Immunoglobin G4-related disease as a rare cause of polycythemia: A case report (notice n° 152196)
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| 000 -LEADER | |
|---|---|
| fixed length control field | 01123cam a2200193 4500500 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20250112030420.0 |
| 041 ## - LANGUAGE CODE | |
| Language code of text/sound track or separate title | fre |
| 042 ## - AUTHENTICATION CODE | |
| Authentication code | dc |
| 100 10 - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Felk, Rime |
| Relator term | author |
| 245 00 - TITLE STATEMENT | |
| Title | Immunoglobin G4-related disease as a rare cause of polycythemia: A case report |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
| Date of publication, distribution, etc. | 2023.<br/> |
| 500 ## - GENERAL NOTE | |
| General note | 53 |
| 520 ## - SUMMARY, ETC. | |
| Summary, etc. | Immunoglobulin 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. |
| 700 10 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Baiche, Farah |
| Relator term | author |
| 700 10 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Belbezier, Aude |
| Relator term | author |
| 700 10 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Bouillet, Laurence |
| Relator term | author |
| 786 0# - DATA SOURCE ENTRY | |
| Note | Cahiers Santé Médecine Thérapeutique | 32 | 4 | 2023-07-01 | p. 189-191 | 2780-8858 |
| 856 41 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="https://shs.cairn.info/journal-cahiers-sante-medecine-therapeutique-2023-4-page-189?lang=en">https://shs.cairn.info/journal-cahiers-sante-medecine-therapeutique-2023-4-page-189?lang=en</a> |
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