Pathology of Benign and Malignant Lumps Flashcards

1
Q
  • Definition of Hemangioma ?
    • common site
A
  • Abnormal proliferation of blood vessels
    • Increased numbers of normal blood vessels filled with blood
      • head and neck is a common site
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2
Q
  • Strawberry hemangioma affects who?
  • How does it grow and regress?
A
  • Benign capillary hemangioma of infancy
    • appears in first few weeks of life
  • Grows rapidly
  • Regress spontaneously
    • by 5-8 years old
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3
Q
  • Appearance of cavernous hemangioma?
    • can involve?
  • Does it regress?
A
  • Appearance:
    • large, dilated vascular channels
      • large cavernous blood filled vascular spaces
    • can involve deep structures
  • NO tendency to regress
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4
Q
  • What is pyogenic granuloma?
  • Where is it found?
    • what is it associated with?
A
  • Polypoid (tumor on a stalk) lobulated capillary hemangioma (benign)
    • can ulcerate and bleed
  • Found on:
    • skin, gingiva or oral mucosa
  • Associated with:
    • trauma
    • pregnancy
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5
Q

How can lymphangiomas be differentiated from hemangioma?

A

absence of RBC

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6
Q
  • What is cystic hygroma?
    • What is it associated with?
A
  • Cystic Hygroma:
    • cavernous lymphangioma (increase lymphatic space)
      • always in head or neck
  • Associated with:
    • Turner’s Syndrome (Monosomy X)
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7
Q
  • What muscle type does Glomus tumor arise from?
  • Where is it commonly found?
A
  • Benign, painful, red-blue tumor
  • Arises from:
    • modified smooth muscle cells of the thermoregulatory glomus body
  • Found:
    • commonly under fingernails
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8
Q
  • How is Nevus Flammeus described?
    • aka?
  • Associated with?
A
  • Benign flat lesion on head and neck (birthmark)
    • a congenital vascular malformation involving mature capillaries, present at birth.
      • Port wine stain
  • Associated with:
    • Sturge-Weber syndrome
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9
Q
  • Hereditary hemorrhagic telangiectasia is also know as Osler-Weber- Rendu syndrome?
    • inherited disorder of?
    • findings?
A
  • Inherited disorder of blood vessels (abnormal blood vessel formation)
    • autosomal dominant
  • Findings:
    • branching skin lesions (telangiectasias)
    • recurrent epitaxis (nose bleed)
    • skin discolorations
    • GI bleeding
    • hematuria
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10
Q
  • Bacillary angiomatosis is?
    • Found in who?
  • Caused by?
  • Frequently mistaken for/ distinguished by?
A
  • Benign capillary skin papule
    • Found in AIDs patients
  • Caused by:
    • Bartonella henselae infections
      • opportunistic infection
  • Frequently mistaken with:
    • Kaposi sarcoma
      • BUT has nuetrophilic infiltrate
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11
Q

What is seen microscopically in Bacillary Angiomatosis?

A

Is a vascular proliferation

  • Granulomatous inflammation
  • Neutrophils
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12
Q
  • Lipoma is?
  • Most common in?
A
  • Benign tumor of adipose tissue
    • Lipo= fat
  • Most common benign soft tissue tumor in adults
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13
Q
  • Nodular Fasciitis is what kind of proliferation?
  • What does it look like microscopically?
A
  • Benign soft tissue lesion most common in upper fascia
    • reactive proliferation of fibroblasts
    • unknown etiology
  • Microscopically
    • plump, randomly oriented spindle cells
    • surrounded by myxoid stroma
    • lots of mitotic activity
    • extravasated (leaked out) RBC
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14
Q
  • What is myositis ossificans?
    • occurs after?
  • Most often seen where on the body?
  • How does it present?
A
  • Heterotropic ossification (presence of bone in soft tissue where bone does NOT exists) of skeletal muscle
    • following muscular trauma
  • Most often seen in:
    • upper or lower extremity
  • May present as:
    • suspicious “mass” at site of known trauma
    • or as incidental finding on radiography
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15
Q
  • What is osteoma?
  • Where does it most commonly arise on?
  • What does it associate with?
A
  • Benign tumor of bone
  • Most commonly arise on:
    • surface of facial bones
  • Assocaited with:
    • Garnder syndrome
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16
Q
  • What is leiomyoma?
    • where is it commonly found?
  • Microscopically see?
A

Benign tumor of smooth muscle

Often arises in:

  • uterus of women
  • skin
  • muscularis of gut

Microscopically

  • whorled pattern of smooth muscle cells
    • well demarcated borders
17
Q
  • What is Baker cyst?
  • Commonly communicates with?
  • Related to?
A
  • Baker cyst:
    • popliteal fluid collection in gastrocnemius-semimembranous bursa in knee
      • herniation of synovium through a join capsule
  • Commonly communicate with:
    • synovial space
  • Related to:
    • chronic joint disease
18
Q
  • Tenosynovial Giant Cell tumor is associated with which translocation?
    • what is overexpressed?
    • result?
  • Where does it commonly affect?
A
  • Chromosomal translocation t(1;2)
    • M-CSF overexpressed
    • tumor infiltrated with lots of macrophages
      • ​macrophage may coalesce into multinucleated giant cells
  • Diffuse type:
    • knee (80%)
    • painful
  • Localized type
    • tendon sheaths along wrist and fingers
    • slow growing, painless
19
Q

Definitions of/ from what tissues:

  • Carcin-
  • Adenocarcin-
  • Sarc-
A
  • Carcin-
    • epithelial cell origin
    • derived from any of the three germ layers
  • Adenocarcin-
    • epithelial cells with glandular growth
  • Sarc-
    • fleshy mesenchymal tissue
20
Q

Sarcoma is?

A

Tumors arising in solid/mesenchymal tissues

21
Q

As a general rule:

  • Sarcomas are usually positive for?
  • Carcinomas are usually positive for?
A
  • Sarcomas positive for vimentin
  • Carcinomas positive for pan-cytokeratin
22
Q
  • Liposarcoma?
  • Most common in?
  • Characteristic cell?
A
  • Malignant tumor of adipose tissue
    • Lipo= fat; sarcoma= malignant mesenchymal tumor
  • Most commom malignant soft tissue tomor in adults
    • 50-60
  • Lipoblast is characteristic cell type
23
Q
  • Fibromatosis refers to?
    • what 3 characteristics do they have in common?
A
  • refers to:
    • a group of benign soft tissue tumors which have certain characteristics in common, including:
      1. proliferation of well-differentiated fibroblasts
      2. an infiltrative growth pattern
      3. aggressive clinical behavior with frequent local recurrence.
  • fibrous overgrowths of dermal and subcutaneous connective tissue develop tumours called fibromas.
    • These fibromas are usually benign (non-cancerous).
24
Q
  • Fibrosarcoma is?
  • Where can it occur?
A
  • Malignant tumor of fibroblasts
  • Can occur anywhere in the body
    • deep soft tissue
25
Rhabdomyoma is?
* Benign tumor of skeletal muscle
26
* Rhabdomyosarcoma is? * Most common in? * What is characteristic cell? * Where on the body is it most common?
* Malignant (aggressive) tumor of skeletal muscle * most common malignant soft tissue tumor in **children** * **Rhabdomyoblast** is the characteristic cell * **​desmin positive** * Common site is head and neck * **vagina** is classic site in young girl (5 yrs)
27
* Leiomyosarcoma is? * Who does it typically effect? * Where does it tend to metastisize?
* Malignant tumor of **smooth muscle** * Affects adults and women more frequently * Metastatic spread especially to **lungs**
28
Neurofibromatosis Type 1 (von Recklinghausen disease): * Disorder? * Characterized by? * Mutation in what gene? * Penetrance and expressivity?
* malignant peripheral nerve sheath tumor * _Characterized by_: * **cafe-au-lait spots** * cutaneous neurofibromas * optic gliomas * pheochromocytomas * **Lisch nodues** (pigmented nodules on iris) * Caused by mutations in the ***NF1*** gene on chromosome 17 * **RAS** is trapped in the active state High penetrance but variable expressivity
30
Neurofibromatosis Type 2: * result in what kind of tumors? * Mutation? * gene product?
* _Result in range of tumors, findings include:_ * bilateral acoustic Schwannomas * multiple meningiomas * Gliomas * ependymomas of spinal cord * juvenile cataracts * Mutation in **NF2 gene on chromosome 22** * **​**product is merlin, cytoskeleton protein that regulate membrane receptor signaling
31
What are 4 associated syndromes of Rhabdomyosarcoma?
1. **Li-Fraumeni** * TP53 gene mutation 2. **Beckwith-Weidemann** * Uniparental Disomy in 11p15 3. **Neurofibromatosis** * NF1 gene mutation 4. **Gorlin syndrome** * PTCH gene mutation skeletal muscle neoplasm
32
* Kaposi sarcoma is a malignancy of? * Caused by? * Presents with? * Associated with/ 3 Typical patients ? * Commonly mistaken for? * how to differentiate?
* low grade malignant proliferation of **endothelial** cells * due to dysregulation of VEGF * _**​**characterized by:_ * Purple patches, plaques and nodules on skin; * can also involve visceral organs (GI) * _Caused by:_ * **HHV-8 Infection** * _Associated with:_ * HIV * Older European males * Transplant Patient * _Mistaken for:_ * * Bacillary angiomatosis (neutrophilic infiltrate) * Kaposi has **lymphocytic** infiltrate
33
What is a KS flare?
* Kaposi sarcoma (KS) flare may occur following therapy with *corticosteroids* * as part of the **immune reconstitution inflammatory syndrome** seen with highly active antiretroviral therapy (**HAART**), and after **rituximab** therapy * The exact mechanism responsible for iatrogenic KS flare is unclear.
34
* What is the mechanism of p53 in apoptosis? * What happens if DNA repair fails? * If it succeeds?
* DNA damage or hypoxia causes **phosphorylation** of p53 by ATM/ATR kinases * this releases p53 from **MDM2** * p53 activates **CDK inhibitor** p21 * cell cycle arrest in G1 * p53 cell apoptosis or senescence results if:* * DNA repair _fails_ * p53 ubiquination and degredation in proteosome if:* * DNA repair _succeeds_
35
* Li-Fraumeni syndrome has abnormalities in which gene? * increases risk for? * associated with which malignancies? * Inheritance pattern?
* Abnormalities in ***TP53*** * multiple malignancies at an early age * Also know as **SBLA** cancer syndrome * sarcoma, breast, leukemia, adrenal gland _Inheritance_: * autosomal dominant
36
* Angiosarcoma is what kind of proliferation? * Common sites? * Associated with exposure to?
* Malignant proliferation of endothelial cells (that line blood vessels) * highly **aggressive** * _Common sites:_ * skin, breast and liver * _Associated with exposure to:_ * **Polyvinal Chloride (PVC),** arsenic and Thorotrast