Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Am J Ther ; 23(2): e583-7, 2016.
Article in English | MEDLINE | ID: mdl-24901901

ABSTRACT

Sunitinib has become a standard treatment agent for metastatic renal cell carcinoma (RCC) for several years. However, various adverse events have been reported. We present a rare adverse effect of hyperammonemic encephalopathy induced by sunitinib. A 66-year-old woman with metastatic RCC referred to the emergency department with confusion that developed 14 days after the initiation of 50 mg/d of sunitinib. Her serum ammonia and thyroid-stimulating hormone levels were markedly elevated (146 µg/dL and 27.27 µIU/mL, respectively). Sunitinib was discontinued, and an enema with lactulose and L-thyroxine were administered. Her mental status and neurologic symptoms were normalized 7 days after the treatment. Serum ammonia level decreased to 61 µg/dL and thyroid stimulating hormone level decreased 22.34 µIU/mL. The incidence of sunitinib-induced hyperammonemia is rarely reported. The relationship between sunitinib and the development of hyperammonemia is not well understood, and the mechanism is unclear. Sunitinib-induced hyperammonemia is very rare, and to the best of our knowledge, this is fourth case hyperammonemia and first case hyperammonemic encephalopathy with hypothyroidism as an adverse effect. Therefore, it is important for clinicians to be aware of hyperammonemia that can occur in several days after the initiation of sunitinib treatment in metastatic RCC.


Subject(s)
Antineoplastic Agents/adverse effects , Brain Diseases/chemically induced , Carcinoma, Renal Cell/drug therapy , Hyperammonemia/chemically induced , Hypothyroidism/chemically induced , Indoles/adverse effects , Kidney Neoplasms/drug therapy , Pyrroles/adverse effects , Aged , Carcinoma, Renal Cell/secondary , Female , Humans , Kidney Neoplasms/pathology , Sunitinib
SELECTION OF CITATIONS
SEARCH DETAIL
...