Chordoma & Lymphoma Flashcards

1
Q

What age group is primarily affected by Chordomas?

A

40-70 yrs

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2
Q

What is the origin of a chordoma?

A

notochord
(NOT spinal cord)

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3
Q

Describe the aggressiveness of a chordoma.

A
  • locally aggressive
  • slow growth rate
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4
Q

What is the only tumor to cross a joint and why?

A

Chordoma
vertebral bodies & discs = notochordal

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5
Q

What are the preferential locations of a chordoma?

A
  • sacrococcygeal (MC)
  • clivus
  • vertebral
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6
Q

What vertebral level is not affected by chordomas?

A

C1 (no vertebral body)

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7
Q

What is the clinical presentation of a sacrococcygeal chordoma?

A
  • age 40-70yrs
  • obstruction of intestines & urinary tract
  • n. root compression (stenosis Sx)
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8
Q

What is the clinical presentation of a clivus chordoma?

A
  • age 40-70yrs
  • headaches
  • endocrine abnormalities
  • visual disturbances (lat. hemianopsia)
    (pressure on pontine, ocular, cerebellar structures)
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9
Q

What are the imaging features of a chordoma?

A
  • central vertebral body destruction
  • lytic destruction
  • amorphous calcification (50%)
  • soft tissue mass (dark on T1 MRI)
  • enlarged presacral space
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10
Q

What follow-up recommendations would you need to indicate a chordoma?

A

MRI w/ contrast + labs

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11
Q

What is on your list of differential diagnoses for a sacrococcygeal, calcified soft tissue mass in a 40 year old patient?

A
  1. chondrosarcoma
  2. chordoma
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12
Q

What is on your list of differential diagnoses for a calcified soft tissue mass coming off the ilium in a 40 year old patient?

A
  1. chondrosarcoma
    (NOT chordoma, b/c not notochordal tissue)
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13
Q

What is the treatment and prognosis of a sacrococcygeal chordoma?

A
  • resection
  • poor 5-yr survival rate (8.7%)
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14
Q

What is the treatment and prognosis of a chordoma in the clivus?

A
  • radiation
  • high rate of local recurrence
  • higher mortality
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15
Q

What is the treatment and prognosis of a spinal chordoma?

A
  • radiation
  • better prognosis than sacrococcygeal or clivus
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16
Q

What percent of patients have skeletal involvement secondary to Non-Hodgkin Lymphoma?

17
Q

What skeletal locations are commonly involved in Non-Hodgkin Lymphoma?

A

red marrow spaces:
- femur
- tibia
- humerus
- pelvis
- spine

18
Q

What age group is primarily affected by Non-Hodgkin Lymphoma?

19
Q

What is the clinical presentation of Non-Hodgkin Lymphoma?

A
  • age 20-40 yrs
  • intermittent local pain
  • pt appears very healthy
  • 50% report Sx >1yr (late stage d/t slow growth)
  • round cell tumor
20
Q

What are the imaging findings of Non-Hodgkin Lymphoma?

A
  • permeative medullary destruction
  • diaphysis (can be in metaphysis)
  • minimal laminated periosteal Rxn
  • soft tissue mass
21
Q

What is the differential diagnosis for Non-Hodgkin Lymphoma on a radiograph?

A

Ewing sarcoma
(need labs to determine)

22
Q

What age group is primarily affected by Hodgkin Lymphoma?

23
Q

What percent of patients with Hodgkin Lymphoma will develop osseous metastasis?

24
Q

What skeletal location is most commonly involved in Hodgkin Lymphoma?

A

vertebral body

25
Q

What type of bony destruction occurs in Hodgkin Lymphoma?

A

75% lytic
15% blastic
10% mixed

26
Q

What radiographic signs may be present in blastic Hodgkin Lymphoma?

A
  • ivory vertebra
  • scalloping of anterior and lateral vertebral body
27
Q

What radiographic characteristics would indicate lymphoma as the first differential diagnosis?

A

Ivory vertebra with anterior vertebral body scalloping

28
Q

Give a list of differentials in order from most to least likely.

A
  1. Mets
  2. Myeloma/plasmacytoma
  3. Chordoma (need MRI w/ contrast)
29
Q

What would prompt you to put lymphoma first on your list of differentials?

A

Anterior body scalloping
(ivory vertebra = IHOP)

30
Q

What is the most likely diagnosis if this lesion is crossing a joint?