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Congenital self-healing Langerhans cell histiocytosis vs benign cephalic histiocytosis: A comprehensive literature review of pediatric cutaneous histiocytoses. [PDF]
JAAD Case RepFekri M, Alavi S, Aghdam MK, Sarraf S.
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Primary cerebral non-Langerhans cell histiocytosis: MRI and differential diagnosis
Neuroradiology, 2002We report a young woman with primary cerebral non-Langerhans cell histiocytosis of the juvenile xanthogranuloma family. The clinical course was complicated by extensive infiltration of cranial nerves and meninges and epi- and intramedullary spinal dissemination.
U, Ernemann +5 more
openaire +4 more sources
Journal of the American Academy of Dermatology, 2009
The advent of electron microscopy and immunohistochemical stains allowed for reclassification of the histiocytoses based on the predominant cell in the infiltrate. Although the current schema simplicity provides a good foundation, some patients display overlapping clinical and immunohistochemical features that defy classification.
Elizabeth K, Satter +2 more
openaire +4 more sources
The advent of electron microscopy and immunohistochemical stains allowed for reclassification of the histiocytoses based on the predominant cell in the infiltrate. Although the current schema simplicity provides a good foundation, some patients display overlapping clinical and immunohistochemical features that defy classification.
Elizabeth K, Satter +2 more
openaire +4 more sources
Non-Langerhans cell histiocytosis
Acta Neurologica Belgica, 2016A 34-year-old man complained of seizures, headache and reduced visual acuity for a month. Physical examination revealed intracranial hypertension. CSF showed high opening pressure, increase of protein (121 mg/dl) and 26 leukocytes per mm, 94 % of which were lymphomononuclear cells, with cytoplasmic and nuclear atypia.
Lívia Nathália Alaite Silveira +2 more
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An unusual case of non-Langerhans cell histiocytosis
Journal of the American Academy of Dermatology, 1994A 28-month-old boy had firm, red nodules for 4 months that were mostly localized to the face. The eruption was preceded by conjunctivitis, eyelid edema, and swelling of the root of the nose. He also had dyspnea, anisocoria with areflexia, swelling of the parotid glands, and hepatosplenomegaly. A bone marrow aspirate showed 25% eosinophils.
R, Caputo +4 more
openaire +2 more sources
A Child with Both Langerhans and Non‐Langerhans Cell Histiocytosis
Pediatric Dermatology, 2002Abstract: The histiocytic syndromes consist of a group of disorders that share in common the proliferation of cells of the monocytic/macrophage lineage. It has been conventional to divide the histiocytoses into two separate groups: Langerhans cell histiocytosis (LCH) and non‐LCH.
Ayelet, Shani-Adir +3 more
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Congenital self-healing non-Langerhans cell histiocytosis
European Journal of Pediatrics, 1988Clinical, morphological, ultrastructural and immunological studies were performed in a case of congenital self-healing non-Langerhans cell histiocytosis. The patient showed several aspects that have not been published before: a large nodule in the vulvar region, vesiculobullous elements and pneumonia (asymptomatic). The relationship of the vesicles and
A P, Oranje +3 more
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Progressive Histiocytosis: Description of a Case of Slow-Course Non-Langerhans Cell Histiocytosis
Dermatology, 2002We describe the case of a 37-year-old male patient who in 1992 started developing a skin eruption characterized by dark red to red-yellow papulonodular lesions that showed no tendency to spontaneous resolution. Visceral organs were not involved and the lipid pattern was basically normal.
R. Caputo +4 more
openaire +2 more sources