Results 1 to 10 of about 2,806 (197)

Rosai‐Dorfman Disease in a 4‐Month‐Old Female Presenting With Cervical Lymphadenopathy [PDF]

open access: yesClinical Case Reports
Rosai‐Dorfman disease is a rare histiocytic disorder that can mimic malignancies. This case highlights the importance of immunohistochemistry in distinguishing RDD from lymphoproliferative neoplasms, ensuring accurate diagnosis and management. Clinicians
Allahdad Khan   +5 more
doaj   +3 more sources

Emperipolesis – A Review [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2014
Emperipolesis is an uncommon biological process, in which a cell penetrates another living cell. Unlike in phagocytosis where the engulfed cell is killed by lysosomal enzymes of the macrophage, the cell exists as viable cell within another in ...
Varun Rastogi   +4 more
doaj   +3 more sources

Genetic deletion of P-selectin prevents fibrosis development by inhibiting the neutrophil megakaryocyte emperipolesis in the Gata1low mouse model for myelofibrosis [PDF]

open access: yesEuropean Journal of Histochemistry
Myelofibrosis (MF) is a rare chronic hematological disorder, within the family of myeloproliferative neoplasms. The MF patients present clinical abnormalities such as anemia, and thrombosis, as well as alterations in the bone marrow (BM ...
Francesca Arciprete   +9 more
doaj   +2 more sources

Emperipolesis: Sternal and femoral microenvironment induces megakaryiocyte emperipolesis in the Wistar strain [PDF]

open access: yesMacedonian Veterinary Review, 2019
Emperipolesis is considered a physiological phenomena often present in various pathophysiological conditions, but its etiology is still unknown. In this study, we analyzed the number of megakaryocytes and the percentage of emperipoletic cells in the ...
Damir Suljević   +2 more
doaj   +2 more sources

Case Report: ALK-positive histiocytosis presenting as an adrenal mass: a diagnostic trap due to unusual morphology [PDF]

open access: yesFrontiers in Oncology
BackgroundThe differential diagnosis of an adrenal mass is critical for clinical management. We report a case that expanded the spectrum of a rare disease and present a novel diagnostic trap for both pathologists and clinicians.MethodsHistopathological ...
Wenjing Ma   +4 more
doaj   +2 more sources

Cutaneous emperipolesis: Rosai–Dorfman disease – An uncommon entity

open access: yesClinical Dermatology Review, 2023
Rosai–Dorfman disease (RDD) is a rare, benign idiopathic, non-Langerhans cell histiocytosis. The most common presentation is massive bilateral painless lymphadenopathy with fever and weight loss.
M B Shashi Kumar   +3 more
doaj   +2 more sources

Emperipolesis

open access: yesRevista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica, 2002
La emperipolesis es la capacidad que tienen los linfocitos, plasmocitos y polimorfonucleares de penetrar al citoplasma de otras células, usualmente gigantes, sin sufrir daño en el proceso. Su significado es desconocido.
Sandra Liliana Cortés Vera   +1 more
doaj   +1 more source

Significant Neutrophilic Emperipolesis in Squamous Cell Carcinoma

open access: yesCase Reports in Oncological Medicine, 2018
A 53-year-old man was admitted for tooth mobility. A mass was identified at the tooth base by CT. Histopathology of the excisional biopsy revealed a moderately differentiated squamous cell carcinoma.
Seza Tetikkurt   +4 more
doaj   +4 more sources

Isolated intracranial Rosai-Dorfman disease in an adult man: Report of a rare case [PDF]

open access: yesJournal of Research in Clinical Medicine, 2020
Background: Isolated intracranial Rosai-Dorfman disease (RDD) is an extremely rare, idiopathic histo-proliferative disorder. RDD is associated with the proliferation of histiocytes and emperipolesis.
Somaye Rezaei   +5 more
doaj   +1 more source

Cerebral CD1a positive Rosai–Dorfman disease with coexistent granulomatous angiitis: A case report

open access: yesGlioma, 2022
Rosai–Dorfman disease (RDD) is a nonneoplastic histiocytic proliferation. RDD is CD1a negative as opposed to Langerhans cell histiocytosis (LCH). The lesion was positive for CD1a immunohistochemistry in our RDD patient, suggesting an overlap with LCH. In
Sweety Vijay Shinde, Asha Sharad Shenoy
doaj   +1 more source

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