Results 31 to 40 of about 289,368 (261)
Sinus Histiocytosis with Massive Lymphadenopathy
Sinus Histiocytosis with Massive Lymphadenopathy is a very rare condition often presenting as neck swelling of unknown etiology. The disease involves extranodal sites in 20-30 percent of cases and histologically characterized by emperiopolesis, non-cohesive and non-epitheloid histocytes with abundant eosinphilic cytoplasm.
, Samiullah +4 more
openaire +3 more sources
An extremely rare case of sinus histiocytosis of the non-Langerhans cell histiocytoses type is described in 55-year-old patient with isolated localization of cutanious lesion on the right cheek without involvement of nodular structures.
E. Sokolovsky +9 more
semanticscholar +1 more source
A rare case of oral multisystem Langerhans cell histiocytosis [PDF]
Langerhans cell histiocytosis (LCH) is a rare disorder characterized by high proliferation of Langerhans dendritic cells. LCH is a solitary or multifocal disease that primarily involves bone tissue and often affects children and young men. A 29 years-old
Facciolo, Maria Teresa +4 more
core +1 more source
Langerhan’s cell histiocytosis (LCH) results from the proliferation of immunophenotypically and functionally immature, morphologically rounded Langerhan’s cells along with eosinophils, macrophages, lymphocytes, and, commonly, multinucleated giant cells ...
Seema Lale +2 more
doaj +1 more source
A Rare Case of a Systemic Non-Langerhans Histiocytosis Presenting with Diabetes Insipidus and a Tentorial Mass [PDF]
Introduction The histiocytoses are a group of clinically diverse diseases distinguished from one another based on the specific immunophenotype of the lesional cells, implying derivation from the same precursor cell.
Barros, MS, Guilherme +5 more
core +2 more sources
Management and treatment of sinonasal inverted papilloma [PDF]
Aims: The aim of this paper is to describe the surgical experience of 35 patients with Inverted Papilloma (IP) of paranasal sinuses and its recurrence rate after a year of follow-up.
Agrillo, Alessandro +6 more
core +1 more source
An unusual Erdheim-Chester disease with orbital involvement: A case report [PDF]
Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multiorgan involvement and a specific tropism for perivascular and fatty connective tissue, of unclear origin, with poor response to therapy. Its identification is difficult because
Bencivinni, F. +5 more
core +2 more sources
Solitary extranodal Rosai-Dorfman disease of the mandible: an exceedingly rare presentation
Sinus histiocytosis with massive lymphadenopathy, generally known by the name of Rosai-Dorfman disease is a rare benign condition principally affecting cervical lymph nodes.
Ameer Hamza +2 more
doaj +1 more source
Langerhans cell histiocytosis (LCH) is a neoplastic disease characterized by aberrant proliferation of the mononuclear phagocyte system, predominantly affecting children under the age of 3 years.
Min-shan Li +3 more
semanticscholar +1 more source
Rosai-Dorfman Disease (Sinus Histiocytosis With Massive Lymphadenopathy): A Case Report
Sinus Histiocytosis with Massive Lymphadenopathy also known as Rosai-Dorfman Disease is a rare histiocytic proliferative disorder of unknown etiology. It presents as massive bilateral painless cervical lymphadenopathy.
F. Ahmed +1 more
semanticscholar +1 more source

