Sarcoma Flashcards

1
Q

FNCLCC Sarcoma histopathology grade depends on

A

FNCLc grading depends on
1. Cell differentiation
2. Mitotic activity
3. Extent of necrosis

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2
Q

Inrease risk of local recurrence in sarcoma

A

Increased risk of local recurrence in
1. Positive margin
2. Tumor site: RPS, H &N
3. Prior local recurrence
4. Age>50
5. Histology: FMS, desmoid, MPNST
Grade

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3
Q

Common RT induced sarcoma are:

A

Common RT induced sarcoma are:
- Angiosarcoma: 21%
- Pleomorphic leiomyosarcoma
- Fibrosarcoma
- MPNST

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4
Q

Histological classification of sarcoma

A

Fibroblastic/myofibroblastic tumor:
a. Malignant: adult fibrosarcoma, low grade fibromyxoid, myxofibrosarcoma, epitheliod
B. Fibrohistocytic tumor
a. Malignant: tensynovial giant cell tumor
C. Adipocytic tumor:
a. Malignant: liposarcoma
i. Dedifferentiated
ii. Myxoid
iii. Pleomorphic
D. Smooth muscle tumor
a. Leiomyosarcoma
E. Skeletal muscle tumor
a. Rhabdomyosarcoma
i. Alveolar
ii. Embryonal
iii. Pleomorphic
I : spindle cell
V: classic
F: vascular
G: perivascular: glomus tumor
H: neural: mpnst
J: GIST
K: uncertain differentiation:
Alveolar soft part sarcoma
Clear cell sarcoma
Desmoplastic
Epithelioid

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5
Q

Histopathologic immunohistochemistry in sarcoma

A

CD34: dermato fibrosarcoma protuberance
CD99: ewing sarcoma family tumor
CD117: GIST
Synaptophysin and NSE: PNET, SMA
Vimentin, desmin= leiomyosarcoma, rhabdomyosarcoma

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6
Q

Common D/D of STS below 30/20 years of age

A

RMS
ES
Desmoplastic
Alveolar
Clear cell and synovial

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7
Q

STS D/D age >40/30

A

MFH
MPNST
DFSP
Fibrosarcoma
Leiomyosarcoma
Desmoid
Liposarcoma
MFH

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8
Q

Common D/D of soft tissue sarcoma in abdomen

A

Midline abdomen: germ cell tumor, lymphoma
Lower abdomen: leiomyosarcoma, RMS
Extra abdominal: desmoid
Thigh: liposarcoma

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9
Q

Common D/D of retroperitoneal mass

A

Germ cell tumor
Lymphoma
MFH
Kidney, GIST

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10
Q

D/D of visceral STS

A

Leiomyosa
• Liposarcoma
• GIST
• Desmoid
• RMS, angiosarcoma
• Haemangiopericytoma

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11
Q

Indication pre op RT in sarcoma

A

Indication of pre operative RT:
1. Borderline operable tumor to improve chance of R0 resection
2. Tumors with anticipated marginal resection (skull base, paranasal sinus, retroperitoneum)
3. Tumors close to neurovascular bundle
4. Situations where post OP Rt volume might leads significant late toxicities
5. RP/visceral sarcoma/ dedifferentiated/ myxoid round cell/LMS/MPNST)

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12
Q

Post OP RT indication in sarcoma

A

Post OP RT: indication:
1. Large tumor >5cm
2. Deep seated tumor
3. High grade tumor (G2-3), margin positive even if <5cm
4. +ve margin: high grade
5. R1/R2 resection
6. Limb conserving wide excision/ limited surgery
7. Virtually all tumors in head and neck (because complete excision unlikely)
8. After surgery for recurrent sarcoma, if not previously irradiated.

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13
Q

Soft tissue sarcoma radiotherapydose

A

Pre operative dose; 50 gy in 25 fractions
Post operative:
Elective ptv:50 gy in 25 daily fraction
Boost ptv: 10 gy in 5 daily fraction
Total dose: 60 gy in 30 daily fractions

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14
Q

Prognostic factors of STS

A

Stage: I: 86%; II: 72%, III:52%
Grade
Tumor size and site
Histologic subtype
Tumor depth
Older age at presentation
Positive margin on resection
Bony oer neurovascular invasion
Gender
Race
Lymph node invovlement

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15
Q

Common sarcoma in retroperitoneum: ajcc

A

Liposarcoma( well differentiated and dedifferentites)
Leiomyosarcoma
Less common
Pleomorphic lps
Undifferentiated Pleomorphic sarcoma
Mpnst
Solitary fibrous tumor

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16
Q

Role of MRI in bone sarcoma

A

Marrow extention
• soft-tissue extension
• Relation with neuro-vascular bundle
• Skip lesion
• Whole-body MRI is a sensitive imaging technique for
the detection of skeletal metastases in patients with small cell neoplasms, Ewing sarcoma, and osteosarcoma