Results 21 to 30 of about 7,890 (255)

Intravenous immunoglobulin–refractory necrobiotic xanthogranuloma successfully treated with tofacitinib 2% cream

open access: yesJAAD Case Reports, 2022
IVIg: intravenous immunoglobulin JAK: janus kinase NXG: necrobiotic xanthogranuloma INTRODUCTION Necrobiotic xanthogranuloma (NXG) is a nonLangerhans cell histiocytosis occurring in association with paraproteinemia.
N. Shahriari, D. Mazori, J. Merola
semanticscholar   +1 more source

An analysis of clinical and pathological features of 32 cases of juvenile xanthogranuloma

open access: yesPifu-xingbing zhenliaoxue zazhi, 2020
Objective: To summarize the clinical and histopathological features of juvenile xanthogranuloma (JXG). Methods: The clinical manifestations and histopathological findings of 32 children with juvenile xanthogranuloma diagnosed and treated in our hospital ...
Cui HU   +6 more
doaj   +1 more source

Long-standing necrobiotic xanthogranuloma limited to the skin: A case report

open access: yesSAGE Open Medical Case Reports, 2021
Necrobiotic xanthogranuloma is a rare non-Langerhans cell histiocytosis with a known association with monoclonal gammopathies and malignant conditions. There is a lack of consensus regarding the management of necrobiotic xanthogranuloma.
Anne-Sophie Smilga   +3 more
doaj   +1 more source

Neuroimaging in Pediatric Patients with Juvenile Xanthogranuloma of the CNS

open access: yesAmerican Journal of Neuroradiology, 2022
BACKGROUND AND PURPOSE: Juvenile xanthogranuloma is a rare clonal, myeloid, neoplastic disorder. Typically, juvenile xanthogranuloma is a self-limited disorder of infancy, often presenting as a solitary red-brown or yellow skin papule/nodule.
B. Serrallach   +11 more
semanticscholar   +1 more source

Adult onset Xanthogranuloma presenting as a solitary laryngeal localization: case report and review of literature

open access: yesArchive of Clinical Cases, 2022
Juvenile Xanthogranuloma (XG) is a rare disorder that belongs to the heterogeneous group of histiocytic neoplasms, characterized by a clonal expansion of non-Langerhans cell histiocytes that share a dermal macrophage phenotype. Although the head and neck
Gianluca Velletrani   +5 more
semanticscholar   +1 more source

Line‐field confocal optical coherence tomography of xanthogranuloma: Correlation with vertical and horizontal histopathology

open access: yesJournal of cutaneous pathology, 2021
Line‐field confocal optical coherence tomography (LC‐OCT) is a new noninvasive technique for a real‐time, vertical, and horizontal imaging of the skin at cellular resolution.
F. Lacarrubba   +5 more
semanticscholar   +1 more source

A Multicenter Cross-Sectional Study and Systematic Review of Necrobiotic Xanthogranuloma With Proposed Diagnostic Criteria.

open access: yesJAMA dermatology, 2020
Importance Necrobiotic xanthogranuloma (NXG) is a non-Langerhans cell histiocytosis classically associated with paraproteinemia attributable to plasma-cell dyscrasias or lymphoproliferative disorders.
C. Nelson   +11 more
semanticscholar   +1 more source

Oral Juvenile Xanthogranuloma: a case report of gingival hyperplasia and osteolysis in male adult patient

open access: yesBMC Oral Health, 2022
Background Juvenile Xanthogranuloma (JXG) is a non-hereditary, self-limiting disease which is usually presented in infancy or early childhood and in males over females.
Long Chen, Lin Feng, Lingling E
doaj   +1 more source

Dermoscopic Patterns in Juvenile Xanthogranuloma Based on the Histological Classification

open access: yesFrontiers in Medicine, 2021
Background: Several dermoscopic features of juvenile xanthogranuloma (JXG) have been previously described in single cases or small case series and need to be further verified in a large sample.
Jiaosheng Xu, Lin Ma
semanticscholar   +1 more source

Clinical outcome of a patient with lysosomal acid lipase deficiency and first results after initiation of treatment with Sebelipase alfa: A case report [PDF]

open access: yes, 2019
We report on a case of very rare autosomal recessive cholesteryl ester storage disease due to lysosomal acid lipase deficiency (LALD). LALD is caused by mutations in the lysosomal acid lipase A (LIPA) gene resulting in cholesteryl ester accumulation in
Bobbert, Thomas   +8 more
core   +1 more source

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