Results 71 to 80 of about 19,037 (201)
A Rare Case Report: A Malignant Histiocytic Tumor in the Form of Ovarian Mass [PDF]
Histiocytic cell malignancies are very rare. Hence, the information about this disease in hematology is limited. In this case report, we present a case of malignant histiocytic tumor affecting the ovary of a 40-year-old virgin female.
Emsal Pinar Topdagi Yilmaz +3 more
core +2 more sources
Abstract Rarely, Rosai–Dorfman disease (RDD) manifests exclusively in the skin, typically as nodules on the trunk and extremities. Recognition of characteristic histopathologic features enables diagnosis of RDD. A 55‐year‐old female presented with a 7‐year history of cutaneous nodules involving the trunk and extremities. A prior skin biopsy specimen at
Joseph Gillam +6 more
wiley +1 more source
ABSTRACT Introduction MGRS are new rare clinical entities, whose recognition and optimal management is evolving. Methods To implement real‐life data, we retrospectively analysed a multicentre cohort of 60 patients with renal biopsy‐proven MGRS receiving mainly novel treatments (between 2006 and 2021) in eight Italian centres.
K. Mancuso +24 more
wiley +1 more source
Neurology and the histiocytoses: a case of Rosai-Dorfman-Destombes disease [PDF]
The histiocytoses are a group of rare disorders characterised by the accumulation of neoplastic or non-neoplastic activated histiocytes in various tissues.
Blake, Julian +11 more
core
children: differentiation using diffusion-weighted magnetic resonance imaging [PDF]
Purpose To evaluate differences in magnetic resonance imaging (MRI) appearance between infantile hemangiomas and rhabdomyosarcomas of the orbit in pediatric patients using diffusion-weighted imaging.
Calloni, Sonia F. +5 more
core +1 more source
Human infection by avian influenza A H5N1 [PDF]
The Southeast Asian outbreak of the highly lethal avian influenza A HSN1 infection in humans is unlikely to abate because of the enormous number of backyard farms providing poultry as the main source of food protein in developing countries.
Wong, SSY, Yuen, KY
core
Erdheim-Chester disease as complex clinical presentation and diagnosis: A case report and concise review of literature [PDF]
Rationale: Erdheim-Chester disease (ECD) is a rare multisystemic disease characterized by the infiltration of multiple organs by foamy CD68 + CD1a-histiocytes. The genetic background consists of gain-of-function somatic mutations in the mitogen-activated
Pegoraro, Francesco, Vaglio, Augusto
core +4 more sources
Indeterminate cell histiocytosis: report of a case.
Indeterminate cell histiocytosis is a very rare disorder of histiocytes proliferation. It has both Langerhans and non-Langerhans cell histiocytosis immunophenotypic features. We described a 45-year-old man with a 2 years history of multiple yellow-brown papules and a few red nodules on his trunk and extremities.
Alireza, Ghanadan +9 more
openaire +1 more source
Myeloid Leukemia and Cutaneous Histiocytosis: fortuitous encounter? [PDF]
Background: Histiocytosis encompass highly heterogeneous proliferative disorders of the mononuclear phagocyte system. Recently they have been reclassified by the Histiocyte Society (2016) and reviewed in WHO classifications of hematopoietic (2017) and ...
Arturo Bonometti +9 more
core
Concomitant Langerhans Cell Histiocytosis and Chronic Myelomonocytic Leukaemia Responding to 5-azacitidine [PDF]
Brændstrup, Peter +4 more
core +1 more source

