Results 51 to 60 of about 4,609,996 (168)
Multisystem ALK-positive histiocytosis: a multi-case study and literature review
Orphanet Journal of Rare Diseases, 2023 Background Anaplastic lymphoma kinase (ALK)-positive histiocytosis, a novel rare histiocytic proliferation, was first described in 2008; it occurs in early infancy with liver and hematopoietic involvement.
Wei Liu +7 more
doaj +1 more source
Bilateral spontaneous hyphaema in juvenile xanthogranuloma
Indian Journal of Ophthalmology, 2006 This report describes a rare occurrence of bilateral, spontaneous, nontraumatic hyphema in a 6 weeks old infant, associated with a small, multiple skin lesions.
Vijayalakshmi P +3 more
doaj
Emergence of solitary juvenile xanthogranuloma on the corneoscleral limbus
Journal of Clinical Ophthalmology and Research, 2018 Juvenile xanthogranuloma (JXG) is the most frequent form of non-Langerhans histiocytosis, a rare benign inflammatory skin disorder. Eye involvement is the most frequent extracutaneous manifestation of the disease.
Raul Alfaro-Rangel +2 more
doaj +1 more source
Case Reports in Dermatology, 2011 Erdheim-Chester disease is a rare non-Langerhans form of histiocytosis with multiple organ involvement. Approximately 20% of patients have xanthoma-like lesions, usually on the eyelids.
Yukako Murakami +6 more
doaj +1 more source
Uterine PEComa With Lymphangioleiomyomatosis (LAM)‐Like Features: A Case Report
Case Reports in Pathology, Volume 2026, Issue 1, 2026.Perivascular epithelioid cell tumors (PEComas) of the uterus are rare mesenchymal neoplasms characterized by myogenic and melanocytic differentiation. These tumors can mimic other uterine mesenchymal tumors in their clinical presentation and morphology. We report a case of a 58‐year‐old woman who presented with abnormal uterine bleeding.
Ramani Raman +4 more
wiley +1 more source
Cerebrotendinous Xanthomatosis In A Family
Indian Journal of Dermatology, 1999 A family consisting of a brother (11 years) and his twin sisters (13 years) with cerebrotendinous xanthomatosis is presented. The brother had bilateral achilles tendon xanthoma, low intelligence, poor memory with early cerebellar signs.
Chatterjee Gobinda +3 more
doaj
A large multilobulated cutaneous nodule in infancy
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Hannah Wahida +2 more
wiley +1 more source
Everolimus in Erdheim-Chester disease
The Egyptian Journal of Internal Medicine, 2013 A 43-year-old man presented with bony pains, repeated pathological fractures with overlying skin ulcerations, and forearm and chest wall swellings. Investigations led to the diagnosis of Erdheim-Chester disease. Treatment with low-dose prednisolone, oral
Mohamed A. Hussein +2 more
doaj +1 more source
Treatment of Xanthoma disseminatum – a systematic literature review
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 9, Page 1061-1069, September 2025.Summary Xanthoma disseminatum is a rare disease from the spectrum of non‐Langerhans cell histiocytoses, which can be categorized into three types and is sometimes associated with systemic involvement. Due to the its rarity, there are no standardized treatment guidelines for this disease, making treatment in everyday clinical practice more difficult ...
Inga Hansen‐Abeck +4 more
wiley +1 more source