osteogenesis Imperfecta
Giant Cell Tumor
Osteoblastoma and Chondroblastoma
Benign Lesions with Potential for Malignant Transformation
Descriptions of various benign lesions and their potential malignant counterparts:
Enchondroma may lead to Chondrosarcoma
Osteochondroma leads to Chondrosarcoma
Fibrous Dysplasia can progress to Fibrosarcoma, Pleomorphic Sarcoma, or Osteosarcoma
Osteomyelitis with chronic draining sinus tract can result in Squamous Cell Carcinoma and Fibrosarcoma
Radiographic Evaluations
Enneking’s Questions for Assessment:
Location of the lesion
Effects of the lesion on the bone
Bone's response to the lesion
Characteristics within the lesion
Patient’s age
Presence of other lesions
Locations of Lesions
Key Locations:
Epiphysis: E.g., Adamantinoma, Osteoid Osteoma
Metaphysis: E.g., Osteochondroma, Ewing Sarcoma, Osteosarcoma
Diaphysis: E.g., Fibrous cortical defect, Adamantinoma, Round cell tumors
Bone Lesion Descriptions
Discusses types of lesions based on radiographic features like:
Geographic: Well-defined with a sclerotic margin.
Moth-Eaten: Lesion margins showing perforated appearance.
Permeative: Invasive lesions that disrupt surrounding bone.
Further Exploration of Lesion Characteristics
Investigates what lesions do to bones including:
Soft Tissue Extension: Distinction between benign containment versus malignant involvement with soft tissues.
Periosteal Reactions: Described by types like uninterrupted, interrupted, and various appearances such as onion-skin or Codman's triangle.
Assessments of Intra-lesion Components
Analysis of what is within the lesions such as:
Abnormal calcifications
Chondroid and Osteoid matrix characteristics (e.g., popcorn-like appearance).
Age Distribution of Bone Malignancies
Specific ages correlated with various malignancies:
1st decade: Ewing’s sarcoma
2nd-3rd decade: Osteosarcoma
4th-5th decade: Chondrosarcoma, Metastasis
6th decade onward: Multiple Myeloma, Metastasis
Diagnosis and Treatment Approaches
Conscious of Signs of Malignancy:
Cortical destruction, wide transitional zones, soft tissue masses, periosteal reactions
Introduces principles of biopsy ensuring minimal disruption for future surgeries.
Classifying Tumors
Categorizes benign/malignant based on behavior and necessary surgical margins (e.g., wide excision for aggressive tumors).
Staging and Treatments for Malignant Bone Tumors: (as per Enneking Classification)
Examples: IA, IB, IIA, IIB, III based on tumor grade and site with associated treatment strategies.
Common Benign Bone Tumors
Detailed descriptions of prominent benign tumors: e.g., Osteochondroma, Enchondroma, Osteoid Osteoma, Unicameral Bone Cyst, Fibrous Dysplasia, Giant Cell Tumor, etc.
Include location, treatment, radiographic presentations, and potential for malignancy.
Common Malignant Bone Tumors
Discusses the most significant malignant bone tumors such as Osteosarcoma, Chondrosarcoma, Ewing’s Sarcoma, and Multiple Myeloma.
Each section includes:
Common locations
Patient demographics
Symptoms
Radiographic findings
Treatment approaches
Metastatic Tumors in Bone
Describes metastatic bone tumors being most common in adults, often originating from cancers of the breast, prostate, lung, kidney, or thyroid.
Identifies common sites for metastasis and presents typical symptoms associated with them and their treatment methodologies.