Results 31 to 40 of about 286,204 (263)
Surgical neurology international, 2019 Background: Langerhans cell histiocytosis (LCH) is a term describing a clonal proliferation of pathologic Langerhans cells (histiocytes), which may manifest as unisystem (unifocal or multifocal) or multisystem disease.
Kacper Kostyra, B. Kostkiewicz
semanticscholar +1 more source
Vestnik Dermatologii i Venerologii, 2019 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]
, 2017 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
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Case Reports in Pathology, 2014 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
Management and treatment of sinonasal inverted papilloma [PDF]
, 2015 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
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An unusual Erdheim-Chester disease with orbital involvement: A case report [PDF]
, 2016 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
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A Rare Case of a Systemic Non-Langerhans Histiocytosis Presenting with Diabetes Insipidus and a Tentorial Mass [PDF]
, 2015 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
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Solitary extranodal Rosai-Dorfman disease of the mandible: an exceedingly rare presentation
Autopsy and Case Reports, 2018 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
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A case report of Rosai–Dorfman disease of the breast
Journal of Current Research in Scientific Medicine, 2023 Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy, is a benign, self-limiting disease. In the majority of cases, there is massive and painless lymphadenopathy in any lymph node group but most commonly in the cervical lymph ...
Rini Francis +3 more
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Discrepancy of target sites between clinician and cytopathological reports in head neck fine needle aspiration: Did I miss the target or did the clinician mistake the organ site? [PDF]
, 2015 The diagnostic accuracy of fine needle aspiration cytology (FNAC) of head and neck lesions is relatively high, but cytologic interpretation might be confusing if the sample is lacking typical cytologic features according to labeled site by physician ...
Aledavood, A +9 more
core +2 more sources