# Unveiling Renal Lipid Deposition: A Rare Case of Hepatic Glomerulosclerosis Resembling Lecithin-Cholesterol Acyltransferase (LCAT) Deficiency Post Liver Transplantation

**Authors:** Aseel Zghayer, Ewa Borys, Maria M Picken, Kavitha Vellanki

PMC · DOI: 10.7759/cureus.64004 · Cureus · 2024-07-07

## TL;DR

A rare case of kidney changes resembling LCAT deficiency is reported in a liver transplant patient, highlighting the link between liver disease and kidney lipid deposition.

## Contribution

This case report highlights a rare histopathological resemblance between hepatic glomerulosclerosis and LCAT deficiency post liver transplantation.

## Key findings

- A patient with ESLD showed kidney biopsy findings similar to LCAT deficiency after liver transplantation.
- The case suggests a potential link between liver disease and lipid-related kidney changes.
- The clinical significance of such renal alterations post-transplant remains unclear and requires further study.

## Abstract

Hepatic glomerulosclerosis, a renal complication of liver cirrhosis, presents challenges in diagnosis and management. This case report discusses the rarity of kidney biopsy findings resembling lecithin-cholesterol acyltransferase (LCAT) deficiency post liver transplantation. We present the case of a patient with end-stage liver disease (ESLD) from alcohol-related cirrhosis, who underwent orthotopic liver transplantation (OLT) with persistent proteinuria after transplantation. Kidney biopsy revealed features of hepatic glomerulopathy resembling both IgA nephropathy (IgAN) and LCAT deficiency. The histopathological similarities between hepatic glomerulosclerosis and LCAT deficiency suggest a potential link between liver disease and lipid deposition in the kidneys. The clinical course and outcomes of such renal alterations post liver transplantation remain uncertain, highlighting the need for further research in glomerular pathology in the context of liver transplantation. This case underscores the importance of kidney biopsy in ESLD patients and the necessity for more attention to glomerular pathology post liver transplantation, especially in the current era of increasing liver transplantation rates.

## Linked entities

- **Proteins:** LCAT (lecithin-cholesterol acyltransferase)
- **Diseases:** LCAT deficiency (MONDO:0018999)

## Full-text entities

- **Diseases:** renal complication (MESH:D007674), liver disease (MESH:D008107), liver cirrhosis (MESH:D008103), IgA nephropathy (MESH:D005922), Hepatic Glomerulosclerosis (MESH:D056486), alcohol-related cirrhosis (MESH:D008104), ESLD (MESH:D058625), proteinuria (MESH:D011507), LCAT deficiency (MESH:D007863)
- **Chemicals:** Lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC11304406/full.md

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Source: https://tomesphere.com/paper/PMC11304406