Results 51 to 60 of about 2,482 (186)
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
Benign and malignant cutaneous nasal lesions
Eye &ENT Research, Volume 1, Issue 2, Page 65-91, December 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
Interdisciplinary Neurosurgery, 2022 Background: Juvenile xanthogranuloma (JXG) is a type of non-Langerhans cell histiocytosis (non-LCH) that primarily affects infants and young children. It mostly occurs in the skin, while the brain is rarely affected.
Haifeng Liu +3 more
doaj +1 more source
Respirology Case Reports, Volume 12, Issue 12, December 2024.A flow volume loop demonstrated classical upper airway obstruction pattern. Abstract Inflammatory myofibroblastic tumour is a rare tumour. We present an atypical case of Inflammatory myofibroblastic tumour which was trachea in location, histocyte rich and ROS1 rearranged.
Chin Tong Kwok +5 more
wiley +1 more source
Japanese classification of pancreatic carcinoma by the Japan Pancreas Society: Eighth edition
Journal 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
Intraocular juvenile xanthogranuloma masquerading as conjunctivitis in an adult
Journal of Clinical Ophthalmology and Research, 2015 A 22-year-old female presented to us with redness, pain and intermittent blurring of vision in the left eye of one month duration. She had been diagnosed as a case of conjunctivitis elsewhere for which she was being treated with topical antibiotics ...
Ramesh Murthy +3 more
doaj +1 more source
Noonan syndrome‐like disorder: Case report and review of the literature
Pediatric 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
CD68-negative nonlipidized juvenile xanthogranuloma
Dermatologica 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
Multiple juvenile xanthogranuloma: A rare case of having clinical appearance mimicking molluscum contagiosum or syringoma [PDF]
JDVI (Journal of General Procedural Dermatology & Venereology Indonesia), 2015 Introduction: Juvenile xanthogranuloma (JXG) is an uncommon benign cutaneous fibrohistiocytic, self healing, class II non-Langerhan’s cell histiocytosis (NLCH). JXG accounts for 80-90% of cases of NLCH.
Heru Nugraha +6 more
doaj +1 more source