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Treatment of pembrolizumab-induced bullous pemphigoid with dupilumab: A case report and review of the literature.
Int J Dermatol
December 2024
Division of Dermatology, Department of Medicine, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
Chronic Treatment-Resistant Annular Rash: A Case of Neutrophilic Figurate Erythema.
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August 2024
General Dermatology, Naval Medical Center Portsmouth, Portsmouth, USA.
Article Synopsis
- - Neutrophilic figurate erythema (NFE) is a rare skin condition that resembles erythema annulare centrifugum (EAC) but is characterized by a neutrophil-dominated inflammatory response in the skin.
- - A case study of a 32-year-old military male showed a chronic skin rash that started five years ago, resistant to multiple antifungal treatments, with no identifiable triggers or improvement post-deployment.
- - Diagnosis of NFE can be challenging due to its rarity, with only 15 known cases, and it may require specific treatment focusing on anti-neutrophil therapy rather than standard antifungal options.
A Classification for Gastric Outlet Obstruction in Childhood: Extending Beyond Infantile Hypertrophic Pyloric Stenosis.
Turk J Gastroenterol
March 2024
Department of Pediatric Surgery, Gazi University School of Medicine, Ankara, Turkey.
Background/aims: Gastric outlet obstruction (GOO) is a rare condition in childhood, with the exception of infantile hypertrophic pyloric stenosis (IHPS). However, no classification exists from a pediatric gastroenterologist's perspective.
Materials And Methods: The patients with a diagnosis of GOO between 2009 and 2020 were reviewed retrospectively.
A case of eosinophilic annular erythema as a presenting sign for primary biliary cholangitis.
An Bras Dermatol
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Department of Dermatology, University General Hospital of Albacete, Albacete, Castilla-La Mancha, Spain.
Sequential occurrence of primary cutaneous indeterminate cell histiocytosis after oesophageal cancer and subsequent bullous pemphigoid: a case report.
Br J Hosp Med (Lond)
July 2024
Department of Dermatology, Zhejiang Provincial Hospital of Dermatology, Huzhou, Zhejiang, China.
Indeterminate cell histiocytosis is a rare proliferative histiocytic disease with an unknown aetiology, which shares immunophenotypic features of both Langerhans cells and macrophages. There is a relationship between indeterminate cell histiocytosis and cancer, while there are no reports about indeterminate cell histiocytosis and bullous pemphigoid. In this study, we reported the rare case of a patient with primary cutaneous indeterminate cell histiocytosis who had been diagnosed with oesophagal cancer and later developed bullous pemphigoid.
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