Cardiac mass as the primary diagnostic clue of Edheim–Chester disease
Clinical Case ReportsKey Clinical Message We introduced one of the rare causes of intra‐cardiac mass, that is, ECD and a new gene mutation (SLC29A3) that is probably related to this disease, and we noted the importance of using several diagnostic methods to rule out other ...
Azin Alizadehasl +6 more
doaj +1 more source
Endocrine manifestations in Langerhans cell histiocytosis
, 2007 Langerhans cell histiocytosis is a rare, multisystem disease that shows a particular predilection for hypothalamo-pituitary axis involvement. Diabetes insipidus is the most frequent permanent consequence of Langerhans cell histiocytosis, developing in ...
Kaltsas, G.A. +4 more
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Malignant Histiocytosis with Nodular Ulcerating, Vasculitic Skin Lesion
, 2002 malignant histiocytosis with nodular ulcerating, vasculitic skin ...
Lawrence, Christine
core
Malignant Histiocytosis with Binuclear Histiocyte in Bone Marrow
, 2002 malignant histiocytosis with binuclear histiocyte in bone ...
Lawrence, Christine
core
Longitudinal Monocyte Subset Dynamics as Biomarker in Adult Histiocytosis: Association With Mutational Status, Kinase Inhibitor Exposure and Relapse Risk. [PDF]
Hematol OncolRazanamahery J +10 more
europepmc +1 more source
Literature review of pediatric Erdheim-Chester disease (ECD) and mixed histiocytosis (Langerhans cell histiocytosis/ECD). [PDF]
Ann Transl MedImashuku S.
europepmc +1 more source
Giant Juvenile Xanthogranuloma Co-Occurring with Langerhans Cell Histiocytosis
The Journal of Pediatrics: X, 2023 Hiroshi Hayashi, MD +2 more
doaj +1 more source
Single-Site ALK-Positive Histiocytosis With TFG-ALK Fusion: Expanding the Clinical Spectrum of This Rare Entity. [PDF]
Am J Case RepDasgupta M +4 more
europepmc +1 more source