Results 71 to 80 of about 319,608 (239)
Rosacea in childhood and adolescence: A review
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 6, Page 684-691, June 2025.Summary Despite presenting with similar symptoms, triggers, and progression patterns as adults, rosacea in children and adolescents is frequently overlooked as a primary differential diagnosis. However, initial manifestations of classic clinical types can be observed from infancy onwards.
Sören Korsing +4 more
wiley +1 more source
Síndrome ocular mascarada devido linfoma intra-ocular: relato de casos [PDF]
, 2007 Ocular masquerade syndrome was diagnosted in two patients with chronic uveitis. The patients presented non-Hodgkin's lymphoma as the final diagnosis two forms of intraocular retinal pigment epithelium involvement was seen.
Abreu, Mariza Toledo +2 more
core +2 more sources
Intraocular juvenile xanthogranuloma of the iris in an adult patient
American Journal of Ophthalmology Case Reports, 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
doaj +1 more source
Disseminated Juvenile Xanthogranuloma: A Case Report
International Journal of Dermatology and Venerology, 2022 Introduction:. Histiocytoses are localized or systemic diseases that can broadly be classified into Langerhans cell histiocytosis and non-Langerhans cell histiocytosis.
Najam Us Saher +2 more
doaj +1 more source
Diagnostic Importance of Cutaneous Manifestations of Neurofibromatosis—A Systematic Review
Neurology and Clinical Neuroscience, Volume 13, Issue 3, Page 165-173, May 2025.ABSTRACT A class of hereditary diseases known as neurofibromatoses results in tumor growth on tissue from nerves. The spinal cord, nerves, and brain are among the parts of the nervous framework where these tumors can form. Similar to other genetic disorders, neurofibromatosis discloses complicated phenotypes, exhibiting varying benign and malignant ...
Hina Aslam +11 more
wiley +1 more source
American Journal of Ophthalmology Case Reports, 2018 Purpose: To report a case of juvenile xanthogranuloma involving the iris and skin that clincally was diagnosed with an obvious cutaneous lesion.
Peter Meyer +4 more
doaj +1 more source
A case report of pediatric systemic juvenile xanthogranuloma
Malignancy Spectrum, Volume 2, Issue 1, Page 53-58, March 2025.Abstract Background Juvenile xanthogranuloma (JXG) is a rare disorder that belongs to the broad group of non‐Langerhans cell histiocytosis. It is characterized by one or more nodules with predilection sites on the head, neck, and trunk, and lesions that may be several millimeters in diameter.
Feifei Liu +4 more
wiley +1 more source
Case Reports in Otolaryngology, Volume 2025, Issue 1, 2025.Background The unusual disorder known as Langerhans cell histiocytosis (LCH), which is most frequently observed in children and young adults, is caused by the clonal proliferation of Langerhans cells. This disease is classified into several types depending on the extent of the lesion.
Yoshifumi Matsumoto +4 more
wiley +1 more source
A Case of Orbital Xanthogranuloma Treated by Surgical Excision [PDF]
, 2010 Orbital xanthogranuloma is an uncommon tumor. It is usually associated with a systemic or hematological disease. This report presents a rare case of orbital xanthogranuloma associated with heart disease and thrombocytopenia.
Fujiwara, Sakuhei +5 more
core +3 more sources
Juvenile Xanthogranuloma of the Nasal Septum: A Case Report
Journal of Clinical Otolaryngology Head and Neck
Surgery, 2021 Juvenile xanthogranuloma is a rare benign lesion that occurs most frequently in infants and children. Histologically, juvenile xanthogranuloma represents an accumulation of non-Langerhans cell histiocytes.
H. Kim, Y. An, Min Ju Kim, J. Choi
semanticscholar +1 more source