Results 81 to 90 of about 6,887 (246)
A 50‐year‐old man with a 12‐year history of extensive pachymeningeal thickening
Brain Pathology, EarlyView.
Alyssa M. Lee +3 more
wiley +1 more source
The Clinicopathologic Spectrum of Rosai–Dorfman–Destombes Disease in Adults: An Analysis of 16 Cases
European Journal of Haematology, Volume 115, Issue 6, Page 555-564, December 2025.ABSTRACT Rosai–Dorfman–Destombes disease (RDD) is a rare histiocytic proliferation with protean clinical manifestations, resulting from the accumulation of activated histiocytes within nodal and extra‐nodal tissues. The diagnosis can be missed, particularly when biopsies are obtained from extra‐nodal sites, where histological features may be less ...
Mark Trinder +8 more
wiley +1 more source
Secondary vs. primary pituitary xanthogranulomas: which yellow is more mellow?
Endocrine JournalPituitary xanthogranulomatomas (XG) are a rare pathological entity caused by accumulation of lipid laden macrophages and reactive granuloma formation usually triggered by cystic fluid leakage or hemorrhage. Our aim was to compare clinical characteristics
Dragana Miljic +15 more
doaj +1 more source
Gingival Juvenile Xanthogranuloma [PDF]
, 2019 Juvenile xanthogranuloma (JXG) is a benign histiocytosis that occurs in the pediatric population. Cutaneous JXG is the most common form, while extracutaneous lesions, including oral JXG, is extremely rare.
김동욱 +8 more
core +1 more source
IMPROVE 2023: The 2nd International Meeting on Pathway‐Related Obesity: Vision & Evidence
Clinical Obesity, Volume 15, Issue 5, October 2025.ABSTRACT A total of 150 clinicians and researchers representing 19 countries came together in person and online to participate in the highly anticipated 2nd International Meeting on Pathway‐Related Obesity: Vision & Evidence (IMPROVE), held on 13–15 December 2023 in Paris, France.
Karine Clément +19 more
wiley +1 more source
Juvenile xanthogranuloma of the cerebellopontine angle: A case report and review of the literature
Otolaryngology Case Reports, 2019 Juvenile xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis, most often presenting with skin lesions of the head, neck, and upper trunk. Intracranial presentations have been previously described, however, due to its rarity, treatment algorithms
Sarah M. Tittman +6 more
doaj +1 more source
Epidermal Nevi and Epidermal Naevus Syndromes
JEADV Clinical Practice, Volume 4, Issue 3, Page 669-680, August 2025.ABSTRACT Epidermal nevi (EN) arise from postzygotic variants in ectoderm‐derived cell lines, such as keratinocytes and cells forming adnexa. EN may be present alone without any associated abnormality or be part of a syndrome. In this review, we will discuss about the clinical and genetics of the main types of EN and related syndromes.
Gianluca Tadini +2 more
wiley +1 more source
Pielonefritis xantogranulomatosa: Estudio retrospectivo de 8 casos
Revista Chilena de RadiologíaHemos revisado las características clínicas, radiológicas y patológicas de la pielonefritis xan-togranulomatosa junto con la evolución de la enfermedad y una revisión bibliográfica de la misma.
Diego Miguel Soriano M +4 more
doaj +1 more source
Emergence of solitary juvenile xanthogranuloma on the corneoscleral limbus
Journal of Clinical Ophthalmology and Research, 2018 Juvenile xanthogranuloma (JXG) is the most frequent form of non-Langerhans histiocytosis, a rare benign inflammatory skin disorder. Eye involvement is the most frequent extracutaneous manifestation of the disease.
Raul Alfaro-Rangel +2 more
doaj +1 more source
A neonatal pustule:Langerhans cell histiocytosis [PDF]
, 2019 Langerhans cell histiocytosis (LCH) is a rare, clinically heterogeneous disease that most commonly occurs in pediatric populations. Congenital self-limited LCH is a benign variant of LCH.
Hogeling, Marcia +4 more
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