Results 211 to 220 of about 7,890 (255)
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Annals of Otology, Rhinology & Laryngology, 1989
The skin of the head and neck is an area of predilection for xanthogranuloma, formerly called nevoxanthoendothelioma. Spontaneous resolution is the usual course for this benign, nonneoplastic lesion that is composed of macrophages and Touton giant cells and occurs principally in infants and children.
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The skin of the head and neck is an area of predilection for xanthogranuloma, formerly called nevoxanthoendothelioma. Spontaneous resolution is the usual course for this benign, nonneoplastic lesion that is composed of macrophages and Touton giant cells and occurs principally in infants and children.
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Recurrent CLTC::SYK fusions and CSF1R mutations in juvenile xanthogranuloma of soft tissue.
BloodJuvenile xanthogranuloma (JXG) is a histiocytic neoplasm that usually presents in the skin. Rarely, extracutaneous localizations occur; the genetic drivers of this clinical variant of JXG remain incompletely characterized.
P. Kemps +25 more
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Genetic Aspects of Necrobiotic Xanthogranuloma.
JAMA dermatologyThis genetic association study examines the genetic aspects of necrobiotic xanthogranuloma in 3 patients in China.
Peng-Yu Chen +6 more
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Journal of Pediatric Ophthalmology & Strabismus, 1991
ABSTRACT Three cases of histologically proven limbal xanthogranuloma are presented. All three cases presented with a yellow raised swelling at the limbus and no other ocular or systemic abnormality. A simple excision of the lesion was carried out in all cases and histological examination revealed features typical of xanthogranuloma.
L M, Collum +3 more
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ABSTRACT Three cases of histologically proven limbal xanthogranuloma are presented. All three cases presented with a yellow raised swelling at the limbus and no other ocular or systemic abnormality. A simple excision of the lesion was carried out in all cases and histological examination revealed features typical of xanthogranuloma.
L M, Collum +3 more
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Seminars in Cutaneous Medicine and Surgery, 2007
Necrobiotic xanthogranuloma (NXG) is an uncommon granulomatous disease involving the skin and extracutaneous tissues. In its typical clinical presentation, it consists of multiple indurate yellow-brownish plaques or nodules, usually located on the periorbital area.
Jesús, Fernández-Herrera +1 more
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Necrobiotic xanthogranuloma (NXG) is an uncommon granulomatous disease involving the skin and extracutaneous tissues. In its typical clinical presentation, it consists of multiple indurate yellow-brownish plaques or nodules, usually located on the periorbital area.
Jesús, Fernández-Herrera +1 more
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Concomitant adult onset xanthogranuloma and IgG4-related orbital disease: a rare occurrence
Orbit, 2020Adult onset xanthogranulomatous disease is a rare orbital disease. IgG4-related disease is a systemic disease that can often manifest in the orbit. In this communication, we present the case of a patient with a xanthelasma-like lesion on the upper eyelid,
A. Andron +4 more
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Nonnecrobiotic Necrobiotic Xanthogranuloma
The American Journal of Dermatopathology, 2007N ...
Ferrara G +4 more
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International Journal of Dermatology, 2020
Juvenile xanthogranuloma (JXG) is a rarely encountered skin disorder, which is characterized by the proliferation of non‐Langerhans cell histiocytes.
Selcen Kundak, Yasemin Çakır
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Juvenile xanthogranuloma (JXG) is a rarely encountered skin disorder, which is characterized by the proliferation of non‐Langerhans cell histiocytes.
Selcen Kundak, Yasemin Çakır
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Disseminated Juvenile Xanthogranuloma
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2006SummaryJuvenile xanthogranuloma (JXG) is the most common type of non‐Langerhans cell histiocytosis occurring predominantly in infants and children. Typical lesions are asymptomatic red‐yellow papules and nodules on the scalp or in the axillae or groins. Multiple lesions are more common in children than in adults.
Uwe, Wollina +2 more
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Clustered Juvenile Xanthogranuloma
Pediatric Dermatology, 2012Abstract: Clustered or agminated juvenile xanthogranuloma (JXG) is an unusual form of JXG characterized by multiple reddish‐brown or yellowish papules and nodules in a coalescent pattern. We report a case of clustered JXG involving the left lower back of a 5‐month‐old boy.
Francesc, Messeguer +4 more
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