Active colitis, mild to moderate
62 year old F with diarrhea.
62 year old F with diarrhea.
Clinical summary
42 yo M with cecal tumor.
48 yo M with jaundice. Whipple
MICROSCOPIC FEATURES
• In adults, usually a nonspecific pattern of chronic hepatitis and cirrhosis
• Eosinophilic hyaline globules can be seen on H+E, predominantly in periportal hepatocytes
• Portal inflammation is variable (predominantly lymphocytic), and interface hepatitis usually mild or absent
• Bile ductular reaction seen only in endstage disease
• In neonates, there may be a picture of neonatal hepatitis, with canalicular cholestasis, giant cell transformation, ballooned hepatocytes, and loss of bile ducts
Read more on Alpha-1 antitrypsin deficiency, cirrhotic stage…
79 year old with gastric tumor and long history of gastritis and duodenitis.
Asian male in his 40’s with jaundice
7 year old with history of previous polyps. F/U colonoscopy shows several new polyps as shown here. Has frequent nosebleeds!
MICROSCOPIC FEATURES
• Marked lymphoplasmacytic infiltrate in the lamina propria, with associated damage of the fundic glands (“lymphoepithelial lesions”)
• Loss of oxyntic glands (parietal and chief cells) may result in “antralization” of body/fundus
• Metaplasia (pyloric, intestinal, and pancreatic) may be seen
• Affects body/fundus but spares the antrum (vs. atrophic gastritis)
• Changes can be variable depending on severity and duration of disease
MISCELLANEOUS
MICROSCOPIC FEATURES
DIFFERENTIAL DIAGNOSIS
Female with dysphagia
Male with dysphagia
MICROSCOPIC FEATURES
• Nests of cells with neuroendocrine features (polygonal cells with round nuclei with “salt-and-pepper” chromatin and no nucleoli)
• The cytoplasm is eosinophilic or amphophilic, and may contain granules
• The cells are monomorphic, and mitoses are rare
• The stroma is usually delicate and vascular but can become dense and fibrous
• May form tubules or acini, with PAS-positive luminal material
Female in her 30’s with iron deficiency anemia. Duodenal biopsy.
MICROSCOPIC FEATURES
• Numerous metaphase mitoses in crypt epithelium, especially “ring” mitoses
• There may also be epithelial pseudostratification, loss of goblet cell polarity, villus blunting, and increased apoptotic figures
DIFFERENTIAL DIAGNOSIS
55 y/o F with gallbladder polyp
34 year old M with diarrhea.
9 y/o M with iron deficiency anemia, weight loss, and diarrhea. Biopsy of distal esophagus
MICROSCOPIC FEATURES
• Marked expansion of portal tracts by lymphocytic infiltrates. The extent of the infiltrate is beyond what is seen in chronic viral hepatitis, where portal tracts tend to have a relatively tight “cuff” of inflammation around them.
• The lymphocytic infiltrate is sheet-like and monotonous, rather than mixed and with a follicle-like architecture, as is usually seen in chronic viral hepatitis. In some cases, the lymphoid cells may show atypia.
• There is no interface hepatitis at the edge of the infiltrate, and there are no apoptotic hepatocytes in the lobule
• There is no associated periportal fibrosis, as is usually seen with the inflammatory infiltrates of chronic viral hepatitis
18 year old F with diarrhea.
MICROSCOPIC FEATURES
• Portal tracts are expanded by a mixed lymphoid infiltrate, which focally extends into the lobules
• The infiltrate contains lymphocytes, plasma cells, eosinophils, and scattered Reed-Stenberg cells
• The infiltrate may also involve bile ducts
• Sinusoidal dilatation and peliosis hepatis may also be present
• Epithelioid granulomas are found in ~10% of cases, usually in the portal tracts
78 yo male with chronic watery diarrhea
65 year old with clinical picture of celiac disease, unresponsive to gluten-free diet.
MICROSCOPIC FEATURES
• Spindle cell proliferation infiltrating the lamina propria, with interspersed ganglion cells, sometimes forming nests
• There may be associated distortion of the crypt architecture
• In ganglioneuromatous polyposis (see below), multiple exophytic polyps are formed
• Diffuse ganglioneuromatosis (see below) is centered in the myenteric plexus and extends into the lamina propria, and can lead to transmural involvement and stricture formation
50 year old with history of multiple skin lesions. Polyp found on routine colonoscopy.
19 yo with small intestinal obstruction. Ileal mass was surgically removed
MICROSCOPIC FEATURES
• Marked lymphoid follicular hyperplasia, with prominent germinal centers, and chronic inflammation of the lamina propria
• Variable crypt inflammation and architectural distortion
• Aphthous ulcers may develop
DIFFERENTIAL DIAGNOSIS
Read more on Diversion colitis, with superimposed ulcerative colitis…
Female in her 40’s with abnormal LFTs.
MICROSCOPIC FEATURES
• Cords, nests, or single tumor cells embedded in myxoid matrix, with variable sclerosis and calcification
• Tumor cells may be dendritic (spindle- or stellate-shaped) or epithelioid, and have intracytoplasmic vascular lumina that may contain erythrocytes. These spaces should not be mistaken for signet-ring cells or glandular spaces
• Often multifocal or composed of confluent nodules
• At the edge, the tumor spares portal tracts and spread along sinusoids, causing atrophy of liver plates, and eventually obliterating central veins
MICROSCOPIC FEATURES
• Nests of large polygonal cells, with abundant eosinophilic granular cytoplasm, separated by fibrous stroma
• The fibrous stroma is composed of thick, hyalinized bundles of collagen, arranged in parallel lamellae
• Cells may have cytoplasmic hyaline globules (containing alpha1-antytripsin), “ground glass”-like pale bodies (containing fibrinogen), Mallory’s hyalin, and bile
• Nuclei are large, hyperchromatic, and vesicular, with prominent nucleoli, but mitoses are uncommon
64 yo M with Barrett’s esophagus. Esophageal biopsy.
Cholecystectomy
22 y/o female with stomach ache
55 y/o M with polyp
MICROSCOPIC FEATURES
• Giardia lamblia trophozoites (pear-shaped organisms, sometimes with two nuclei) seen on the luminal surface, with no tissue invasion
• Usually normal-appearing intestinal mucosa, but can sometimes see villous blunting, and a mixed inflammatory infiltrate in the lamina propria (neutrophils, lymphocytes, and plasma cells)
Male in his 30’s, s/p bone marrow transplant. Liver biopsy.
Female in her 30’s with an esophageal ulcer. Esophageal biopsy.
MICROSCOPIC FEATURES
• Non-caseating epithelioid granulomas in association with features of H. pylori gastritis (see below)
• Diffuse superficial chronic inflammation
• Neutrophils present at the neck region (“pititis”)
• Large lymphoid follicles may be present
• Regenerative epithelial changes with foveolar hyperplasia
• Proliferation of bland-appearing hepatocytes arranged in cords, without portal tracts or biliary epithelium
• Abnormal-appearing arteries (“unpaired arteries”) and thin-walled vessels are scattered throughout the tumor
• Cells may form pseudorosettes around canaliculi, but not acini
• Cells often contain fat or glycogen, so that the lesion looks paler than adjacent normal liver
• Bile production, hyaline globules, megamitochondria, and Mallory’s hyaline may be present
• May occasionally display focal mild atypia (especially when associated with androgenic steroid use) but mitoses are almost never seen
• May show various degenerative changes: evidence of prior hemorrhage; sinusoidal dilatation; large blood-filled (pelioid) spaces; myxoid stroma; fibrosis; necrosis; infarction
• Usually solitary but can be multi-focal; when >10, sometimes referred to as adenomatosis
MICROSCOPIC FEATURES
• Composed of blood-filled spaces lined by a single layer of bland endothelium
• Contains variable amounts of fibrous stroma
• Vascular spaces may contain organizing fibrin or thrombi
• May undergo various degenerative changes with time, such as sclerosis, calcification, and involution
MICROSCOPIC FEATURES
• Non-caseating epithelioid granulomas centered in portal tracts
• Lymphoplasmacytic “cuff” of inflammation surrounding granulomas
• Necrosis is uncommon, and tuberculomas are very rare
• Hepatic parenchyma is otherwise fairly normal in appearance