Results 1 to 10 of about 70 (67)

Histiocitosis sinusal con linfadenopatía masica (enfermedad de Rosai Dorfman) Sinusal histiocytosis with massive lymphadenopathy: report of a case

open access: yesIatreia, 1995
<p class="MsoNormal"><span style="font-size: 10pt; font-family: Arial">Se presenta el caso de una Joven de 14 años con adenomegalias cervicales bilaterales masivas, con diagnóstico clínico de linfoma y cuyo estudio anatomopatológico demostró ...
Alejandro Vélez Hoyos   +1 more
doaj  

Emperipolesis: Sternal and Femoral Microenvironment Induces Megakaryiocyte Emperipolesis in the Wistar Strain [PDF]

open access: yesMacedonian Veterinary Review, 2019
Abstract 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 sternal and femoral bone marrow of Wistar rats.
Damir Suljević   +2 more
openaire   +2 more sources

Emperipolesis – A Review

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 emperipolesis and can exit at any time without any structural or functional abnormalities for either of them ...
Varun Rastogi   +4 more
openaire   +3 more sources

Histiocytosis development and clinical variation through the lens of genomics

open access: yesThe Journal of Pathology, EarlyView.
Abstract Histiocytic neoplasms are rare haematologic diseases characterised by clonal expansions of cells with a monocyte, macrophage or dendritic cell phenotype. Their clinical manifestations are diverse, ranging from indolent lesions to aggressive systemic disease.
Paul G Kemps   +3 more
wiley   +1 more source

Updates and controversies in contemporary grading of clear cell renal cell carcinoma and papillary renal cell carcinoma

open access: yesHistopathology, EarlyView.
New concepts, innovations and some issues have emerged since the adoption a decade ago of WHO/ISUP grading for CCRCC and PRCC. Continued use of the WHO/ISUP grading for CCRCC and PRCC has been upheld by newer studies, and practice guidance for some of the grading issues, where data are available, is provided.
Gladell P. Paner   +4 more
wiley   +1 more source

Autoimmune Hepatitis Following COVID‐19 Vaccination in a Patient With Ulcerative Colitis: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Autoimmune hepatitis (AIH) following COVID‐19 vaccination is a rare adverse event. We present the case of a 55‐year‐old male with a history of ulcerative colitis (UC) who developed AIH 3 weeks after receiving his second dose of the Pfizer–BioNTech mRNA vaccine. He presented with jaundice and significantly elevated liver enzymes. A liver biopsy
Marwah Algodi   +6 more
wiley   +1 more source

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. Es un rasgo morfológico muy útil en el diagnóstico histopatológico de algunas enfermedades como la de Rosai-Dorfman, la micosis ...
Sandra Liliana Cortés Vera   +1 more
openaire   +1 more source

Clinicopathological Features, Treatment Response, and Outcome of Rosai‐Dorfman Disease in Two Children

open access: yesClinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Rosai‐Dorfman disease is a rare non‐Langerhans cell histiocytic disorder. It is common in male children and young adults of African descent. It is classified into sporadic and familial types. The most common clinical presentation is massive bilateral cervical lymphadenopathy associated with constitutional symptoms. Histiocytic emperipolesis is
George Evele   +2 more
wiley   +1 more source

Striking emperipolesis in megakaryocytes of gray platelet syndrome [PDF]

open access: yesBlood, 2019
![Figure][1] An 11-year-old girl was diagnosed with gray platelet syndrome (GPS) with compound heterozygous NBEAL2 mutations after presenting with recurrent epistaxis and thrombocytopenia. Bone marrow examination was performed to evaluate for myelofibrosis.
Eric McGinnis, Kate M. Chipperfield
openaire   +2 more sources

Autoimmune Hepatitis: Histopathological Diversity and Its Clinical Implications

open access: yesHepatology Research, Volume 56, Issue 2, Page 139-147, February 2026.
ABSTRACT Autoimmune hepatitis (AIH) is a chronic inflammatory liver disease characterized by diverse clinical and histological manifestations. Accurate histopathological evaluation plays a critical role in determining disease activity, guiding treatment strategies, and predicting prognosis.
Mina Komuta, Kenichi Harada
wiley   +1 more source

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