专题:Histiocytic Disorders and Treatments

This cluster of papers focuses on the classification, diagnosis, and treatment of histiocytic disorders, including Langerhans Cell Histiocytosis and Erdheim-Chester Disease. It explores the role of BRAF mutations, immunohistochemical approaches to classification, and consensus guidelines for clinical management. The papers also delve into the pathogenesis, molecular characterization, and therapy intensification for multisystem involvement.
最新文献
Case Report: Focal xanthogranulomatous pyelonephritis in children: diagnostic pitfalls and the role of conservative management

article Full Text OpenAlex

Refractory Tumorous and Neurodegenerative Histiocytosis Treated With Intra-Arterial Chemotherapy

article Full Text OpenAlex

Recent Advances in the Histopathology, Molecular Biology, and Treatment of Kaposi Sarcoma: A Contemporary Review

review Full Text OpenAlex

Integrative functional genomics analysis of Kaposi sarcoma cohorts

article Full Text OpenAlex

Thymic Rosai-Dorfmann disease: a case report

preprint Full Text OpenAlex

Challenging Diagnosis in a Pediatric Eyelid Mass: Resection of a Subcutaneous Pyogenic Granuloma Versus Sarcoma

article Full Text OpenAlex

A patient with Eradheim-Chester disease presenting with progressive cystic lung lesions and confirmed pulmonary artery hypertension: a case report

article Full Text OpenAlex

Mortality in Tuberous Sclerosis Complex in the United Kingdom, 2016–2022

article Full Text OpenAlex

Retrospective nationwide survey of pediatric RDD in Japan: a high prevalence of mutations in the kinase pathway genes

article Full Text OpenAlex

A Stepwise decision tree model for differential diagnosis of Kimura’s disease in the head and neck

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近5年高被引文献
The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms

review Full Text OpenAlex 3359 FWCI601.49233209

Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management Recommendations

article Full Text OpenAlex 604 FWCI67.89335258

Lung-selective mRNA delivery of synthetic lipid nanoparticles for the treatment of pulmonary lymphangioleiomyomatosis

article Full Text OpenAlex 417 FWCI74.67048945

International expert consensus recommendations for the diagnosis and treatment of Langerhans cell histiocytosis in adults

article Full Text OpenAlex 217 FWCI39.13020841

Novel somatic mutations in UBA1 as a cause of VEXAS syndrome

letter Full Text OpenAlex 215 FWCI40.69617297

Estimated Prevalence and Clinical Manifestations of UBA1 Variants Associated With VEXAS Syndrome in a Clinical Population

article Full Text OpenAlex 199 FWCI81.66451453

Senolytics dasatinib and quercetin in idiopathic pulmonary fibrosis: results of a phase I, single-blind, single-center, randomized, placebo-controlled pilot trial on feasibility and tolerability

article Full Text OpenAlex 189 FWCI63.76387227

Castleman disease

review Full Text OpenAlex 158 FWCI11.00730683

Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis

article Full Text OpenAlex 156 FWCI39.01071554

Azacitidine for patients with Vacuoles, E1 Enzyme, X‐linked, Autoinflammatory, Somatic syndrome (VEXAS) and myelodysplastic syndrome: data from the French VEXAS registry

article Full Text OpenAlex 153 FWCI26.90469213