Results 171 to 180 of about 323,828 (213)

Clustered Juvenile Xanthogranuloma

Pediatric Dermatology, 2012
Abstract:  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, Anna, Agustí-Mejias, Isabel, Colmenero, Angela, Hernández-Martin, Antonio, Torrelo   +4 more
openaire   +2 more sources

Subcutaneous juvenile xanthogranuloma

Journal of Cutaneous Pathology, 1995
A 1‐month‐old female infant was seen in consultation because of a congenital subcutaneous nodule, 2×3 cm in diameter, in the right retroauricular area. The nodule was surgically excised. Histologically, a large subcutaneous nodular mass was well delimited but not encapsulated.
E, Sánchez Yus, L, Requena, C, Villegas, P, Valle   +3 more
openaire   +2 more sources

Ocular Juvenile Xanthogranuloma

Optometry and Vision Science, 2015
To report the clinical and histopathologic characteristics and prognoses of three ocular juvenile xanthogranuloma (JXG) cases.Three cases were included in this study. The first case involved a 5-year-old girl with an enlarging yellowish mass at the limbus with corneal involvement.
Liangliang, Niu, Chaoran, Zhang, Fanrong, Meng, Rongrong, Cai, Yingwen, Bi, Yan, Wang, Jianjiang, Xu   +6 more
openaire   +2 more sources

Hemosiderotic Juvenile Xanthogranuloma

The American Journal of Dermatopathology, 2017
Abstract: Juvenile xanthogranuloma is a non-Langerhans cell lesion mostly limited to the skin but occasionally presenting in extracutaneous locations or associated with systemic conditions. Lesions need to be distinguished mainly from dermatofibroma, xanthoma, Langerhans cell histiocytosis, or reticulohistiocytoma.
Angel, Fernandez-Flores, Ina, Nicklaus, Fiona, Browne, Isabel, Colmenero   +3 more
openaire   +2 more sources

Role of FDG PET/CT in the Evaluation of Therapy Response in Systemic Juvenile Xanthogranuloma.

Clinical Nuclear Medicine, 2022
Juvenile xanthogranuloma, a rare type of non-Langerhans cell histiocytosis, is mostly seen in childhood and adolescence and generally manifests as widespread skin lesions. It rarely shows systemic involvement.
Mehmet Emin Mavi, Başak Turan, B. Salancı, M. Bozkurt   +3 more
semanticscholar   +1 more source

Intraoral juvenile xanthogranuloma

Oral Surgery, Oral Medicine, Oral Pathology, 1978
A case of juvenile xanthogranuloma of the gingiva is presented. This uncommon, benign disorder has rarely been histologically documented in the oral cavity, and rarely have oral lesions been described as presenting symptoms prior to this report. The pertinent literature is reviewed and possible etiologic factors are discussed.
R E, Christensen, R S, Hertz, H M, Cherrick   +2 more
openaire   +2 more sources

Juvenile Xanthogranuloma: A Comparative Immunohistochemical Study of Factor XIIIa, CD11c, and CD4

American journal of dermatopathology, 2022
: Juvenile xanthogranuloma is a group C and L non-Langerhans cell histiocytosis, and its cell of origin is still debatable. The expression of CD11c, a more recently described macrophage marker, and CD4 have not been studied comprehensively.
B. Salari, L. Dehner
semanticscholar   +1 more source

Juvenile xanthogranuloma: three cases

Pediatric Surgery International, 1996
Juvenile xanthogranuloma (JX) is a regressing fibrous histiocytoma occurring during infancy and characterized by cutaneous papules and nodules and less often by additional lesions in deep tissue and organs. It has a special place among childhood masses by presenting different outcomes and spontaneous regression.
Gork, S, Ariturk, E, Baris, S, Ariturk, N, Bernay, F, Rizalar, R, Gurses, N   +6 more
openaire   +2 more sources

Notable therapeutic response in a patient with systemic juvenile xanthogranuloma with KIF5B‐ALK fusion

Pediatric Blood & Cancer, 2021
To the Editor, Juvenile xanthogranuloma (JXG) is classified as ahistiocytosis that is generally diagnosed on the basis of the presence of cutaneous nodules in infancy. It has been considered benign and can undergo spontaneous regression without therapy.1
Minako Sugiyama, Shinsuke Hirabayashi, Yukitomo Ishi, J. Kikuchi, Ayako Ishikura, Hiroaki Motegi, Y. Ueda, Saori Sawai, K. Hara, Yukayo Terashita, Yuko Cho, E. Takakuwa, Shohei Honda, S. Yamaguchi, I. Kinoshita, A. Manabe   +15 more
semanticscholar   +1 more source

Recurrent CLTC::SYK fusions and CSF1R mutations in juvenile xanthogranuloma of soft tissue.

Blood
Juvenile 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, Hans J Baelde, R. Vorderman, Ellen Stelloo, Joost F Swennenhuis, K. Szuhai, M. Lamers, Boyd Kenkhuis, M. Al-Hussaini, I. B. Briaire-de Bruijn, S. W. Lam, J. Bovée, A. Cleven, R. M. Verdijk, C. V. van Noesel, Marijke van Dijk, M. Scheijde-Vermeulen, Annette H Bruggink, Jan Am van Laar, A. D. de Vries, Wim Tissing, C. van den Bos, Andreas von Deimling, T. van Wezel, A.G.S. van Halteren, P.C.W. Hogendoorn   +25 more
semanticscholar   +1 more source