Results 31 to 40 of about 287,512 (253)

Aggressive Neoplasms That Mimic Chronic Endodontic Lesions: A Multi-Institutional Case Series. [PDF]

Aust Endod J
ABSTRACT This study aimed to report sociodemographic, clinicopathologic and radiological features of 12 cases of aggressive neoplasms that were clinically diagnosed as chronic endodontic lesions. The series comprised seven females (58.33%) and five males (41.67%), with a mean age of 48.9 ± 19.19 years (range: 16–75 years).
Macedo NG, Pappen FG, da Fonseca Orcina B, Mascarenhas G, Dos Santos JN, da Silva Santos PS, Vieira CC, Garcia AS, Soares AC, Schuch LF, Gomes APN, Vasconcelos ACU.   +11 more
europepmc   +2 more sources

Orbital involvement in Rosai-Dorfman disease [PDF]

, 2011
A doença de Rosai-Dorfman (DRD) ou histiocitose sinusal com linfadenopatia maciça é uma entidade clínica idiopática, rara e benigna, caracterizada pela proliferação histiocitária com linfofagocitose. Geralmente se apresenta com linfoadenomegalia cervical,
GONÇALVES, Allan C. Pieroni, MONTEIRO, Mário Luiz Ribeiro, MOURA, Frederico Castelo, OLIVEIRA, Cristiana Dumaresq de, Rossato, Luiz Angelo   +4 more
core   +2 more sources

Sinus Histiocytosis: An Uncommon Presentation of an Uncommon Condition [PDF]

, 2015
Introduction Rosai–Dorfman Disease (RDD), also known as Sinus Histiocytosis with Massive Lymphadenopathy (SHML), is a rare, benign, proliferative disorder of macrophages and monocytes that was first described by Rosai and Dorfman in 1969.
Greco, MD, Allison, Kane, MD, Gregory
core   +2 more sources

Rosai–Dorfman disease presenting as internal jugular vein thrombosis and middle lobe collapse-consolidation

Lung India, 2020
Rosai–Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy, is a rare and benign disease that usually presents as massive and painless cervical lymphadenopathy.
Ambika Sharma, Deepika Hemrajani, Sheetu Singh, Kapil Bhardwaj, Chand Bhandari, R K Jenaw   +5 more
doaj   +1 more source

Unusual presentation of Rosai-Dorfman disease in a 14-month-old Italian child: a case report and review of the literature [PDF]

, 2016
Background: Rosai-Dorfman disease (RDD) is a rare form of histiocytosis characterized by histiocyte proliferation within lymph nodes and extranodal tissue. Here we report an unusual presentation of RDD in an Italian toddler.
Bruzzi, Patrizia, Coccolini, Elena, Di Dio, Francesco, Iughetti, Lorenzo, Mariotti, Ilaria, Predieri, Barbara   +5 more
core   +2 more sources

Rosai-Dorfman Disease: Rare Pulmonary Involvement Mimicking Pulmonary Langerhans Cell Histiocytosis and Review of the Literature

Case Reports in Radiology, 2018
Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare nonmalignant lymphohistiocytic proliferative disorder.
Rashid AL Umairi, Danielle Blunt, Wedad Hana, Matthew Cheung, Anastasia Oikonomou   +4 more
doaj   +1 more source

A Rare Case of Multiorgan Involvement of Rosai Dorfman Disease in an Elderly Female

Journal of Nepal Medical Association, 2014
Sinus histiocytosis with massive lymphadenopathy (SHML), Rosai-Dorfman Disease, is a rare histiocytic syndrome first described by Rosai and Dorfman, most frequently seen in children and young adults.The disease is more common in males and in individuals ...
Rakesh Digambar Waghmare
doaj   +1 more source

Histocytopathological diagnosis of Rosai–Dorfman disease: Case report

Clinical Case Reports, 2022
Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) being a rare benign proliferative self‐limiting disease of the cells of macrophage‐histiocyte family is of unknown etiology and presents with massive lymphadenopathy.
Zephania Saitabau Abraham, Zerd Francis, Advera Isaac Ngaiza, Aveline Aloyce Kahinga, Faustine Bukanu   +4 more
doaj   +1 more source

Asymptomatic flow of Rosai-Dorfman disease [PDF]

, 2014
Introduction. Sinus histiocytosis with massive lymphadenopathy is a rare benign self-limiting disease of unknown etiology. The salivary gland involvement, indicating the extranodal character of the disease, often presents a diagnostic dilemma ...
Bjelaković Bojko, Kesić Ljiljana, Kostić Miloš, Mihailović Dragan, Mijovićć Žaklina, Petrović Dragan, Petrović Milica, Petrović Slađana, Stanković Ana, Vučković Ivica, Živković Nikola   +10 more
core   +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, Gaglioti, Domenico, Gallenzi, Patrizia, Patini, Romeo, Riva, Francesco   +4 more
core   +1 more source