Results 161 to 170 of about 2,482 (186)

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
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Glaucoma in Juvenile Xanthogranuloma

Seminars in Ophthalmology, 2006
Juvenile xanthogranuloma (JXG) is a benign histiocytic skin disorder mainly encountered during infancy. Approximately 10% of cases exhibit ocular manifestations leading to serious complications. Specifically, secondary glaucoma can result in severe and blinding eye disease.
Zarmeena Vendal, Teresa Chen, David S. Walton   +2 more
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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
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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.
Fiona Browne, Angel Fernandez-Flores, Ina Nicklaus, Isabel Colmenero   +3 more
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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
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Juvenile xanthogranuloma of the tongue

Journal of the American Academy of Dermatology, 1995
Oral juvenile xanthogranuloma is a rare condition, with only 10 histologically proven cases previously described. A histologically unusual variant is reported here, diagnosis of which was aided by the use of immunohistochemical stains. Previously reported cases are reviewed, and their characteristics are tabulated and discussed.
Sarah J Satow, Kenneth H. Dawson, Allen M. Gown, Dolphine Oda, Philip Worthington, Sui Zee   +5 more
openaire   +3 more sources

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.
Teruto Isayama, Sansen Yo, A. Matsuzaki
openaire   +3 more sources

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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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 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,
O. V. Golubeva, T. V. Yanchenko, A. A. Yarovoy, S. S. Kleyankina   +3 more
openaire   +3 more sources