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Case Reports
. 1995 Oct;36(10):1199-203.

[Hemophagocytic syndrome with syndrome of inappropriate secretion of antidiuretic hormone (SIADH)]

[Article in Japanese]
Affiliations
  • PMID: 8531331
Case Reports

[Hemophagocytic syndrome with syndrome of inappropriate secretion of antidiuretic hormone (SIADH)]

[Article in Japanese]
A Ohmoto et al. Rinsho Ketsueki. 1995 Oct.

Abstract

A 69-year-old female was admitted to the hospital because of fever, hyponatremia and anemia. Laboratory data showed hemoglobin 8.6 g/dl, indirect bilirubin 1.9 mg/dl and Na 122 mEq/l. Urine osmolality was elevated and urinary excretion of sodium was increased. Furthermore, antidiuretic hormone (ADH) level was elevated. Renal function and hormonal data were within normal limit. Therefore, she was diagnosed as having syndrome of inappropriate secretion of antidiuretic hormone (SIADH). On the other hand, bone marrow aspiration showed hemophagocytosis and the diagnosis of hemophagocytic syndrome (HPS) was also made. High dose prednisolone and pulse therapy of cyclophosphamide were administered, nevertheless high grade fever persisted. Fever alleviation was acquired by Etoposide. But she died of pneumonia. An autopsy revealed hemophagocytosis in bone marrow, lymphnodes and spleen, but malignant tumor was not detected. And hypophysis was intact. The pathogenesis of SIADH in this case was not clarified. This report is seemed to be the first case of HPS associated with SIADH.

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