Results 61 to 70 of about 2,635 (192)
Endoscopic treatment of mediastinal pancreatic pseudocyst using lumen apposing metal stents - Case report [PDF]
, 2023 Mediastinal pancreatic pseudocyst (PP) is a rare complication of acute alcoholic pancreatitis. Endoscopic drainage has become widely used in the management of PPs and novel lumen apposing metal stents (LAMS) could provide more effective ...
Kralj, Dominik +2 more
core +2 more sources
Epidermal Nevi and Epidermal Naevus Syndromes
JEADV Clinical Practice, Volume 4, Issue 3, Page 669-680, August 2025.ABSTRACT Epidermal nevi (EN) arise from postzygotic variants in ectoderm‐derived cell lines, such as keratinocytes and cells forming adnexa. EN may be present alone without any associated abnormality or be part of a syndrome. In this review, we will discuss about the clinical and genetics of the main types of EN and related syndromes.
Gianluca Tadini +2 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
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
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
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
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
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
A neonatal pustule:Langerhans cell histiocytosis [PDF]
, 2019 Langerhans cell histiocytosis (LCH) is a rare, clinically heterogeneous disease that most commonly occurs in pediatric populations. Congenital self-limited LCH is a benign variant of LCH.
Hogeling, Marcia +4 more
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