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Author Spotlight: Alleviating Nausea and Vomiting in Pregnancy with Safe and Effective Auricular Acupuncture
Published on: August 4, 2023
[A female patient with earache, polyuria and polydipsia]
Nora Bidner1, Christoph Schnack1, Johanna M Brix1
11. Medizinische Abteilung mit Diabetologie, Endokrinologie und Nephrologie und Karl Landsteiner Institut für Adipositas und Stoffwechselerkrankungen, Klinik Landstraße, Wien.
Langerhans cell histiocytosis, a rare bone marrow neoplasia, can present subtly. Early recognition of its association with diabetes insipidus in cranial bone cases is crucial for timely diagnosis and better outcomes.
Area of Science:
- Oncology
- Histopathology
- Endocrinology
Background:
- Langerhans cell histiocytosis (LCH) is a rare neoplastic proliferation of cells resembling Langerhans cells.
- It commonly affects bone, lung, and skin, but its varied presentation can delay diagnosis.
- Cranial bone involvement in LCH is frequently linked with central diabetes insipidus.
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