Results 51 to 60 of about 1,911 (163)

PRESENTACIÓN DE UN PACIENTE CON ADENOPATÍAS MÚLTIPLES: UN DIAGNÓSTICO COMPLEJO

Revistas Argentina de Medicina, 2016
Un varón de 65 años se presenta con adenopatías cervicales bilaterales de seis meses de evolución con antecedente de lesión osteolítica en húmero derecho (fractura patológica asentada varios años antes de la consulta y pseudoartrosis de hombro) y ...
Lucía Lossetti, Daniela Piedrabuena, Oscar Furlong, Natalia Bassi, Fernando Tortosa   +4 more
doaj   +2 more sources

Presentation of Neurological Rosai–Dorfman Disease Over 12 Years: A Case Report

Case Reports in Neurological Medicine, Volume 2026, Issue 1, 2026.
Rosai–Dorfman disease (RDD) is a rare, non‐Langerhans cell histiocytosis that classically presents with cervical lymphadenopathy. Neurological involvement occurs in less than 5% of cases and is often associated with extra‐axial lesions. Diagnosis of RDD in the setting of neurological deficits is challenging, as RDD often mimics meningioma and ...
Sam E. Gary, Serdar Akkol, Harshadayani J. Kumar, Christina Appin, Xiaosi Han, Suraiya Saleem   +5 more
wiley   +1 more source

Extra nodal Rosai Dorfman disease of nasal septal mucosa without lymphadenopathy

Journal of Pathology of Nepal, 2016
Rosai–Dorman disease, also known as sinus histiocytosis with massive lymphadenopathy, typically presents as massive enlargement of lymph nodes accompanied by systemic symptoms. Extranodal involvement is also known usually in head and neck regions. Rarely
P Raje, P Vyas
doaj   +1 more source

Rosai - Dorfman disease: a rare entity diagnosed at autopsy

Autopsy and Case Reports, 2013
Rosai-Dorfman disease (RDD) or Sinus histiocytosis with massive lymphadenopathy is a rare and benign histiocytic proliferative disorder first described by Juan Rosai and Ronald Dorfman in 1969, whose etiology remains unknown.
João da Costa Veloso Neto, Sheila Aparecida Coelho Siqueira, Maria Claudia Nogueira Zerbini   +2 more
doaj   +1 more source

Primary tibial bone involvement in Rosai Dorfman Disease treated with surgery and radiotherapy; case report and literature review

Journal of Orthopaedic Reports
Rosai-Dorfman disease is a rare benign disease that is characterized by over-production and accumulation of white blood cells, known as (histiocytes) in the lymph nodes (nodal) or any other areas of the body (extranodal). It usually presents as painless,
Abdullah F. Alotaibi, Talal Alrawaf, Osama Alshaya, Hassan Sawan, Muath Aljufayr   +4 more
doaj   +1 more source

Emperipolesis, entosis and cell cannibalism: Demystifying the cloud

Journal of Oral and Maxillofacial Pathology, 2017
There are intense published data in literature related to cell engulfment phenomena such as emperipolesis, entosis and cell cannibalism. All these are closely related phenomena with a very fine line of differences. Its correct identification has a significant diagnostic and prognostic value.
Gupta, Nidhi, Jadhav, Kiran, Shah, Vandana   +2 more
openaire   +3 more sources

Histological and immunohistochemical evaluations of the bone marrow from femur and sternal manubrium of dogs reactive for leishmaniasis by DPP® and ELISA tests

Ciência Animal Brasileira, 2022
As the bone marrow is one of the most organs affected by canine visceral leishmaniasis (CVL), samples from this are frequently taken for parasitological tests, with occurrence of myelodysplastic changes, with consequent anemia, leukopenia, and ...
Aline Oliveira de Magalhães, Lucilandia Maria Bezerra, Diego Pereira Araújo, Bruna Siqueira Gomes de Lima, Leandro do Prado Assunção, Rodrigo Caldas Menezes, Veridiana Dignani Moura   +6 more
doaj  

Cutaneous sinus histiocytosis of face of the non-Langerhans cell histiocytoses type (cutaneous Rosai — Dorfman disease)

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. V. Sokolovsky, G. N. Mikheev, M. G. Rybakova, E. B. Manasheva, V. A. Seredina   +4 more
doaj   +1 more source

Persistent Generalized Lymphadenopathy: A Diagnostic Conundrum—Case Report and Review of Literature

Indian Journal of Medical and Paediatric Oncology
Generalized lymphadenopathy is a nonspecific sign with heterogenous etiology including infective, inflammatory, and malignant causes. We present the case of a child who presented with generalized lymphadenopathy, involving the cervical, axillary ...
Mahin Mundra, Vaishnavi Sreenivasan, Nisha Swami, Kawaldeep Kaur, Bhavika Rishi, Aroonima Misra, Sumit Mehndiratta, Amitabh Singh   +7 more
doaj   +1 more source

Characteristics of histiocytic neoplasms presenting as breast masses

British Journal of Haematology, Volume 208, Issue 1, Page 358-362, January 2026.
Theodore Vougiouklakis, Marc K. Rosenblum, Matthew Cannavo, Kimberly Feigin, Andrew E. Rosenberg, Frederick Wittlin, Sonia Mahajan, Edi Brogi, Maria E. Arcila, Hannah Y. Wen, Eli L. Diamond   +10 more
wiley   +1 more source