# An Atypical Cause of a Child Limp: A Gorham-Stout Disease with a Vanishing Hip

**Authors:** Hanene Lassoued Ferjani, Yasmin Makhlouf, Dorra Ben Nessib, Kaouther Maatallah, Dhia Kaffel, Wafa Hamdi

PMC · DOI: 10.1055/s-0042-1757962 · Revista Brasileira de Ortopedia · 2023-07-31

## TL;DR

This paper reports a rare case of Gorham-Stout disease in a child's hip and iliac crest, highlighting the disease's severity and lack of established treatment.

## Contribution

The contribution is a new clinical case report of Gorham-Stout disease in a pediatric patient with hip involvement.

## Key findings

- Gorham-Stout disease was diagnosed in a child's hip and iliac crest.
- The case highlights the disease's destructive nature and lack of effective treatment strategies.

## Abstract

Gorham-Stout disease (GSD) is a rare bone disease characterized by an abnormal proliferation of endothelial-lined vessels and destruction of the affected bone. As it affects commonly children and young adults, it is associated with significant morbidity and mortality. To date, there is no established treatment strategy for GSD.

We report through this observation a rare case of GSD in a child located in the hip and the iliac crest.

A síndrome de Gorham-Stout (SGS) é uma doença óssea rara caracterizada pela proliferação anormal de vasos endoteliais e destruição do osso acometido. Por ser comum em crianças e adultos jovens, causa morbidade e mortalidade significativas. Até o momento, não há estratégia terapêutica estabelecida para a SGS.

Relatamos um caso raro de SGS no quadril e na crista ilíaca de uma criança.

## Linked entities

- **Diseases:** Gorham-Stout disease (MONDO:0007414), SGS (MONDO:0008426)

## Full-text entities

- **Diseases:** Vanishing Hip (MESH:D056784), GSD (MESH:D010015), bone disease (MESH:D001847)
- **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/PMC11254440/full.md

## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC11254440/full.md

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Source: https://tomesphere.com/paper/PMC11254440