Results 201 to 210 of about 316,660 (233)
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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   +5 more
openaire   +3 more sources

Juvenile Xanthogranuloma of the Pancreas in a Pediatric Patient Mimicking Pancreatic Neoplasm With High CA 19-9: Case Report and Literature Review

Journal of pediatric hematology/oncology, 2021
Juvenile xanthogranuloma (JXG) is a rare, non–Langerhans cell histiocytosis. It is usually a benign and self-limiting condition. The most common sites are skin and soft tissue. Pancreatic involvement is extremely rare.
Eman Al-Antary   +4 more
semanticscholar   +1 more source

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   +2 more
openaire   +3 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.
Fiona Browne   +3 more
openaire   +2 more sources

Iris Juvenile Xanthogranuloma Presenting with Hypopyon

Ocular immunology and inflammation, 2021
Purpose To report a case an iris juvenile xanthogranuloma presenting with hypopyon. Case report A 45-day-old infant was referred to our clinic for unilateral hypopyon.
Mine Esen Baris   +3 more
semanticscholar   +1 more source

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 ...
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

Bilateral retinal involvement in juvenile xanthogranuloma—Successful treatment with clofarabine

Pediatric Blood & Cancer, 2021
To the Editor Juvenile xanthogranuloma (JXG) is a disorder belonging to a group of non-Langerhans cell histiocytes that typically affects children.
M. Mifsud, S. Picton, J. Ainsworth
semanticscholar   +1 more source

Juvenile Xanthogranuloma of the Sellar Region with a 5-Year Medical History: Case Report and Literature Review

Pediatric Neurosurgery, 2021
Introduction: Xanthogranuloma of the sellar region is a rare benign lesion, and there are few cases reported in children. Its histogenesis is controversial, and it is difficult to strictly differentiate it from craniopharyngioma (CP), Rathke’s cleft cyst,
Dekui Cheng   +4 more
semanticscholar   +1 more source

Refractory Extracutaneous Juvenile Xanthogranuloma With Multiple Intracranial Nodular Lesions Successfully Treated With 2-Chlorodeoxyadenosine

Journal of pediatric hematology/oncology, 2021
Juvenile xanthogranulomatosis (JXG) is a rare histiocytic disease that is usually limited to the skin, but some JXG cases involve other organs. JXG involving the central nervous system (CNS) is rare and its treatment is inadequate.
Y. Matsukawa, K. Sakamoto, Y. Shioda
semanticscholar   +1 more source

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