Results 91 to 100 of about 5,266 (225)

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  

Ovarian endometroid adenocarcinoma in pregnancy [PDF]

open access: yes, 2011
Background. Ovarian cancer is very rare in pregnancy. It is mainly of epithelial origin, low grade and low malignant potential. Case report. We presented a patient in which ultrasound confirmed the presence of clearly limited tumor in the left ovary when
Dimitrijević Aleksandra   +5 more
core   +1 more source

Sinus Histiocytosis with Massive Lymphadenopathy

open access: yesSouth African Medical Journal, 2017
Two cases of a recently described entity, 'sinus histiocytosis with massive lymphadenopathy,' occurring in Black males, are reported. Prominent cervical adenopathy was the main presenting feature in both. Histologically, these nodes were characterised by pronounced proliferation of sinus histiocytes which showed phagocytosis of blood cells ...
Sinclair-Smith, C.C.   +2 more
openaire   +2 more sources

An unusual and malignant intussusception in a child [PDF]

open access: yes, 2016
Intussusception is a common cause of bowel obstruction in the pediatric population. Malignant lesions account for up to 30 % of all cases of intussusception in the small intestine. We herein report an interesting case of ileo-colic intussusception caused
Carmelo Romeo   +9 more
core   +1 more source

Spatial distribution variation and probabilistic risk assessment of exposure to chromium in ground water supplies; a case study in the east of Iran [PDF]

open access: yes, 2018
A high concentration of chromium (VI) in groundwater can threaten the health of consumers. In this study, the concentration of chromium (VI) in 18 drinking water wells in Birjand, Iran, s was investigated over a period of two yearsNon-carcinogenic risk ...
Adli, Abolfazl   +6 more
core   +1 more source

Extranodal manifestation of Rosai-Dorfman disease with bilateral ocular involvement

open access: yesJournal of Cytology, 2011
Rosai-Dorfman disease, that is, sinus histiocytosis with massive lymphadenopathy is a benign systemic proliferative disorder of histiocytes. The typical clinical presentation of the disease includes bilateral painless massive lymphadenopathy, fever and ...
Chayanika Kala   +2 more
doaj   +1 more source

PET-CT-guided interventions in the management of FDG-positive lesions in patients suffering from solid malignancies: initial experiences [PDF]

open access: yes, 2018
Positron emission tomography-computed tomography (PET-CT) has gained widespread acceptance as a staging investigation in the diagnostic workup of malignant tumours and may be used to visualize metabolic changes before the evolution of morphological ...
Guevara, Carlos   +5 more
core  

Sinus Histiocytosis

open access: yes, 2006
The author describes a case of massive lynphadenopathy, fever, astenia and sweating, with 3 weeks evolution. The patient was investigated in a health unit in Sapiranga – RS, Brazil, where he diagnosed with sinus histiocytosis (Rosai-Dorfman disease). After initial treatment in the health unit, the patient was transferred to a reference service.
openaire   +1 more source

Rosai–Dorfman disease as chronic bilateral granulomatous anterior uveitis: A case report

open access: yesSAGE Open Medical Case Reports
Rosai–Dorfman disease is a rare non-Langerhans cell histiocytosis disorder, also known as sinus histiocytosis, with massive lymphadenopathy. Rosai–Dorfman disease is classified into nodal and extranodal diseases.
Yaninsiri Ngathaweesuk   +1 more
doaj   +1 more source

Rosi-Dorfman Syndrome; A case Report [PDF]

open access: yes
Rosai-Dorfman disease1,2 ( RDD or sinus histiocytosis with massive lymphadenopathy, SHML) is a rare, benign proliferative disorder of histiocytes, sometimes showing familiar incidence, it is etiology is uncertain.
جوانپور, حنانه   +1 more
core  

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