Results 101 to 110 of about 11,417 (249)
Isolated unilateral eyelid Rosai–Dorfman disease
Oman Journal of Ophthalmology, 2018 Isolated eyelid Rosai–Dorfman disease without orbital disease or systemic involvement is very rare and needs a high degree of suspicion. In this report, we describe a 16-year-old boy who presented with isolated eyelid Rosai–Dorfman disease involving the ...
Nandini Bothra +3 more
doaj +1 more source
Foot & Ankle Orthopaedics, 2021 Rosai-Dorfman disease (RDD), otherwise known as sinus histiocytosis with massive lymphadenopathy (SHML), is a very rare and typically benign disorder of unknown etiology with
Jasmin Mansoori DPM +4 more
doaj +1 more source
Adhesion and transcellular migration of neutrophils and B lymphocytes on fibroblasts [PDF]
, 2009 During tissue inflammation, infiltrated leukocytes may have physical contacts with fibroblasts. We observed that neutrophils and B lymphocytes adhered in a larger proportion than T cells on cultured fibroblasts.
Couture, Patrick +3 more
core +2 more sources
The Neuroimaging Spectrum of Neurosarcoidosis
Clinical Neuroimaging, Volume 2, Issue 1, 2025.ABSTRACT Among its many forms, involvement of the nervous system in sarcoidosis ranks as one of the most severe and potentially disabling manifestations of the disease, and timely recognition and accurate diagnosis are critical for its optimal treatment.
Spencer K. Hutto, Gabriela A. Bou
wiley +1 more source
BMC Neurology, 2021 Background The term “Tolosa-Hunt syndrome” (THS) has been used to refer to painful ophthalmoplegia associated with nonspecific inflammation of the cavernous sinus and many processes can result in a similar clinical picture, including infectious ...
Paulo Ribeiro Nóbrega +8 more
doaj +1 more source
The rare cancer network: ongoing studies and future strategy. [PDF]
, 2014 The Rare Cancer Network (RCN) was formed in the early 1990's to create a global network that could pool knowledge and resources in the studies of rare malignancies whose infrequency prevented both their study with prospective clinical trials.
Atalar, B. +15 more
core +2 more sources
A Rare Case of Primary Intraparenchymal Rosai‐Dorfman Disease
iRADIOLOGY, Volume 3, Issue 5, Page 370-371, October 2025.
Lin Chen, Rui Zhou
wiley +1 more source
Case Reports in Otolaryngology, Volume 2025, Issue 1, 2025.Background The unusual disorder known as Langerhans cell histiocytosis (LCH), which is most frequently observed in children and young adults, is caused by the clonal proliferation of Langerhans cells. This disease is classified into several types depending on the extent of the lesion.
Yoshifumi Matsumoto +4 more
wiley +1 more source
Orbital Rosai-Dorfman disease initially diagnosed as IgG4-related disease: a case report [PDF]
, 2020 Nishanth S. Iyengar +12 more
openalex +1 more source
Benign and malignant cutaneous nasal lesions
Eye &ENT Research, Volume 1, Issue 2, Page 65-91, December 2024.Abstract The nose is a structure of both cosmetic and functional importance. Cutaneous lesions of the nose occasionally represent a diagnostic challenge and involve the expertise of several specialties from dermatology, otolaryngology—head and neck surgery, infectious disease, and pathology, among others.
Hamed Sarikhani +4 more
wiley +1 more source