Langerhans Cell Histiocytosis (LCH) Associated With Helicobacter Pylori Infection

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dc.FacultyEndemic Diseasesen_US
dc.contributor.authorElhassan, Ahmed M.
dc.contributor.authorALhassan, Lamyaa
dc.contributor.author., et al
dc.contributor.otherMolecular Biologyen_US
dc.date2011-06
dc.date.accessioned2015-11-29T11:49:12Z
dc.date.available2015-11-29T11:49:12Z
dc.date.issued2015-11-29
dc.date.submitted2015
dc.description.abstractLangerhans cell histiocytosis (LCH) is defined as a clonal proliferation of Langerhans phenotypic-like cells. Letterer-Siwe disease is the most common and serious of these entities, affecting mainly infants up to two years of age. We report an interesting, previously misdiagnosed and relapsing case of adult skin limited to LCH in a 25 years old female patient presented with well defined erythematous, dry scaly plaques in the face, trunk and extremities for 10 years duration, and then remains stable over the time. The case is diagnosed and confirmed histopathologically, considered to be the second case of LCH and first case as adult Letterer Siwe been reported in Sudan.en_US
dc.identifier.urihttp://khartoumspace.uofk.edu/123456789/17354
dc.language.isoenen_US
dc.publisherUOFKen_US
dc.subjectImmunology, Langerhans cell histiocytosis, lymphoid, Helicobacter pylorien_US
dc.titleLangerhans Cell Histiocytosis (LCH) Associated With Helicobacter Pylori Infectionen_US
dc.typePublicationen_US

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