Cutaneous Rosai-Dorfman disease with spontaneous partial involution. [PDF]
Porter J, Subhadarshani S.
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Pulmonary Langerhans cell histiocytosis with multiple cavitary nodules after lung cancer surgery. [PDF]
Sugihara M, Okamoto S, Taniguchi T.
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Overlap syndrome of Erdheim-Chester disease and Langerhans cell histiocytosis: A case report.
Ding Y, Chen S, Huang G, Guo X.
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Extracorporeal membrane oxygenation in the treatment of critical Pneumocystis jirovecii pneumonia in a child with Langerhans cell histiocytosis: a case report and literature review. [PDF]
Zou Z+5 more
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Circulating Tumor DNA Combining with Imaging Analysis for Lesion Detection of Langerhans Cell Histiocytosis in Children. [PDF]
Liu S+9 more
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The Role of Bronchoscopy in the Diagnosis of Interstitial Lung Disease: A State-of-the-Art Review. [PDF]
Peralta AR, Shadid AM.
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Case report: Primary subcutaneous Rosai-Dorfman-Destombes of the scalp with intra-cranial involvement: diagnosis and treatment of a rare case with literature review. [PDF]
Zhenwei Q+8 more
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Gastrointestinal LCH: a rare manifestation of Langerhans cell histiocytosis. [PDF]
Thapaliya I+4 more
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An unusual case of non-Langerhans cell histiocytosis [PDF]
A 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.
Ramon Grimalt+4 more
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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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