Results 61 to 70 of about 7,890 (255)

A Rare Case of Cutaneous Crystal‐Storing Histiocytosis With Kappa Light Chain Restriction and Unusual BCL6 Expression

open access: yesJournal 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 Presenting as Bilateral Non-Infiltrative Extraconal Superior Orbital Tumour in a 27 Year Old Nigerian Woman: Features, Management and Outcome

open access: yesClinical Medicine Insights: Case Reports, 2012
Introduction Orbital masses in adults are often caused by systemic diseases or are associated with systemic manifestations. Juvenile xanthogranuloma as a cause is rare and unreported in Africa.
Okosa Michael Chuka   +1 more
doaj   +1 more source

An exuberant case of necrobiotic xanthogranuloma

open access: yesIndian 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

Xanthogranulomatous hypophysitis: A rare presentation in a young female patient

open access: yesClinical Case Reports, 2022
Hypophysitis is a rare inflammatory condition that may present both clinically and radiologically as a neoplastic lesion. Xanthogranulomas are rare intracranial lesions with controversial etiology.
Mohammad Ali Yaghoubi   +4 more
doaj   +1 more source

Inflammatory pseudotumor of the kidney: a case report [PDF]

open access: yes, 2011
Introduction Inflammatory pseudotumors, also known as inflammatory myofibroblastic tumors, are uncommon benign tumors of unknown etiology which may develop at several anatomical sites. In the urogenital tract, inflammatory pseudotumor usually
Abdelhak Khallouk   +7 more
core   +1 more source

Necrobiotic Xanthogranuloma [PDF]

open access: yesMayo Clinic Proceedings, 2021
Andrew J. Portuguese   +2 more
openaire   +2 more sources

Validation of the German version of Infants and Toddlers Dermatology Quality of Life (InToDermQoL) Questionnaire

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background and Objectives Skin diseases can greatly impair quality of life (QoL) of pediatric patients and their families. The Infants and Toddlers Dermatology Quality of Life questionnaire (InToDermQoL) is the first skin‐generic instrument assessing QoL in children ≤ 4 years, as reported by their caregiver. This study aimed to psychometrically
Juliane Traxler   +8 more
wiley   +1 more source

Baby with neonatal systemic juvenile xanthogranuloma born within a cross-cousin marriage

open access: yesDermatologica Sinica, 2015
Juvenile xanthogranuloma is a non-Langerhans cell histiocytosis seen most commonly in childhood and adolescence. Extracutaneous involvement is rare. We report an interesting and extremely rare case of systemic (skin, lung, spleen, and colon) “juvenile ...
Hikmet Tekin Nacaroglu   +6 more
doaj   +1 more source

Necrobiotic xanthogranuloma successfully treated with autologous stem cell transplantation [PDF]

open access: yes, 2018
Paraproteinemia can be complicated by necrobiotic xanthogranuloma. Therapeutic options for this progressive disease are limited, and there is no agreement on a single best strategy.
Dispenzieri, Angela   +7 more
core  

Management of pediatric uveitis [PDF]

open access: yes, 2014
Pediatric uveitis is a topic of special interest not only because of the unique diagnostic and therapeutic challenges but also because of the lifetime burden of vision loss if the problem is not adequately treated, as well as the economic and ...
Foster, C. Stephen   +2 more
core   +1 more source

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