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
- Increased numbers of normal blood vessels filled with blood

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

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
- large, dilated vascular channels
- NO tendency to regress

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

5
Q
How can lymphangiomas be differentiated from hemangioma?
A
absence of RBC
6
Q
- What is cystic hygroma?
- What is it associated with?
A
- Cystic Hygroma:
- cavernous lymphangioma (increase lymphatic space)
- always in head or neck
- cavernous lymphangioma (increase lymphatic space)
-
Associated with:
- Turner’s Syndrome (Monosomy X)

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

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
- a congenital vascular malformation involving mature capillaries, present at birth.
-
Associated with:
- Sturge-Weber syndrome

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

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
-
Bartonella henselae infections
-
Frequently mistaken with:
- Kaposi sarcoma
- BUT has nuetrophilic infiltrate
- Kaposi sarcoma

11
Q
What is seen microscopically in Bacillary Angiomatosis?
A
Is a vascular proliferation
- Granulomatous inflammation
- Neutrophils

12
Q
- Lipoma is?
- Most common in?
A
- Benign tumor of adipose tissue
- Lipo= fat
- Most common benign soft tissue tumor in adults
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

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

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

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
-
popliteal fluid collection in gastrocnemius-semimembranous bursa in knee
-
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:
- proliferation of well-differentiated fibroblasts
- an infiltrative growth pattern
- aggressive clinical behavior with frequent local recurrence.
- a group of benign soft tissue tumors which have certain characteristics in common, including:
- 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