Ch 18 Pathoma - MSK Pathology Flashcards

1
Q

_____ is impaired cartilage proliferation in the growth plate, due to an activating mutation in the ______. It is autosomal dominant/recessive. Most mutations are inherited/sporadic and related to increased _____.

A

Achondroplasia; fibroblast growth factor receptor 3 (FGFR3 - overexpression inhibits growth); dominant; sporadic; paternal age

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2
Q

Clinical features of achondroplasia include short ____ with normal-sized ___ and ___, due to poor ____ bone formation. ____ bone formation is not affected. Mental function, life span, and fertility are/are not affected.

A

extremities; head and chest; endochondral; intramembranous; are not

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3
Q

____ bone formation is characterized by formation of a cartilage matrix, which is then replaced by bone; it is the mechanism by which ____ bones grow.

A

Endochondral; long

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4
Q

____ bone formation is characterized by formation of bone without a preexisting cartilage matrix; it is the mechanism by which ____ bones grow

A

Intramembranous; flat (skull and rib cage)

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5
Q

_____ is a congenital defect of bone formation resulting in structurally weak bone. Most commonly due to an autosomal/x-linked, dominant/recessive defect in ____ synthesis. Name the three clinical features

A

Osteogenesis imperfecta; autosomal dominant; collagen type I; multiple fractures of bone (can mimic child abuse w/o bruising), blue sclera (thinning of scleral collagen shows choroidal veins), hearing loss (bones of middle ear fracture)

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6
Q

_____ is an inherited defect of bone resorption resulting in abnormally thick, heavy bone that fractures easily. Due to poor ___ function. ____ mutation leads to loss of acidic microenvironment needed for bone resorption (removing calcium). Tx is ___.

A

Osteopetrosis; osteoclast; Carbonic anydrase II; bone marrow transplant (b/c osteoclasts are derived from monocytes)

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7
Q

Name the five clinical features of osteopetrosis

A

bone fracture (b/c no proper bone remodeling due to osteoclasts dysfunction); anemia, thrombocytopenia and leukopenia with extra medullary hematopoiesis; vision/hearing impairment (impingement on CNs); hydrocephalus (narrowing of foramen magnum); renal tubular acidosis (lack of carbonic anhydrase > dec tubular reabsorption of HCO3-)

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8
Q

___ and ___ cause defective mineralization of osteoid due to a ____ deficiency. Which one is seen in adults and which one in kids

A

Rickets; osteomalacia; vitamin D
(osteoid produced by osteoblasts is normally mineralized with calcium and phosphate to form bone). Rickets in kids; osteomalacia in adults

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9
Q

Vitamin D is derived from skin upon exposure to ___ and from ___. Activation requires _____ by the liver, followed by ___ by the PCT cells of the kidney. Vitamin D raises serum ___ and ___ by acting on intestine, kidney, and bone (mechanism)

A

sunlight (85%), diet (15%); 25-hydroxylation; 1-alpha-hydroxylation; calcium; phosphate; intestine: inc absorption; kidney: inc reabsorption; bone: inc resorption

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10
Q

Osteomalacia results in ___ bone with an increased risk of ___. Labs include low ___ and ___ and high ___ and ___.

A

weak; fractures (esp in weight bearing bones: vertebral bodies or hip); calcium, phosphate; PTH, alk phos (needed to create an alkaline environment to lay down calcium on bone)

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11
Q

_____ is a reduction in trabecular bone mass, which results in ___ bone with increased risk for fracture. Risk of it is based on ____ and ___ that follows thereafter. Most common forms are __ and __

A

Osteoporosis; porous; peak bone mass; rate of bone loss; senile; postmenopausal

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12
Q

Peak bone mass is achieved by ___ years of age and is based on these three things. Thereafter, slightly less than __% of bone mass is lost each year; lost more quickly with these three things.

A

30; genetics (vit D receptor variants); diet; exercise; 1; lack of weight bearing exercise (space travel); poor diet; decreased estrogen (menopause)

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13
Q

Name the the clinical feature of osteoporosis. Bone density can be measured using ___. Tx includes __, __, and __ to limit bone loss, __ to induced apoptosis of osteoclasts. ___ are contraindicated, and ___ would in theory be helpful but not recommended.

A

Bone pain/fractures (in weight bearing areas like vertebrae, hip, distal radius - height loss, kyphosis); DEXA scan; exercise, vit D, calcium; bisphosphonates; glucocorticoids; estrogen replacement therapy

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14
Q

How can you tell apart osteomalacia and osteoporosis?

A

In osteomalacia, you have decreased calcium and phosphate and increased PTH and alk phos; in osteoporosis labs are normal

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15
Q

____ is an imbalance between osteoclast and osteoblast function usually seen in late adulthood (>60). It’s etiology is unknown though it is possibly ___. It involves one or more bone/entire skeleton. Tx includes ___ to inhibit osteoclast function and ___ to cause osteoclast apoptosis.

A

Paget disease of bone; viral; one or more; calcitonin; bisphosphonates

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16
Q

Name the 3 distinct stages of Paget disease of bone. The end result is __, __ bone that ___ easily. Bx reveals a ___ pattern of lamellar bone.

A

1) osteoclastic; 2) mixed osteoblastic-osteoclastic; 3) osteoblastic; thick, sclerotic; fractures; mosaic

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17
Q

Name the five clinical features of Paget disease of bone. Name the two complications.

A

1) bone pain (due to micro fractures); 2) increasing hat size; 3) hearing loss (impingement on CN); 4) lion like facies (craniofacial bones); 5) isolated elevated alkaline phosphatase; high output cardiac failure (due to AV shunts in bone); Osteosarcoma (blasts are going cray)

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18
Q

____ is an infection of marrow and bone; it usually occurs in ____. Most commonly ____; arises via hematogenous spread. _____ bacteremia (children) seeds ___. _____ bacteremia (adults) seeds ___. Dx is made by ____.

A

Osteomyelitis; children; bacterial; transient; metaphysis; open wound; epiphysis; blood culture

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19
Q

Causes of osteomyelitis; most common, seen in sexually active, seen in sickle cell dx, seen in diabetics/IV drug abusers; associated with cat/dog bite; involves vertebrae (Pott dx)

A

staph aureus; N gonorrhoeae; salmonella; pseudomonas; pasteurella; mycobacterium tuberculosis

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20
Q

Clinical features of osteomyelitis include __ pain with ___ signs of infxn; and a ___ surrounded by ___ of bone on X-ray

A

bone; systemic (fever, leukocytosis); lytic focus (abscess); sclerosis (lytic focus is called sequestrum and sclerosis is called involucrum)

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21
Q

Avascular (aseptic) necrosis is _____ necrosis of bone and bone marrow. Name five causes. ___ and ___ are major complications

A

ischemic; trauma, fracture (most common), steroids, sickle cell anemia, cassion disease; osteoarthritis; fracture

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22
Q

____ is a benign tumor of bone. It is most commonly found on the surface of ____. It is associated with ___ syndrome.

A

Osteoma; facial bones; Gardner (familial adenomatous polyposis, fibromatosis, and osteoma of facial bones)

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23
Q

____ is a benign tumor of osteoblasts (that produce osteoid) surrounded by a rim of reactive bone. Occurs in __ years of age (more commonly females/males), arises in ___ of ___ bones. Presents as bone pain that resolves with ___.

A

Osteoid osteoma; less than 25; males; cortex; long; aspirin

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24
Q

Osteoblastoma vs Osteoid osteoma

Which one is >2 cm? Which one arises in vertebrae vs long bones? In which one does bone pain respond to aspirin?

A

Osteoblastoma; osteoblastoma; osteoid osteoma; osteoid osteoma

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25
Q

___ is a malignant proliferation of osteoblasts. It’s peak incidence is seen in ____ and less commonly also seen in ___. It arises in ___ of long bones (usually the distal femur or proximal tibia).

A

Osteosarcoma; teenagers; elderly; metaphysis

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26
Q

Name three risk factors of osteosarcoma

A

familial retinoblastoma; Paget disease; radiation exposure

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27
Q

Osteosarcoma presents as a ___ or ___ with swelling. Imaging revealed a destructive mass with a ___ appearance, and lifting of the ____ (known as ____ triangle). Bx reveals ____ cells that produce ____.

A

pathologic fracture; bone pain; sunburst; periosteum; Codman; pleomorphic (variability in size/shape of nucleus); osteoid

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28
Q

Ewing Sarcoma is malignant proliferation of well/poorly differentiated cells derived from _____. It arises in the ____ of long bones; usually in female/male children/adults. A ____ translocation is characteristic and it often presents locally/with metastases and is responsive/unresponsive to chemo.

A

poorly; neuroectoderm; diaphysis; male children (less than 15 yrs of age); 11;22; metastasis; responsive

29
Q

This bone tumor has an onion-skin appearance on X-ray and on bx it reveals small, round blue cells that resemble lymphocytes. It can therefore easily be confused with lymphoma or chronic osteomyeletis.

A

Ewing Sarcoma

30
Q

____ is a tumor comprised of multinucleated giant cells and stromal cells. It occurs in ___. It arises in the ____ of long bones (usually the distal femur or proximal tibia).

A

Giant cell tumor; young adults; epiphysis

31
Q

On xray, a giant cell tumor has a ___ appearance. It is locally aggressive and may recur.

A

soap bubble

32
Q

___ is a benign tumor of cartilage; ___ is a malignant cartilage forming tumor. Both arise in the ___ of bones.

A

chondroma; chondrosarcoma; medulla

33
Q

This cartilage tumor arises in the medulla of the pelvis or central skeleton.

A

Chondrosarcoma

34
Q

This cartilage tumor arises in the medulla of small bones of the hands and feet

A

Chondroma

35
Q

Which is more common, primary bone tumors or bone metastases?

A

bone metastases

36
Q

Bone mets usually result in ___ lesions, however prostate carcinoma classically produces ___ lesions.

A

osteolytic (punched out); osteoblastic lesions

37
Q

A joint is a _____. ____ joints are tightly connected to provide structural strength. ____ joints have a joint space to allow for motion.

A

connection btwn two bones; solid; synovial

38
Q

The articular surface of adjoining bones is made of ____ cartilage (type __) that is surrounded by a ____. Synovium lining the joint capsule secretes fluid rich in ____ to lubricate the joint & facilitate smooth motion

A

hyaline; II; joint capsule; hyaluronic acid

39
Q

______ is a progressive degeneration of articular cartilage (aka ____), most often due to ____. Major risk factor is ___ and others include ___ and ___. Classic presentation is ____ in the morning that gets better/worsens during the day.

A

Degenerative joint disease; osteoarthritis; wear and tear; age (common after 60); obesity; trauma; joint stiffness; worsens (different from RA)

40
Q

What is the most common types of arthritis?

A

Osteoarthritis (degenerative joint disease)

41
Q

Osteoarthritis affects a limited number of joints (oligoarticular), most commonly these 5

A

hips, lower lumbar spine, knees, DIP joints, PIP joints

42
Q

Name three pathologic features of degenerative joint disease (osteoarthritis)

A

1) disruption of cartilage that lines the articular surface (fragments of cartilage are called joint mice); 2) eburnation of the subchondral bone (bony sclerosis that occurs when bone rubs bone); 3) osteophyte formation (reactive bony outgrowths - arises in DIP (heberden nodes) and PIP (bouchard nodes)

43
Q

The hallmark of rheumatoid arthritis is ___ leading to formation of a ____. These then leads to further destruction of cartilage and ___ (fusion) of the joint

A

synovitis; pannus (inflamed granulation tissue –> bv’s, fibroblasts, and myofibroblasts that contract and fuse the joint); ankylosis

44
Q

Rheumatoid arthritis is a chronic, systemic ___ disease that classically arises in middle aged women/men. It is associated with ____. There is symmetric/asymmetric involvement of the joints Name the 5 joints commonly involved.

A

autoimmune; women; HLA-DR4; symmetric; PIP joints (swan-neck deformity), wrists (radial deviation), elbows, ankles, knees

45
Q

HLA-DR4 is associated with this disorder

A

Rheumatoid arthritis

46
Q

Which type of arthritis presents with joint stiffness in the morning? In which type does it get better with activity?

A

Osteoarthritis and RA; RA

47
Q

Name the 6 clinical features of RA

A

1) morning stiffness, improves with activity; 2) symptoms of inflammatory process (fever, malaise, weight loss, myalgia); 3) rheumatoid nodules (central zone of necrosis surrounded by epithelial histiocytes); 4) vasculitis; 5) baker cyst (swelling of bursa behind knee); 6) pleural effusions, lymph adenopathy, and interstitial lung fibrosis

48
Q

Laboratory findings for RA will show a ___ autoantibody against __ portion of ___ (rheumatoid factor). It is a marker of tissue damage and disease activity. You can also see ___ and high ___ in synovial fluid.

A

IgM; Fc; IgG; neutrophils; protein

49
Q

Complications of rheumatoid arthritis include ___ and ___.

A

anemia of chronic disease (hepcidin); secondary amyloidosis (SAA –> AA, which deposits in tissues)

50
Q

_______ are a group of joint disorders characterized by lack of rheumatoid factor, axial skeleton involvement, and a HLA-___ association. Name three

A

Seronegative spondyloarthropathies; B27; ankylosing spondyloarthritis; reiter syndrome; psoriatic arthritis

51
Q

Ankylosing spondyloarthritis involves the ___ joints and ___. It arises in young/old adults, most often female/male. It presents with ___ pain. Fusion of the ___ eventually arises (bamboo spine). Extra-articular manifestations include __ and __.

A

sacroiliac; spine; young; male; low back; vertebrae; uveitis; aortitis (leading to aortic regurgitation)

52
Q

Reiter syndrome (aka reactive arthritis) is characterized by the triad of ___, ___, and ___. Arises in young/old adults, usually females/males, weeks after a GI or ____ infxn.

A

arthritis, urethritis, conjuctivitis (can’t see, can’t pee, can’t climb a tree); young; males; chlamydia trachomatis

53
Q

Psoriatic arthritis is seen in __% of cases of psoriasis. Involves ___ and ___ joints. Most commonly affected joints are ___.

A

10; axial and peripheral; DIP joints (leads to sausage fingers or toes)

54
Q

Infectious arthritis is due to an infectious agent usually ___. Name two cause and who you see them in. Classically involves asymmetric/symmetric joint, most typically the ___. Presents as a ___ joint with limited range of motion. Also often see __, increased ___, and elevated ___.

A

bacterial; N gonorrhoeae (young adults; most common); S aureus (older children and adults; 2nd most common); asymmetric (single joint); knee; warm; fever; WBC; ESR (erythrocyte sedimentation rate)

55
Q

Gout is a deposition of ____ crystals in tissues, especially the joints due to ___. ___ is derived from purine metabolism and is excreted by the kidney. Primary gout is the most common form and the etiology of hyperuricemia is ___.

A

monosodium urate; hyperuricemia; uric acid; unknown

56
Q

Name three disorders that cause secondary gout

A

Leukemia and myeloproliferative disorders (increased cell turnover lead to hyperuricemia); Lesch Nyhan syndrome (HGPRT is used to salvage purines, and they have deficiency); Renal insufficiency (decreased excretion)

57
Q

Lesch Nyhan syndrome is an x-linked deficiency of _____, which presents with these three symptoms

A

hypoxanthine-guanine phosphoribosyltransferase (HGPRT); mental retardation, self mutilation, secondary gout

58
Q

Acute gout presents as painful arthritis of the ___ (aka ___); MSU crystals deposit in joint, and activate ___, triggering an acute inflammatory reaction. ___ or ___ may precipitate this.

A

great toe; podagra; neutrophils; alcohol; consumption of meat (lots of RNA and DNA in meat)

59
Q

Chronic gout leads to development of ___, white chalky aggregates of uric acid crystals with fibrosis and giant cell reaction in the soft tissues and joints. Can also lead to ___ due to crystals depositing in the kidney tubules

A

tophi; renal failure

60
Q

Tophi are ___, ___ aggregates of uric acid crystals with ___ and ___ reaction in the soft tissues and joints

A

white, chalky; fibrosis; giant cell

61
Q

In gout, synovial fluid shows ___ shaped crystals with positive/negative birefringence under polarized light. When laying flat the crystals appear ___.

A

needle; negative; yeLLow (lay low - also yellow in paraLLel light)

62
Q

Pseudogout, resembles gout clinically but is due to deposition of ____. Synovial fluid shows ___ shaped crystals and weakly positive/negative birefringence under polarized light.

A

calcium pyrophosphate dihydrate (CPPD); rhomboid; positive

63
Q

What is the most common benign soft tissue tumor in adults?

A

Lipoma

64
Q

What is the most common malignant soft tissue tumor in adults?

A

liposarcoma

65
Q

What is the most common malignant soft tissue tumor in children?

A

rhabdomyosarcoma

66
Q

___ is a benign tumor of adipose tissue. ___ is a malignant tumor of adipose tissue and ___ is the characteristic cell.

A

Lipoma; liposarcoma; lipoblast

67
Q

___ is a benign tumor of skeletal muscle. Cardiac ____(same as above) is associated with ____.

A

Rhabdomyoma x 2; tuberous sclerosis

68
Q

___ is a malignant tumor of skeletal muscle and ___ is the characteristic cell. On IHC staining, ___ is positive. Most common site is ____; ___ is classic site in young girls.

A

Rhabdomyosarcoma; rhabdomyoblast; desmin; head and neck; vagina (grape like mass)

69
Q

Rickets most commonly arises in children ___ years of age, and presents with these 4 findings

A

less than 1; pigeon breast deformity (inward bending of ribs with anterior protrusion of the sternum); frontal bossing (enlarged forehead - due to osteoid deposition on skull); rachitic rosary (due to deposition at costochondral junction); bowing of legs (in ambulating children)