Results 51 to 60 of about 2,232,149 (123)
BMC OphthalmologyBackground The “C group” of the histiocytic disorders is characterized by non-Langerhans-cell histiocytic lesions in the skin, mucosal surfaces, or both, out of which Juvenile xanthogranuloma (JXG) is the most common typically affecting the skin. The eye
Hind Manaa Alkatan +3 more
doaj +1 more source
Intraocular juvenile xanthogranuloma of the iris in an adult patient
, 2017 Purpose: Juvenile xanthogranuloma (JXG) is a rare histiocytic skin disease primarily of young children, which may also affect ocular structures and in particular the iris.
Elias Flockerzi +2 more
core +1 more source
, 2008 Background: Thrombotic thrombocytopenic purpura (TTP) is most commonly associated with deficiency or inhibition of von Willebrand factor-cleaving protease (ADAMTS-13) activity.
Cohen, H. +7 more
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Multiple generalized xanthogranuloma in adult: Case report and treatment
, 2011 Xanthogranuloma is a benign, asymptomatic, and self-healing disorder of non-Langerhans cell histiocytosis, affecting mostly infants, children, and rarely adults. Diagnosis is easy in typical cases but become more complex in unusual forms.
Mallika Pal +4 more
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Unusual aspects of juvenile xanthogranuloma
, 1993 We describe three unusual features of juvenile xanthogranuloma that were observed in three different children. We also describe the mixed and clustered forms of juvenile xanthogranuloma and a giant juvenile xanthogranuloma of the ...
R. Grimalt +3 more
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Case report Adult-onset Still’s disease as a mask of Hodgkin lymphoma
, 2015 Adult-onset Still’s disease is a rare disorder, which creates difficulties in making a proper diagnosis. Ambiguous symptoms and results of auxiliary tests, lack of unequivocal diagnostic tests and the need to exclude other causes of the disease are major
Katarzyna Pawlak-Buś +2 more
core +1 more source
Puzzle histiocytosis (solitary mononuclear xanthogranuloma with LCH component). A case report*
, 2017 We report a case of 40-year-old Caucasian man presented with an asymptomatic nodule localized on his arm. The puzzle histiocytosis composed of juvenile xanthogranuloma and Langerhans cell histiocytosis was diagnosed.
Katarzyna Woszczyna-Mleczko +5 more
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, 2012 Amir Mohsenin,1 John Sinard,1,2 John J Huang11Department of Ophthalmology and Visual Science, 2Department of Pathology, Yale University School of Medicine, New Haven, CT, USAAbstract: This report describes a unique case of coexisting necrobiotic ...
Huang JJ, Sinard J, Mohsenin A
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A case report of a man with adult-onset idiopathic hypogonadotrophic hypogonadism
, 2017 Background Adult-onset idiopathic hypogonadotrophic hypogonadism is a rare condition. It includes men who have no recognizable central nervous system abnormality nor other identifiable cause. They generally demonstrate age-appropriate puberty and normal
Davoren, Peter, Tang, Chee
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Late Onset Juvenile Xanthogranuloma
, 1999 A 19 year old female was seen with multiple skin coloured and hyperpigmented macules, discrete as well as grouped papules and nodules of varying sizes distributed over the face, neck, extensor and flexor aspects of both upper and lower extremities ...
Sentamilselvi G +3 more
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