# Novel Development of a Large Cerebral Cavernous Malformation in an Adolescent With a History of Familial Cerebral Cavernous Malformation Syndrome

**Authors:** Mary G McIntosh, Laura L Hayes

PMC · DOI: 10.7759/cureus.52591 · 2024-01-19

## TL;DR

A 16-year-old girl with a family history of cerebral cavernous malformations developed a new large lesion in her brain during adolescence.

## Contribution

This case highlights the potential for new cavernoma development in adolescents with familial CCM syndrome.

## Key findings

- A large cavernoma was found in the right frontal lobe of a 16-year-old girl with familial CCM.
- The lesion was not present in an MRI scan from eight years earlier.
- The case shows that new cavernomas can develop later in adolescence.

## Abstract

Cerebral cavernous malformations (CCM) are capillary vascular malformations of the central nervous system (CNS). These lesions can be either familial or sporadic. We present a case of a 16-year-old girl with familial CCM syndrome who presented with a six-month history of chronic headaches. A magnetic resonance imaging (MRI) scan revealed a large cavernoma in the right frontal lobe that had not been present on a prior scan performed eight years earlier. This case presentation demonstrates the possibility of significant novel cavernoma development further into adolescence.

## Linked entities

- **Diseases:** cerebral cavernous malformations (MONDO:0020724)

## Full-text entities

- **Diseases:** chronic headaches (MESH:D020773), CCM (MESH:D020786), capillary vascular malformations of the central nervous system (MESH:D020785), Familial Cerebral Cavernous Malformation Syndrome (MESH:C536610)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC10874682/full.md

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Source: https://tomesphere.com/paper/PMC10874682