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Histiocytosis X: Langerhans’ Cell Histiocytosis
Histiocytosis X is a complex and poorly understood entity. Nevertheless, it would appear as if certain themes are found recurrently throughout the literature dealing with this disease and a review of them serves as a useful summary. 1. Problems with Nomenclature.
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Langerhans Cell Histiocytosis [PDF]
Sandra Camelo-Piragua+2 more
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Langerhans’ cell histiocytosis diagnosed due to dermatological perianal lesion
Langerhans’ cell histiocytosis is a rare disease characterized by proliferation of Langerhans cells in the body. It affects mainly males, predominantly in childhood. Ulcerated plaques are one of the cutaneous forms of presentation.
Bruno Lorenzo Scolaro+5 more
doaj
Skull base Langerhans cell histiocytosis presenting as persistent ear discharge with granulation-like tissue in the external ear canal. [PDF]
Saad MME, Thompson CSG, Alsalem M.
europepmc +1 more source
A Metastasis-Tumour-Like Pulmonary Langerhans Cell Histiocytosis With Association to Positron Emission Tomography/Computed Tomography Finding Confirmed With Surgical Resection. [PDF]
Chuang TY, Liao KS, Hsie YS, Lee SW.
europepmc +1 more source
Utilizing Computer-assisted Planning for Split Calvarial Bone Cranioplasty of an Infant With Occipital Langerhans Cell Histiocytosis. [PDF]
Whittles JR+5 more
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Solitary Langerhans Cell Histiocytosis of the Femur in a Nine-Month-Old Girl. [PDF]
Abdullah F, Alabd K, Carpenter C.
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