49,006
edits
m (→Images: altered image notation) |
(→Fulminant hepatic necrosis: split out) |
||
(10 intermediate revisions by 2 users not shown) | |||
Line 307: | Line 307: | ||
==Autoimmune hepatitis with obstruction - combined changes== | ==Autoimmune hepatitis with obstruction - combined changes== | ||
A. [[File:1 AIH OBS 1.tif|Low power shows inflammation; portal triads, lobules, central veins cannot be distinguished (40X).]] | |||
[[File:1 AIH OBS 1.tif|Low power shows inflammation; portal triads, lobules, central veins cannot be distinguished (40X). | |||
<br> | <br> | ||
[[File: | B. [[File:2 AIH OBS 1.tif|Trichrome shows central venous sclerosis (red arrowhead), periportal fibrosis (green arrowhead), & space of Disse collagenization (yellow arrowhead); juxtaposition of central vein & portal tract indicates collapse, no definite bridging was seen (100X)]] | ||
<br> | <br> | ||
[[File:5 AIH OBS 1.tif|Proliferating bile ductules (blue arrows) with occasional neutrophils (fucsia arrows), indicative of obstruction, but not acute cholangitis, which requires inflamed bile duct itself, best diagnosed with associated blood vessel (400X).]] | C. [[File:3 AIH OBS 1.tif|Central vein is inflamed with a rare plasma cell (cyan arrowhead) (400X).]] | ||
[[File:6 AIH OBS 1.tif|Rare distorted rosettes with greenish brown strands of bile (left arrow) or bile plugs (right arrow) (400X).]] | <br> | ||
D. [[File:4 AIH OBS 1.tif|Interface hepatitis with plasma cells (yellow arrows) and ballooned hepatocytes (red arrows). Lobule is disorganized (400X).]] | |||
Patient with SLE and obstructive jaundice that resolved with apparent passage of stone. Low power shows inflammation; portal triads, lobules, central veins cannot be distinguished | <br> | ||
E. [[File:5 AIH OBS 1.tif|Proliferating bile ductules (blue arrows) with occasional neutrophils (fucsia arrows), indicative of obstruction, but not acute cholangitis, which requires inflamed bile duct itself, best diagnosed with associated blood vessel (400X).]] | |||
<br> | |||
F. [[File:6 AIH OBS 1.tif|Rare distorted rosettes with greenish brown strands of bile (left arrow) or bile plugs (right arrow) (400X).]] | |||
<br> | |||
Patient with SLE and obstructive jaundice that resolved with apparent passage of stone. A. Low power shows inflammation; portal triads, lobules, central veins cannot be distinguished. B. Trichrome shows central venous sclerosis (red arrowhead), periportal fibrosis (green arrowhead), & space of Disse collagenization (yellow arrowhead); juxtaposition of central vein & portal tract indicates collapse, no definite bridging was seen. C. Central vein is inflamed with a rare plasma cell (cyan arrowhead). D. Interface hepatitis with plasma cells (yellow arrows) and ballooned hepatocytes (red arrows). Lobule is disorganized. E. Proliferating bile ductules (blue arrows) with occasional neutrophils (fucsia arrows), indicative of obstruction, but not acute cholangitis, which requires inflamed bile duct itself, best diagnosed with associated blood vessel. F. Rare distorted rosettes with greenish brown strands of bile (left arrow) or bile plugs (right arrow). | |||
==Autoimmune hepatitis-primary biliary cirrhosis overlap syndrome== | ==Autoimmune hepatitis-primary biliary cirrhosis overlap syndrome== | ||
Line 331: | Line 333: | ||
===Microscopic=== | ===Microscopic=== | ||
:See: ''[[autoimmune hepatitis]]'' and ''[[primary biliary cirrhosis]]''. | :See: ''[[autoimmune hepatitis]]'' and ''[[primary biliary cirrhosis]]''. | ||
A. [[File:1 AIH PBC 1 680x512px.tif|Expanded portal tracts with fuzzy edges (40X).]] | |||
[[File:1 AIH PBC 1 680x512px.tif|Expanded portal tracts with fuzzy edges (40X).]] | <br> | ||
[[File:2 AIH PBC 1 680x512px.tif|Interface hepatitis with plasma cells (400X).]] | B. [[File:2 AIH PBC 1 680x512px.tif|Interface hepatitis with plasma cells (400X).]] | ||
<br> | |||
C. [[File:3 AIH PBC 1 680x512px.tif|Loose granuloma (400X).]] | |||
<br> | |||
D. [[File:4 AIH PBC 1 680x512px.tif|Damaged bile duct (400X).]] | |||
<br> | <br> | ||
AIH/PBC overlap. AMA & ANA positive with Alkaline phosphatase > 2 upper limit of normal & one ALT > 5 times upper limit of normal. A. Expanded portal tracts with fuzzy edges. B. Interface hepatitis with plasma cells. C. Loose granuloma. D. Damaged bile duct. | |||
AIH/PBC overlap. AMA & ANA positive with Alkaline phosphatase > 2 upper limit of normal & one ALT > 5 times upper limit of normal. Expanded portal tracts with fuzzy edges | |||
==Primary sclerosing cholangitis== | ==Primary sclerosing cholangitis== | ||
Line 384: | Line 386: | ||
=Other= | =Other= | ||
==Primary Systemic Sclerosis== | |||
[[File:5 05168051 sl 1.png |Primary systemic sclerosis in the liver]] | |||
[[File:5 05168051 sl 2.png |Primary systemic sclerosis in the liver]] | |||
[[File:5 05168051 sl 3.png |Primary systemic sclerosis in the liver]] | |||
[[File:5 05168051 sl 4.png |Primary systemic sclerosis in the liver]] | |||
[[File:5 05168051 sl 5.png |Primary systemic sclerosis in the liver]] | |||
[[File:5 05168051 sl 6.png |Primary systemic sclerosis in the liver]] | |||
<br> | |||
Primary systemic sclerosis in a 67 year old White, non-Hispanic man who had undergone renal transplantation for idiopathic nodular glomerusclerosis, which had recurred in 2013. He had been scheduled to receive a second transplantation, but had not yet received one. The patient had a positive anti-nuclear antigen study, with a positive scleroderma antibody (SCL-70), a high SCL-70 antibody index of 3.9, and negative DNA, Chromatin, Anti-Riboscomal P, SS-A, SS-B, anti Smith, RNP, JO-1, anticentromere antibody and rheumatoid factor serologic studies. Hepatitis A, B, and C serologic studies were negative. Liver function tests showed normal albumin and total bilirubin levels with alkaline phosphatase of 712 IU/L (35-129 normal range), alanine aminotransferase 59 IU/L (5-41 normal range), and aspartate aminotransferase 68 IU/L (5-37 normal range). This case provisions many of the features known to be present in primary systemic sclerosis as seen in the skin. A. At low power, triads appear almost as white ghosts against a relatively normal set of hepatocyte lobules. B. Closer examination reveals some triads to be expanded, with peripheral bile ductular proliferation and modest associated chronic inflammation without interface hepatitis. C. Portal arterioles had thick walls; inflammation included lymphocytes and occasional plasma cells. D. Trichrome failed to stain the material in the triads blue, but did show space of Disse collagenization. E. PAS with diastase showed positive staining of the material with emphasis on the arteriole walls. F. Hemosiderosis was seen on iron stain. | |||
==Budd-Chiari syndrome== | ==Budd-Chiari syndrome== | ||
*[[AKA]] ''hepatic vein obstruction''. | *[[AKA]] ''hepatic vein obstruction''. | ||
Line 434: | Line 447: | ||
*[[CK7]] -ve. | *[[CK7]] -ve. | ||
**Marks bile ducts. | **Marks bile ducts. | ||
==Hepatic Graft versus Host Disease (L-GVHD)== | |||
[[File:3 579232643 sl 1.png| Hepatic graft versus host disease (L-GVHD)]] | |||
[[File:3 579232643 sl 2.png| Hepatic graft versus host disease (L-GVHD)]] | |||
[[File:3 579232643 sl 3.png| Hepatic graft versus host disease (L-GVHD)]] | |||
[[File:3 579232643 sl 4.png| Hepatic graft versus host disease (L-GVHD)]] | |||
[[File:3 579232643 sl 5.png| Hepatic graft versus host disease (L-GVHD)]] | |||
[[File:3 579232643 sl 6.png| Hepatic graft versus host disease (L-GVHD)]] | |||
[[File:3 579232643 sl 7.png| Hepatic graft versus host disease (L-GVHD)]] | |||
<br> | |||
Hepatic graft versus host disease (L-GVHD) in a 22 yo man who underwent bone marrow transplantation after developing ALL. A. Low power view shows brownish discoloration in triad, but is otherwise of little interest. B. Arterioles in triads were accompanied by bile ducts in only 30% of cases; this image shows an arteriole without a bile duct. Note the pigment and the accompanying macrophage/lymphocyte inflammation, not extreme. The added chronic inflammation is a feature of chronic L-GVHD. C. Bile ducts, when shown, showed extensive damage, here seen as loss of cytoplasm, and nuclear pleomorphism and hyperchromasia (other degenerative changes, not seen here, include nuclear dropout or necrosis, cytoplasmic eosinophilia, loss of duct lumen). Lymphocytosis into the ducts was not seen. D. Ballooned hepatocytes and dilated canaliculi were seen. E. Pigment was present, but mostly in Kupffer cells, not hepatocytes or as bile plugs. F. Up to two foci of spotty necrosis were seen in a 100X field (field shown is 200X); not shown are rare apoptotic hepatocytes. G. An iron stain showed the pigment represented extemsive iron deposition, with emphasis on Kupffer cells and portal triad macrophages, frustrating definite assessment of bile plugs in canaliculi. The hemosiderosis resulted from the many blood transfusions the patient had received. | |||
==Extrahepatic biliary obstruction== | ==Extrahepatic biliary obstruction== | ||
A. [[File:1 OBS 3 680x512px.tif|Sinusoidal dilatation, circular spaces of hepatocytes, small portal triads(40X).]] | |||
[[File:1 OBS 3 680x512px.tif|Sinusoidal dilatation, circular spaces of hepatocytes, small portal triads(40X).]] | <br> | ||
[[File:2 OBS 3 680x512px.tif|Bile in hepatocytes about central vein & in plugs in canaliculi [yellow arrowhead] (400X).]] | B. [[File:2 OBS 3 680x512px.tif|Bile in hepatocytes about central vein & in plugs in canaliculi [yellow arrowhead] (400X).]] | ||
<br> | |||
C. [[File:3 OBS 3 680x512px.tif|Trichrome shows fibrosis about central vein (400X).]] | |||
<br> | |||
D. [[File:4 OBS 3 680x512px.tif|PAS with diastase shows portal triads with mild edema and chronic inflammation, without tortuous bile duct (400X).]] | |||
<br> | |||
Early extrahepatic biliary obstruction, demonstrated radiographically, transient, with rise in bilirubin, alkaline phosphatase, and transaminases. Pure canalicular cholestasis near terminal hepatic venules also seen in acute hepatitis, drug reactions, benign recurrent cholestasis, pregnancy, sepsis, & lymphomas. A. Sinusoidal dilatation, circular spaces of hepatocytes, small portal triads. B. Bile in hepatocytes about central vein & in plugs in canaliculi [yellow arrowhead]. C. Trichrome shows fibrosis about central vein. D. PAS with diastase shows portal triads with mild edema and chronic inflammation, without tortuous bile duct. | |||
<br> | <br> | ||
A. [[File:1 OBS 2 680x512px.tif|Expanded inflamed portal triads, swollen hepatocytes (40X)]] | |||
[[File:1 OBS 2 680x512px.tif|Expanded inflamed portal triads, swollen hepatocytes (40X | |||
<br> | <br> | ||
[[File: | B. [[File:2 OBS 2 680x512px.tif|Edematous stroma, proliferating ductules [yellow arrowheads], PAS-D macrophages [red arrowhead] (PAS with diastasse, 200X)]] | ||
<br> | <br> | ||
[[File:3 | C. [[File:3 OBS 2 680x512px.tif|Disordered, often swollen hepatocytes,some with feathery degeneration (net like spaces in cytoplasm [blue arrowhead], rare Councilman body [green arrowhead] (400X)]] | ||
<br> | <br> | ||
D. [[File:4 OBS 2 1360x1024px.tif|Bile in hepatocytes [cyan arrrowhead] & in canaliculi [purple arrowheads]. Empty acinar spaces bounded by hepatocytes [orange arrowhead] (400X, higher pixel),]] | |||
[[File: | |||
<br> | <br> | ||
Changes of extrahepatic biliary obstruction, months duration. A. Expanded inflamed portal triads, swollen hepatocytes. B. Edematous stroma, proliferating ductules [yellow arrowheads], PAS-D macrophages [red arrowhead]. C. Disordered, often swollen hepatocytes,some with feathery degeneration (net like spaces in cytoplasm) [blue arrowhead], rare Councilman body [green arrowhead]. D. Bile in hepatocytes [cyan arrrowhead] & in canaliculi [purple arrowheads]. Empty acinar spaces bounded by hepatocytes [orange arrowhead]. | |||
<br> | <br> | ||
A. [[File:1 Bd obs 4 680x512px.tif|Expanded, light colored portal triads (arrows)(20X).]] | |||
<br> | <br> | ||
B. [[File:2 Bd obs 4 680x512px.tif|Proliferating bile ductules (cyan arrows) with neutrophils (yellow arrows), not specific for acute cholangitis, of assistance with large bile duct obstruction (400X)..]] | |||
<br> | <br> | ||
C. [[File:3 Bd obs 4 680x512px.tif|Uninflamed interlobular duct (yellow arrow) with, accompanying blood vessel (red arrow) (400X)]] | |||
<br> | <br> | ||
D. [[File:4 Bd obs 4 680x512px.tif|Bile infarct with pyknotic nuclei (arrows)(400X).]] | |||
<br> | <br> | ||
E. [[File:5 Bd obs 4 680x512px.tif|Bile (arrow) in interlobular bile duct with disordered nuclei (400X).]] | |||
<br> | <br> | ||
F. [[File:6 Bd obs 4 680x512px.tif|Bile plugs in cannaliculi (red arrows), feathery degeneration producing foamy macrophage like hepatocytes (yellow arrows)(400X).]] | |||
<br> | <br> | ||
F. | Large bile duct obstruction. A. Expanded, light colored portal triads (arrows). B. Proliferating bile ductules (cyan arrows) with neutrophils (yellow arrows), not specific for acute cholangitis, of assistance with large bile duct obstruction. C. Uninflamed interlobular duct (yellow arrow) with, accompanying blood vessel (red arrow). D. Bile infarct with pyknotic nuclei (arrows). E. Bile (arrow) in interlobular bile duct with disordered nuclei. F. Bile plugs in cannaliculi (red arrows), feathery degeneration producing foamy macrophage-like hepatocytes (yellow arrows). | ||
==Congestive hepatopathy== | |||
{{Main|Congestive hepatopathy}} | |||
==Drug-induced liver disease== | ==Drug-induced liver disease== | ||
Line 616: | Line 602: | ||
==Peliosis hepatis== | ==Peliosis hepatis== | ||
{{Main|Peliosis hepatis}} | |||
{| | |||
Peliosis hepatis | |||
==Total parenteral nutrition== | ==Total parenteral nutrition== | ||
Line 677: | Line 644: | ||
Image:Hepatic_amyloidosis_-_very_high_mag.jpg | Amyloidosis of the liver - very high mag. (WC) | Image:Hepatic_amyloidosis_-_very_high_mag.jpg | Amyloidosis of the liver - very high mag. (WC) | ||
</gallery> | </gallery> | ||
A. [[File:1 AMY 1 680x512px.tif|Amorphous material replaces hepatic parenchyma [4X]]] | |||
[[File:1 AMY 1 680x512px.tif|Amorphous material replaces hepatic parenchyma [4X | |||
<br> | <br> | ||
[[File:3 AMY 1 680x512px.tif|Material stains red on unpolarized Congo Red [40X]]] | B. [[File:2 AMY 1 680x512px.tif|Material barely stains blue on trichrome [10X]]] | ||
[[File:4 AMY 1 680x512px.tif|Material stains apple green on polarized Congo Red [40X]]] | <br> | ||
C. [[File:3 AMY 1 680x512px.tif|Material stains red on unpolarized Congo Red [40X]]] | |||
Amyloidosis. Amorphous material replaces hepatic parenchyma | <br> | ||
D. [[File:4 AMY 1 680x512px.tif|Material stains apple green on polarized Congo Red [40X]]] | |||
<br> | |||
Amyloidosis. A. Amorphous material replaces hepatic parenchyma. B. Material barely stains blue on trichrome. C. Material stains red on unpolarized Congo Red. D. Material stains apple green on polarized Congo Red. | |||
===Stains=== | ===Stains=== | ||
Line 690: | Line 658: | ||
==Fulminant hepatic necrosis== | ==Fulminant hepatic necrosis== | ||
{{Main|Fulminant hepatic necrosis}} | |||
{| | |||
==Secondary hemochromatosis== | ==Secondary hemochromatosis== |
edits