Treatment of primary defective iron-reutilization syndrome: revisited

被引:5
作者
Besa, EC
Kim, PW
Haurani, FI
机构
[1] Med Coll Penn & Hahnemann Univ, Med Coll Penn Hosp, Dept Med, Div Hematol Oncol, Philadelphia, PA 19129 USA
[2] Thomas Jefferson Univ, Cardeza Fdn Hematol Res, Dept Med, Philadelphia, PA 19107 USA
关键词
ACD; primary defective iron-reutilization syndrome; Danazol;
D O I
10.1007/s002770000180
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
We encountered two patients who presented with hypochrornic-microcytic anemia and were refractory to iron therapy. The symptoms were suggestive of anemia of chronic disease (ACD): however, there was no evidence of ally such disease, either inflammatory or malignant. These patients were reminiscent of patients originally described as having primary defective iron reutilization. The hematologic picture consisted of hypochrotnic-microcytic anemia, low serum iron, low to normal iron binding capacity, high serum ferritin, and increased bone marrow iron in the absence of ringed sideroblasts. These patients had symptomatic anemia and received danazol (200 mg orally) three times per day to which they responded very well with an increase of approximately 3 g in the hemoglobin concentration over 1 year and amelioration of their symptoms. Danazol was well tolerated and did not cause any virilizing side effects. Doses were lowered in maintenance after 1 year to 200 mg once per week, and responses were sustained up to 36 months of follow-up duration. In the differential diagnosis of hypochromic-microcytic anemia, especially in postmenopausal women, one has to consider this type of treatable anemia when more common types such as iron deficiency, chronic inflammation, malignancy, sideroblastic anemia, or thalassemia have been ruled out.
引用
收藏
页码:465 / 468
页数:4
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