Results 91 to 100 of about 316,660 (233)
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
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 +3 more
core +1 more source
Dermatology Research and Practice, Volume 2024, Issue 1, 2024.Background. Granulomatous dermatoses, particularly on facial skin, pose a diagnostic challenge, as similar histologic patterns can be produced by different causes. Aim. To evaluate the correlation between clinical suspicion and histopathological findings in various facial granulomatous dermatoses. Materials and Methods.
Zeinab Aryanian +7 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
Management of pediatric uveitis [PDF]
, 2014 Pediatric uveitis is a topic of special interest not only because of the unique diagnostic and therapeutic challenges but also because of the lifetime burden of vision loss if the problem is not adequately treated, as well as the economic and ...
Foster, C. Stephen +2 more
core +1 more source
Juvenile xanthogranuloma-diagnostic challenge on fine-needle aspiration cytology
Journal of Cytology, 2011 Juvenile xanthogranuloma (JXG) is a rare cutaneous lesion with paucity of literature on its cytological features. We report one such case which on fine-needle aspiration cytology yielded a mixed population of foamy histiocytes, multinucleated giant cells
Arghya Bandyopadhyay +2 more
doaj +1 more source
The association between juvenile xanthogranulomas in neurofibromatosis type 1 patients and the development of leukemia: A systematic review [PDF]
, 2023 Neurofibromatosis type 1 (NF1) is an inherited tumor syndrome caused by heterozygous germline mutations in the NF1 gene, occurring in approximately 1/2600 individuals.
Kiuru, Maija +4 more
core
Rare association of juvenile xanthogranuloma and acute lymphoblastic leukemia
Indian Journal of Paediatric Dermatology, 2020 Juvenile xanthogranuloma (JXG) is a rare non-Langerhans cell histiocytosis that usually occurs during infancy and early childhood. It is seen in combination with juvenile chronic myelomonocytic leukemia and/or neurofibromatosis type 1.
Palvi Singla, Rima Joshi, Bela J Shah
doaj +1 more source
Cranial unifocal langerhans cell histiocytosis in a female child: a difficult case with S-100 and CD1a immunonegativity [PDF]
, 2015 A 13-years old female child was carried to Dr. Sardjito General Hospital, Yogyakarta by her mother with chiefcomplaint of a mass on her forehead. Since eight months prior to her visiting, she had a mass on her forehead whichbecame larger slowly without ...
Soeripto, J Bras, Hanggoro Tri Rinonce Sagiri Mangunsudirdjo
core +1 more source
Juvenile xanthogranuloma of the cerebellopontine angle: A case report and review of the literature
Otolaryngology Case Reports, 2019 Juvenile xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis, most often presenting with skin lesions of the head, neck, and upper trunk. Intracranial presentations have been previously described, however, due to its rarity, treatment algorithms
Sarah M. Tittman +6 more
doaj