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Clinical and biochemical stabilization of Nelson’s syndrome with long-term low-dose cabergoline treatment

✍ Scribed by Ilana Shraga-Slutzky; Ilan Shimon; Ruth Weinshtein

Book ID
106497195
Publisher
Springer US
Year
2006
Tongue
English
Weight
249 KB
Volume
9
Category
Article
ISSN
1386-341X

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Idiopathic pulmonary hemosiderosis (IPH) is a rare disease of unknown etiology characterized by recurrent episodes of pulmonary symptoms such as cough, hemoptysis, and dyspnea. Our study consisted of 23 patients: 12 males and 11 females with IPH. The diagnosis was based on history, presence of anemi