000 | 01123cam a2200193 4500500 | ||
---|---|---|---|
005 | 20250112030420.0 | ||
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 |