Celiac Disease Histopathology - prior to Tx Flat biopsy with surface damage Increased Intraepithelial lymphocytes Increased lamina propria inflammation.

Slides:



Advertisements
Similar presentations
Celiac Disease This session introduces you to the intestinal malady known as celiac disease or celiac sprue. There are three reasons for looking at this.
Advertisements

The “Great Mimic” Disease
A.M. Report 5/5/09 Jason Haag, M.D.
Upper GI quiz PBL 28.
Celiac disease Prepared by :Maha Hmeidan nahal.
Research Techniques Made Simple: T-Cell Receptor Gene Rearrangement
SCREENING FOR CELIAC DISEASE IN EGYPTIAN CHILDREN SCREENING FOR CELIAC DISEASE IN EGYPTIAN CHILDREN Prof. Dr: Mona Abu Zekry -Professor of Pediatrics Head.
Chapter 18 Autoimmune Diseases 1. 1.Immunological homeostasis: To self Ag, our immune system is in tolerance and immune response won’t take place. Immune.
HPI 35 year old caucasian female presents to your clinic with 3 month history of diarrhea, bloating, and fatigue. What else would you like to know?
Pathology of the Large Intestine Dr. Shaun Walsh Ninewells Hospital Dundee.
Dr. Adnan Hamawandi Professor of Pediatrics
Celiac Disease and tropical sprue
GASTRO INTESTINAL DISORDERS Dr.linda maher. GIT(GASTRO INESTINAL TRACT)  it is a tube with muscle walls throughout its length. it is lined by an epithelium.
Lecture 22 Autoimmunity.
In Vitro Gliadin Challenge: Diagnostic Accuracy and Utility for the Difficult Diagnosis of Celiac Disease Am J Gastroenterol 2012; 107:111–117; Raffaella.
Raneen Omary. Contents Definition Pathogenesis Epidemiology Acute Radiation Enteritis Chronic Radiation Enteritis Risk Factors Diagnosis DD Medical Management.
Dr Nisha Verma Department of Immunology Royal Free Hospital, London
18-1 Important terms: Hypersensitivity – immune responses that causes tissue damage Autoimmune disease – immune responses to self-antigens Immunodeficiency.
Should we Screen for Celiac Disease in IBS? Brennan Spiegel, MD, MSHS.
Ben Greenfield 28 September Epidemiology 1% of the population in North America More common in the Caucasian population, very rare in Asian and African.
A Patient with Recurring Infections Julia Wright, M.D. Clinical Associate Professor of Medicine Section of General Internal Medicine.
Gastric carcinoma.
The Role of TCR gamma-delta T cells in Celiac Disease Columbia University, College of Physicians and Surgeons By: Nertila Ujkaj Littin Kandoth Sandra.
Premalignant states n Tubular GI Tract: 1. Esophagus – Barrett’s epithelium 1. Esophagus – Barrett’s epithelium 2. Stomach – dysplasia, IM due to 2. Stomach.
Lecture #13 Aims Describe autoimmune diseases, concentrating on the role of immunity in their pathogenesis. Readings: Robbins, Chapter 5.
Crohn’s Disease & Mycobacterial Infections Kimberly Persley, MD October 19, 2005.
AIM OF THIS PRESENTATION  Introduce the important components of the Autoimmune Diseases.  Demonstrate what happens when things go wrong & the body turns.
Part B Autoimmune Diseases Part B Autoimmune Diseases Effector mechanisms of autoimmune disease Endocrine glands as special targets.
Principles of Immunology Autoimmunity 4/25/06. Organs Specific Autoimmune Diseases  Hashimoto’s thyroiditis DTH like response to thyroid Ags Ab to thyroglobulin.
Tissue Transglutaminase, Endomysial Antibodies, and Celiac Disease
Doudenum Histopathological diagnosis of gluten sensitive entropathy.
Celiac Disease.
JESSIE BUTTS AMANDA SCHUESSLER Celiac Disease. What is Celiac Disease? Genetically based autoimmune disease  Of all 8 0, only one with a known trigger.
Immunological Disease of the Gastrointestinal Tract
SERUM CYTOKINE PATTERNS IN CELIAC DISEASE Shabab Naqvi & Ibrahim Ibrahim Mentor: Dr. Sanil Manavalan Columbia University, College of Physicians and Surgeons.
Celiac Disease Gluten Sensitive Enteropathy. Celiac Disease: Immune mediated enteropathy caused by permanent sensitivity to gluten in genetically susceptible.
By Dr. Gehan Mohamed Dr. Abdelaty Shawky
ESPGHAN COMMITTEE to revise the diagnostic protocol of Celiac Disease Prof. Riccardo Troncone, President March 2010.
Immune system Chp. 16 (pp ) ~20,000 genes affect immunity, usually polygenic or multifactorial traits.
Celiac Sprue Common cause of malabsorption of one or more nutrients in Caucasians, especially those of European descent Also known as non-tropical sprue,
(Review Articles). An increased intraepithelial lymphocyte density in an architecturally normal proximal small intestinal mucosal biopsy is a common finding.
Immune Disorders and Imbalances. Organ Transplants There are 4 major varieties of grafts – Autografts: tissue transplanted from one body site to another.
Normal stomach. Fundic mucosa with parietal & chief cells Antral mucosa with mucin secreting glands Stomach - Histology.
Celiac Disease and Autoimmune Diseases
1-Helicobacter pylori gastritis
Gastrointestinal system
Effect of Elemental Diet on Mucosal Immunopathology and Clinical Symptoms in Type 1 Refractory Celiac Disease  Richard Willfred Olaussen, Astrid Løvik,
Compliant with neg bx (6) Compliant with pos bx (3)
Gastric carcinoma.
By Dr. Abdelaty Shawky Assistant professor of pathology
Celiac Disease: An Immunological Jigsaw
© The Author(s) Published by Science and Education Publishing.
A Single Center Experience of Treatment of
Immunosuppressive related indolent
Coeliac Disease at ABCD
Malabsorption syndrome
Effect of Elemental Diet on Mucosal Immunopathology and Clinical Symptoms in Type 1 Refractory Celiac Disease  Richard Willfred Olaussen, Astrid Løvik,
AUTOIMMUNE DISEASES.
DIAGNOSTIC TESTS Endoscopy: enables your surgeon to examine the lining of the esophagus (swallowing tube), stomach and duodenum (first portion of the small.
Associated Conditions
Overview and pathogenesis of celiac disease
Malabsorption Work-up: Utility of Small Bowel Biopsy
Adult Autoimmune Enteropathy: Mayo Clinic Rochester Experience
Neutrophil Recruitment and Barrier Impairment in Celiac Disease: A Genomic Study  Begoña Diosdado, Harm van Bakel, Eric Strengman, Lude Franke, Erica van.
Volume 129, Issue 1, Pages (July 2005)
Pathology and mechanisms of malabsorption
Celiac disease Journal of Allergy and Clinical Immunology
Inflammatory bowel disease and Ulcerative colitis
© The Author(s) Published by Science and Education Publishing.
Inflammation process and possible routes of probiotic action in the maintenance of CD. In CD patients, increased epithelial tight junction permeability.
Presentation transcript:

Celiac Disease Histopathology - prior to Tx Flat biopsy with surface damage Increased Intraepithelial lymphocytes Increased lamina propria inflammation –Plasma cells Increased crypt mitoses

Flat bx with lots of IELS – fully developed sprue-like changes

Note surface damage with lots of IELS

Activated T-cells in surface epithelium

Increased mitoses in the crypts

The mucosal thickness doesn’t change as there is crypt hyperplasia

Classification of Celiac Lesions Marsh 3A Marsh 3B Marsh 3C

Celiac Disease Histopathology - Shortly after Tx Marked clinical improvement Surface epithelium restored Slight return of villi Other findings unchanged

Gluten Free Diet - 2 Weeks

Celiac Disease Histopathology - Long term Tx Continued clinical improvement Further return of villi Mitotic rate subsides Chronic inflammation subsides

Villi are present but abnormal, hard to get all gluten out of diet

Better but not normal histology still eating some gluten??

Celiac Disease Gluten Challenge Epithelial lymphocytes increase Epithelial damage to upper villi Full-blown lesion develops later

Celiac Disease Pathogenic Factors Genetic Aspects –Familial Occurrence (11-22% first degree relative) –Identical Twin Concordance (70%) –HLA Associations ( DQ2, B8) Environmental Factors –Dietary Gluten –Twin non-concordance rate of 30%; separate onsets –?Viral exposure (Adenovirus type 12)

Protein Sequence Homology adenovirus type 12 induces molecular mimicry due to homology?

Serologic Markers In Celiac Disease MarkerSensitivitySpecificity Anti-gliadin31-100%85-100% Anti-reticulin42-100%95-100% Anti-endomysium60-100%95-100% Tissue Transglut % 92-97%

Schuppan D. Gastroenterol 2000:119; Ugh - immunology

Schuppan et al. Gastro 2009;137: Pinier et al, Am J Gastroenterol 105: ;2010

Normal on the right versus too many IELS on the left This is the Marsh 1 lesion

Marsh 1 = Nl villi with too many IELs

How many IELs are abnormal? >25/100 epithelial cells – new threshold for flat biopsies >40/100 epithelial cells – old threshold for flat biopsies >12/20 epithelial cells on the tips of villi (for Marsh 1) –Decrescendo pattern is normal –Diffuse pattern is abnormal –Goldstein Am J Clin Pathol 116;63-71,2001 >8/20 epithelial cells in the tips of villi (for Marsh 1) –CD3 stains –Biagi et al J Clin Pathol 57; , 2004

CD3 stain highlighting a Marsh 1 lesion Don’t get this stain unless you are used to what it looks like in a normal biopsy!

But what does it all mean? 2-3 % of small bowel biopsies have normal architecture with increased IELs Depending on the type of study and the country the study was carried out in, anywhere from 9 to 40% of such cases represent (pre) celiac disease. –Whether such patients need any therapy is controversial Brown I,et al. Arch Pathol Lab Med 130; , 2006

Normal Architecture Increased IELs Gluten Sensitive Enteropathy –Early type 1 lesion or treated sprue Other food hypersensitivity H. Pylori (usually only in bulb) Autoimmune conditions (RA, SLE, MS, Graves, Hashimoto’s, Diabetes) Post-infection Drugs (NSAIDs, PPIs??) Bacterial Overgrowth Obesity Crohn’s disease and Ulcerative colitis

Results Other Diagnoses: Graft versus Host Disease, Combined Variable Immunodeficiency, Diabetes mellitus 1, Juvenile Rheumatoid Arthritis, Systemic Lupus Erythematosis, Tropical Sprue, Ulcerative Colitis

Celiac Disease Complications Refractory Celiac Disease Ulcers of Small Bowel Collagenous Sprue Malignancy –T cell Lymphoma of gut and regional nodes –Adenocarcinoma of small bowel –Squamous cell carcinoma of esophagus and oropharynx

Refractory Celiac Disease Develops in about 5% of celiac patients –Malabsorption, diarrhea, pain, wt loss Divided into types I and II Type I RCD: IELs are normal / not clonal –better prognosis –Can progress to Type II Type II RCD: IELs are aberrant / clonal –50% mortality rate

Refractory Celiac Disease IELs in Celiac disease and type I RCD are CD3 + and CD8 + IELs in type II RCD are CD3 + and CD8 - –Will have T-cell gene rearrangements –Will also loose staining for T-cell receptor αβ

Loss of CD8 in type 2 refractory sprue CD3CD8

Collagenous Sprue

LYMPHOMA IN CELIAC DISEASE

EATCL with lots of eos

Celiac Disease Histologic Mimics Celiac-related –Lymphoma (EATCL) –Collagenous Sprue Other luminal antigens other than gluten/gliadin –Soy protein General –Peptic duodenitis* = most commonly mis dxed as sprue –Tropical Sprue, Bacterial overgrowth –Autoimmune enteropathy –Infections/immunodeficiencies –Crohn’s disease

Looks like sprue, but this is peptic duodenitis – no IELs

Peptic Duodenitis with polys instead of IELS

More peptic duodenitis Note gastric metaplasia