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In this study, researchers found that high-dose tryptophan ingestion before symptom onset may be linked to clinical features resembling eosinophilia-myalgia syndrome in patients with eosinophilic fasciitis.

Resident memory T cells and necroptosis may drive fibrosis in eosinophilic fasciitis and morphea.

In this study, researchers found histopathological similarities between L-tryptophan eosinophilic myalgia syndrome and idiopathic eosinophilic fasciitis, with certain unique inflammatory features present in the former.

This case report discusses a 56-year-old female patient with multiple risk factors, including diabetes mellitus and liver cirrhosis, who developed necrotizing fasciitis, emphasizing the complexity and high cost of treatment required.

In this case report, a 7-month-old girl with suspected acrodermatitis enteropathica and severe dermatitis experienced a tragic outcome despite zinc treatment, highlighting the challenges of diagnosing and managing this rare genetic disorder.