- Case report
- Open Access
- Open Peer Review
Hyperuricemia and acute kidney injury secondary to spontaneous tumor lysis syndrome in low risk myelodysplastic syndrome
© Feng et al.; licensee BioMed Central Ltd. 2014
- Received: 22 July 2014
- Accepted: 9 October 2014
- Published: 11 October 2014
This is a rare instance of acute kidney injury caused by hyperuricemia due to spontaneous tumor lysis syndrome and also the first case of spontaneous tumor lysis syndrome reported in association with myelodysplastic syndrome.
A 53-year-old man presented with abrupt oliguria. Laboratory findings on admission included hyperuricemia, hyperphosphatemia, hypocalcemia, metabolic acidosis and rapidly rising serum creatinine, which were consistent with acute tumor lysis syndrome in the absence of precipitating chemotherapy or radiotherapy. After hemodialysis and oral uric acid lowering therapy, serum uric acid levels returned to normal range and renal function rapidly recovered. The patient was diagnosed as myelodysplastic syndrome eleven months later.
Occult malignancy including solid tumors and hematological malignancies should be carefully evaluated in the case of unexplainable acute kidney injury with hyperuricemia. Aggressive investigations should be thoroughly considered and repeated in this population.
- Acute kidney injury
- Myelodysplastic syndrome
- Spontaneous tumor lysis syndrome
Acute tumor lysis syndrome (TLS) is a metabolic disorder manifesting as abrupt occurrence of acute kidney injury (AKI), metabolic acidosis and electrolyte disturbances which include hyperuricemia, hyperphosphatemia, hyperkalemia and hypocalcemia . TLS most commonly results from treatment of malignancies, especially high turnover rate hematologic malignancies. Spontaneous tumor lysis syndrome (STLS) before chemotherapy is a rare event which has been mostly reported in Burkitt lymphoma and non T-cell acute lymphoblastic leukemia . Here we report a rare case of STLS in myelodysplastic syndrome (MDS) which presented with marked hyperuricemia and AKI months before the diagnosis of MDS.
Laboratory investigation results
5 days before admission/after LC
1 day before admission
1 day after admission
3 days after admission
At the current admission, physical examination showed a chronically ill-appearing man in no acute distress, with stable vital signs. The patient was awake, alert and oriented. There was no increase in jugular venous pressure. Pulmonary and cardiac examinations were unremarkable. Abdominal examination showed well healed small scars left by the LC. Mild bilateral pretibial pitting edema was present in both lower limbs. Neurological examination was unremarkable.
The patient visited the clinic every 2-3 months after discharge. Investigations showed HGB was fluctuating in the range of 7.5-9.0 g/dL while SCr and UA remained normal. Chest/abdominal CTs were done 3 months and 9 months later with unremarkable findings. However, the patient complained of persistent progressively worsening malaise. Eleven months later, he was admitted again because of refractory anemia. At this time, bone marrow smear indicated erythroid hyperplasia and significant dyshaematopoiesis of all three lineages. The major loss of the D20S108 signal suggesting 20q- along with minor gains of D8Z2 signal was discovered by fluorescence in situ hybridization (FISH), which was consistent with a G banding karyotype. MDS was confirmed and the patient was classified as low-moderate risk group, hence no chemotherapy. He has been on regular clinic follow-up and the condition has not deteriorated.
The most commonly used diagnostic laboratory and clinical criteria for TLS are those proposed by Cairo and Bishop . A clinical diagnosis of TLS includes one clinical symptom and two laboratory criteria, and at least two laboratory criteria must be present for three days before treatment or up to seven days after treatment. In our case, the patient fulfilled one clinical symptom (acute renal failure) and two laboratory criteria (hyperphosphatemia, hyperuricemia), thus meeting the clinical diagnostic criteria for TLS. In the absence of precipitating chemotherapy or radiotherapy, we considered this as a STLS case.
Acute TLS is usually observed after the initiation of cytotoxic chemotherapy of malignancies, especially hematological malignancies with a high turnover rate. The severity of TLS depends on tumor burden, tumor type, proliferation rate, baseline uric acid level and the sensitivity of the tumor to chemotherapeutic agents . STLS prior to the initiation of chemotherapy is rare, especially in the absence of evidence of a tumor, including hematological malignancies and solid tumor. According to previous studies, STLS most commonly occurrs in Burkitt lymphoma and non T-cell acute lymphoblastic leukemia , but it has also been reported in acute lymphoblastic leukemia (ALL) , acute myeloid leukemia(AML) , myelofibrosis , metastatic germ cell tumor  and solid tumors .
To the best of our knowledge, our case is the first STLS reported in association with MDS. The initial presentations of significant hyperuricemia, hyperphosphatemia, metabolic acidosis, AKI and relative hypocalcemia were all consistent with STLS. In 2003, Yang et al.  reported a 32-year-old man who had been diagnosed as MDS with refractory anemia and excess blasts in transformation subtype developed TLS after a single 1.0 g dose of methylprednisolone. However, in our case, the patient did not fulfill the diagnostic criteria for MDS at the onset of STLS. Instead, he was diagnosed as MDS almost one year after the episode of STLS. When the STLS occurred, repeated bone marrow cytology and biopsy did not show evidence of a large tumor burden or of tumor types which had been reported in association with STLS. The etiology in our case is inconclusive. Potential causes for STLS include endogenous secretion of glucocorticoid with infection  and fever . In Daisuke et al.’s case of STLS in ALL , it was believed the STLS might have been triggered by a febrile gastroenteritis-like illness one month prior to the first admission and accelerated by the concomitant urinary tract infection. In our case, the patient had experienced abdominal pain consistent with cholecystitis before the admission and it had been only one weeks after a surgery when the AKI developed. The endogenous secretion of glucocorticoid triggered by the prior infection and the stress of the operation could be considered to be causes of the STLS.
We report an adult presenting with AKI and laboratory features of acute TLS months before his diagnosis of MDS, in the absence of precipitating chemotherapy and radiotherapy. It has been suggested occult malignancy should be considered in the case of unexplainable AKI with hyperuricemia . Aggressive examination for malignancies, including solid tumors and hematological malignancies should be thoroughly performed and regularly repeated in this population, and patients without a definite diagnosis should be closely followed-up in the clinic.
Written informed consent was obtained from the patient for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
This work was supported by grant from the Program of Sichuan Provincial Department of Health (13130153), China. The funder had no role in study design, data collection and analysis, decision to publish, or manuscript preparation. We thank Dr. Nathan W. Levin for correcting the English writing. We also thank Dr. Hanlu Ding for help in preparing the manuscript.
- Jasek AM, Day HJ: Acute spontaneous tumor lysis syndrome. Am J Hematol. 1994, 47: 129-131. 10.1002/ajh.2830470212.View ArticlePubMedGoogle Scholar
- Hsu HH, Chen YC, Tian YC, Chan YL, Kuo MC, Tang CC, Fang JT, Lee SY, Yang CW: Role of serum sodium in assessing hospital mortality in cancer patients with spontaneous tumor lysis syndrome inducing acute uric acid nephropathy. Int J Clin Pract. 2009, 63: 751-756. 10.1111/j.1742-1241.2007.01264.x.View ArticlePubMedGoogle Scholar
- Cairo MS, Bishop M: Tumour lysis syndrome: new therapeutic strategies and classification. Br J Haematol. 2004, 127: 3-11. 10.1111/j.1365-2141.2004.05094.x.View ArticlePubMedGoogle Scholar
- Kobayashi D, Wofford M, McLean TW, Lin JJ: Spontaneous tumor lysis syndromes in a child with T-cell acute lymphoblastic leukemia. Pediatr Blood Cancer. 2010, 54: 773-775.PubMedGoogle Scholar
- Riccio B, Mato A, Olson EM, Berns JS, Luger S: Spontaneous tumor lysis syndrome in acute myeloid leukemia: two cases and a review of the literature. Cancer Biol Ther. 2006, 5: 1614-1617. 10.4161/cbt.5.12.3610.View ArticlePubMedGoogle Scholar
- Sile S, Wall BM: Acute renal failure secondary to spontaneous acute tumor lysis syndrome in myelofibrosis. Am J Kidney Dis. 2001, 38: E21-View ArticlePubMedGoogle Scholar
- Pentheroudakis G, O'Neill VJ, Vasey P, Kaye SB: Spontaneous acute tumor lysis syndrome in patients with metasitatic germ cell tumors. Report of two cases. Support Care Cancer. 2001, 9: 554-557. 10.1007/s005200100276.View ArticlePubMedGoogle Scholar
- Levin M, Cho S: Acute tumor lysis syndrome in high grade lymphoblastic lymphoma after a prolonged episode of fever. Med Pediatr Oncol. 1996, 216: 417-418.View ArticleGoogle Scholar
- Yang SS, Chau T, Dai MS, Lin SH: Steroid-induced tumor lysis syndrome in a patient with preleukemia. Clin Nephropathy. 2003, 59: 201-205. 10.5414/CNP59201.View ArticleGoogle Scholar
- Chen RL, Chuang SS: Transient spontaneous remission after tumor lysis syndrome trigged by a severe pulmonary infection in an adolescent boy with acute lymphoblastic leukemia. J Pediatr Hemotol Oncol. 2009, 31: 76-79. 10.1097/MPH.0b013e31818ab30c.View ArticleGoogle Scholar
- Sharma SK, Malhotra P, Kumar M, Sharma A, Varma N, Singh S: Spontaneous tumor lsis syndrome in acute lymphoblastic leukemia. J Assoc Physicians India. 2005, 53: 828-830.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2369/15/164/prepub
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