Begnin Mesenchymal Tumors Flashcards

(57 cards)

1
Q

Lesion is categorized border line tumor

A

Chondroma

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2
Q

Why chondroma is called border line tumor

A

Because its like well diferentiated type of chondrosarcoma

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3
Q

Site of chondroma

A

Anterior maxilla، posterior manduble، symphysis menti , coronoid process ,condyle

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4
Q

Hp of chondroma

A

Lobules of mature hyaline cartilage

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5
Q

Most common site of osteoma

A

Skull

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6
Q

Site of periosteal osteoma ,but site of endosteal osteoms

A

Surface of bone
Intrabony

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7
Q

RF of osteoma

A

Well circumscribed radioopaue mass

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8
Q

Types of osteomas Hp

A

Compact dense bone with minimal marrow tissue
Cancellous : bone trabeculae

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9
Q

What is Choriostoma?

A

A tumor-like growth of normal tissue in an abnormal location, typically near the foramen cecum.

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10
Q

Where is Choriostoma commonly found?

A

In the tongue, mainly in the posterior third.

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11
Q

What are the symptoms of Choriostoma?

A

Asymptomatic except for gagging, dysphagia, and speaking difficulty.

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12
Q

What is the composition of Choriostoma?

A

Dense lamellar bone and mature cartilage, surrounded by dense fibrous connective tissue.

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13
Q

What is Gardner syndrome?

A

An autosomal dominant trait characterized by multiple intestinal polyps and other features.

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14
Q

What are the key features of Gardner syndrome?

A

Multiple intestinal polyps, epidermoid and sebaceous cysts, desmoid tumors, adrenal gland tumors, supernumerary teeth, and pigmented lesions on ocular fundus.

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15
Q

What are the types of tumors associated with Gardner syndrome?

A

Desmoid tumors and adrenal gland tumors.

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16
Q

What dental abnormalities are associated with Gardner syndrome?

A

Supernumerary teeth and impacted teeth.
ملحوظة : نقص الأسنان مع ectodermal dysplasia syndrome

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17
Q

What type of cysts are associated with Gardner syndrome?

A

Epidermoid and sebaceous (epithelial) cysts.

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18
Q

What is CHRPE?

A

Pigmented lesions on the ocular fundus associated with Gardner syndrome.

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19
Q

What are the key features of Neurofibromatosis type 1?

A
  1. Café au lait macules.
  2. Neurofibromas.
  3. Freckling in axillary or inguinal regions (Crowe’s sign).
  4. Two or more iris hamartomas (Lisch nodules) -> brown pigmented spots in the iris.
  5. Optic glioma.
  6. Bone changes → thinning of long bone cortex.
  7. First degree relative diagnosed with neurofibromatosis type 1.
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20
Q

What is a granular cell tumor?

A

A soft tissue tumor originating from Schwann cells, composed of large cells with eosinophilic, granular cytoplasm.

Very rare, benign soft tissue tumor.

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21
Q

What is the most Histopathological feature of granular cell tumor (schwannoma)

A

Cells : syntial pattern
Cytoplasm : abundant cytoplasm with coarse granules (representing phagolysosmes )

Pseudocarcinomatus appearance(pseudoepithelimatus hyperplasia)

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22
Q

Lesion شبه ال granular cell tumor(granular cell scwanoma) وبتيجي مع ال new born

A

Congenital epulis of new born

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23
Q

Age ,site of congenital epulis newborn

A

New born
Anterior alveolar ridge of maxilla,and madible usually canine lateral incisor

24
Q

Hp of congenital epulis of new born

A

Epithelium :atrophic
No pseudoepithelimatus appearance
Negative to s100

25
What is the Site of traumatic meuroma ?
26
Other name of neurolemmoma
27
Neurolemmoma is associated with which syndrome
28
What is the Hp of neurolemmoma?
29
What is the difference between Antoni A and antoni B
30
What is the definition of of verocay bodies ?and associated with each lesion ?
31
Neurofibroma is associated with which syndrome?
32
What are the components of neurofibroma?
33
What is the shape of collagen bundles in neurofibroma?
Shredded carrot collagen
34
Is fibroma capsulated?
False
35
The most common bengin neoplasm of oral cavity
Fibroma
36
If fibroma reactive to secondary irritation is called
Irritational,traumatic ,focal fibrous hyperpla6
37
What is Giant Cell Fibroma?
A benign, sessile or pedunculated lesion of oral mucosa seen predominately in the third decades of life with a slight female predilection. ## Footnote It presents as a localized reactive proliferation of fibrous tissue, resembling irritation fibroma rather than a neoplastic proliferation.
38
What characterizes the cells in Giant Cell Fibroma?
The presence of large stellate-shaped, sometimes multinucleated fibroblasts that tend to occur near the overlying epithelium. ## Footnote The surface epithelium is thin with narrow elongated rete ridges.
39
What is Fibrous Histiocytoma?
A benign fibrohistocytic tumor that arises within the subcutaneous or deep soft tissues and rarely metastasizes. ## Footnote BFH is reported at any age with predominance in males adults older than 25 years and with a mean age of 40 years.
40
What are the clinical features of oral BFH?
Painless solitary tumor, slowly enlarging. ## Footnote The tumor typically does not cause discomfort or pain.
41
What is the histological appearance of Fibrous Histiocytoma?
spindle shaped fibroblasts in a storiform pattern intermixed with rounded histiocyte-like cells. ## Footnote Multinucleated giant cells and scattered lymphocytes may also be present.
42
True or False: Giant Cell Fibroma is a neoplastic proliferation.
False. ## Footnote It is a localized reactive proliferation rather than a neoplastic growth.
43
Fill in the blank: Giant Cell Fibroma resembles _______ rather than a neoplastic proliferation.
irritation fibroma. ## Footnote The resemblance indicates its reactive nature.
44
What age group is predominantly affected by Fibrous Histiocytoma?
Adults older than 25 years, with a mean age of 40 years. ## Footnote There is a noted predominance in males.
45
What is a lipoma?
A benign lesion composed largely of fat tissue ## Footnote Lipomas are one of the most common neoplasms but are rarely seen in the oral cavity.
46
In which demographic are oral lipomas more commonly found?
More often in males than in females, particularly in patients past the age of 40 years ## Footnote This demographic trend highlights the age and gender predisposition for the occurrence of oral lipomas.
47
What is the most common site for oral lipomas?
The cheek ## Footnote Oral lipomas can occur at any site but the cheek is the predominant location.
48
What is the histopathological characteristic of a lipoma?
Lobular mass of mature fat cells with collagen in between ## Footnote This histopathological structure is typical for lipomas.
49
What appearance do fat cells in a lipoma have?
Characteristic signet ring appearance ## Footnote This distinctive appearance aids in the identification of lipomas during histopathological examination.
50
What does significant fibrous tissue in a lipoma give rise to?
Fibro-lipoma ## Footnote The presence of fibrous tissue alters the classification of the lipoma.
51
What is formed when the endothelial element is obvious in a lipoma?
Angiolipoma ## Footnote Angiolipomas are a variant of lipomas characterized by more vascular components.
52
When does Strawberry hemangioma typically present?
At birth or within a few weeks ## Footnote Strawberry hemangiomas can appear immediately at birth or shortly after, distinguishing them from other types.
53
When do Infantile hemangiomas typically appear?
Within a month after birth ## Footnote Unlike Strawberry hemangiomas, Infantile hemangiomas manifest after birth.
54
What is a common characteristic of both Strawberry and Infantile hemangiomas?
They often show self involution ## Footnote Both types of hemangiomas are known to regress on their own over time.
55
What may larger hemangiomas require?
Surgical excision ## Footnote Larger lesions that do not involute may need to be surgically removed.
56
What is the histology of Capillary Hemangioma?
Proliferation of small blood vessels ## Footnote Capillary hemangiomas are characterized by a dense network of small blood vessels.
57
What is the histology of Cavernous Hemangioma?
Proliferation of large blood vessels and communicating with each other ## Footnote Cavernous hemangiomas consist of larger vascular channels that are interconnected.