Results 31 to 40 of about 1,167 (171)
Adult onset xantogranulomatous disease associated with vitiligo
Indian Dermatology Online Journal, 2019 Adult Onset Xanthogranulomatous Disease represents an umbrella term encompassing 4 distinct entities with partially overlapping clinicopathological features: adult-onset xanthogranuloma, adult-onset asthma with periocular xanthogranuloma, Erdheim-Chester
Rashmi Sriram +2 more
doaj +1 more source
Indian Journal of Ophthalmology. Case Reports, 2021 Juvenile xanthogranuloma (JXG) is a benign histiocytic disorder that belongs to the non-Langerhans cell group. Extracutaneous involvement in the eye usually involves the iris and presents as recurrent spontaneous episodes of hyphema or secondary glaucoma.
Rachna Meel +2 more
doaj +1 more source
A case of adult-onset asthma and periocular xanthogranuloma treated with systemic steroids
Indian Journal of Ophthalmology. Case Reports, 2022 Adult orbital xanthogranulomatous disease is a rare disorder which may or may not be associated with a systemic involvement. Herein, we report a 60-year-old male who presented with periocular swelling around the eyes for six years with history of asthma ...
S Gajashree +4 more
doaj +1 more source
An exuberant case of necrobiotic xanthogranuloma
Indian Dermatology Online Journal, 2020 Necrobiotic xanthogranuloma (NXG) is a rare form of inflammatory granulomatous disease of the skin characterized by the presence of pruritic to painful lesions, generally located in the periorbital area, although trunk and proximal extremities may also ...
Sofia Lopes +5 more
doaj +1 more source
ADULT ONSET XANTHOGRANULOMA – CASE REPORT AND REVIEW OF LITERATURE [PDF]
Romanian Medical Journal, 2019 Juvenile xanthogranuloma represents the most common form of non-Langerhans cell histiocytosis. It is tipically a childhood disorder, over 80% of cases developing in the first year of life.
Liliana Gabriela Popa +5 more
doaj +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
core +1 more source
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
core +1 more source
Histiocytosis development and clinical variation through the lens of genomics
The Journal of Pathology, EarlyView.Abstract Histiocytic neoplasms are rare haematologic diseases characterised by clonal expansions of cells with a monocyte, macrophage or dendritic cell phenotype. Their clinical manifestations are diverse, ranging from indolent lesions to aggressive systemic disease.
Paul G Kemps +3 more
wiley +1 more source
Journal of Cutaneous Pathology, EarlyView.ABSTRACT Crystal‐storing histiocytosis (CSH) is a rare histopathologic phenomenon characterized by the accumulation of crystalline material within histiocytes, most often associated with lymphoplasmacytic or plasma cell neoplasms. Cutaneous involvement is uncommon and may present diagnostic challenges.
Liangli Wang +8 more
wiley +1 more source
JUVENILE XANTHOGRANULOMA: A CASE REPORT
, 2019 Objective: To report a rate case of Juvenile xanthogranuloma in a newborn infant. Case description: We present the case of a 31-week preterm newborn with multiple skin lesions whose clinical, histological and immunohistochemical findings allowed the ...
Marta Almeida Pereira (6403391) +5 more
core +3 more sources