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  1. 201
    “…Erdheim–Chester disease (ECD) is a rare systemic disease characterized by non-Langerhans histiocytosis. …”
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    Endoscopic Transsphenoidal Resection of Suprasellar Histiocytosis in a Patient with Erdheim–Chester Disease: A Case Report
  2. 202
    “…Erdheim-Chester disease (ECD) is a rare and systemic non-Langerhans cell histiocytosis. …”
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    A Patient With Erdheim-Chester Disease Presenting With Intestinal Obstruction as the Initial Symptom: A Case Report
  3. 203
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    PD-1/PD-L1 expression is frequent and correlated with lymphocyte density in Erdheim-Chester disease
  4. 204
    “…Erdheim-Chester disease (ECD) is a rare histiocytosis, considered to be an inflammatory myeloid neoplasm. …”
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    Serum vascular endothelial growth factor is associated with cardiovascular involvement and response to therapy in Erdheim-Chester disease
  5. 205
    “…Erdheim-Chester disease (ECD) is a rare progressive disease affecting multiple systems. …”
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    Case report of a patient with Erdheim-Chester disease presenting with neuro-endocrine symptoms and negative for BRAF mutation
  6. 206
    “…Erdheim–Chester disease (ECD), a rare form of non-Langerhans histiocytosis, is a multisystem disorder. …”
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    Incidental Diagnosis of Oligosymptomatic Bilateral Perirenal Erdheim–Chester Disease during Emergency Investigation for COVID-19 Infection
  7. 207
    “…Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis characterized by xanthoma/xanthogranuloma infiltration in various organs and a broad spectrum of clinical presentations, including bone lesions, central diabetes insipidus and renal failure. …”
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    Erdheim-Chester Disease With BRAF V600E Mutation and Central Diabetes Insipidus Successfully Treated With Glucocorticoid
  8. 208
    “…BACKGROUND: Erdheim-Chester disease (ECD) is a rare non–Langerhans cell histiocytosis characterized histologically by foamy histiocytes and Touton giant cells in a background of fibrosis. …”
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    Recurrent petit mal seizures in Erdheim-Chester disease mimicking an intra-axial brain tumor: illustrative case
  9. 209
    “…Patient: Female, 54-year-old Final Diagnosis: Erdheim-Chester disease (ECD) Symptoms: Bilateral flank pain • renal mass presentation Clinical Procedure: CT scan • histopathology • kidney biopsy Specialty: Pathology OBJECTIVE: Rare disease BACKGROUND: Erdheim-Chester disease (ECD), a form of non-Langerhans-cell histiocytosis, is extremely rare. …”
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    Erdheim-Chester Disease with Renal Mass Presentation: Report of the First Case From Palestine and a Review of the Literature
  10. 210
    “…Erdheim-Chester disease (ECD) is a rare form of non-Langerhans cell histiocytosis, with multisystem manifestation such as bone pain, being the most common presenting symptom, cardiovascular or central nervous system involvement, interstitial lung disease, skin and orbital lesions, adrenal enlargement, retroperitoneal fibrosis and renal impairment as well fever, and weight loss. …”
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    A new role for fluorine-18-fluorodeoxyglucose positron-emission tomography/computed tomography in Erdheim-Chester disease
  11. 211
    “…Background: Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis affecting multiple organs, including the endocrine system. …”
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    MON-605 Hypothyroidism in Erdheim-Chester Disease: Experience from a Tertiary Care National Referral Center
  12. 212
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    3D culture of Erdheim-Chester disease tissues unveils histiocyte metabolism as a new therapeutic target
  13. 213
    “…Erdheim-Chester disease (ECD) is a rare type of non-Langerhans cell histiocytosis and is characterized by the diffuse histiocytic infiltration of multiple organs. …”
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    Retroperitoneal Erdheim-Chester disease without skeletal bone involvement mimicking uterine sarcoma with multiple organ involvement
  14. 214
    “…BACKGROUND: Erdheim–Chester disease (ECD) is a non-Langerhans histiocytosis that results in multi-organ disease involving the skin, bones, lungs and kidneys. …”
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    Intracranial mass lesions and skin discoloration in the armpits as unusual clues to Erdheim-Chester disease: a case report
  15. 215
    “…BACKGROUND: Erdheim Chester disease (ECD) is very rare in pediatrics with no standard treatment guidelines. …”
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    A rare presentation of Erdheim Chester disease in a pediatric patient subsequently cured on the LCH III protocol
  16. 216
    “…Chester step test (CST) estimates the exercise capacity through a submaximal response, which can limit its application in the prescription of exercise. …”
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    Adapted Chester Step Test Can Have Maximal Response Characteristics for the Assessment of Exercise Capacity in Young Women
  17. 217
    “…Erdheim-Chester disease (ECD) is a rare non-Langerhans histiocytosis that is classified as a malignancy of myeloid progenitor cells, with only 1,000 confirmed cases in the literature so far. …”
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    Urologic Manifestations and Hydronephrosis as Initial Presentation of Erdheim-Chester Disease: A Rare Form of Non-Langerhans Histiocytosis
  18. 218
    “…These findings led to consideration of Erdheim-Chester disease (ECD), a form of non-Langerhans cell histiocytosis, where there is abnormal proliferation of histiocytes which causes tissue fibrosis and sclerosis of the long bones. …”
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    Erdheim-Chester disease: a rare cause of bilateral renal artery stenosis, mimicking large vessel vasculitis
  19. 219
    “…Neurological involvement is relatively common in Erdheim–Chester disease (ECD), a rare clonal disorder of histiocytic myeloid precursors characterized by multisystem involvement. …”
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    Neurological Erdheim–Chester Disease Manifesting with Subacute or Progressive Cerebellar Ataxia: Novel Case Series and Review of the Literature
  20. 220
    por Himes, Chester B., 1909-
    Publicado 1977
    Libro
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