Results 171 to 180 of about 2,710 (215)

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
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Dermoscopy of Juvenile Xanthogranuloma

Dermatology, 2020
<b><i>Background:</i></b> Dermoscopy is useful for the evaluation of juvenile xanthogranuloma (JXG). The classical “setting sun” pattern is characteristic of JXG, but its sensibility appears to be limited. An extensive description of other dermoscopic findings is not available in the literature. <b><i>Objectives:</
Leonardo Peruilh-Bagolini, Mariana Silva-Astorga, María Jesús Hernández San Martín, Magdalini-Sofia Manoli, Chryssoula Papageorgiou, Zoe Apalla, Aimilios Lallas   +6 more
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Juvenile xanthogranuloma of the eye

Vestnik oftal'mologii, 2018
Juvenile xanthogranuloma (JX) is a benign growth of fibrohistiocytoma range that mainly affects children. The most frequent localization of the tumor is skin integument. Non-cutaneous forms of JX are found in 5-10% of cases; they are manifested as deep lesions of soft tissues, involvement of various organs (oropharynx, lungs, liver, spleen, pericardium,
A A, Yarovoy, O V, Golubeva, S S, Kleyankina, T V, Yanchenko   +3 more
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Juvenile xanthogranuloma of the kidney

Pediatric Radiology, 1988
Juvenile xanthogranuloma is a benign histiocytosis of infancy and childhood characteristically involving the skin, the eye, and, rarely, the lungs, liver and mesothelial structures. This report documents the first known case of renal involvement which is demonstrated by ultrasound and computed tomography.
T J, Gilbert, B R, Parker
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Juvenile Xanthogranuloma on the Sole

Pediatric Dermatology, 2000
Abstract: Juvenile xanthogranulomas are benign, typically self‐limiting tumors that most commonly occur on the head and trunk. We report one such tumor with an atypical clinical appearance, occurring at an unusual site, the sole of the foot.
L R, Whittam, E H, Higgins
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Juvenile Xanthogranuloma of the Scrotum

Journal of Urology, 1983
Abstract We report a rare case of juvenile xanthogranuloma affecting the scrotum, that did not follow the usually benign course. Surgical excision is recommended in those cases that do not have a benign and self-limited course.
F J, Goulding, R A, Traylor
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Juvenile Xanthogranuloma of the Hand

Journal of Hand Surgery, 1984
A case of juvenile xanthogranuloma in the hand is reported. The lesion was atypical clinically, being sited in the hand and the tumour was so large that it extended from the palmar to the dorsal surface. Curettage was performed at seven weeks after birth and histological examination established a diagnosis of juvenile xanthogranuloma.
A, Matsuzaki, S, Yo, T, Isayama
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Juvenile Xanthogranuloma of the Finger

Pediatric Dermatology, 2006
Abstract:  We present an unusual instance of juvenile xanthogranuloma occurring in the hand. A 23‐month‐old girl had a mass on the radial aspect of the right third finger at the distal interphalangeal joint that extended to the collateral ligament.
Duncan B, Hughes, Matthew M, Hanasono, William B, Nolan   +2 more
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Segmental Juvenile Xanthogranuloma

Pediatric Dermatology, 2013
AbstractA 5‐month‐old boy had erythematous nodules over the left side of his trunk with a segmental arrangement since birth. Histopathologic examination revealed sheets of foamy histiocytes infiltrating the dermis and subcutaneous fat, admixed with multinucleated giant cells and lymphocytes, making this an unusual case of juvenile xanthogranuloma ...
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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
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