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International Journal of Surgical Pathology, ISSN 1066-8969, 12/2019, Volume 27, Issue 8, pp. 836 - 843
Langerhans cell histiocytosis (LCH) is characterized by clonal proliferation of Langerhans cells and has been classified as a hematolymphoid tumor. BRAF V600E... 
head and neck Sanger sequencing | immunohistochemistry | Langerhans cell histiocytosis | BRAF V600E mutation | SURGERY | MAP2K1 MUTATIONS | PATHOLOGY
Journal Article
BMC cancer, ISSN 1471-2407, 05/2019, Volume 19, Issue 1, pp. 514 - 8
Crystal-storing histiocytosis (CSH) is a rare lesion characterized by sheets of crystal-laden non-neoplastic histiocytes. CSH shows a prominent association... 
Immunoglobulins | Genetic aspects | Lymphomas | Research | Histiocytosis | Multiple myeloma | Monoclonal gammopathy | Immunoglobulin | Crystal-storing histiocytosis | Diffuse large B-cell lymphoma
Journal Article
by Zhao, SS and Yan, LF and Feng, XL and Du, P and Chen, BY and Dong, WT and Gao, Y and He, JB and Cui, GB and Wang, W
JOURNAL OF ORTHOPAEDIC SURGERY AND RESEARCH, ISSN 1749-799X, 05/2019, Volume 14, Issue 1, p. 123
Journal Article
Radiology Case Reports, ISSN 1930-0433, 12/2019, Volume 14, Issue 12, pp. 1478 - 1482
Langerhans Cell Histiocytosis (LCH) is a rare disorder characterized by neoplastic proliferation of Langerhans-type dendritic cells. LCH is most frequently... 
Skull lesion | Elderly patient | Langerhans Cell Histiocytosis
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 01/2019, Volume 14, Issue 1, pp. 11 - 8
Journal Article
by Wang, X and Li, PF and Zhou, P and Fu, YY and Lai, YT and Che, GW
BMC PULMONARY MEDICINE, ISSN 1471-2466, 01/2019, Volume 19, Issue 1, pp. 8 - 4
BackgroundCystic lung lesions involving both lungs include a variety of diseases, such as pulmonary Langerhans cell histiocytosis, lymphangioleiomyomatosis and... 
Cystic | Metastasis | Computed tomography | RESPIRATORY SYSTEM | Pulmonary meningioma | Diagnosis | Lung diseases | Meningioma
Journal Article
BMC PEDIATRICS, ISSN 1471-2431, 04/2019, Volume 19, Issue 1, pp. 128 - 9
BackgroundJuvenile xanthogranuloma (JXG) belongs to the heterogeneous group of non-Langerhans cell histiocytosis and is caused by an accumulation and... 
Non-Langerhans cell histiocytosis | Case report | Histopathology | Blueberry muffin baby | DISEASE | UNCOMMON | PEDIATRICS | Juvenile xanthogranuloma | Systemic | LESIONS | Case studies | Causes of | Care and treatment | Diagnosis | Histiocytosis | Literature reviews | Nervous system | Ultrasonic imaging | Skin | Birth weight | Congenital diseases
Journal Article
Annals of Diagnostic Pathology, ISSN 1092-9134, 12/2019, Volume 43, p. 151403
Crystal-storing histiocytosis (CSH) is a rare manifestation of monoclonal gammopathy in which histiocytes containing monoclonal proteins in their cytoplasm are... 
Kidney biopsy | Crystal-storing histiocytosis (CSH) | Plasma cell dyscrasia | Dysproteinemia | Multiple myeloma
Journal Article
Journal Article
by Lee, YK and Chao, SC and Lee, CN and Hung, JH
BMC OPHTHALMOLOGY, ISSN 1471-2415, 07/2019, Volume 19, Issue 1, pp. 144 - 5
BackgroundRosai-Dorfman disease is a rare non-Langerhans cell histiocytosis. Ocular involvement is even rarer, mostly involving the orbit and eyelids, although... 
OPHTHALMOLOGY | Epibulbar tumor | Histiocytosis | Rosai-Dorfman disease | Scleritis | Development and progression | Care and treatment | Immunotherapy | Uveitis | Tumors | Cornea | Cheek | Neutrophils | Family medical history | Patients | Stains & staining | Eye | Immunosuppression | Ulcers | Ophthalmology | Rosacea
Journal Article
Journal of Cutaneous Pathology, ISSN 0303-6987, 12/2019, Volume 46, Issue 12, pp. 945 - 948
Histiocytoses are a group of rare disorders characterized by a proliferation of monocytes/macrophages and dendritic cells. We present a case of a 3‐year‐old... 
indeterminate cell histiocytosis | S‐100 | CD1a+ S‐100‐indeterminate cell histiocytosis | CD1a | Cell proliferation | Monocytes | Dendritic cells | Biopsy | Bone marrow | Histiocytosis | Macrophages
Journal Article
Journal of Medical Case Reports, ISSN 1752-1947, 03/2019, Volume 13, Issue 1, pp. 67 - 4
Langerhans cell histiocytosis previously known as histiocytosis X is a rare disease of children and young adults with a very broad clinical spectrum. In... 
Langerhans cell histiocytosis | Pediatric bone lesion | Forearm | Immunohistochemistry | Care and treatment | Usage | Langerhans-cell histiocytosis | Diagnosis | Health aspects | Girls | Proteins | Pediatrics | Chemotherapy | Nuclear magnetic resonance--NMR | Hospitals | Pain | Biopsy | Bones | Family medical history | Localization | Cancer therapies
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 317 - 9
Accurate risk stratification according to the extent of Langerhans cell histiocytosis (LCH) determined on whole-body evaluation is important for determining... 
FDG-PET | MANAGEMENT | MULTIDISCIPLINARY SCIENCES | LIVER | INVOLVEMENT | VOLUME | EXPERIENCE | AGREEMENT | COMPUTED-TOMOGRAPHY | CHILDREN | Accuracy | Nuclear magnetic resonance--NMR | Magnetic resonance imaging | Tomography | Histiocytosis | Bone imaging | Patients
Journal Article
Experimental and Molecular Pathology, ISSN 0014-4800, 12/2019, Volume 111, p. 104320
V600E is the predominant oncogenic driver of L-group histiocytoses, which includes Erdheim-Chester disease (ECD); however, limited data exist on the prevalence... 
Xanthogranuloma | BRAF | Erdheim-Chester disease | Langerhans cell | Histiocytosis | Reticulohistiocytoma
Journal Article