26 morph Flashcards

1
Q

bone lacks medullary canal = no hematopoetic marrow

A

osteopetrosis

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2
Q

erlenmeyer flask deformity

A

osteopetrosis

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3
Q

neural foramina small

A

osteopetrosis

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4
Q

nml bine, but decreased quantity of trabecular bone

A

osteoporosis

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5
Q

Mosaic pattern of lamellar bone. ‘Jigsaw puzzlelike’ d/t unusually prominent cement lines orienting lamellar bone

A

sclerotic phase Paget Disease (osteitis deformans)

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6
Q

‘Cotton wool’ appearance.

A

Paget Disease (osteitis deformans)

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7
Q

wedge shaped empty lacunae that are surrounded by ruptured adipocytes, which can have assoc fat saponification (may remain for life).

A

Osteonecrosis (avascular necrosis)

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8
Q

tissue paper cells

A

goucher dis: Osteonecrosis (avascular necrosis)

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9
Q

Involucrum: .
o : . (pic)
o : .

A

pyogenic osteomelitis

=subperiosteal new bone encasing the inflamm focus

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10
Q

Brodie abscess

A

pyogenic osteomelitis

=small, walled off intracortical abscess

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11
Q

gummas

A

Skeletal Syphilis (congenital)

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12
Q

well circumscribed nodules of translucent cortical, interlacing woven bone (nidus) rimmed by osteoblasts; surrounded by vasc and loose CT

A

osteoid osteoma and osteobalstoma

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13
Q

formation of bone by tumor cells*; fine, lace-like pattern or may be deposited in broad sheets

A

osteosarcoma

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14
Q

sessile/peduncleated solitar, cartilage cap mass; cortex of the stalk merges with the cortex of the host bone so that the 2 medullary cavities are continuous.

A

Osteochondroma (exostosis)

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15
Q

multiple cartilaginous tumors of hands and feet

A

chondroma

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16
Q

 Translucent gray-blue tumors, < 3cm with limited growth potential.
 Well-circumscribed nodules of benign hyaline cartilage.
 Peripheral portion of the nodules may undergo enchondral ossification and the center can calcify and infarct.

A

chondroma

17
Q

spindle cell hemangioma

A

maffucci synd

18
Q

malig tumor producing cartilage on the axial skeleton (pelvis, shoulder, ribs)

A

chondrosarcoma

19
Q

 Transluscent cartilage w gelatinous or myxoid matrix (may ooze from cut surfaces).
 Spotty calcifications.

A

chondrosarcoma

20
Q

homer-Wright rosettes

A

Ewing Sarcoma Family Tumors (ESFT) (including PNET)

21
Q

tumor rich in glycogen, hem, necrosis

A

Ewing Sarcoma Family Tumors (ESFT) (including PNET)

22
Q

onion-skinning

A

Ewing Sarcoma Family Tumors (ESFT) (including PNET)

23
Q

expansile lesion w well defined margins at metaphysis of long bones

A

Aneurysmal Bone Cyst (ABC)

24
Q

.5cm on metaphysis of distal femur, prosimal tibia, storiform (pinwheel) pattern and foamy mfs clustered in giant cells

A

Fibrous Cortical Defect (metaphyseal fibrous defects) and non-ossifying fibromas

25
Q

 Curvilinear trabeculae of woven bone that resemble Chinese characters.
 Cystic degeneration, hemorrhage and foamy Mf.

A

Fibrous Dysplasia

26
Q

Mature adipocytes and scattered spindle cells w hyperchromatic nuclei

A

well-diff liposarcoma

27
Q

Myxoid matrix, ‘chicken wire’ vessels, round cells, lipoblasts.

A

myxoid liposarcoma

28
Q

eos cells interecting at right angles

A

leiomyoma

29
Q

o Pleomorphic eosinophilic spindle cells.

o Blunt-ended hyperchromatic nuclei in interweaving fascicles.

A

leiomyosarcoma