Results 11 to 20 of about 5,167 (181)

Characteristics of histiocytic neoplasms presenting as breast masses. [PDF]

Br J Haematol
British Journal of Haematology, Volume 208, Issue 1, Page 358-362, January 2026.
Vougiouklakis T, Rosenblum MK, Cannavo M, Feigin K, Rosenberg AE, Wittlin F, Mahajan S, Brogi E, Arcila ME, Wen HY, Diamond EL.   +10 more
europepmc   +2 more sources

Region-Based Segmentation of Lymph Node Metastases in Whole-Slide Images of Colorectal Cancer: A Pilot Clinical Study. [PDF]

Cancer Med
ABSTRACT Background Digital technologies and artificial intelligence (AI) are transforming medical diagnostics, particularly in pathology. This study presented a two‐stage computer vision model designed to detect colorectal cancer metastases in whole slide images (WSIs) of lymph nodes.
Fayzullin A, Savelov N, Balkivskiy A, Ivanova E, Timakova A, Funtikov V, Shelomentseva E, Panchenko N, Spiridonov I, Korkonishko I, Makhina M, Kutuzova E, Meretukov D, Kretova N, Demura T, Timashev P, Parchiev R.   +16 more
europepmc   +2 more sources

Tumoral Stage of Mycosis Fungoides, Misdiagnosed With Wells Syndrome and Langerhans Cell Histiocytosis Histologically: A Challenging Case and Review of the Literature. [PDF]

Cancer Rep (Hoboken)
ABSTRACT Background Mycosis fungoides (MF) is a type of cutaneous T‐cell lymphoma (CTCL) with slow progression, usually presenting with patches and plaques. The infiltration of histiocytes and eosinophils in skin cancers can mask the underlying condition, posing a diagnostic challenge.
Vahabi SM, Montazeri S, Pourgholi E, Bahramian S, Ghanadan A, Hesari KK, Etesami I.   +6 more
europepmc   +2 more sources

New cases expand the genotype, phenotype and therapeutic landscape of H syndrome. [PDF]

Br J Haematol
British Journal of Haematology, Volume 208, Issue 1, Page 363-366, January 2026.
Triaille C, Beauchemin J, Campeau PM, Chapdelaine H, Dery J, Kondyli M, Mitchell G, Powell J, Turpin S, Cros G, Touzot F.   +10 more
europepmc   +2 more sources

The Clinicopathologic Spectrum of Rosai-Dorfman-Destombes Disease in Adults: An Analysis of 16 Cases. [PDF]

Eur J Haematol
ABSTRACT Rosai–Dorfman–Destombes disease (RDD) is a rare histiocytic proliferation with protean clinical manifestations, resulting from the accumulation of activated histiocytes within nodal and extra‐nodal tissues. The diagnosis can be missed, particularly when biopsies are obtained from extra‐nodal sites, where histological features may be less ...
Trinder M, Pryma C, Leung E, Slack GW, Farinha P, Young S, Ozkaya N, Carruthers M, Chen LYC.   +8 more
europepmc   +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

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

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

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