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15 Cards in this Set

  • Front
  • Back
Lipoma
Benign uniform proliferation of mature apdipocytes.

Most common soft tissue tumor of adults.

Commonly seen in subcutis of proximal extremities and trunk.

Soft, mobile, painless (except angiolipomas) lesions.
Liposarcomas
One of the most common sarcomas of adults.

Usually arises in the deep soft tissues of the proximal extremities and retroperitoneum.

Four variants:
- Well differentiated: indolent
- Dedifferentiated: intermediate
- Myxoid/round-cell: intermediate
- Pleomorphic: aggressive and frequently metastasize.

Recognition of lipoblast in the tissue section is important for diagnosis (round clear cytoplasmic vacuoles of lipid that scallop the nucleus).

Gross: from large multinodular mass with yellow cut surface. Some admixed white or gelatinous areas may be seen.
What is the most common malignant tumor of the bone?
A metastasis.
What type of bone cancer does Gaucher's disease cause? Paget's disease?
Sarcoma. Sarcoma.
c/c osteoblastoma and osteoid osteoma
Osteoid osteomas are <2 cm, posterior spine, appendicular skeleton; localized pain that is relieved by NSAIDs, worst at NIGHT.

Osteoblastomas are >2 cm; pain is dull, achy and is NOT relieved by NSAIDs; involve the spine more frequently.
Osteosarcoma
Most common bone sarcoma (20%)

Bimodal age distribution
- Children, young adults (75% <20 y.o.)
- Elderly (Paget's, radiation)

Location: Metaphyseal in youth, flat bones in elderly

Path:
70% from genetic causes (Li-Fraumeni, Retinoblastoma, others)

Gross:
Large tumor with white-tan, gritty cut surface. Hemorrhagic and cystic areas.

Infiltrates cortex, lifts periosteum and forms soft tissue masses in the areas surrounding the bone.

Histo:
Varies, hyperchromatic nuclei, mitoses, necrosis common.
What are the bone-forming tumors? Which are benign? Malignant?
Osteoid osteoma (B)
Osteoblastoma (B)
Osteosarcoma (M)
Osteochondroma (Exotosis)
Most common benign bone tumor.

Benign cartilage-capped tumor that is attached to the underlying skeleton by a bony stalk.

Adolescents, young adults

May develop in any bone in which endochondral ossification happens.

Metaphysis.

Assumed to arise from displaced fragments of the growth plate.

Histo:
Mimics an epiphyseal growth plate
Enchondromas
Benign tumors of hyaline cartilage that usually occur in bones with endochondral ossificiation.

Most common in medullary cavity of small tubular bones of hands/feet, also in metaphysis/diaphysis of larger bones.

Adolescents and young adults.

May erode (but not invade) bone cortex; lesion usually solitary.

CP: pathological fracture.

Gross: lytic, lobulated appearance, ring-like calcifications.

Histo: the border of an enchondroma with surrounding cortex is sharp. No cytological atypia of chondrocytes is seen.
Ollier's disease and Mafucci's syndrome
Multiple enchondromas.

Ollier's: may develop osteosarcoma

Mafucci's: Multiple enchondromas and hemangiomas of soft tissue and viscera. May develop chondrosarcoma, angiosarcoma and other extraskeletal tumors
Chondrosarcoma
>40 y.o.

Central skeleton (pelvis, scapula, ribs)
Met/diaphysis of long bones (femur, humerus)

In contrast to enchondroma, chondrosarcoma rarely involves the distal extremities.

About 15% of osteosarcomas arise from preexisting enchondroma or osteochondroma.

Gross: gray-white nodules glistening filling medullary cavity.

Histo: hypercellular compared to chondromas. Pleo, hyperchromasia. Binucleated nuclei are commonly seen.
What cancers send mets to bones?
BLT And a Kosher Pickle

Breast
Lung
Thyroid
Adrenal
Kidney
Prostate
Metastatic tumors to bone
Most common malignant lesion

May be osteoblastic or osteolytic.
Ewing's sarcoma / Primitive neuroectodermal tumors (ES/PNET)
Frequently histologically indistinguishable

Children and adolescents

Diaphyses of long bones, pelvis, soft tissues

(11;22) translocation, causes fusion of EWS gene and FLT1. EWS-FLT1 acts as a dominant oncogene --> cell proliferation.

Tx: chemo and surgery +/- radiation therapy.
DDx of "small round blue cell tumors"
Ewing's sarcoma/PNET
Lymphoma, non-Hodgkin's
Alveolar rhabdomyosarcoma
Wilm's Tumor
Malignant melanoma (smal cell variant)
Small cell carcinoma (poorly differentiated neuroendocrine carcinoma)
Mesenchymal chondrosarcoma/Small cell osteosarcoma