Bone tumors

Introduction
       Bone tumor is neoplastic tissue growth in bone . abnormal growth can benign or malignant.
       Average five year survival in us after diagnose with bone & joint cancer is 70%.
CLASSIFICATION
v  Tumor  as primary tumors, which originate in bone derive cells & tissue .it may be neoplastic, development, traumatic, infectious & inflammatory etiology.
v  Secondary tumor originate in other sites & spread to skeleton.
v  Prostate Carcinomas, breasts, lungs, thyroid & kidneys most commonly.
Secondary malignant bone tumor estimated to be 50 to 100 times as primary



TISSUE TYPES
BENIGN
MALIGNANT
SITE
INCIDENCE
Chondrogenic (cartilage-forming tumors
OSTEOCHONDROMA
Chondroma
 Pelvis, scapula, ribs
Hands, feet, ribs, spine, sternum, or long bones.
 Higher in males
Age  30 to 50 , higher in males.
Chondrosarcoma
femur., pelvis, ribs, epiphysis of long bones
13% of malignant bone tumors
Middle age & older higher in males.
Osteogenic  (bone forming tumors)
Osteoid
Osteoma
Diaphysis of long bone (femur , tibia)
Age 20 to 30 higher in males
Osteosarcoma
(most common malignant)
Long bones, knee
38% of malignant bone tumors, Predominant in adolscents & people age 50 to 60
Collagenic (collagen forming tumors)
Fibrosarcoma
Femur, tibia
4% malignant bone tumors, wide but usually 40 to 60, higher in males.
Myelogenic (bone marrow tumors)
Giant cell tumor
Diaphysis of long bones
4 to 5% , higher in males

q  Primary tumor divide in benign & cancers
Common benign bone tumors may neoplastic, developmental, traumatic, infectious or inflammatory etiology.
Example of benign tumours as osteoma, osteoid osteoma, osteochondroma, enchondroma, giant cell tumor, aneurysmal bone cyst, fibrous dyspasia of bone

BENIGNS

1. Osteoma - new piece of bone grows on another piece.
2. Osteoid osteoma- arise from osteoblast cells , size is less than 1.5 cm.
3. Osteochondroma– tumor form of cartilage capped bony projections or outgrowth on  bone surface.
4. Osteoblastoma– uncommon osteoid tissue forming  , primary neoplasm of bone.
5.  Enchondroma- cartilage cyst found  in  bone marrow.
6.Giant cells  tumor – multinucleated
7.ABC- osteolytic bone neoplasma as several sponge like blood or serum filled, generally non- endothelialized spaces of various diameters.
8.Fibrous dysplasia- normal bone & marrow replaced with fibrous  tissue.

MALIGNANT

1.Osteosarcoma- cancerous tumor in bone , aggressive malignant neoplasm that arise from  primitive transformed cells of mesenchymal origin.
2.Chondrosarcoma- cancer composed of cells  derived from transformed cells produce cartilage.
3.Ewing’s sarcoma– malignant small, round, blue cell tumor in bone or soft tissue.
4.Fibrosarcoma-  malignant mesenchymal tumor derived from fibrous  connective tissue.

SECONDARY BONE TUMORS



Ø  All secondary  tumor  are metastatic lesions.
Ø  Have spread from other organ , most commonly carcinomas of  breast,  lungs & prostate.

  PATHOPHYSIOLOGY  :-

  Due to risk factors & unknown etiology
     |
      Increase bone activity
                          |   connection
  Development of primary bone growth
                            | FREQUENTLY
  Primary bone tumors
                    CAUSES
  Bone breakdown (osteolysis)
  |
  Weakens bone results bone fractures
  |
  Increase  pressure of tumor by alterations
  |
  Altered bone surface & enlarge tumor growth areas
                  |  develop
  Malignant tumor invade & destroy adjacent bone tissue
 |
  Pathological features

CLINICAL MANIFESTATION
ü  Bone pain
ü  Weakness
ü  Slightly tenderness
ü  Swelling
ü  Sirm lump on bones
ü  Fatigue
ü  Fever
ü  Weight loss
ü  Anemia

MANIFESTATION OF NEOPLASMS

TYPES
SITES
MANIFESTATIONS
bony sarcomas
q Upper, lower extremities
 or pelvis
q Metaphysis of distal femur,
 proximal tibia, proximal
 humerus & pelvis
q Worsening deep bony
 pain, pain at night or 
during rest may radiate 
or become severe, muscular
 weakness or atrophy,
q  soft tissue mass 
extends from bone with
 erythematous or warm skin
 over tissue mass,
q Change in ability to ADLs,
 fever.
soft tissue sarcomas
q Upper or lower extremity
 & pelvis.
q Thigh ; shoulder
 & pelvis
q pelvis
q Enlarging firm mass  with
 regular borders, which cause
 pain in surrounds soft tissue  
structure.
q Erythema, warmth & 
venous dilation over skin.
q Muscular weakness, atrophy 
limited motion range & change
 in gait.
q Paresthesia with neurologic 
 involvement & distal swelling.
q Palpable local lymph nodes.
q Altered bowel & bladder
 habits or pain with intercourse.

DIAGNOSTIC EVALUATIONS

X –rays
CT scan
MRI
Needle biopsy

 LABORATORY TEST –

Alkaline phosphatase (elevate with malignant bone tumor)
Calcium level (increase with massive bone destruction)

TREATMENT

Tumor treated with chemotherapy, radiotherapy & surgery.

Ø Chemotherapy –
Administered  to shrink  the malignant tumor before.
To control recurrence of tumor growth after surgery.

v Chemotherapeutic agents-

Alkylating agents- ifosfamide, cyclophosphamide
Antibiotics- doxorubicin, bleomycin
Antimetabolites- methotrexate
Plant alkaloids – vincristine
Synthetic agents- cisplatin

MEDICATIONS

o   Non hormonal BISPHOSPHONATES  / once a week/ pills/ increase bone strength.
o   METASTRON (STRONTIUM-89) CHLORIDE / IV medication/ in three month interval/ in pain.
o   GENERIC STRONTIUM CHLORIDE Sr- 89 injection
o   SURGICAL TREATMENT
o   Amputation – limb amputation, limb sparing surgery (combination  with chemotherapy & radiation therapy)
o   Limb sparing surgery, limb salvage surgery in two ways.
o   (a)Bone graft – bone is taken from elsewhere on body.
o   (b)Artificial bone – IN surgery of uper leg .
o   ratationplasty

o   TYPES OF AMPUTATION:-

o   LEG- above knee, below knee, symes, hip disarticulation, hemipelvectomy 
o   ARM:- below elbow, above elbow, shoulder disarticulation forequarter (amputation of whole arm, along with shoulder blade & clavicle)
o  
      HEMICORPORECTOMY
   trans lumbar  or waist amputation , which removes legs, pelvis, urinary system, excretory system & genital area.




Tags

Post a Comment

1 Comments
* Please Don't Spam Here. All the Comments are Reviewed by Admin.
  1. આણંદ ભાઈ24 February, 2017

    ખૂબ જ ઉપયોગી માહિતી

    ReplyDelete

Thank you for comments.
we are trying to give our best