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Clinical Images: Erdheim-Chester disease presenting with fever, enlarged lymph nodes, and monoallelic BRAF (V600E) mutation. [PDF]
ACR Open RheumatolGan L, Zhang Q, Yan H, Bai H, Tang X.
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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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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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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
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Progressive nodular histiocytosis – rare variant of cutaneous non‐Langerhans cell histiocytosis
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2006SummaryProgressive nodular histiocytosis is an extremely rare skin disease is clinically characterized by the coincidence of two distinct lesions, namely, superficial xanthomatous papules up to 5 mm and deep nodules and tumors 1–3 cm. Histologically the nodules represent spindle cell xanthogranulomas.
Matthias, Lüftl +3 more
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Fibroblastic rheumatism: fibromatosis rather than non‐Langerhans cell histiocytosis
Journal of Cutaneous Pathology, 2010Background: Fibroblastic rheumatism is a unique fibro‐proliferative disease affecting the skin and joints. It is characterized by distinctive clinical and histological features related to benign spindle‐shaped cells proliferation. Pediatric reports are scarce in the literature.
Nicolas, Kluger +4 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
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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
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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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