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: two cases of idiopathic plasmacytic lymphadenopathy subtype of idiopathic multicentric Castleman disease with xanthelasma palpebrum from a Canadian center

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Laboratory Evaluation of Peripheral Blood Involvement in Mycosis Fungoides and Sézary Syndrome: Evolution of Flow Cytometry and Morphology Quantification and Interpretation

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Hearing loss in Langerhans cell histiocytosis: close association with central nervous system consequences

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Management of a Pediatric Patient With Langerhans Cell Histiocytosis Using General Anesthesia

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Facial Cutaneous Rosai-Dorfman Disease Misdiagnosed as Sporotrichosis: A Case Report and Literature Review

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The use of MEK inhibitors in pediatric patients presenting with respiratory distress and laryngeal Rosai-Dorfman Disease: Two case reports

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Cutaneous Rosai–Dorfman disease: a comprehensive literature review and two case reports

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A Rare Presentation of A Common Dermatosis; Unilateral Blaschko-Linear Erythema Multiforme

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Mastocytosis: Imaging Spectrum and Diagnostic Insights

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Extranodal Rosai–Dorfman Disease With Increased IgG4-Positive Plasma Cells Involving the Breast: A Case Report With Review of the Literature

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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 3617 FWCI552.0255

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

article Full Text OpenAlex 451 FWCI49.5426

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

article Full Text OpenAlex 236 FWCI26.5407

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

article Full Text OpenAlex 213 FWCI54.6036

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 211 FWCI55.3419

Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis

article Full Text OpenAlex 165 FWCI27.0748

Epstein–Barr Virus History and Pathogenesis

review Full Text OpenAlex 109 FWCI25.4227

A Phase II prospective trial of azacitidine in steroid-dependent or refractory systemic autoimmune/inflammatory disorders and VEXAS syndrome associated with MDS and CMML

letter Full Text OpenAlex 86 FWCI14.3012

Updates on Sturge-Weber Syndrome

review Full Text OpenAlex 86 FWCI17.8761

Tazemetostat for tumors harboring SMARCB1/SMARCA4 or EZH2 alterations: results from NCI-COG pediatric MATCH APEC1621C

article Full Text OpenAlex 80 FWCI12.5754