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F anconi's Syndrome and Nephrogenic Diabetes Insipidus in an Adult Treated with Ifosfamide
Author(s) -
Ingemi Amanda I.,
Bota Vasile M.,
Peguero Anyeri,
Charpentier Margaret
Publication year - 2012
Publication title -
pharmacotherapy: the journal of human pharmacology and drug therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.227
H-Index - 109
eISSN - 1875-9114
pISSN - 0277-0008
DOI - 10.1002/phar.1013
Subject(s) - ifosfamide , medicine , nephrogenic diabetes insipidus , diabetes insipidus , fanconi syndrome , urology , pediatrics , gastroenterology , endocrinology , kidney , chemotherapy , etoposide
F anconi's syndrome is a serious condition characterized by type II proximal renal tubular dysfunction, with urinary loss of glucose, amino acids, phosphate, bicarbonate, and potassium. Ifosfamide‐induced F anconi's syndrome is reported in about 1.4–5% of children being treated for solid tumors, yet only a few cases have been reported in adults. We describe a 54‐year‐old man who came to the hospital with symptoms of neutropenic fever 4 days after his fourth cycle of ifosfamide and doxorubicin treatment for recurrent sarcoma with metastases to the lung. During admission, he was noted to have severe renal tubular dysfunction; ifosfamide‐induced nephrogenic diabetes insipidus and F anconi's syndrome were suspected. He received supportive therapy that resulted in incomplete resolution of signs and symptoms. The patient was discharged after a 5‐day hospital stay when his white blood cell count increased from 0.1–2.5 × 10 3 /mm 3 and his fever had resolved. Use of the Naranjo adverse drug reaction probability scale indicated a probable relationship (score of 7) between the patient's development of diabetes insipidus and F anconi's syndrome and his use of ifosfamide. This dual diagnosis of diabetes insipidus and F anconi's syndrome in an adult makes this case unusual, as well as therapeutically challenging. We conducted a review of the existing literature regarding ifosfamide‐induced F anconi's syndrome and describe the proposed mechanisms and therapeutic options. This case suggests that patients treated with ifosfamide should be monitored closely for renal function to identify, and perhaps prevent, these rare adverse events. Preliminary animal models show promise for adding N ‐acetylcysteine to ifosfamide treatment, but more research is necessary before using this drug as a therapeutic option.

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