Results 51 to 60 of about 4,922,335 (121)
Expert Perspective: Diagnosis and Treatment of Castleman Disease
Castleman disease (CD) is a major diagnostic challenge for rheumatologists. Unicentric CD (UCD) involves one enlarged lymph node region, whereas multicentric CD (MCD) involves multiple enlarged lymph node regions. Both UCD and MCD may exhibit a wide range of symptoms that overlap with other immune‐mediated conditions.
Luke Y. C. Chen +2 more
wiley +1 more source
Background Cutaneous metastases are uncommon but clinically significant manifestations of internal malignancies and may indicate advanced disease or, in certain cases, represent the initial sign of cancer. Their variable clinical and histopathologic presentations can pose diagnostic challenges, particularly when the primary tumor is unknown.
Qiannan Jia +3 more
wiley +1 more source
Indeterminate Cell Histiocytosis: Report of a Case
- Indeterminate cell histiocytosis is a very rare disorder of histiocytes proliferation. It has both Langerhans and non-Langerhans cell histiocytosis immunophenotypic features.
Mahsa Ansari +11 more
core
Extraosseous langerhans cell histiocytosis in children
Langerhans cell histiocytosis, a rare disease that occurs mainly in children, may produce a broad range of manifestations, from a single osseous lesion to multiple lesions involving more than one organ or system.
Letovanec, I. +26 more
core +1 more source
Langerhans cell histiocytosis (LCH) is rare unique disorder of the reticuloendothelial system characterized by an abnormal proliferation of histiocytes and eosinophilic leukocytes.
S Jayachandran, N Balaji
core +1 more source
Uncommon preputial localization of Langerhans cell histiocytosis
International audienceWe report a rare case of a 14-year-old boy with Langerhans cell histiocytosis localized to the prepuce. The patient was treated with a topical corticosteroid followed by imiquimod cream resulting in significant clinical improvement ...
Sebastien Barbarot +11 more
core +1 more source
[Unusual pulmonary presentation of systemic Langerhans cell histiocytosis]
An 80-year-old nonsmoking man was referred to our hospital with bilateral perihilar pulmonary opacities. He had a history of epilepsy, sclerosing cholangitis, cutaneous lesions previously diagnosed as localised Langerhans cell histiocytosis.
Schuller, A +11 more
core +1 more source
Uncommon variants of Non-Langerhans Cell Histiocytosis [PDF]
Background: Histiocytosis are rare disorders of the mononuclear phagocyte system, characterized by a derangement in differentiation, proliferation or function of monocytes and dendritic cells.
Chiara Moltrasio +9 more
core +2 more sources
Langerhans cell histiocytosis of the orbit
Purpose: The management of Langerhans cell histiocytosis is controversial.
KIRATLI, HAYYAM +2 more
core +1 more source
Langerhans cell histiocytosis; an institutional study [PDF]
Background: Langerhans cell histiocytosis is a complex rare disease of the dendritic cell system.The disease can occur at any age, with a peak at 5-10 years.
Shovana Karki, Aasia Rajbhandari
core +1 more source

