Begnin Mesenchymal Tumors Flashcards
(57 cards)
Lesion is categorized border line tumor
Chondroma
Why chondroma is called border line tumor
Because its like well diferentiated type of chondrosarcoma
Site of chondroma
Anterior maxilla، posterior manduble، symphysis menti , coronoid process ,condyle
Hp of chondroma
Lobules of mature hyaline cartilage
Most common site of osteoma
Skull
Site of periosteal osteoma ,but site of endosteal osteoms
Surface of bone
Intrabony
RF of osteoma
Well circumscribed radioopaue mass
Types of osteomas Hp
Compact dense bone with minimal marrow tissue
Cancellous : bone trabeculae
What is Choriostoma?
A tumor-like growth of normal tissue in an abnormal location, typically near the foramen cecum.
Where is Choriostoma commonly found?
In the tongue, mainly in the posterior third.
What are the symptoms of Choriostoma?
Asymptomatic except for gagging, dysphagia, and speaking difficulty.
What is the composition of Choriostoma?
Dense lamellar bone and mature cartilage, surrounded by dense fibrous connective tissue.
What is Gardner syndrome?
An autosomal dominant trait characterized by multiple intestinal polyps and other features.
What are the key features of Gardner syndrome?
Multiple intestinal polyps, epidermoid and sebaceous cysts, desmoid tumors, adrenal gland tumors, supernumerary teeth, and pigmented lesions on ocular fundus.
What are the types of tumors associated with Gardner syndrome?
Desmoid tumors and adrenal gland tumors.
What dental abnormalities are associated with Gardner syndrome?
Supernumerary teeth and impacted teeth.
ملحوظة : نقص الأسنان مع ectodermal dysplasia syndrome
What type of cysts are associated with Gardner syndrome?
Epidermoid and sebaceous (epithelial) cysts.
What is CHRPE?
Pigmented lesions on the ocular fundus associated with Gardner syndrome.
What are the key features of Neurofibromatosis type 1?
- Café au lait macules.
- Neurofibromas.
- Freckling in axillary or inguinal regions (Crowe’s sign).
- Two or more iris hamartomas (Lisch nodules) -> brown pigmented spots in the iris.
- Optic glioma.
- Bone changes → thinning of long bone cortex.
- First degree relative diagnosed with neurofibromatosis type 1.
What is a granular cell tumor?
A soft tissue tumor originating from Schwann cells, composed of large cells with eosinophilic, granular cytoplasm.
Very rare, benign soft tissue tumor.
What is the most Histopathological feature of granular cell tumor (schwannoma)
Cells : syntial pattern
Cytoplasm : abundant cytoplasm with coarse granules (representing phagolysosmes )
Pseudocarcinomatus appearance(pseudoepithelimatus hyperplasia)
Lesion شبه ال granular cell tumor(granular cell scwanoma) وبتيجي مع ال new born
Congenital epulis of new born
Age ,site of congenital epulis newborn
New born
Anterior alveolar ridge of maxilla,and madible usually canine lateral incisor
Hp of congenital epulis of new born
Epithelium :atrophic
No pseudoepithelimatus appearance
Negative to s100