# Isolated Cutis Marmorata Telangiectatica Congenita in a Full-Term Neonate: A Case Report

**Authors:** Afnan Maashi, Ghadah Khormi, Laila Alali, Abdulaziz Rajhi, Najlaa Alsudairy

PMC · DOI: 10.7759/cureus.82137 · Cureus · 2025-04-12

## TL;DR

A full-term baby girl was born with a rare skin condition called CMTC, which was diagnosed after ruling out other possible disorders and managed with regular check-ups.

## Contribution

This case highlights the clinical presentation and management of isolated CMTC in a neonate with no associated anomalies.

## Key findings

- The neonate exhibited nonblanching, marble-like skin changes that did not resolve with warming.
- Comprehensive testing ruled out other vascular and systemic conditions, confirming isolated CMTC.
- At six months, the skin changes had partially faded with no complications or developmental delays.

## Abstract

Cutis marmorata telangiectatica congenita (CMTC) is a rare condition present at birth, marked by a persistent, net-like purplish discoloration of the skin caused by abnormal blood vessels. We report a case of a full-term female neonate born following an uneventful pregnancy, who exhibited widespread, nonblanching, marble-like skin changes involving the trunk, limbs, and face. These findings were present at rest, did not resolve with warming, and were more prominent during crying. Physical examination revealed no associated limb asymmetry, neurologic abnormalities, or dysmorphic features. A comprehensive diagnostic workup, including laboratory tests, echocardiography, skeletal survey, and Doppler ultrasonography, ruled out neonatal lupus, Klippel-Trénaunay syndrome, and capillary malformation-arteriovenous malformation syndrome. Based on clinical features and exclusion of other conditions, a diagnosis of isolated CMTC was made. The patient was managed conservatively with parental education and scheduled follow-up. At six months of age, the skin changes had faded partially, and no complications or developmental delays were observed. This case emphasizes the importance of recognizing CMTC as a benign condition that warrants thorough evaluation to exclude associated anomalies and benefit from early, structured monitoring.

## Linked entities

- **Diseases:** neonatal lupus (MONDO:0018360), Klippel-Trénaunay syndrome (MONDO:0007864), capillary malformation-arteriovenous malformation syndrome (MONDO:0012016), Cutis marmorata telangiectatica congenita (MONDO:0009055)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** capillary malformation-arteriovenous malformation syndrome (MESH:C564254), Klippel-Trenaunay syndrome (MESH:D007715), limb asymmetry (MESH:D005146), CMTC (MESH:C536226), dysmorphic features (MESH:D000013), neurologic abnormalities (MESH:D009461), developmental delays (MESH:D002658), neonatal lupus (MESH:C536397)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12068003/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12068003/full.md

## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12068003/full.md

---
Source: https://tomesphere.com/paper/PMC12068003