Results 71 to 80 of about 2,665 (208)
A 50‐year‐old man with a 12‐year history of extensive pachymeningeal thickening
Brain Pathology, EarlyView.
Alyssa M. Lee +3 more
wiley +1 more source
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
Istiocitoma fibroso maligno. Caso clinico [PDF]
, 2010 L’istiocitoma fibroso maligno è un sarcoma aggressivo dei tessuti molli, che compare più frequentemente nei muscoli degli arti e nella cavità addominale o nel retroperitoneo di giovani adulti.
Fabrizio, T. +3 more
core
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
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
Puzzle histiocytosis (solitary mononuclear xanthogranuloma with LCH component). A case report*
Polish Journal of Pathology, 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
doaj +1 more source
JEADV Clinical Practice, Volume 5, Issue 1, Page 303-305, March 2026.
Flora Balieva +5 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
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