Results 121 to 130 of about 9,764 (249)

Unique Presentation of Rosai-Dorfman Disease as Concomitant Appendiceal and Rectal Masses with IgG4-Positive Plasma Cells Diagnosed by Core Needle Biopsy

open access: yesCase Reports in Oncological Medicine, 2020
Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy, is a rare non-Langerhans cell histiocytosis. We report a case of a 69-year-old male with concurrent appendiceal and rectal masses who underwent CT-guided percutaneous ...
Jenna J. Poldemann   +2 more
doaj   +1 more source

Cytophagic Histiocytic Panniculitis (CHP) in a Patient with SLE Found after Autopsy: When a Rash Is "Complicated!" [PDF]

open access: yes, 2019
Introduction: Cytophagic histolytic panniculitis (CHP) is a clinical disorder characterized by nodular panniculitis of the subcutaneous adipose tissue. It was first described in 1980 by Winkelmann.
Abbas, Hafsa   +4 more
core   +1 more source

Employment Situation of Parents of Long-Term Childhood Cancer Survivors [PDF]

open access: yes, 2016
BACKGROUND: Taking care of children diagnosed with cancer affects parents' professional life. The impact in the long-term however, is not clear. We aimed to compare the employment situation of parents of long-term childhood cancer survivors with control ...
Ansari, M.   +7 more
core   +6 more sources

Extra-osseous involvement of Langerhans' cell histiocytosis in children [PDF]

open access: yes, 2018
The predominant clinical and radiological features of Langerhans' cell histiocytosis (LCH) in children are due to osseous involvement. Extra-osseous disease is far less common, occurring in association with bone disease or in isolation; nearly all ...
Eich, Georg   +5 more
core  

Apresentação clínica e análise molecular do gene da arginina-vasopressina neurofisina II de pacientes com diabetes insípido central idiopático com longo seguimento [PDF]

open access: yes, 2010
INTRODUCTION: Central diabetes insipidus (DI) characterized by polyuria, polydipsia and inability to concentrate urine, has different etiologies including genetic, autoimmune, post-traumatic, among other causes. Autosomal dominant central DI presents the
ANTUNES-RODRIGUES, Jose   +5 more
core   +2 more sources

Multisystem Langerhans cell histiocytosis in an adult non‐smoker treated with steroid therapy [PDF]

open access: gold, 2020
Haruka Ito   +5 more
openalex   +1 more source

A RARE CASE OF PULMONARY NON-LANGERHANS CELL HISTIOCYTOSIS [PDF]

open access: yesChest, 2020
Victoria Gonzalez   +3 more
openaire   +1 more source

Langerhans cell histiocytosis of the thyroid mimicking thyroiditis in a boy: a case report and literature review

open access: yesBMC Pediatrics
Background Langerhans cell histiocytosis affecting the thyroid commonly presents with nonspecific clinical and radiological manifestations. Thyroid Langerhans cell histiocytosis is typically characterized by non-enhancing hypodense lesions with an ...
Yu Fan Cheng   +4 more
doaj   +1 more source

An unusual acute myeloid leukemia associated with hyper IgE: another case of AML‐M5c? [PDF]

open access: yes, 2001
Haematologica. 2001 Feb;86(2):216-7. An unusual acute myeloid leukemia associated with hyper IgE: another case of AML-M5c? Lima M, Orfão A, Coutinho J, Ferreira G, Freitas I, Silvestre F, Justiça B.
COUTINHO, J.   +6 more
core  

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