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Updated: Jan 22, 2026

Author Spotlight: Investigating the Pathophysiology of Eosinophilic Esophagitis
Published on: May 10, 2024
Morphoea-like plaques revealing an eosinophilic (Shulman) fasciitis
C Moulin1, A Cavailhes, B Balme
1Dermatology Service, Centre Hospitalier de Valence, Valence, France.
Abstract:
Eosinophilic fasciitis (EF) is a connective-tissue disease characterized by thickened fascia. Involvement of the dermis may occur during the progression of the disease, characterized clinically by morphoea-like plaques (MLPs). This more superficial feature of EF carries a poor prognosis, suggestive of refractory EF that requires intensive therapy. We report a case in which morphoea-like plaques occurred before the EF. This case and previous cases of MLPs show some differences between MLPs and classic morphoea. Clinically, MLPs present with ill-defined brown plaques, with no lilac ring or ivory colour. Histologically, there is a more marked inflammatory infiltrate and an increase in the number of eosinophils. The discovery of MLPs at an early stage should prompt examination of the fascia with magnetic resonance imaging or surgical biopsy, and aggressive treatment.
Insights
Eosinophilic fasciitis (EF) can present with morphoea-like plaques (MLPs) before fascial thickening. Early detection of MLPs indicates aggressive EF requiring prompt, intensive treatment.
Area of Science:
- Rheumatology
- Dermatology
- Pathology
Background:
- Eosinophilic fasciitis (EF) is a connective tissue disease primarily affecting the fascia.
- Dermal involvement in EF can manifest as morphoea-like plaques (MLPs).
- MLPs in EF are associated with a poor prognosis and refractory disease.
Observation:
- This report details a unique case where MLPs preceded the characteristic fascial thickening of EF.
- Clinical presentation of MLPs differs from classic morphoea, lacking lilac or ivory hues and exhibiting ill-defined borders.
- Histological examination reveals a pronounced inflammatory infiltrate with increased eosinophils in MLPs.
Findings:
- Morphoea-like plaques can be an early indicator of eosinophilic fasciitis.
- MLPs associated with EF exhibit distinct clinical and histological features compared to classic morphoea.
- Early identification of MLPs necessitates advanced imaging or biopsy for fascia evaluation.
Implications:
- Prompt diagnosis of MLPs can lead to earlier detection of EF.
- Aggressive treatment initiated early in EF, guided by MLP identification, may improve patient outcomes.
- Recognizing MLPs as an early sign aids in differentiating EF from other connective tissue diseases.
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