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. 1999 Aug;45(2):301–305. doi: 10.1136/gut.45.2.301

Spur cell anaemia and hepatic iron stores in patients with alcoholic liver disease undergoing orthotopic liver transplantation

A Pascoe 1, P Kerlin 1, C Steadman 1, A Clouston 1, D Jones 1, L Powell 1, E Jazwinska 1, S Lynch 1, R Strong 1
PMCID: PMC1727602  PMID: 10403746

Abstract

BACKGROUND—Following orthotopic liver transplantation (OLT) histological examination of explant livers from patients with alcoholic liver disease (ALD) sometimes shows extensive iron deposits in a distribution suggestive of homozygous haemochromatosis.
AIMS—To use haemochromatosis gene (HFE) assays to distinguish between ALD with notable siderosis and hereditary haemochromatosis. To evaluate the possible influence of spur cell haemolytic anaemia on hepatic iron loading.
PATIENTS—Thirty seven patients with ALD were abstinent for at least six months prior to OLT. Twenty three patients had transferrin saturations greater than 55%, 16 also had increased serum ferritin (>350 µg/l). Eight of 37 (22%) explant livers had grade 3 or 4 hepatic iron deposition, predominantly in hepatocytes. Of these, four had a hepatic iron index greater than 1.9 and most seemed to have spur cell haemolytic anaemia.
METHODS—Mutation analysis for C282Y and H63D mutations was performed on DNA extracts from peripheral blood or explant liver. Spur cell haemolytic anaemia was diagnosed when the haemoglobin was 105 g/l in the presence of notable acanthocytosis.
RESULTS—None of the eight patients with grade 3 or 4 hepatic iron had evidence of the C282Y mutation. Two of the eight were heterozygous for H63D. None of the remaining 28 patients tested showed homozygous HFE mutations. Spur cell anaemia was present in six of the eight patients with heavy iron deposition and only one of the remaining patients.
CONCLUSIONS—The HFE mutation was not present in these patients with advanced ALD and heavy iron loading. Spur cell haemolytic anaemia provides an alternative potential mechanism for the heavy iron loading.


Keywords: alcoholic liver disease; haemochromatosis; hepatic iron index; orthotopic liver transplantation

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Figure 1  .

Figure 1  

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Grade 4 siderosis in two patients with alcoholic liver disease and spur cell anaemia, showing predominantly hepatocyte deposition. Patients OLTx 313 (A) and OLTx 392 (B) are homozygous normal for the C282Y and H63D mutations and have no family history of haemochromatosis. Both have spur cell anaemia. (Perls' stain; original magnification × 250).

Figure 2  .

Figure 2  

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Deposition of iron in bile duct epithelium (d) and arteriolar walls (a) in a patient (OLTx 401) with spur cell anaemia and normal C282Y and heterozygous H63D gene analysis (Perls' stain; original magnification × 400). v, vein.

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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