national liver histopathology eqa scheme · 2010. 9. 1. · 1 hepatitis secondary to sle (only...
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National Liver Histopathology
EQA SchemeEQA Scheme
Circulation A1
December 2009
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Circulation A1, meeting 10.12.09
• Present were 30 members and 9 guests
• Of members present, 6 had been unable to view the slides
and send responses because the slides had not been sent to
them in time. If you have slides at a busy time, please send
straight on to the next person in your cell and inform Sophia, straight on to the next person in your cell and inform Sophia,
who will re-arrange the circulation.
• Responses with marks deducted are shown in brown italics in
the slides below, and explanation and discussion on the
following slide.
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Case 326
Female 76 years4 week history of painless jaundice.
Bili12umol/L, ALT 40iu/L, AP 349iu/L, alb 41g/l, GGT 498ui/L, negative for HBV, HCV,.
Bili12umol/L, ALT 40iu/L, AP 349iu/L, alb 41g/l, GGT 498ui/L, negative for HBV, HCV,.
Immunology: ANA 160, other serology negative (AMA, LKM etc.) IgG 23.4g/L (6-13) IgA 8.73g/L (0.8-3)
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326
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326
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326
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Responses
Morphology:
19 acute hepatitis
11 acute hepatitis with bridging or confluent necrosis
14 hepatitis
7 chronic active hepatitis
1 active hepatitis
Aetiology:
19 autoimmune hepatitis with no differential
25 autoimmune hepatitis most likely
25 differential includes drugs
10 differential includes viral hepatitis
326
1 active hepatitis
2 overlap autoimmune hepatitis/cholangitis
1 hepatitis secondary to SLE (only diagnosis)
1 autoimmune cholangitis (no mention of hepatitis)
34 any of above with specific mention of prominent plasma cells
10 differential includes viral hepatitis
5 autoimmune hepatitis among differential, not most likely
1 lupoid hepatitis, no differential
1 no mention of autoimmune hepatitis in differential
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Scoring and discussion.
Score 5 points for any answer including hepatitis except as indicated above. This case
showed confluent bridging necrosis which is an important indicator of severity and
should be included in the report. Chronicity requires connective tissue stains for
accurate evaluation, so points were not deducted for diagnoses of chronic disease,
although the consensus for this case was of acute disease. There were no
histological or clinical features to suggest overlap with biliary disease. Hepatitis is
rarely a component of the multisystem disease of SLE, and the serology given does
not point to SLE.
326
Prominent plasma cells are an important feature contributing to the overall clinical
diagnosis of autoimmune hepatitis and should be included in the report, but was
not included in the EQA scoring.
Aetiology: 5 points deducted for failure to include autoimmune in the diagnosis;
lupoid hepatitis is an old terminology, and may be misleading – the current
terminology is for a diagnosis of autoimmune hepatitis with additional comment
on severity of necrosis, interface activity and chronicity.
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Submitting pathologist’s diagnosis:
Autoimmune hepaititis with bridging fibrosis
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Follow up: after the biopsy the patient received prednisolone and
azathioprine, and the LFTs returned to normal, confirming the diagnosis of
autoimmune hepatitis.
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Case 327
Female 61 years
Unexpected cirrhosis at lap chole
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327
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327
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327
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327
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327
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327
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Responses
16 nodular regenerative hyperplasia as definite diagnosis
11 possible nodular regenerative hyperplasia
3 possible or definite cirrhosis, as morphological diagnosis
4 cirrhosis, likely clinical diagnosis despite not being confirmed by this biopsy
11 non-diagnostic biopsy, needs special stains
4 chronic biliary disease/obstruction
1 primary biliary cirrhosis
327
1 primary biliary cirrhosis
1 hepatoportal sclerosis
1 hyperplastic nodular process
1 no specific abnormality, fatty change only
1 lipogranulomas (as main diagnosis)
1 amyloid
2 iron overload and mild steatosisCase not scored
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Scoring and discussion:
This case had insufficient consensus for scoring.
The submitted and most popular diagnosis was nodular
regenerative hyperplasia. It was commented that
macronodular cirrhosis could not be completely excluded by
needle biopsy, and more clinico-pathological correlation was
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needle biopsy, and more clinico-pathological correlation was
required to reach a diagnosis in this case.
Submitting pathologist’s diagnosis:
Nodular regenerative hyperplasia
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Case 328
Female 53 years
Lateral left liver lobe cyst ?cystadenoma
Specimen: Lateral liver lobectomy
Macroscopic description: Partial hepatectomy
containing a unilocular cyst 100X85mm in containing a unilocular cyst 100X85mm in
which abundant red/brown material is present.
Background liver looks normal.
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328
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328
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328
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328
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328
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Responses
14 primary biliary cystic tumour, no differential diagnosis
17 biliary cystic tumour, differential diagnosis including
metastatic thyroid carcinoma
4 metastatic thyroid carcinoma with differential diagnosis
1 metastatic papillary carcinoma, differential pancreas, kidney,
lung, thyroid
328
lung, thyroid
14 metastatic thyroid carcinoma, no differential given but
immunohistochemistry requested
5 metastatic thyroid carcinoma, no immunos.
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Scoring and discussion
Discussion over whether there was sufficient consensus to
include scoring on this case. Members voted to accept
diagnoses that included the possibility of metastatic
carcinoma. The clear, overlapping nuclei of the papillary
tumour were very characteristic of papillary thyroid
carcinoma.
328
carcinoma.
Further information from submitting pathologist – this patient
had a thyroid FNA showing papillary carcinoma two weeks
before this surgery – there was a lack of communication of
this result between clinical teams. The tumour is
immunohistochemically positive for TTF.
Submitting pathologist’s diagnosis: metastatic papillary
carcinoma of the thyroid
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Case 329
Female 79 years
Presented with cholestatic liver function tests
with an ALP of 319. Known to have conjestive
cardiac failure. Liver screen normal. Not obese. cardiac failure. Liver screen normal. Not obese.
CT scan showed no evidence of biliary dilation
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329
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329
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329
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329
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Responses
30 amyloid, includes clinical comment about need for investigation of
cause
21 amyloid, no comment about clinical investigation
2 amyloid or light chain disease
1 cardiac cirrhosis, need to exclude amyloid, do congo red
1 pseudo-amyloidosis ? cause, not typical of cardiac cirrhosis or
amyloid.
329
amyloid.
Comment: several suggested cardiac failure may be due to cardiac
amyloid
Several commented on bilirubinostasis.
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Scoring and discussion
All responses scored 10.
Congo red confirmed the diagnosis of amyloid. There is no
indication of the type – immunohistochemistry for kappa and
lamda both positive. The patient did not survive long. The
possibility of cardiac involvement by amyloidosis was raised at
329
possibility of cardiac involvement by amyloidosis was raised at
the time, but was not further investigated.
Submitting pathologist’s diagnosis: hepatic amyloidosis
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Case 330
Female 47 years
Known ulcerative colitis, elevated alk phos.
?PSC/other pathology
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330
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330
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330
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330
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330
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330
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330
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Responses
34 venous outflow obstruction/Budd Chiari syndrome
1 veno-occlusive disease as only diagnosis
1 sinusoidal obstruction syndrome
1 obstructive portal venopathy
1 peliosis
1 portal vein thrombosis
2 nodular regenerative hyperplasia
1 sinusoidal obstruction suggestive of portal vein thrombosis
12 no mention of vascular abnormality
330
Of which: 9 PSC definite, or consistent with, as only diagnosis
1 ductopaenia, ?sclerosing cholangitis
1 minimal chronic hepatitis, PSC not excluded
1 description, no diagnosis,
1 PSC main diagnosis, ? recent viral hepatitis
2 PSC as secondary diagnosis
1 ? early PBC check autoantibodies
8 PSC possible, not excluded
18 specifically commented on absence of features of PSC
12 no mention of PSC
Case not scored
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Scoring and discussion
Case not suitable for scoring – too complicated.
This is a good example of the clinically important features of venous
outflow obstruction. The zone 3 hepatocyte loss and red cell
extravasation characteristic of Budd Chiari syndrome are well seen.
330
This led to imaging and pressure studies which confirmed the
diagnosis of Budd Chiari syndrome. The hepatic vein was stented
and the patient is on warfarin and remains well. ? evidence for PSC
as well??
Submitting pathologist’s diagnosis: Budd Chiari syndrome
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Case 331
Female 64 years
Haemochromatosis, 3 litres drained from
ascites
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331
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331
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331
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331
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331
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331
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Responses
54 cirrhosis
1 cirrhosis not mentioned
54 haemochromatosis
1 siderosis (not further qualified)
331
9 specifically commented on absence of
dysplasia/malignancy
7 also ? fatty liver disease
1 large cell dysplasia
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Scoring and discussion
Both cirrhosis and haemochromatosis needed to be included for
full marks.
Submitting pathologist’s diagnosis: cirrhosis, haemochromatosis
331
Submitting pathologist’s diagnosis: cirrhosis, haemochromatosis
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Case 332
Female 55 years
Liver resection for adenoma
Specimen: Liver resection
Macroscopic description: Nodular segment of Macroscopic description: Nodular segment of
liver measuring 3.8x2x1.8cm. on section
there was a multinodular lesion 2.2x2x.1.4cm
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332
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332
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332
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332
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Responses
52 focal nodular hyperplasia
1 FNH or FNH-like adenoma
1 benign liver adenoma
1 follicular nodular hyperplasia
332
1 follicular nodular hyperplasia
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Scoring and discussion
This case showed unequivocal characteristic features of a focal nodular
hyperplasia, including stellate fibrosis with thick walled artery,
ductular reaction and chronic inflammation.
Score 0 for adenoma or ‘FNH or FNH-like adenoma’ – this case did not
have the features of a telangiectatic FNH, the type of FNH which is
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have the features of a telangiectatic FNH, the type of FNH which is
now re-classified as an adenoma. Score 5 marks for ‘follicular
nodular hyperplasia’ – presumed a typographical error.
Submitting pathologist’s diagnosis:
Focal nodular hyperplasia
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Case 333
Female 34 years
Acute abnormal LFT’s. Increased IgG
(40).Positive ANA and SMA. Negative other
serology. Likely autoimmune hepatitis
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Responses
Morphology:
6 acute hepatitis
17 acute hepatitis with bridging/confluent necrosis
12 hepatitis,
4 acute on chronic hepatitis
10 chronic active hepatitis
4 chronic hepatitis
1 autoimmune hepatitis and cirrhosis
1 lupoid hepatitis
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1 lupoid hepatitis
37 specifically commented on prominence of plasma cells
Aetiology:
40 Autoimmune hepatitis as only diagnosis
9 autoimmune hepatitis as main diagnosis, with differential
1 lupoid hepatitis
4 autoimmune hepatitis/primary biliary cirrhosis overlap
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Scoring and discussion
For full marks, needed mention of activity of hepatitis, and of
autoimmune aetiology. Responses with chronic hepatitis or
cirrhosis without a comment on activity of disease were
deducted 5 marks. Lupoid hepatitis is obsolete terminology,
replaced by autoimmune hepatitis. There were neither
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replaced by autoimmune hepatitis. There were neither
histological or clinical features to suggest an additional
component of an overlap syndrome with PBC.
Submitting pathologist’s diagnosis: florid autoimmune hepatitis
with prominent confluent /submassive necrosis
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Case 334
Male 34 years
Hepatitis B positive. Fatty liver? Cause.
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Responses
3 Chronic hepatitis, NOS
18 chronic hepatitis, minimal
28 chronic hepatitis, mild
1 hepatitis B carrier
1 ‘hepatitis B infection’ – no mention of chronic hepatitis histologically
1 no portal or acinar inflammation
1 ‘no portal or parenchymal inflammation. No evidence of NASH or active hepatitis B hepatitis’
1 ‘no changes of active viral hepatitis’ (ground glass not mentioned)
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50 ground glass hepatocytes / hepatitis B mentioned
4 ground glass/hepatitis B not mentioned
45 steatosis, mild
1 steatosis, moderate
3 steatosis, NOS
1 no steatosis
1 steatohepatitis
1 micro and macrovesicular steatosis, ? drug
2 steatosis not mentioned
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Scoring and discussion
For full marks, responses needed to include the presence of
chronic hepatitis, ground glass hepatocytes, and steatosis.
Although mild there was sufficient portal inflammation in some
portal tracts to support a diagnosis of chronic hepatitis. The
clinical information queried fatty liver, and a comment on the
presence of steatosis was therefore required for full marks.
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presence of steatosis was therefore required for full marks.
There were no ballooned hepatocytes or other features of
steatohepatitis.
Submitting pathologist’s diagnosis: minimal chronic hepatitis B,
stage 0, no steatosis
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Case 335
Female 25 years
beta Thalassaemia. Increased ferritin
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Responses
51iron overload, pattern consistent with transfusion siderosis
3 iron overload NOS
1 no mention of iron
32 fibrosis present
13 no mention of fibrosis
1 ‘not yet cirrhosis’
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1 ‘not yet cirrhosis’
7 need connective tissue stain to assess fibrosis
33 extra-medullary haematopoiesis
1 ‘haemosiderosis and haemochromatosis, not established cirrhosis. HFE gene studies’
Few commented on need to exclude hepatitis C
Several - need HFE genetics as well?
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Scoring and discussion
Full marks for all responses including iron overload. The presence of fibrosis was not
scored, since this was considered to require connective tissue stains for evaluation.
There was evidence of extra-medullary haematopoiesis on the scanned slide
photographed, but it is unknown whether this was present on all slides, and
therefore was not required for full marks.
Discussion – it was presumed that the patient had iron overload following multiple
transfusions because of thalassaemia. The presence of extra-medullary
haematopoiesis supported this, as it implied insufficient bone marrow
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haematopoiesis supported this, as it implied insufficient bone marrow
haematopoises to keep pace with haemolysis from thalassaemia.
Clinicopathological discussion is required to confirm transfusions.
The distribution of iron in macrophages/Kupffer cells as well as hepatocytes can also
be seen in some inborn errors of iron metabolism e.g. ferropontin/ferroportin
deficiency. Specialist investigations for this are not currently available in the UK –
some members had sent samples to Italy for further investigation. Genetic tests
for haemochromatosis would only be indicated if the iron could not be explained
by multiple transfusions.
Submitting pathologist’s diagnosis: Grade 4 siderosis, Ishak stage 2 fibrosis. Extra-
mdullary haematopoieses, consistent with stated history.
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Case 336
Female 34 years
Non-anatomical resection. Previous partial
excision for simple cyst. This is completion
excision of remainder.
Specimen: Liver and gall bladder
Macroscopic description: A- liver cyst-the
specimen weighs 260 grams, comprising
previously opened thick walled unilocular cyst
13 cms in diameter, received in a collapsed
state without contents.
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Responses
42 hepatobiliary cystadenoma, with specialised/mesenchumal
stroma
7 hepatobiliary cystadenoma (no mention of stroma)
1 mucinous cystadenoma
1 benign biliary cyst, ? hamartomatous
1 solitary unilocular cyst, biliary epithelium
2 endometriotic cyst
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2 endometriotic cyst
1 adenofibroma or mucinous cystadenoma
24 granuloma/granulomatous hepatitis
27 no mention of granuloma
7 further medical investigations suggested for granulomatous
inflammation
Several attributed granuloma to previous surgery.
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Scoring and discussion
This cyst wall showed cellular stroma characteristic of
hepatobiliary cystadenoma.
Half the responses did not include mention of the granuloma in
the adjacent liver tissue; it is possible that this feature was not
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the adjacent liver tissue; it is possible that this feature was not
present in all sections, and so is not included in the scoring
Submitting pathologist’s diagnosis: hepatobiliary cystadenoma
with mesenchymal stroma
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Case 337
Female 50 years
Hepatitis C, plus cirrhosis secondary to alcohol.
1cm hypoechoic lesion segment 4, core biopsy
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Responses
49 cirrhosis
5 no mention of cirrhosis
44 hepatocellular carcinoma
of which: 14 well differentiated
5 moderately differentiated
25 no grade included
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25 no grade included
1 probable HCC
7 dysplastic nodule suspicious of HCC
1 liver cell dysplasia (nil else)
2 adenoma vs. Well differentiated HCC
10 ? iron overload, needs Perl’s stain
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Scoring and discussion
Both the presence of background cirrhosis and of hepatocellular
carcinoma in the biopsy were required for full marks. There were
considered to be sufficient features of HCC (cytological and
architectural) to make the diagnosis on this slide. The presence of
arteries within the lesion, the cytology compared with the
hepatocytes in the background liver, and the large rosettes/pseudo-
acinar pattern were features that supported the diagnosis of HCC.
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acinar pattern were features that supported the diagnosis of HCC.
The differential is with dysplastic nodule, and not with adenoma, in
the context of a cirrhotic liver.
This patient went on to have radio-frequency ablation, but
subsequently developed several other small nodules. For a while
she was within transplant criteria (up to 3 lesions <3cm diameter.
Submitting pathologist’s diagnosis: cirrhosis, well differentiated
hepatocellular carcinoma.
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The end