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041 _afre
042 _adc
100 1 0 _aFelk, Rime
_eauthor
700 1 0 _a Baiche, Farah
_eauthor
700 1 0 _a Belbezier, Aude
_eauthor
700 1 0 _a Bouillet, Laurence
_eauthor
245 0 0 _aImmunoglobin G4-related disease as a rare cause of polycythemia: A case report
260 _c2023.
500 _a53
520 _aImmunoglobulin G4 (IgG4) disease is a recently described condition with a growing list of associated disorders. The most common manifestations are pancreatitis, infiltration of the salivary or lacrimal glands (Mikulicz syndrome), and retroperitoneal fibrosis. We present the case of a patient in whom polycythemia was secondary to IgG4 disease. Through a review of the literature, we discuss the clinical, radiological, and therapeutic aspects of this rare condition.
786 0 _nCahiers Santé Médecine Thérapeutique | 32 | 4 | 2023-07-01 | p. 189-191 | 2780-8858
856 4 1 _uhttps://shs.cairn.info/journal-cahiers-sante-medecine-therapeutique-2023-4-page-189?lang=en
999 _c152196
_d152196