Tumor/Path Flashcards
t(X:18)
synovial sarcoma
t(12:16)
myxoid liposarcoma
pleomorphic cells with high mitotic index, occasional bizarre multinucleated giant cells
malignant fibrous histiocytoma/undifferentiated pleomorphic sarcoma/spindle cell sarcoma
CD34 positive stain
dermatofibrosarcoma
tumors treated with neoadjuvant chemotherapy, wide resection, adjuvant chemotherapy (2)
MFH, osteosarcoma
sunburst new bone formation and aggressive periosteal reaction on radiograph
osteosarcoma
smoke in a chimney stack
bone infarct
where are chondroblastomas found (2)
epiphyseal or apophyseal regions of bones
radiolucent lesion with mineralization and a well-marginated rim of reactive bone
chondroblastoma
sheets of immature chondroblasts, chicken-wire matrix calcifications, cobblestone pattern
chondroblastoma
treatment with curettage and bone grafting (4)
chondroblastoma, giant cell tumor, chondromyxoid fibroma, osteoblastoma
four commonly used chemotherapy agents
doxorubicin, cisplatin, methotrexate, ifosfamide
osteoblasts with a small amount of lacy malignant osteoid
intramedullary osteosarcoma
Enneking’s 4 radiographic questions
location, tumor-bone interaction, bone-tumor interaction, matrix
multiple destructive lesions in middle-aged and older patients (> 40 years old) ddx (3)
metastatic disease, multiple myeloma, lymphoma
multiple lytic and oval lesions in young patients (< 30 years old) in the same extremity (1)
hemangioendothelioma
multiple destructive lesions in a young child (< 5 years old) ddx (3)
neuroblastoma, Wilms tumor, Langerhans cell histiocytosis
multiple destructive lesions in any age group ddx (2)
fibrous dysplasia, Paget disease
tumors primarily affecting epiphysis (3)
chondroblastoma, giant cell tumor, clear cell chondrosarcoma
tumors primarily affecting metaphysis (3)
osteosarcoma, chondrosarcoma, metastatic disease
tumors primarily affecting diaphysis (6)
AEIOUY: adamantimoma, eosinophilic granuloma, infection, osteoid osteoma/osteoblastoma, Ewing sarcoma, myeloma/lymphoma/fibrous dysplasia
tumors primarily affecting flat bones (5)
chondrosarcoma, fibrous dysplasia, hemangioma, Paget disease, Ewing sarcoma
tumors primarily affecting the anterior column of the spine (2)
giant cell tumor, metastatic disease
tumors primarily affecting the posterior column of the spine (2)
osteoid osteoma/osteoblastoma, aneurysmal bone cyst
tumors primarily affecting the sacrum (4)
midline: chordoma; eccentric: aneurysmal bone cyst/giant cell/metastatic disease
t(2;13)
alveolar rhabdomyosarcoma
t(12;22)
clear cell sarcoma
t(11;22)
Ewing sarcoma/peripheral neuroectodermal tumor
t(9;22)
extraskeletal myxoid chondrosarcoma
tumor suppressor genes mutated in osteosarcoma (2)
Rb (35%) and p53 (20-65%)
hereditary cancer syndromes associated with osteosarcoma (2)
Li-Fraumeni (p53) and congenital bilateral retinoblastoma
hereditary cancer syndromes associated with chondrosarcoma (1)
multiple hereditary exostoses (EXT 1-3)
hereditary cancer syndromes associated with malignant peripheral nerve sheath tumor (1)
NF1
histological grading is based upon these 3 things
nuclear atypia, pleomorphism, nuclear hyperchromasia
nuclear atypia definition
degree of loss of structural differentiation
pleomorphism definition
variations in size and shape
nuclear hyperchromasia definition
increased nuclear staining
most common soft tissue sarcomas in young patients (2)
synovial sarcoma, rhabdomyosarcoma