Results 61 to 70 of about 2,482 (186)
Pilomatricoma in the infraorbital region
Clinical Case Reports, Volume 12, Issue 8, August 2024.Key Clinical Message Pilomatricoma, a rare benign skin tumor arising from hair follicle matrix cells, warrants consideration in the evaluation of subcutaneous nodules or masses, especially when presenting as painless and firm lesions. Accurate diagnosis hinges on histopathological examination, underscoring the significance of clinician vigilance and ...
Dilasha Dhungel +3 more
wiley +1 more source
Cysts and tumours of the iris: Diagnostic tools and key management considerations—A review
Clinical &Experimental Ophthalmology, Volume 52, Issue 6, Page 665-683, August 2024.Abstract The iris is a unique structure, with exquisite variations in colour and form. Pathological changes, specifically including iris cysts and tumours are relatively uncommon, difficult to diagnose, and yet potentially blinding or life‐threatening.
Bia Z. Kim +2 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
Brain imaging in children with neonatal cholestatic liver disease: A systematic review
Acta Paediatrica, Volume 113, Issue 6, Page 1168-1185, June 2024.Abstract Aim To determine if children with neonatal cholestatic liver disease had concurrent and later findings on brain imaging studies that could be attributed and the cholestasis to contribute to the understanding of the impaired neuropsychological development.
Thora Wesenberg Helt +6 more
wiley +1 more source
Histopathology, Volume 84, Issue 5, Page 837-846, April 2024.From 1993 to 2022, more than 4000 patients with a pathologist‐assigned diagnosis of a histiocytic disorder were registered in the Dutch Nationwide Pathology Databank. This unique dataset provides an unbiased look into the demographic characteristics and additional haematologic cancers of patients diagnosed with histiocytic disorders in The Netherlands.
Paul G Kemps +11 more
wiley +1 more source
Journal of Cosmetic Dermatology, Volume 23, Issue 3, Page 970-977, March 2024.Abstract Background Surgical excision combined with radiotherapy is considered an effective treatment for keloids, while the efficacy and safety of this regimen for huge keloids in patients who need reconstruction after excision is still unclear. Therefore, this study aimed to evaluate the efficacy and safety of surgical excision and reconstruction ...
Wenfang Dong +3 more
wiley +1 more source
Cataract surgery in juvenile xanthogranuloma: Case report and a brief review of literature
Indian Journal of Ophthalmology, 2013 There is limited literature on the management of cataracts in juvenile xanthogranuloma (JXG). A 2-month-old girl presented to us with hyphema, secondary glaucoma OU and skin nodules suggestive of JXG.
R Muralidhar +5 more
doaj +1 more source
Juvenile Xanthogranuloma [PDF]
Ophthalmology, 2015 Krishna R, Surapaneni +2 more
openaire +2 more sources
A Subcutaneous Juvenile Xanthogranuloma in a 4-Year-Old Girl Who Presented with a Lower Eyelid Mass
Case Reports in Ophthalmology, 2019 Juvenile xanthogranuloma (JXG) is a relatively uncommon, benign, histiocytic proliferative cutaneous disorder that typically affects children, with the head and neck being the most common sites.
Amjad A. Saifaldein +3 more
doaj +1 more source
Juvenile Xanthogranuloma of the Ear: A Case Report [PDF]
, 2008 Mohamed Amir Mrad +3 more
openalex +2 more sources