Linear‐agminated juvenile xanthogranulomas
International Journal of Dermatology, 2008 An 8‐month‐old girl presented with an asymptomatic skin lesion on the right popliteal fossa, which had been present for approximately 6 months. The child had a past medical history of a urinary tract infection at the age of 1 month and had been on daily cotrimoxazole since. There was no history of trauma to the site.
Kiorpelidou, D. +3 more
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The association between juvenile xanthogranulomas in neurofibromatosis type 1 patients and the development of leukemia: A systematic review [PDF]
, 2023 Neurofibromatosis type 1 (NF1) is an inherited tumor syndrome caused by heterozygous germline mutations in the NF1 gene, occurring in approximately 1/2600 individuals.
Kiuru, Maija +4 more
core
Cranial unifocal langerhans cell histiocytosis in a female child: a difficult case with S-100 and CD1a immunonegativity [PDF]
, 2015 A 13-years old female child was carried to Dr. Sardjito General Hospital, Yogyakarta by her mother with chiefcomplaint of a mass on her forehead. Since eight months prior to her visiting, she had a mass on her forehead whichbecame larger slowly without ...
Soeripto, J Bras, Hanggoro Tri Rinonce Sagiri Mangunsudirdjo
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NTRK1-rearranged histiocytosis:clinicopathologic and molecular features [PDF]
Non-Langerhans cell histiocytoses are a diverse group of histiocytic diseases. Different entities are defined based on clinical, histopathologic, and/or molecular characteristics. This study aimed to define NTRK-rearranged histiocytosis.
Babor, Florian +34 more
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Juvenile Xanthogranuloma With Hydrocephalus
Indian Journal of Dermatology, 2004 Juvenile xanthogranuloma (JXG) is a rare, benign, self-healing tumor of unknown etiology arising from non-Langerhans†cell histiocytes.
Ghosh Arghyaprasun +4 more
doaj
Orbital inflammation:IgG4-related disease, xanthogranulomatous disease and Graves’ orbitopathy: three of a kind [PDF]
Orbital inflammation can arise from various conditions, making diagnosis tricky due to similar symptoms. This thesis dives into understanding and treating three specific types: IgG4-related orbital disease (IgG4-ROD), orbital xanthogranulomatous disease (
Detiger, Sanne
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Late Onset Juvenile Xanthogranuloma
Indian Journal of Dermatology, 1999 A 19 year old female was seen with multiple skin coloured and hyperpigmented macules, discrete as well as grouped papules and nodules of varying sizes distributed over the face, neck, extensor and flexor aspects of both upper and lower extremities ...
Punithwavathy K +3 more
doaj
Juvenile xanthogranuloma in an adult
Indian Journal of Dermatology, 2009 Juvenile xanthogranuloma (JXG), a rare benign histiocytic disorder, primarily seen in the first two decades of life as a solitary cutaneous lesion. Though in majority of cases lesions are confined to the skin, systemic forms can occur in rare instances ...
Nayak Surajit +3 more
doaj
Bilateral spontaneous hyphaema in juvenile xanthogranuloma
Indian Journal of Ophthalmology, 2006 This report describes a rare occurrence of bilateral, spontaneous, nontraumatic hyphema in a 6 weeks old infant, associated with a small, multiple skin lesions.
Vijayalakshmi P +3 more
doaj
Giant Juvenile Xanthogranuloma Co-Occurring with Langerhans Cell Histiocytosis. [PDF]
J Pediatr X, 2023 Hayashi H, Makimoto A, Matsuoka K.
europepmc +1 more source