Results 61 to 70 of about 1,911 (167)
Characteristics of histiocytic neoplasms presenting as breast masses
British Journal of Haematology, Volume 208, Issue 1, Page 358-362, January 2026.
Theodore Vougiouklakis +10 more
wiley +1 more source
Isolated localization of Rosai Dorfman disease as renal mass: a case report and review of literature
We report a rare case of an elderly woman presented with right renal mass with invasion of renal vein and several small lymphadenopathy in the hilar area .the diagnosis of kidney cancer is suspected and the patient underwent open radical nephrectomy ...
Aziz El Majdoub +5 more
doaj +1 more source
Images in hematology emperipolesis [PDF]
K, Samii, E, Pasteur
openaire +2 more sources
Soft Tissue Rosai-Dorfman Disease: Case report
Rosai-Dorfman disease (RDD) is a rare benign proliferative histiocytic disorder characterised by massive lymphadenopathy. While extranodal involvement can occur in generalised RDD, isolated soft tissue RDD (STRDD) is extremely rare.
Rubyath C. Rajib +3 more
doaj +1 more source
Persistent Generalized Lymphadenopathy: A Diagnostic Conundrum—Case Report and Review of Literature
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 +7 more
doaj +1 more source
Se presenta una paciente de 50 años de edad con lesión tumoral redondeada, no dolorosa en región inguinal, con crecimiento progresivo y formación de una placa eritematosa, con áreas de pigmentación e infiltración de tejidos profundos, así como aparición ...
Yaniurka Cruz-Camejo +4 more
doaj
Megakaryocyte emperipolesis in B‐lymphoblastic leukaemia [PDF]
Mark Gurney +2 more
openaire +2 more sources
EMPERIPOLESIS BY MEGAKARYOCYTES IN BLOOD LOSS [PDF]
openaire +2 more sources
Rosai-Dorfman disease in a 12-year-old Nigerian male
Rosai-Dorfman disease is a rare disorder of systemic histioproliferation, first described in 1969 by Juan Rosai and Ronald Dorfman. It is characterised by massive lymphadenopathy, particularly of the head and neck region, and it is sometimes associated ...
Jacintha Chinyere Elo-Ilo +2 more
doaj

