Normal Lab Values

Gastrointestinal Tract - Readings from Robbins Basic Pathol, 10th ed. (equivalent readings in 9th ed in parentheses)

by TUESDAY
by THURSDAY
 
 
pages
topics
pages
topics
 
Lab Sections 1, 2, and 3
pp 583 - 607
(9e: 551 - 573)
Ch 14 intro - GI Stromal Tumors

pp 573 - 576

Intestinal Obstruction - Hemorrhoids
 
 
pp 611 - 620
(9e: 576 - 587)
Diarrheal diseases - Sigmoid Diverticulitis
pp
587 - 601
Inflammatory Bowel Disease - Ch 14 end
 
           
Lab Sections 4 and 5

pp 607 - 610
(9e: 573 - 576)

Intestinal Obstruction - Hemorrhoids
pp
551 - 573
Ch 14 intro - GI Stromal Tumors
 
 
pp 620 - 635
(9e: 587 - 601)
Inflammatory Bowel Disease - Ch 14 end
pp 576 - 587
Diarrheal diseases - Sigmoid Diverticulitis
 
           

Case assignments by lab group and class day:

  TUESDAY THURSDAY
Labs 1, 2, & 3
Labs 4 & 5

 

CASE NUMBER 129
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Clinical History: A 70-year-old man was referred to a gastroenterologist due to a six-month history of slowly worsening dysphagia. Esophagogastroduodenoscopy was performed and revealed a friable, necrotic, ulcerated mass. An esophagectomy was performed.

 

129-1. What is the differential diagnosis?

ANSWER 

 

Image Gallery:

(Summary of Gross Findings)
The resected esophagus contained a firm, raised, pink-gray, friable and necrotic 3.5 x 4.5 cm tumor mass, completely encircling the esophagus and producing a marked stenosis.
(Summary of Microscopic Findings)
At one end of the section the squamous epithelium of the esophagus shows marked atypia, pleomorphism and loss of polarity, but no submucosal invasion. These changes represent carcinoma in situ. By following the mucosal lining, one comes upon an area where the cords and nests of poorly differentiated squamous cells are seen to invade the mucosa and submucosa reaching the muscular layer. At one margin of the section the tumor cells are better differentiated with production of keratin and formation of so-called epithelial pearls. Associated with the tumor are marked fibrous proliferation and intense chronic inflammatory infiltration in the stroma. The tumor invades into, but not through the muscularis externa.
(Review Normal Histology)
Slide UCSF 226 (esophagus, H&E) WebScope ImageScope
Slide UMich 126 40x (trachea & esophagus, H&E) WebScope ImageScope
Slide UMich 153 20x (esophagus, H&E) WebScope ImageScope
Slide UMich 155 40x (gastro-esophageal junct, H&E) WebScope ImageScope

For the purpose of histological descriptions, the esophagus is subdivided into upper (entirely skeletal muscle in the muscularis externa), middle (mixed smooth and skeletal muscle) and lower (entirely smooth muscle) portions. Slide UCSF 226 is from the upper 1/3; slides 126 and 153 are from the middle 1/3; and slide 155 is from the lower 1/3 (at the esophageal-cardiac junction). The esophageal epithelium [example] is the non-keratinized stratified squamous type and is supported by a connective tissue lamina propria. Note the presence of isolated lymphoid nodules [example] and scattered leukocytes in the lamina propria. A rather thick layer of longitudinally arranged smooth muscle fibers form the muscularis mucosae [example]. The connective tissue of the submucosa consists of mostly collagenous fibers with some elastic fibers and varying amounts of fat as well as submucosal sero-mucous glands which can be readily observed in both slide 126 [example] and slide 153 [example] (those in slide 155 are not very well preserved).

In the upper esophagus, as shown in Slide UCSF 226, the muscularis externa consists of both inner and outer layers of skeletal muscle only. In the middle esophagus, the muscularis externa contains a mixture of skeletal and smooth muscle as seen in slide 126 [example], whereas in the lower esophagus only smooth muscle is found as seen in slide 155 [example]. Present in all regions of the esophagus (upper, mid, and lower) is the myenteric (Auerbach’s) plexus [example] between the two layers of the muscularis externa (W pg 267, 14.3). For most of its extent, the esophagus is retroperitoneal, so its outermost layer consists of a connective tissue adventitia which merges with the adjacent connective tissue associated with nearby structures (such as the trachea as shown in slide 126). Below the diaphragm, however, the esophagus is suspended within abdominal cavity and is therefore covered by a connective tissue serosa as shown in slide 155.

129-2. Which of the following is the most significant risk factor for developing this disease?

  1. Alcohol and tobacco use
  2. Barrett esophagus
  3. Gastroesophageal reflux disease
  4. Helicobacter pylori infection
  5. PTEN mutation

ANSWER

 

129-3. Intestinal metaplasia (Barrett esophagus) at the gastroesophageal junction is most closely associated with which of the following esophageal lesions?

  1. Adenocarcinoma
  2. Eosinophilic esophagitis
  3. Esophageal varices
  4. Squamous cell carcinoma
  5. Squamous papilloma

ANSWER

 

CASE NUMBER 253
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Clinical History: A 60-year-old woman was referred to a gastroenterologist due to a one-year history of weight loss with new onset abdominal pain. Physical exam revealed occult blood present in her stool. Upper endoscopy showed a fungating, ulcerated mass in the gastric antrum and the patient underwent a partial gastrectomy. Gross and microscopic images are provided.

 

253-1. What is the differential diagnosis?

ANSWER

 

Image Gallery:

(Summary of Gross Findings)
The resected portion of the stomach showed a large fungating, partially ulcerated tumor mass in the antrum. Regional lymph nodes and a liver biopsy were free of tumor.
(Summary of Microscopic Findings)
There is a rather abrupt change of the normal stomach mucosa to malignant tumor tissue, projecting into the lumen as a cauliflower-like mass. The tumor forms abundant irregular acini, lined by one or more layers of atypical cells with mostly large irregular nuclei and poorly defined eosinophilic cytoplasm. Atypical mitoses are moderately frequent. The tumor has infiltrated through the muscularis mucosa and the edematous submucosa and has invaded the muscle layers. The invading tumor had elicited a rather marked neutrophilic and plasma cell response.
(Review Normal Histology)
Norm No. 16 Stomach, fundus
Slide UCSF 242 40x (pyloro-duodenal junction, H&E) WebScope ImageScope
Slide UMich 162 40x (pyloro-duodenal junct, H&E) WebScope ImageScope

In these slides, you can see the transition from pylorus of the stomach to duodenum of the small intestine. The pyloric region of the stomach is characterized by a thick wall due to the presence of the pyloric sphincter muscle [example], which is comprised primarily of the inner circular layer of the muscularis externa. Compare its wall thickness with that of the adjacent duodenum (W pg 273, 14.15). The pyloric glands [example] at the base of each gastric pit [ORIENTATION] are also composed again of a mostly HOMOGENEOUS population of mucous cells that are similar in appearance to those in cardiac glands although the pits are much deeper compared to cardiac glands. Present, but not seen, are stem cells and endocrine cells. An occasional parietal cell may be also found. Note that the bases of the pyloric glands abut the muscularis mucosae whereas in the duodenum, you will see abundant glands (Brunner’s glands) DEEP to the muscularis mucosae (i.e. in the SUBMUCOSA).

 

253-2. Which of the following risk factors has the most significant association with this disease?

  1. Alcoholism
  2. Cigarette smoking
  3. Helicobacter pylori infection
  4. Nitrites from nitrates in food and water
  5. Ulcerative colitis

ANSWER

 

 

253-3. Germline mutations in which of the following genes are associated with development of this tumor?

  1. APC
  2. CDHI
  3. KRAS
  4. MAML2
  5. NOD2

ANSWER

 

 

253-4. Infection with which of the following is associated with the development of this disease?

  1. Candida albicans
  2. Epstein-Barr virus
  3. Escherichia coli O157:H7
  4. Herpes simplex virus type 1
  5. Human papillomavirus

ANSWER

 

 

253-5. Metastasis of this tumor to a supraclavicular lymph node is called which of the following?

  1. Horner syndrome
  2. Krukenberg tumor
  3. Pancoast tumor
  4. Sister Mary Joseph nodule
  5. Virchow node

ANSWER

 

 

 

CASE NUMBER 10

Clinical History: A 73-year-old woman who lives in a nursing home is brought to her primary care physician with a 3-day history of fever and mild confusion. She is quite debilitated at baseline, and she has a chronically indwelling bladder catheter for urinary incontinence. One week ago, she was treated for a catheter-associated urinary tract infection with documented clearance of her pyuria. She has no respiratory symptoms, but she reports mild, diffuse abdominal pain and diarrhea (4 loose, non-bloody stools daily). A colonoscopy was performed.

 

10-1. What is the differential diagnosis?

ANSWER

Image Gallery:

Summary of Endoscopic Findings)
Pseudomembranes are present.
 

 

 

Clinical History (continued): The patient died of unrelated causes. A section of colon is provided for your review.

Virtual Slide and Image Slide Gallery (slide courtesy of the University of Leeds):
Slide 237042: [ImageScope] [WebScope]

(Summary of Gross Findings)
Yellowish plaques/pseudomembranes are scattered across the mucosal surface.
(Summary of Microscopic Findings)
There is acute colitis with a mucopurulent exudate that appears to be “erupting” from the crypts. There is karyorrhectic and neutrophilic debris in a linear distribution above the crypts. Superficially, there is necrosis and dilation of the crypts with areas of epithelial denudation. Areas of normal epithelium have an overlying pseudomembrane.
(Review Normal Histology)
Norm No. 16 Stomach, fundus
Slide UCSF 242 40x (pyloro-duodenal junction, H&E) WebScope ImageScope
Slide UMich 162 40x (pyloro-duodenal junct, H&E) WebScope ImageScope

In these slides, you can see the transition from pylorus of the stomach to duodenum of the small intestine. The pyloric region of the stomach is characterized by a thick wall due to the presence of the pyloric sphincter muscle [example], which is comprised primarily of the inner circular layer of the muscularis externa. Compare its wall thickness with that of the adjacent duodenum (W pg 273, 14.15). The pyloric glands [example] at the base of each gastric pit [ORIENTATION] are also composed again of a mostly HOMOGENEOUS population of mucous cells that are similar in appearance to those in cardiac glands although the pits are much deeper compared to cardiac glands. Present, but not seen, are stem cells and endocrine cells. An occasional parietal cell may be also found. Note that the bases of the pyloric glands abut the muscularis mucosae whereas in the duodenum, you will see abundant glands (Brunner’s glands) DEEP to the muscularis mucosae (i.e. in the SUBMUCOSA).

10-2. Which of the following tests would be most helpful in confirming the diagnosis?

  1. Antigen analysis of stool
  2. Assay for fecal leukocytes
  3. Oil red O stain
  4. Small intestinal biopsy
  5. White blood cell count

ANSWER

 

 

Clinical history, part 2 (click here to open)

 

 

CASE NUMBER 111 (slide courtesy of UMich)
[ImageScope] [WebScope]

Clinical History: A 31-year-old woman with a ten-year history of bloody diarrhea that was adequately managed by immunosuppressant therapy presented to her primary care physician with worsening symptoms. She underwent a partial colectomy. Gross and microscopic images are provided.

 

111-1. What is the differential diagnosis?

ANSWER

Image Gallery:

(Summary of Gross Findings)
The mucosa showed an area of edema and hyperemia distally. This was sharply demarcated from the remainder of the colon. A superficial mucosal lesion was noted.
(Summary of Microscopic Findings)
This section shows fulminant ulcerative colitis with areas of ulceration extending into the submucosa and also some areas of hemorrhage. While deep ulceration is seen, there is no fissuring necrosis, fibrous expansion of the submucosa, or transmural chronic inflammation, which differentiates this lesion from Crohn disease. The base of the ulcerated areas is covered by necrotic debris and fibrinopurulent or sanguinous exudate. Glands are distorted in shape and lined by regenerating epithelium. There are rare crypt abscesses and focal cryptitis.
(Review Normal Histology)
Norm No. 27 Colon
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The colon is lined by glandular epithelium with numerous mucin secreting goblet cells. The epithelium is infolded into straight tubular glands of uniform diameter to increase the surface area available for secretion and absorption.

 

111-2. Which of the following findings is most supportive of this diagnosis?

  1. Noncaseating granulomas
  2. Perianal fistula
  3. Rectal disease progressing proximally
  4. Strictures
  5. Transmural inflammation

ANSWER

 

 

111-3. Which of the following is more common in this disease than in other types of inflammatory bowel disease?

  1. Ankylosing spondylitis
  2. Erythema nodosum
  3. Migratory polyarthritis
  4. Primary sclerosing cholangitis
  5. Uveitis

ANSWER

 

 

111-4. Which of the following is associated with partial relief of symptoms in patients with this disease?

  1. Ciprofloxacin
  2. Clostridium difficile infection
  3. Estrogen therapy
  4. Radiation
  5. Smoking

ANSWER

 

 

CASE NUMBER 133
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Clinical History: A 39-year-old man presented to his gastroenterologist with a one-day history of cramping, lower abdominal pain and bloating that he noticed about five hours after a meal.  He also reported bloody diarrhea. His clinical history is significant for an 8-year history of enteritis and a one-year history of a non-healing rectal fistula. Large bowel obstruction was suspected and he underwent a partial colon resection. Gross and microscopic images are provided.

 

133-1. What is the differential diagnosis?

ANSWER

 

Image Gallery:

(Summary of Gross Findings)
The colon showed extensive ulcerations separated by pedunculated areas of hypertrophic mucosa. The intestinal wall was swollen and edematous. The serosa was thickened with fibrous adhesions.
(Summary of Microscopic Findings)
There are broad areas of ulceration extendint into the submucosa. The surface of the ulcers is covered by fibrinopurulent exudate overlying granulation tissue. Neutrophils infiltrate glands in the adjacent mucosa, some of which are lined by regenerating epithelium. A few crypts are distorted in shape and crypt abscesses are present. These features differ little from those seen in ulcerative colitis (Case No. 111). However, this section also shows transmural chronic inflammation in the form of lymphoid aggregates and granulomatous inflammation.
(Review Normal Histology)
Norm No. 27 Colon
[ImageScope] [WebScope]

The colon is lined by glandular epithelium with numerous mucin secreting goblet cells. The epithelium is infolded into straight tubular glands of uniform diameter to increase the surface area available for secretion and absorption.

 

133-2. Which of the following is most commonly seen in this disease?

  1. Abundant pseudopolyps
  2. Rectal involvement
  3. Superficial ulceration
  4. Toxic megacolon
  5. Transmural inflammation

ANSWER

 

 

133-3. Which of the following is most accurate regarding colitis-associated neoplasia in patients with this disease?

  1. Degree of dysplasia is associated with extent of granuloma formation
  2. Incidence is greatest in patients with left-side only colitis
  3. Increased active disease is associated with lower risk
  4. Primary sclerosing cholangitis is associated with increased risk
  5. Risk increases sharply 5 years after disease initiation

ANSWER

 

 

CASE NUMBER 84
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Clinical History: A 64-year-old woman presented to her primary care physician with a six-month history of weakness and weight loss and recent onset colicky abdominal pain and distention. Physical exam revealed occult blood in her stool and a mass was palpated in the rectum. The patient underwent total colectomy. Gross and microscopic images are provided.

 

 

84-1. What is the differential diagnosis?

ANSWER

 

Image Gallery:

(Summary of Gross Findings)
A tumor was present 4 cm from the anus. It was hard and had completely surrounded the bowel, reducing the lumen to less than 0.5 cm in diameter. Small tumor implants were present over the peritoneum and mesentery nearby. No distant metastases were noted.
(Summary of Microscopic Findings)
The the lumen of the bowel can be recognized. Note the thickened bowel wall and masses of tumor surrounding fat. Under low power note the tendency in some areas toward a gland-like structure. There is considerable variation in nuclear staining, size and shape. In some areas clumps of tumor cells are in the midst of mucus which the tumor cells are producing. Note the relatively large amount of dense collagen which accompanies the tumor cells in the fat.
(Review Normal Histology)
Norm No. 27 Colon
[ImageScope] [WebScope]

The colon is lined by glandular epithelium with numerous mucin secreting goblet cells. The epithelium is infolded into straight tubular glands of uniform diameter to increase the surface area available for secretion and absorption.

 

84-2. Which of the following is the most important prognostic indicator for this disease?

  1. Depth of invasion
  2. Number of mitotic figures
  3. Presence of necrosis
  4. Tumor diameter
  5. Tumor site

ANSWER

 

 

84-3. Which of the following is the gene that is usually the first to be mutated in the adenoma-carcinoma progression?

  1. APC
  2. KRAS
  3. P53
  4. SMAD2
  5. Telomerase

ANSWER

 

 

84-4. Increased consumption of which of the following is associated with decreased risk of this disease?

  1. Alcohol
  2. Aspirin
  3. Coffee
  4. Red meat
  5. Saturated fats

ANSWER

 

 

84-5. Which of the following is the most common clinical presentation for a right-sided colonic adenocarcinoma?

  1. Constipation
  2. Cramping epigastric pain
  3. Diarrhea
  4. Iron deficiency anemia
  5. Nausea and vomiting

ANSWER


GI SYSTEM Review Items

Key Vocabulary Terms (click here to search any additional terms on Stedman's Online Medical Dictionary)

achalasia gastritis, chronic idiopathic necrotizing enterocolitis (NEC)
acute gastritis gastroesophageal reflux disease (GERD) odynophagia
adhesion Helicobacter pylori peptic ulcer
angiodysplasia hematemesis pernicious anemia
appendicitis, acute hematochezia Peutz-Jegher syndrome
atresia hemorrhoids Plummer-Vinson syndrome
Barrett esophagus hernia pseudomembranous colitis
carcinoid syndrome Hirschsprung disease pseudomyxoma peritonei
carcinoid tumor hypergastrinemia pyloric stenosis
chronic gastritis hyperplastic polyp reflux esophagitis
chronic inflammatory bowel disease inflammatory polyp Schatzki ring
Crohn disease intestinal metaplasia signet ring cell
Cushing ulcer intrinsic factor sprue (celiac, tropical, nontropical)
d-xylose absorption test intussusception steatorrhea
diarrhea ischemic enteritis or colitis stress ulcer
diverticulum juvenile polyp  superficial gastritis
dysentery Krukenberg tumor transmural inflammation
dysphagia linitis plastica tubular adenoma
dysplasia malabsorption ulcer
enterocolitis Mallory-Weiss syndrome ulcerative colitis
enterotoxin Meckel diverticulum villous adenoma
erosion Mediterranean lymphoma Virchow node
esophageal varices megacolon volvulus
esophagitis melena Whipple disease
gastritis, atrophic mucocele Zenker diverticulum
gastritis, autoimmune napkin ring lesion

LEARNING OBJECTIVES - Gastrointestinal Tract Pathology

Goal 1: Embryology of the Gut
Apply knowledge of the embryology of the foregut, midgut and hindgut to summarize the morphological features and clinical presentation of developmental anomalies.

Objective1.1: Congenital Disorders of the Gut
Outline the clinicopathological features of tracheoesophageal fistula, pyloric stenosis, intestinal atresia, and Hirschprung diseases.

 

Goal 2: Anatomy and Blood Supply of the Gut
Apply knowledge of the gross anatomy of the GI tract and hemodynamic principles to discuss vascular disorders.

Objective 2.1: Ischemic Disorders of the Gut
Outline the pathogenesis and clinicopathological features for common disorders of the GI tract that arise from hypoxia or ischemia.

 

Goal 3: Gastrointestinal Neoplasia
Apply knowledge of the molecular basis of neoplasia to explain the clinical presentation, inheritance risk, biologic behavior, morphologic appearance, classification, diagnosis, prognosis and targeted therapy of gastrointestinal neoplasms.

Objective 3.1: Precursors to Bowel Carcinoma
Outline the precursor lesions, risk factors, and hereditary cancer syndromes that lead to GI neoplasia.

Objective 3.2: Molecular Basis of Bowel Neoplasms
Summarize the molecular basis and clinicopathologic features, local and systemic, for esophageal cancer, gastric cancer, GI lymphoma, GIST, colon and anal cancer.

Objective 3.3: Esophageal Carcinoma
Describe the location of adenocarcinomas versus squamous cell carcinomas of the esophagus and list the major risk factors for each.

Objective 3.4 Gastric Polyps
Compare and contrast the different types of gastric polyps in terms of risk factors, etiology, clinical presentation, histologic findings, treatment and risk for malignant transformation.

Objective 3.5 Gastric Carcinoma
Compare and contrast the different types of gastric carcinoma in terms of risk factors, epidemiology, etiology, clinical presentation, histologic findings, prognosis and treatment.

Objective 3.6: Colonic Polyps
Describe the different types of polyps and the risk of developing cancer.

Objective 3.7: Colon Carcinoma
List the most important prognostic factors for colon cancer and explain why they are most important.

 

Goal 4: Features of Gastrointestinal Neoplasms
Apply knowledge of the gross anatomy of the GI tract and its blood supply to describe presenting signs and symptoms, and pattern of spread of gastrointestinal neoplasms.

Objective 4.1: Right- and Left-sided Colon Carcinoma
Distinguish between carcinomas arising in the left and right colon in terms of symptoms and morphology.

Objective 4.2: Staging of Colon Carcinoma
Describe how colon cancers are staged and list the common sites of metastases.

 

Goal 5: Immune-Related Disorders of the Bowel
Apply knowledge of immune system dysregulation to discuss specific immune-related disorders.

Objective 5.1: Inflammatory Bowel Disease
Compare and contrast the pathophysiology and clinicopathological features of inflammatory bowel disease.

Objective 5.2: Celiac Disease
Explain the pathophysiology of gliadin hypersensitivity (Celiac disease).

 

Goal 6: Malabsorption
Apply knowledge of gastrointestinal anatomy and physiology to summarize the clinicopathologic features, diagnostic criteria, and therapy of disorders presenting with malabsorption.

Objective 6.1: Pancreaticobiliary Causes of Malabsorption
Outline disorders of the pancreas and bile acid metabolism, and discuss how they lead to malabsorption.

Objective 6.2: Inflammatory Causes of Malabsorption
Explain how Celiac disease, sprue, gastroenteritis, and inflammatory bowel disease lead to malabsorption.

 

Goal 7: Bowel Infections
Apply knowledge of common pathogens and principles of immunity to describe the morphological features and clinical presentation of infectious diseases affecting immunocompetent and immunocompromised patients.

Objective 7.1: Bowel Infections
Compare the underlying mechanism and clinicopathologic features of GI tract involvement by common bacterial, fungal and parasitic pathogens.

Objective 7.2: Helicobacter Infection
Relate the clinicopathologic features of Helicobacter to chronic gastritis and ulcer formation.

 

Goal 8: Mechanical Disorders of Bowel
Apply knowledge of GI anatomy and physiology to explain the clinicopathologic features, diagnostic criteria and therapy of disorders resulting in acid reflux, abnormal GI motility and gastrointestinal tract obstruction.

Objective 8.1: Dysphagia
Describe the pathophysiology and clinicopathological features of disorders presenting with dysphagia.

Objective 8.2: Bowel Obstruction
Compare and contrast the pathophysiology of gastrointestinal disorders that present with GI obstruction.

Objective 8.3: Diverticulosis
Describe the complications of diverticulosis.

 

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