Results 61 to 70 of about 31,396 (267)
Primary unifocal thymic Rosai-Dorfman disease: an extremely rare challenge in diagnostic practice
Journal of Cardiothoracic Surgery, 2023 Rosai-Dorfman disease (RDD) is currently considered a group of neoplastic diseases of unknown etiology, with monoclonal proliferation of histiocytes, showing unique histopathologic features and varying clinical presentation.
Qian Liu +4 more
doaj +1 more source
Immunohistological analysis of Rosai-Dorfman histiocytosis. A disease of S-100 + CD1-histiocytes
, 1987 Five cases of Rosai-Dorfman histiocytosis (RDH) (also called Sinus Histiocytosis with Massive Lymphoadenopathy; SHML) have been studied by immunohistochemical methods with heteroantisera and monoclonal antibodies.
Pier-Giuseppe Pelicci +19 more
core +1 more source
Xanthogranulomatous endometritis: A benign uncommon masquerader of malignancy
Journal of Mid-Life Health, 2019 Xanthogranulomatous endometritis is an uncommon benign lesion characterized by the destruction of endometrium and replacement by the sheets of foamy histiocytes, lymphocytes, plasma cells, multinucleated giant cells, fibrosis, calcification, and ...
Vipra Malik +3 more
doaj +1 more source
, 1986 Cell suspensions from 16 tumour-free axillary lymph nodes from breast cancer patients were prepared, using collagenase digestion to free the sinus histiocytes from the fibrous stroma of the nodes. The histiocytic cells so obtained were then characterized
Steele, R. J. C., Brown, M., Eremin, O.
core +1 more source
HISTOCHEMICAL AND ULTRASTRUCTURAL OBSERVATION OF THE PIGMENT IN PIGMENTED LIPID HISTIOCYTES OF CHRONIC GRANULOMATOUS DISEASE [PDF]
, 1977 Pigmented lipid histiocytes (PLH) of chronic granulomatous disease (CGD) were examined by histochemistry and electron microscopy. The yellowish brown pigments were stainable with Sudan III and IV even in paraffin sections, and the sudanophilia was kept ...
Tsuchiyama, Hideo +7 more
core +1 more source
Histiocytosis development and clinical variation through the lens of genomics
The 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
Diagnostic Pathology, 2023 Lennert lymphoma (LeL) is a rare variant of peripheral T-cell lymphoma, not otherwise specified (PTCL/NOS) that is rich in epithelioid histiocytes. LeL may pose great diagnostic and therapeutic challenges to the pathologist and clinician.
Ying Yin +5 more
doaj +1 more source
histiocytic Necrotizing Lymphadenitis
Apollo Medicine, 2006 We are presenting a case of histiocytic necrotizing lymphadenitis (Kikuchi disease), which is characterized by involvement of lymph nodes, skin, liver and spleen. A 21-year-old girl presented with 27 days history of prolonged fever, left cervical painless lymphadenitis and maculo-papular skin rashes.
Vijay Kumar Aneja +2 more
openaire +1 more source
Inflammatory infiltrates are composed of MAC-2 expressing histiocytes.
, 2014 A. H&E-stained section of meninges for orientation of serial sections (B–D). B. Infiltrating cells are negative for CD3 (T-cells). C. Few cells within the thickened meninges are positive (brown) for the B cell marked CD45R (B220).
Jessica M. Snyder (630641) +7 more
core +1 more source
Prenatal Diagnosis, EarlyView.ABSTRACT Objective To investigate uterine healing at delivery after fetoscopic myelomeningocele (MMC) closure in an ovine model. Methods This descriptive study was conducted in Romane ewes. Fetal MMC lesions were created after hysterotomy at 75 days of gestation.
Enora Parc +5 more
wiley +1 more source