Results 41 to 50 of about 248,416 (166)
Intraocular juvenile xanthogranuloma of the iris in an adult patient
American Journal of Ophthalmology Case Reports, 2017 Purpose: Juvenile xanthogranuloma (JXG) is a rare histiocytic skin disease primarily of young children, which may also affect ocular structures and in particular the iris.
Elias Flockerzi +2 more
doaj +1 more source
Pediatric Blood &Cancer, Volume 73, Issue 10, October 2026.ABSTRACT Juvenile xanthogranuloma (JXG) of the central nervous system (CNS) is a rare non‐Langerhans cell histiocytosis. CSF1R mutations have been reported for peripheral JXG, but not in CNS JXG. A 3‐month‐old male presented with fever, lymphadenopathy, and macrocephaly with bulging fontanelles.
Sima Vazquez +8 more
wiley +1 more source
American Journal of Ophthalmology Case Reports, 2018 Purpose: To report a case of juvenile xanthogranuloma involving the iris and skin that clincally was diagnosed with an obvious cutaneous lesion.
Peter Meyer +4 more
doaj +1 more source
ADULT ONSET XANTHOGRANULOMA – CASE REPORT AND REVIEW OF LITERATURE [PDF]
Romanian Medical Journal, 2019 Juvenile xanthogranuloma represents the most common form of non-Langerhans cell histiocytosis. It is tipically a childhood disorder, over 80% of cases developing in the first year of life.
Liliana Gabriela Popa +5 more
doaj +1 more source
Disseminated Juvenile Xanthogranuloma: A Case Report
International Journal of Dermatology and Venerology, 2022 Introduction:. Histiocytoses are localized or systemic diseases that can broadly be classified into Langerhans cell histiocytosis and non-Langerhans cell histiocytosis.
Najam Us Saher +2 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 10, October 2026.ABSTRACT Some of the rarest diseases with cell accumulation in different organs are histiocytoses. Since these diagnoses are uncommon, other differential diagnoses must be excluded. We report a case of a 42‐year‐old man with episodes of knee pain and fever.
Maris Tulk +4 more
wiley +1 more source
Histiocytosis development and clinical variation through the lens of genomics
The Journal of Pathology, Volume 270, Issue 1, Page 23-39, September 2026.Abstract Histiocytic neoplasms are rare haematologic diseases characterised by clonal expansions of cells with a monocyte, macrophage or dendritic cell phenotype. Their clinical manifestations are diverse, ranging from indolent lesions to aggressive systemic disease.
Paul G Kemps +3 more
wiley +1 more source
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 9, Page 1251-1262, September 2026.Summary Background and Objectives Skin diseases can greatly impair quality of life (QoL) of pediatric patients and their families. The Infants and Toddlers Dermatology Quality of Life questionnaire (InToDermQoL) is the first skin‐generic instrument assessing QoL in children ≤ 4 years, as reported by their caregiver. This study aimed to psychometrically
Juliane Traxler +8 more
wiley +1 more source
Juvenile Xanthogranuloma: Case Report and Review of the Literature
, 2008 The present case report describes a juvenile xanthogranuloma in a five-month-old girl. A circumscribed papule was located below the right nasal ala and above the right vermilion border.
Tatiana Karine Simon Cypel +1 more
core +1 more source
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 9, Page 1251-1263, September 2026.Zusammenfassung Hintergrund und Zielsetzung Hauterkrankungen können die Lebensqualität (quality of life; QoL) von pädiatrischen Patienten und ihren Familien erheblich beeinträchtigen. Der Fragebogen zur Lebensqualität in der Dermatologie bei Säuglingen und Kleinkindern (Infants and Toddlers Dermatology Quality of Life questionnaire; InToDermQoL) ist ...
Juliane Traxler +8 more
wiley +1 more source