Week 7: Polyps Flashcards
ID
Polyp
What percent of polyps are benign?
95%
ID
Hyperplastic Polyp
Serrations (blue circle), tapering at the crypt base (yellow trapezoid), and no dysplasia
ID
Inflammatory Polyp
Lymphocytes (yellow arrows) and dilated crypts (cyan arrow)
ID
Hamartomatous Polyp
ID
Hamartomatous Polyp
Dilated crypts (cyan ellipse), abundant and inflamed stroma (yellow arrow), and surface erosion (orange arrows)
What mutation is associated with Juvenile Polyps/Juvenile Polyposis Syndrome?
Autosomal Dominant SMAD4/ BMPR1A mutation
ID
Juvenile Polyp
Dilated crypts (cyan circle), abundant and inflamed stroma (yellow arrow), and surface erosion (orange arrow). Essentially a Hamartomatous Polyp, but in a child.
An 11-year-old female presented to the emergency department with severe abdominal pain and was found to have intussusception of the small bowel. She was taken for emergent bowel resection. Physical exam had revealed dark blue to brown macules on the lips, nostrils and palmar surfaces of the hands.
Peutz-Jeghers Syndrome (PJS)
Hamartomatous Polyposis with arborizing smooth muscle
ID
Peutz-Jeghers Syndrome (PJS)
Broad bands of smooth muscle (yellow arrows). Hamartomatous Polyposis with arborizing smooth muscle
ID
Peutz-Jeghers Syndrome (PJS)
Broad bands of smooth muscle (yellow arrows). Hamartomatous Polyposis with arborizing smooth muscle
ID
Peutz-Jeghers Syndrome (PJS)
Type of Hamartomatous Polyp. Smooth muscle creates an aborization.
ID
Peutz-Jeghers Syndrome (PJS)
Hamartomatous Polyposis with arborizing smooth muscle
What mutation is associated with Peutz-Jeghers Syndrome (PJS)?
Loss-of-function in STK11/LKB1 gene
What are three manifestations of a PTEN Hamartoma-Tumor Syndrome
dark freckles on the penis in AMAB only
- Macrocephaly
- Telangectasia
- Lipomas
What mutation is associated with PTEN Hamartoma-Tumor Syndrome
Phosphate and Tensin homolog deletion
ID
Trichillemmoma
ID
Lipoma
ID
Macrocephaly
Hamartomatous polyps of the GI tract, nail atrophy, alopecia, skin hyperpigmentation, diarrhea, cachexia and anemia
Cronkhite-Canada Syndrome
ID
Cronkhite-Canada Syndrome
Skin hyperpigmention (left) and nail atrophy (right)
ID
Cronkhite-Canada Syndrome
ID
Facial Angiofibromas
Tuberous Sclerosis - TSC1 and TSC2 gene
ID
Cortical Tubers
Tuberous Sclerosis - TSC1 and TSC2 gene