Results 71 to 80 of about 316,660 (233)

MRI features of juvenile xanthogranuloma

open access: yesAsian Journal of Surgery, 2023
Yimeng Kang, Weijian Wang, Yong Zhang
doaj   +3 more sources

Clinical Analysis of Pediatric Systemic Juvenile Xanthogranulomas: A Retrospective Single-Center Study [PDF]

open access: yes, 2021
Objective: To investigate the clinical characteristics, treatment, and prognosis of children with systemic juvenile xanthogranuloma (JXG).Methods: Clinical data of children with JXG who were hospitalized in Beijing Children's Hospital, Capital Medical ...
Ang Wei   +44 more
core   +1 more source

A case report of pediatric systemic juvenile xanthogranuloma

open access: yesMalignancy 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

Intraocular juvenile xanthogranuloma of the iris in an adult patient

open access: yesAmerican 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

Japanese classification of pancreatic carcinoma by the Japan Pancreas Society: Eighth edition

open access: yesJournal of Hepato-Biliary-Pancreatic Sciences, Volume 31, Issue 11, Page 755-768, November 2024.
Ishida and colleagues report that the eighth edition of the Japanese classification of pancreatic carcinoma retains the T category, introduces new lymph node names, incorporates peritoneal cytology into the M category, and addresses endoscopic ultrasound‐guided fine‐needle aspiration biopsy and post‐therapy effects.
Masaharu Ishida   +26 more
wiley   +1 more source

Non-Melanocytic Benign Skin Tumors in Children [PDF]

open access: yes, 2007
Background: Dermatologists often attend children with benign skin tumors and cysts. The decision to perform dermatologic surgery in children may be difficult to make, especially in cases of benign tumors.
Belinchón , Isabel   +6 more
core   +1 more source

Noonan syndrome‐like disorder: Case report and review of the literature

open access: yesPediatric Dermatology, Volume 41, Issue 6, Page 1203-1210, November/December 2024.
Abstract Of patients with a Noonan syndrome phenotype, only about 1% are found to be related to pathological variants in CBL, also known as Noonan syndrome‐like disorder (NSLD). We present a case of a 4‐year‐old boy diagnosed with NSLD, presenting with multiple melanocytic nevi and superficial neurofibromas.
Kristie Mar, Joseph M. Lam
wiley   +1 more source

Disseminated Juvenile Xanthogranuloma: A Case Report

open access: yesInternational 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

Benign and malignant cutaneous nasal lesions

open access: yesEye &ENT Research, Volume 1, Issue 2, Page 65-91, September 2024.
Abstract The nose is a structure of both cosmetic and functional importance. Cutaneous lesions of the nose occasionally represent a diagnostic challenge and involve the expertise of several specialties from dermatology, otolaryngology—head and neck surgery, infectious disease, and pathology, among others.
Hamed Sarikhani   +4 more
wiley   +1 more source

CD68-negative nonlipidized juvenile xanthogranuloma

open access: yesDermatologica Sinica, 2017
Juvenile xanthogranuloma (JXG) belongs to the group of non-Langerhans cell histiocytosis. JXG is typically factor XIIIa- and CD68-positive. Nonlipidized JXG (NJXG) is a rare, mononuclear variant of JXG that shows few or absence of foam cells or Touton ...
Tzu-Kun Lo   +3 more
doaj   +1 more source

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