Results 191 to 200 of about 316,660 (233)

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

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.
Luis Requena, C Villegas, Pilar Valle, E. Sanchez Yus   +3 more
openaire   +3 more sources

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.
Anna Agustí-Mejias, Francesc Messeguer, Isabel Colmenero, Angela Hernández-Martín, Antonio Torrelo   +4 more
openaire   +3 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.
Fanrong Meng, Liangliang Niu, Chaoran Zhang, Yan Wang, Yingwen Bi, Rong-rong Cai, Jianjiang Xu   +6 more
openaire   +3 more sources

Fatal Disseminated Multiple Intracranial Juvenile Xanthogranuloma without Cutaneous and Other Organ Involvement: A Rare Case Report

Pediatric Neurosurgery, 2021
Introduction: Juvenile xanthogranuloma (JXG) is a disorder of histiocytic proliferation that affects young children and usually presents as spontaneously regressing cutaneous lesions.
Emre Bilgin, A. I. Ökten
semanticscholar   +1 more source

Juvenile Xanthogranuloma and Neurofibromatosis

Archives of Dermatology, 1973
The finding of neurofibromatosis in patients or in relatives of patients with juvenile xanthogranuloma is intriguing. To our knowledge, this association has not been emphasized in the American dermatologic literature.
Gordon B. Newell, J. Fred Mullins, Orville J. Stone   +2 more
openaire   +3 more sources

Treatment of juvenile xanthogranuloma [PDF]

Pediatric Blood & Cancer, 2008
AbstractJuvenile xanthogranuloma (JXG) is generally a benign, self‐limited histiocytic disorder of the skin. We report two cases of multisystem JXG presenting with clinical features more commonly seen in Langerhans cell histiocytosis (LCH), including diabetes insipidus and lytic bony lesions.
Daniel G. Stover, Curtis Turner, Osvaldo Regueira, Srilatha Alapati, James A. Whitlock   +4 more
openaire   +2 more sources

Pediatric Orbital Juvenile Xanthogranuloma: A Case Series and Review of the Literature

Ophthalmic Plastic and Reconstructive Surgery
Purpose: Juvenile xanthogranuloma (JXG) is a subtype of histiocytosis characterised histologically by foamy non-Langerhan cells with Touton giant cells.
Ming-Han H Lee, Ebony J Smith, Thomas G. Hardy, Nicole Graf, Krishna Tumuluri   +4 more
semanticscholar   +1 more source

Juvenile Xanthogranuloma of the Testis

Journal of Urology, 1985
A 7-month-old boy presented with numerous xanthomatous skin lesions and a hard irregular swelling of the right testis. Clinically, the testicular lesion was impossible to distinguish from a malignant neoplasm. Histological examination of a skin biopsy and of the testis following orchiectomy showed lesions typical of juvenile xanthogranuloma.
A. Gledhill, N.H. Townell, T. Robinson, P. Hopewell   +3 more
openaire   +3 more sources

Ocular Juvenile Xanthogranuloma With BRAF V600E Mutation in a Child.

Journal of pediatric ophthalmology and strabismus, 2021
The authors present a case of bilateral painless progressive proptosis. A diagnosis of ocular juvenile xanthogranuloma was made based on clinical manifestations, histopathology, and immunohistochemistrical staining.
Chengyue Zhang, Z. Feng, C. Solarte, Li Li   +3 more
semanticscholar   +1 more source