# Radiological Manifestations of Lymphangioleiomyomatosis: A Local Patient Cohort Analysis

**Authors:** Luca Conti, Darlene Mercieca, Gianluca Gatt, Luca Sant Fournier, Peter Fsadni

PMC · DOI: 10.7759/cureus.87292 · Cureus · 2025-07-04

## TL;DR

This study compares lung and other imaging features of two types of LAM in a Maltese patient group, highlighting differences in complications.

## Contribution

The paper presents a local cohort analysis of LAM in Malta, comparing sporadic and TSC-associated cases with detailed radiological findings.

## Key findings

- All LAM patients showed diffuse thin-walled cysts in CT scans.
- Chylous pleural effusions were exclusive to the s-LAM group.
- TSC-LAM patients had extra-pulmonary manifestations like renal angiomyolipomas.

## Abstract

Background: Lymphangioleiomyomatosis (LAM) is an ultra-rare neoplastic cystic disease primarily affecting females of reproductive age, characterized by the infiltration of smooth muscle cells into the lungs and the formation of cystic lesions. This study aims to compare the radiological findings in patients with sporadic LAM (s-LAM) and those with LAM associated with tuberous sclerosis complex (TSC-LAM) in the Maltese population.

Methods: A retrospective observational study was conducted at Mater Dei Hospital, Malta, involving eight patients diagnosed with LAM between 2014 and 2024. Thoracic and abdominal CT scans were reviewed, and findings were categorized based on the presence of s-LAM or TSC-LAM.

Results: The cohort included five patients with s-LAM and three with TSC-LAM, alongside 15 patients with tuberous sclerosis complex (TSC) but no LAM. All LAM patients exhibited diffuse thin-walled cysts, with sizes ranging from 7 to 72 mm. Notably, chylous pleural effusions were observed only in the s-LAM group. The TSC-LAM group demonstrated significant extra-pulmonary manifestations, including renal angiomyolipomas, with some requiring intervention.

Conclusion: This study highlights the distinct radiological features and complications associated with s-LAM and TSC-LAM. The findings underscore the necessity for vigilant screening and monitoring in TSC patients to manage potential LAM-related complications effectively. A multidisciplinary approach is essential for optimizing patient outcomes and addressing the broader implications of TSC and LAM on health.

## Linked entities

- **Diseases:** Lymphangioleiomyomatosis (MONDO:0006277), tuberous sclerosis complex (MONDO:0001734)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** chylous pleural effusions (MESH:D010996), LAM (MESH:D018192), TSC (MESH:D014402), cystic disease (MESH:C563237), renal angiomyolipomas (MESH:D018207), cystic lesions (MESH:D052177), neoplastic (MESH:D009369), cysts (MESH:D003560)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12318564/full.md

## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC12318564/full.md

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Source: https://tomesphere.com/paper/PMC12318564