Module 2: Crohn's, Ulcerative colitis, Juvenile Polyp, Neoplastic, FAP, HNPCC, Carcinoid Flashcards Preview

Pathology Post Midterm > Module 2: Crohn's, Ulcerative colitis, Juvenile Polyp, Neoplastic, FAP, HNPCC, Carcinoid > Flashcards

Flashcards in Module 2: Crohn's, Ulcerative colitis, Juvenile Polyp, Neoplastic, FAP, HNPCC, Carcinoid Deck (40):

Now moving onto the inflammatory bowel diseases. The first disease to discuss is Crohn's Disease/Terminal ileitis/Regional enteritis/Granulomatous Colitis. What is the etiology?

Etiology: Diagnosis of exclusion
--most common is Ashkenazi Jews (due to imbreding in the past and Young Adults
--Pre-disposing factors: genetic predisposition, abnormal host reactivity (autoimmune destruction by CD4 T cells) and microbial infections
-more common in women and has a bimodal distribution in terms of age (young adults and older females)


What is the pathogenesis for Crohn's?

Chronic, transmural inflammation with non-caseating granulomas which can affect anywhere from the mouth to the anus
--Produces SKIP lesions (not continous therefore not able to be fixed by sx)
---Most common location: terminal ileum and proximal colon (but can happen anywhere)
--Typically spares the rectum


What is the presentation for Crohn's?

Abdominal Pain
Bloody/watery diarrhea
--blood = colon
---watery = small bowel
Weight loss


What is seen on gross, barium enema and biopsy for Crohn's patients? (pic 15a&b)?

Gross: Linear and serpentine ulcers with cobblestoning and creeping fat (due to fibrosis and the mesenteric fat coming over the serosa), skip lesions, transmural
Biopsy: pic to left: transmural so there is mucosal ulceration and lots of CD4 T cells within lamina propria all the blue dotted cells, PMNs, submucosa (fibrosis and fibroblasts), muscularia propria (thickening and fibrosis) and in serosa = non caseating granulomas
pic to right: blue dotted cells higher mag are lymphocytes aggregates of CD4 T cells, swallow and then deep ulcers (Also called fissures), blood vessels (angiogenesis and type III collagen)
Barium: See a string sign (that is due to luminal narrowing due to fibrosis) (pencil stools)
--note do the colonoscopy during remission not during an acute on chronic flare


What extraintestinal manifestations are seen with Crohn's patients?

Eyes (uveitis and iritis)
Skin (erythema nodusum and pyoderma gangrene)
Joints (Arthritis)
Kidney ( stones --- oxilic)
Cholesterol gallstones ( bile salt absorption problems in terminal ileum)


What are the complications of Crohn's?

Colon Cancer --- Adenocarcinoma
Colon Obstruction --- due to strictures (Seen in pic), perforation
Malabsorption of iron, bile salts, water and B12 aka everything
Toxic Megacolon -- exposing meisners and auerbach's plexus
Perianal Abscesses: sterile abscess


What is the treatment for Crohn's Disease?

Immunosuppressive Therapy
--surgery does not work due to skipping and recurrence


Now onto Ulcerative Colitis. What is the etiology for this?

Etiology: Idiopathic
--most common in Ashkenazi Jews
Pre-Disposing factors: Genetic, microbial infection, abnormal post reactivity (autoimmune destruction by CD4 T cells)
--bimodal distribution and more common in females
--associated with HLA-DRB1


What is the pathogenesis for Ulcerative Colitis?

Starts in the rectum (proctitis) and moves proximally and goes to distal part of ileum (Backwash ilitis)
---no skipped lesions (so curable)
--spares the anus
--not transmural just mural (First two layers)


What is the presentation for patients with Ulcerative Colitis?

Abdominal Pain
Bloody Diarrhea
Weight Loss
Acute on chronic inflammation


On histology and gross image slide 16a,b what is seen in Ulcerative Colitis ?

Gross: no skip lesions; pseudopolyps on gross (due to regenerating mucosa)
Colonoscopy with biopsy: Mucosa CD4 T cells, abnormal morphology of crypts, ulceration of mucosa, granulation tissue and fibrosis of submucosa. (no granulomas thats Crohns)
16b: crypt abscesses with neutrophil exudate in the lumen of the crypts
PSC: periductal onion skining fibrosis and beaded appearance of biliary tree


On barium enema what do you see in Ulcerative Colitis?

Lead pipe appearance
--loss of hostra


What are the extraintestinal manifestations of Ulcerative Colitis?

Crohn's manifestions + Primary sclerosis cholangitis
--in biliary tract they get PSC (fibrosis in the biliary tree of both the intra and extra hepatic bile ducts, so what backs up is conjugated bilirubin so you get jaundice)
--only time you will see jaundice in Ulcerative Colitis
--PSC also causes malabsorption and PANCA positive


What are additional complications of Ulcerative Colitis besides Primary Sclerosis Cholangitis?

Colon Cancer (After about 10 years with dysplastic crypts as the precursor lesion)
Toxic Megacolon (damages meisners plexus) --- peritonitis
Vit A,D,E,K deficiency due to malabsorption during PSC
PCS -- malabsorption -- osteomalacia
Liver Cancer --- hepatocellular carcinoma


Now moving onto GIT polyps, the most common in children is Juvenile Polyp or Retention Polyp. what is the etiology?

Seen in children under 5
--Juvenile Polyposis syndrome (AD): leads to increased risk of malignancy in other areas
--Single, sporadic poly however had no malignant potential (No dysplastic features): lobulated with stalk


What is seen on histology for Juvenile Polyp?

Lamina Propria forms the bulk and encloses abundant cystically dilated glands
(+ or - inflammatory cells)


The next GIT poly is Peutz Jegher's Polyp or Hammartomatous Polyp. What is the etiology/pathogenesis for this?

Peutz Jegher (AD BLK1 mutation)
--Multiple polyps in entire GI tract
--Melanotic Pigmentation of lips (black), peri-oral areas, face, genitalia and uterus


What is seen on histology for Peutz Jegher Polyp?

Arborizing network of smooth muscle extending into the polyp intermixed
--glands are lined by non-dysplastic epithelium rich in goblet cells
--no malignant potential in the colon, can have carcinomas in other places though


Next topic is Carcinoid Tumors. Most commonly found where? And what are the origin in cells?

Submucosa of the small bowel and appendix
--Origin: enterochromaffin/Kuchitsky/neuroendocrine cells
--same origin as small cell carcinoma of the lung
Appendix tumors usually benign and Small bowl usually malignant (non specific abd pain/mass)
small bowel more common then appendix


What are the three different types of Carcinoid Syndrome?

Type I: Autoimmune Chronic Gastritis and Achlorhydria (decreased acid)
---hypergastrinemia due to ECL cell hyperplasia
--Usually benign
Type II: Zollinger-Elison Syndrome: gastrinoma in the pancreas
---usually in men1
---Hypergastrinemia: due to increased acid and no negative feedback leading to multiple large duodenal ulcers (partial cells)
Type III: Malignant: very aggressive and sporadic
--mets to liver and will do carcinoid syndrome


What is the best investigation for carcinoid tumor? (Slide 17)

Biopsy: sheets of uniform cells with stippled oval nuclei and salt and pepper appearance in the submucosa


What is seen in the urine for Carcinoid tumor and what are the tumor markers?

Urine: 5-HIAA
Tumor Markers: synaptophysin, chromogranin and CD56 (All for confirmation)


One complication of Carcinoid syndrome, explain the pathogenesis for this

Only happens when there is metastasis to the liver or cirrhosis of the liver b/c normal liver can metabolize serotonin but damaged liver can not.
--Present with: episodic flushing, diarrhea and wheezing


What are additional complications of Carcinoid syndrome?

Metastasis: regional lymph nodes, liver, ovaries, peritoneum and spleen
Fibrosis (Due to increased collagen) of the right sided heart valves (tricupsid and pulmonary)
--not on left side due to lack of bio-amines on left side


Next topic to discuss is Neoplastic Polyps (adenomas). What are the two types?

Pedunculated: stalk (pic on right 18) and sessile (pic to left 18) (Described as cauliflower)


What is the most common location of these Neoplastic Polyps?

Colon (Can be left or right sided)


Describe some features of the Neoplastic Masses

Both are Benign but have dysplastic lining the glands
--lined by tall, hyperchromatic and disordered epithelium
Pedunculated: tubular adenoma (has a stalk and can cause obstruction)
Sessile: villous adenoma (flat and therefore more dangerous) (Secretes mucus)


How does a patient present with Neoplastic Polyps?

Asymptomatic commonly
--incidental finding on colonoscopy
--Rarely: bleeding, obstruction, bloody diarrhea, and mucoid diarrhea


what do you see on biopsy for Neoplastic Polyps? slide 18b

Tubular Adenoma (pedunculated): on left: adenoma means benign tumor of glands and is lined by dysplastic glands and thats why it becomes cancer (Not yet cancer in pic because its still on mucosal surface)
Sessile Polyp (on right): finger like projections (Villous adenoma) lined by dysplastic cells but again still benign


What are complications of these Neoplastic Polyps?

Intestinal obstruction
Bloody diarrhea ( iron deficiency anemia)
mucoid diarrhea (hypokalemia and hypoalbuminemia)


What are the three factors that lead to increased malignant potential?

Size: greater than 2cm
Villous Architecture (aka sessile)
Degree of Dysplasia


The last topic dealing with multiple polyps (polyposis) is FAP. what is the etiology for FAP?

Genetic AD
--2 hits on APC gene (tumor suppressor gene) only born with one hit and later in life you get the second hit and this second hit leads to multiple polyps.
--mutation in KRAS --- mutation in p53 --- adenocarcinoma


What are some features of FAP?

Left side of colon
Start screening at age of 12 if there is a family history of left sided colon cancer at a young age
--later stages: bright red blood and mucoid diarrhea (intestinal obstruction and LLQ pain)


What kind of polyps are present in FAP?

Pedunculated, benign polyps (tubular adenoma on histology)
--100% chance of becoming malignant with KRAS (proto oncogene so 1 hit) or p53 mutation (tumor suppressor gene)
--follows the beta catenin pathway


What are the complications for FAP?

Diameter of left colon is smaller --- napkin ring constriction -- intestinal obstruction


What is Gardner's Syndrome?

FAP + multiple osteomas + desmoid tumors and epidermal cysts


What is Turcot's Syndrome?

FAP + CNS glioma (medullablastoma in kids)


Finally lets finish this section with a discuss on HNPCC/Lynch Syndrome. What are some features?

Few polyps but on the right side
Gross: sessile serrated morphology ---- villous adenocarcinoma because it goes straight to cancer (no benign polyps) (invades submucosa and muscularis propria)
--Exophytic mass
--DNA mismatch repair genes (MLH1,MSH2,MSH6,PMS2)
--microsatellite instability: start screening at 25


What do patients present with who have HNPCC?

Initially no symptoms because of occult bleeding, fatigue and iron deficiency anemia due to chronic blood loss
---Older male and post menopausal women think right sided colon cancer


What is the spread of HNPCC?

Lymph nodes, liver, and then lungs

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