Abstract
Langerhans cell histiocytosis is a rare disease characterized by various clinical patterns: from isolated lung lesions to severe involvement of other organs. This clinical case demonstrates a rare combination of pulmonary Langerhans cell histiocytosis and Guillain—Barre syndrome due to possible common mechanisms of the disease development mediated by the CD1A expression.
Highlights
Langerhans cell histiocytosis is a rare disease characterized by various clinical patterns: from isolated lung lesions to severe involvement of other organs
This clinical case demonstrates a rare combination of pulmonary Langerhans cell histiocytosis and Guillain—Barré syndrome due to possible common mechanisms of the disease development mediated by the CD1A expression
Существуют формы заболевания, при которых наблюдается изолированно функций для Синдром Гийена-Барре (СГБ) не характерны и могут наблюдаться у прикованных к постели больных, в основном в виде задержки мочеиспускания
Summary
Е.В. Ефремова*1, А.В. Васильчев2, А.М. Шутов1, А.С. Подусов1, И.Ю. Трошина1, А.А. Тимофеев1 1 — кафедра терапии и профессиональных болезней медицинского факультета Института медицины, экологии и физической культуры ФГБОУ ВО «Ульяновский государственный университет», Ульяновск, Россия 2 — ГУЗ «Центральная городская клиническая больница г. Ульяновска» Ульяновск, Россия СЛУЧАЙ СИНДРОМА ГИЙЕНА-БАРРЕ У БОЛЬНОГО ЛЕГОЧНЫМ ГИСТИОЦИТОЗОМ ИЗ КЛЕТОК ЛАНГЕРГАНСА E.V. Efremova*1, A.V. Vasil’chev2, A.M. Shutov1, A.S. Podusov1, I.Yu. Troshina1, A.A. Timofeev1 1 — Department of General Medicine and Occupational Diseases, Medical Faculty, Institute of Medicine, Ecology and Physical Education, Federal State Budgetary Educational Institution «Ulyanovsk State University», Ulyanovsk, Russia 2 — State Budgetary Healthcare Institution «Ulyanovsk Central City Clinical Hospital», Ulyanovsk, Russia
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