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*Immature hematopoeitic cells adjacent to the bone. | *Immature hematopoeitic cells adjacent to the bone. | ||
=Infectious= | |||
==Osteomyelitis== | |||
General | General | ||
*Hematogenous - often in children. | *Hematogenous - often in children. | ||
*Direct entry (skin defect) - adults with diabetes. | *Direct entry (skin defect) - adults with diabetes. | ||
===Microscopic=== | |||
*PMNs. | *PMNs. | ||
==Chronic osteomyelitis== | |||
*Plasma cells. | *Plasma cells. | ||
**May be sterile, i.e. no organisms. | **May be sterile, i.e. no organisms. | ||
=Bone tumours= | |||
General | ==General== | ||
*Metastasis:primary bone tumours = >20:1.<ref>WMSP P.632.</ref> | *Metastasis:primary bone tumours = >20:1.<ref>WMSP P.632.</ref> | ||
===Common malignant=== | |||
*Osteosarcoma. | |||
*Chondrosarcoma. | |||
*Ewing's sarcoma. | |||
*Multiple myeloma. | |||
*Metastases. | |||
**Most common tumours metastatic to bone (mnemonic: ''BLT with Ketchup & Pickles''): | |||
***Breast. | |||
***Liver. | |||
***Thyroid. | |||
***Kidney. | |||
***Prostate. | |||
Epidemiology:<ref>TN05 OR42.</ref> | |||
*Osteosarcoma -> 2nd decade. | |||
*Ewing's ->5-20 yrs. | |||
*Chondrosarcoma -> from enchondroma or osteochrondroma -- patients over 40 yrs. | |||
*Multiple myeloma -> most common primary bone tumour in adults. | |||
===Malignant bone tumours by age=== | |||
Most common by age:<ref>TN05 OR42.</ref> | |||
*<1 year old - neuroblastoma. | |||
*1-10 years old - Ewing's of tubular bones. | |||
*10-30 years old - osteosarcoma, Ewing's of flat bones. | |||
*30-40 years old - reticulum cell sarcoma, fibrosarcoma, parosteal osteosarcoma, malignant giant cell tumour, lymphoma. | |||
*>40 years old - mets, multiple myeloma, chondrosarcoma. | |||
===Benign aggressive bone tumours=== | |||
*Giant cell tumours. | |||
*Osteoblastoma. | |||
**Thought to be related to osteoid osteoma. | |||
**If in long bones often diaphyseal. | |||
Ref.:<ref>TN05 OR41.</ref><ref>URL: [http://www.emedicine.com/RADIO/topic494.htm http://www.emedicine.com/RADIO/topic494.htm].</ref> | |||
==Giant cell tumour== | ==Giant cell tumour== | ||
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**Neuroblastoma (possibly). | **Neuroblastoma (possibly). | ||
*Several other translocations exist. | *Several other translocations exist. | ||
==Osteosarcoma== | ==Osteosarcoma== | ||
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**Tumours typically very cellular - when compared to normal bone. | **Tumours typically very cellular - when compared to normal bone. | ||
*Large (multinucleated) osteoclast-like giant cells may be seen.<ref>{{cite journal |author=Papalas JA, Balmer NN, Wallace C, Sangueeza OP |title=Ossifying dermatofibroma with osteoclast-like giant cells: report of a case and literature review |journal=Am J Dermatopathol |volume=31 |issue=4 |pages=379-83 |year=2009 |month=June |pmid=19461244 |doi=10.1097/DAD.0b013e3181966747 |url=}}</ref> | *Large (multinucleated) osteoclast-like giant cells may be seen.<ref>{{cite journal |author=Papalas JA, Balmer NN, Wallace C, Sangueeza OP |title=Ossifying dermatofibroma with osteoclast-like giant cells: report of a case and literature review |journal=Am J Dermatopathol |volume=31 |issue=4 |pages=379-83 |year=2009 |month=June |pmid=19461244 |doi=10.1097/DAD.0b013e3181966747 |url=}}</ref> | ||
=Other= | |||
==Pigmented villonodular synovitis== | |||
*Commonly abbreviated: ''PVNS''. | |||
*Course: benign. | |||
===Microscopy=== | |||
Features:<ref>[http://www.wheelessonline.com/ortho/pigmented_villonodular_synovitis http://www.wheelessonline.com/ortho/pigmented_villonodular_synovitis]</ref> | |||
*Subsynovial nodules composed of cells with: | |||
**Abundant cytoplasm. | |||
**Pale nuclei. | |||
*Multinucleated giant cells. | |||
*Hemosiderin-laden macrophages. | |||
*Foam cells. | |||
==Adamantinoma== | ==Adamantinoma== | ||
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Features: | Features: | ||
*Fibrous tumour. | *Fibrous tumour. | ||
==Brown cell tumour== | ==Brown cell tumour== |
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