Results 81 to 90 of about 324,303 (208)

Juvenile xanthogranuloma involving concurrent iris and skin: Clinical, pathological and molecular pathological evaluations

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, Elisabeth Graeff, Corina Kohler, Francis Munier, Elisabeth Bruder   +4 more
doaj   +1 more source

Dermatofibroma: a curious tumor. [PDF]

, 2012
A tumor, such as a dermatofibroma, causes consternation among many patients, but it rarely creates problems on its own. Also called a histiocytoma, it remains one of the most common mesenchymal growths.
Lambert, Peter C, Lambert, W Clark, Parish, Lawrence, Yazdanian, Shideh   +3 more
core   +1 more source

Solitary Xanthogranuloma of the Upper Cervical Spine in a Male Adult [PDF]

, 2012
We present the rare case of solitary xanthogranuloma in the upper cervical column mimicking a Brown-Sequard syndrome. A 29-year-old man complained with right hemiparesis and left hypoesthesia after a car accident.
Jo, Dae Jean, Kim, Sung Min, Lee, Seung Hwan, Lee, Sun Joo   +3 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, Beatrice Carcano, Michela Brena   +2 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, Karola Stieler, Uwe Pleyer, Ulrike Blume‐Peytavi, Annika Vogt   +4 more
wiley   +1 more source

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, Kukić, Sandro, Pavić, Tajana   +2 more
core   +2 more sources

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, Inshal Jawed, Ali Farhan, Vikash Karmani, Agha Muhammad Wali Mirza, Farah Alam, Hina Khan, Abdul Haseeb, Mohammad Omer Alam, Javed Iqbal, Brijesh Sathian, Abu Huraira Bin Gulzar   +11 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, Kato, Aiko, Sato, Haruaki, Shimizu, Fumiaki, Takeo, Naoko, Taneda, Hiroko   +5 more
core   +3 more sources

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, Man Hu, Rui Zhang, Zhigang Li, Hongyun Lian   +4 more
wiley   +1 more source

A Rare Case of Juvenile Xanthogranuloma in 8 Months Old Baby with Dyslipidemia

Bioscientia Medicina : Journal of Biomedicine and Translational Research, 2021
Background: Juvenile xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis disease of childhood. But due to rarity of non Langerhans cell hystiosis itself, the exact prevalence of juvenile xanthogranuloma remain unknown with only a few ...
J. Saiful, Rina Gustia
semanticscholar   +1 more source