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Letterer-Siwe disease presenting with gastrointestinal and cutaneous manifestations.
Dermatol Online J
December 2023
Federal State Autonomous Educational Institution of Higher Education "Peoples' Friendship University of Russia" of the Ministry of Education and Science of the Russian Federation, Children's City Clinical Hospital named after PER, Bashlyaeva, Moscow Department of Health, Moscow, Russia.
Histiocytosis is a set of distinct proliferative illnesses defined by the proliferation and infiltration of varied numbers of dendritic cells, macrophages, and monocytes in the afflicted tissues. The skin and other organs may be impacted by the inflammatory infiltration. It can occur at any age.
View Article and Find Full Text PDFGastrointestinal: Letterer Siwe disease: An uncommon gastrointestinal presentation.
J Gastroenterol Hepatol
June 2016
Division of Gastroenterolgy and Hepatology, Department of Medicine, Hamad General Hospital, Doha, Qatar.
A rare case of langerhans cell histiocytosis of the gastrointestinal tract.
World J Gastroenterol
March 2012
Internal Medicine, Mount Sinai School of Medicine at Queens Hospital Center, Jamaica, NY 11432, USA.
Langerhans cell histiocytosis (LCH) is a group of idiopathic disorders characterized by the proliferation of specialized, bone marrow-derived langerhans cells and mature eosinophils. The clinical spectrum ranges from an acute, fulminant, disseminated disease called Letterer-Siwe disease to solitary or few, indolent and chronic lesions of the bone or other organs called eosinophilic granuloma. Involvement of the gastrointestinal tract is very rare in LCH.
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