 |
| About Bioline | All Journals | Testimonials | Membership | News |
|
||||||
|
||||||
European Journal of General Medicine, Vol. 7, No. 1, January-March, 2010, pp. 114-117 Case Report Massively enlarged kidneys due to leukemic infiltration in a child Murat Doğan1 , Ali Bay2 , Aydın Bora3 , Mehmet Açıkgöz1 , Ahmet F. Öner2 Yuzuncu Yil University, School of Medicine, Departments of Pediatrics1 , Pediatric Hematology2 and Radiology3 , Van, Turkey Code Number: gm10021 Abstract A few cases with bilateral renal enlargement in acute lymphoblastic leukemia were reported in literature. In this article, we reported an unusual case of a child with precursor B-ALL presenting with massively enlarged bilateral unobstructed kidneys and acute renal failure. Renal involvement of ALL should be taken into consideration in case with massively enlarged bilateral kidneys in radiological examination. Based on radiological, clinical and laboratory findings including bone marrow aspirate examination, the patient could be diagnosed as ALL without renal biopsy.Keywords: Acute lymphoblastic leukemia, bilateral kidney enlargement, renal failure, diagnosis Introduction Acute lymphoblastic leukemia (ALL) is the most common malignancy in children, representing nearly one third of all pediatric cancers. Although a small percentage of cases are associated with inherited genetic syndromes, the cause of ALL remains largely unknown [1] . The precursor B-cell form accounted for 80 % of all acute lymphoblastic leukemia [2] . In most of B-ALL patients present with anemia, neutropenia, bone pain, and arthralgia. Acute renal failure (ARF) and nephromegaly, lymphomatous infiltration of the kidneys, are very rare manifestations of ALL in children [3],[4] . In this article, we reported an unusual case of a boy with precursor B-ALL presenting with massively enlarged bilateral unobstructed kidneys and ARF. Case A 14 year-old boy with severe anemia was referred to our hospital. He had been suffered from generalized muscle pain, headache, paleness, and weight loss for the last 30 days. The diagnosis of iron deficiency anemia had established at another hospital and oral iron treatment had been started. Because there was no response to iron supplementation on the 15th day of the treatment, the patient has referred to our hospital. He had a significant pallor, tachycardia (130/min) and a few petechiael eruptions on the lower extremities. His blood pressure was 130/80 mmHg. He had an enlarged liver and spleen both palpable 5 cm below the costal margin at the midclavicular line. The kidneys were bilaterally palpated as two solid tumor masses with smooth surface engaging the whole abdomen. There was no evidence of lymphadenopathy. The results of the complete blood count were as follows: hemoglobin 2.9 g/dl, mean corpuscular volume (MCV): 62 fl, white blood cell count 4,2x 109/1, and platelet count 60 x 109/1. A peripheral blood smear revealed 80% lymphocyte, 2% monocyte and 18% neutrophil with inadequate platelets. Urine microscopy revealed no haematuria and there was no detectable proteinuria. Serum biochemistry, coagulation parameters (prothrombin time, activated partial thromboplastin time and fibrinogen level), vitamin B1 2, and folic acid levels were in the normal range except for elevated serum creatinine (1.4 mg/dl), uric asit (12 mg/dl), LDH (1100 U/L) levels. These elevated values returned to normal ranges after the treatment following anti-cancer chemotherapy (serum creatininine:0.9 mg/ dl, uric acit: 3.3 mg/dl, LDH: 514 U/L). Serological tests including EBV, CMV, HIV, rubella, parvovirus, and hepatitis B virus antibodies were found to be negative. In computed tomography (CT) examination, massively enlarged bilateral unobstructed kidneys with normal shape was revealed which was strongly suggested an infiltrative process [Figure - 1]. There was no other abnormal CT finding in abdomen and thorax except moderate hepatosplenomegaly. Examination of the bone marrow aspiration showed 95% blast cells that were characteristic of ALL, L1 type morphology. Immunophenotypic analysis of the bone marrow aspirate showed that the blast population consisted of predominately of CD1 0 and CD1 9, consistent with PreB cell acute lymphoblastic leukemia. Based on these findings, acute lymphoblastic leukemia (ALL) concomitant with acute renal failure was diagnosed. After red blood cell transfusion, chemotherapy against ALL was started. He received chemotherapy according to the previously described ALL BFM 2000 protocol. In general, compliance with chemotherapy was good, with no major delays or reductions in dosage. Renal failure resolved within 3 days after the start of chemotherapy. Abdominal ultrasonography (US) was repeated at 3 weeks after the initial diagnosis and a progressive reduction on the kidney dimensions was observed [Figure - 2]. During the follow up period of 2 months, he had been in remission and continued to receive chemotherapy for ALL. Discussion Precursor B-cell acute lymphoblastic leukemia is defined as a neoplasm of lymphoblasts committed to the B-cell lineage, typically composed of small-to medium sized blast cells with scant cytoplasm, moderately condensed to dispersed chromatin and inconspicuous nucleoli [5] . The disease involves bone marrow and blood. In our case, we suspected the leukemia because of the common clinical feature of ALL such as anemia, thrombocytopenia and fatigue. Therefore, peripheral blood smear and bone marrow aspiration were performed in the patient. Although no blast was seen in peripheral blood smear, in bone marrow examination 95% lymphoblast had characteristic features of ALL, L1 type morphology. Although renal involvement is not uncommon, only a few cases of renal failure secondary to a diffuse bilateral parenchyma[ infiltration have been reported in the literature. Tumor infiltration into the kidneys can occur via by hematogen route. This infiltration of tumor cells into the kidneys is usually associated with evidence of malignancy elsewhere as identified by physical examanition, imaging studies, and examination of the peripheral smear or bone marrow [4],[6],[7],[8],[9] . The development of acute renal failure in patients with hematological malignancies can present a major clinical problem, and generally develops as a direct invasion of the hematological malignant cells, e.g. obstruction of the ureters, or renal artery or vein thrombosis. Other more indirect causes of renal failure include hyperuricemia, sepsis, hemolysis, and paraproteinemia with deposits of paraprotein. Cryoglobulinemia, amyloid formation, nephrosis or nephritis may also be encountered [10] . Our patient had nephromegaly and hematologic abnormalities on admission. So he was examined about the cause of nephromegaly. Peripheral blood smear examination was normal but 95% blast cells that were characteristic of ALL, L1 type morphology were found on the bone marrow examination. In addition of this, abdominal CT showed the tumoral infiltration of the kidneys. Bilateral cellular infiltration of the renal interstitium may be seen in hematological malignancies. Ultrasound and CT are the main imaging modalitites suggesting the search for any cellular infiltration within the renal parenchyma. In most cases, the US findings in leukemia or lymphoma include renal enlargement and diffuse or focal areas of homogenous hypoechogenicity [11],[12],[13] . In our patient, the US and CT image of both kidneys impressed by their dimensions and by the thickness of parenchyma, which significantly exceeded the age reference values. Renal failure resolved within 3 days after the start of chemotherapy. Abdominal US was repeated at 3 weeks after the initial diagnosis and a progressive reduction on the kidney dimensions was observed. Renal biopsy is not indicated in cases which are suspected the hematopoietic malignancy presenting with renal insufficiency. Standard procedures (physical exam, radiographic studies, and examination of the peripheral smear or bone marrow.) firstly should be performed to explain the etiology. When these procedures do not show the cause of ARF and nephromegaly, a renal biopsy is mandatory for rapid diagnosis and therapy [14] . In our case we followed these suggestions. As a conclusion, a few cases with bilateral renal enlargement in ALL were reported in literature. Renal involvement of ALL should be taken into consideration in case massively enlarged bilateral kidneys in radiologic examination. Based on radiological, clinical and laboratory data including bone aspirate examination, the patient can be diagnosed without renal biopsy. References
Copyright 2010 - European Journal of General Medicine The following images related to this document are available:Photo images[gm10021f2.jpg] [gm10021f1.jpg] |
| |||||||||
![[Figure - 1]](/showimage?gm/photo/gm10021f1.jpg){kind=link}
![[Figure - 2]](/showimage?gm/photo/gm10021f2.jpg){kind=link}