• Advances in pediatric surgery
• /
• 제20권2호
• /
• pp.53-57
• /
• 2014

Purpose: Neonatal neuroblastoma (NBL) is the most common malignant tumor in neonates, but there have been few studies about it. The purpose of this study was to investigate the clinical features of NBL and to compare prenatal and postnatal diagnosed groups. Methods: Nineteen patients who were diagnosed with NBL prenatally or within 28 days after birth from February 1986 to February 2013 in Seoul National University Hospital were enrolled in the study. The patients were categorized according to the International Neuroblastoma Staging System (INSS) and Children's Oncology Group (COG). Retrospective medical-record reviews were performed on these patients. The operative date, complication, pathological stage, and overall survival of the prenatally diagnosed group and the postpartum diagnosed group were compared. Results: Tumor was detected via prenatal ultrasonography in 8 patients (42.1%), and 11 patients (57.9%) were diagnosed within 28 days after birth. Based on INSS, the patients were divided into the stage I (n=8), stage II (n=1), stage III (n=3), stage IV (n=4), and stage IVs (n=3) groups, respectively. Based on COG, on the other hand, the patients were divided into the low-risk (n=8), intermediate-risk (n=8), and high-risk (n=3) groups. The postoperative complication rate was 29%. One patient died from complications from chemotherapy. The other 18 patients' mean follow-up period was 77.7 months. The differences between the postoperative complication rate, proportion of early-stage tumor, and overall survival of the prenatal and postnatal groups were not statistically significant (p=0.446, p=0.607, p=0.414). Conclusion: NBL showed favorable outcomes but relatively higher postoperative complications. There seem to be no significant statistical differences in the postoperative complications, proportion of early-stage tumor, and overall survival between the prenatally diagnosed group and the postpartum diagnosed group.

• Asian Pacific Journal of Cancer Prevention
• /
• 제13권5호
• /
• pp.2285-2289
• /
• 2012

Multidrug resistance (MDR) is a main cause of failure in the chemotherapeutic treatment of malignant disorders. One of the well-known genes responsible for drug resistance encodes the multidrug resistance-associated protein (MRP1). The association of MRP1 with clinical drug resistance has not systematically been investigated in Iranian pediatric leukemia patients. We therefore applied real-time RT-PCR technology to study the association between the MRP1 gene and MDR phenotype in Iranian pediatric leukemia patients. We found that overexpression of MRP1 occurred in most Iranian pediatric leukemia patients at relapse. However, no relation between MRP1 mRNA levels and other clinical characteristics, including cytogenetic subgroups and FAB subtypes, was found.

• Asian Pacific Journal of Cancer Prevention
• /
• 제16권8호
• /
• pp.3351-3354
• /
• 2015

Background: Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in the pediatric age group. All patients with RMS regardless of their initial stage or group receive combination chemotherapy as 'standard therapy' consisting of vincristine, actinomycin-D and cyclophosphamide. Actinomycin-D was not readily available in Turkey at one time. Carboplatin was used instead in order to prevent delays in treatment. The aim of this report is to present the results of patients with rhabdomyosarcoma receiving carboplatin or actinomycin-D therapy. Materials and Methods: Twenty four patients with rhabdomyosarcoma treated between December 2000 and June 2011 were included in this retrospective study. The patients were treated according to International Rhabdomyosarcoma Study Group guidelines. Eleven patients were treated with actinomycin-D and 13 with carboplatin ($250mg/m^2/dose$ for 2 days). The two groups were then compared in terms of 2- and 5-year overall survival (OS) and hematological and non-hematological toxicities. Results: Age, sex, stage and the mean duration of follow-up were similar in both groups (p>0.05). Two- and five-year OS levels were 68.2% in the carboplatin group and 78.0% and 40.0%, respectively, in the actinomycin-D group. There was no statistical difference in the number of febrile episodes (p=0.86) and no other hematological and non-hematological adverse effects were recorded in both groups. Conclusions: The findings show that carboplatin can be used as an alternative drug in the primary treatment of rhabdomyosarcoma in the event that actinomycin-D is unavailable or not tolerated.

• 인간행동과 음악연구
• /
• 제5권2호
• /
• pp.67-92
• /
• 2008

이 연구는 노래 만들기가 소아암을 치료받고 있는 과정중의 어린 환자들에게 어떻게 음악치료적인 목적으로 적용되어왔는지를 보여주는 연구이다. 본 연구자는 소아혈액종양학과에서 음악치료 인턴을 하면서 노래 만들기를 통하여 쉽게 표현하지 못했던 자신들의 생각과 느낌을 표현하는 것을 볼 수 있었다. 또한 노래 만들기를 통해 환자들과 음악치료사가 깊은 믿음을 바탕으로 건강한 치료적 관계가 형성되었으며, 그 관계는 환자가 병원환경에 좀 더 효과적으로 적응할 수 있도록 도와주었다. 본 연구의 사례연구에서는 환자 N이 소아 뇌종양을 치료를 받고 있는 자신의 삶에 대한 감정과 생각들을 노래 만들기를 통해 표현하였으며, 더 나아가 환자 N은 자신의 창조성과 내면의 힘(inner strength)을 자신이 만들어낸 음악을 통해 의식함으로써 자존감을 증진시키게 되었다.

• Child Health Nursing Research
• /
• 제12권2호
• /
• pp.268-276
• /
• 2006

Purpose: this study is attempted to provide basic data on development of systematic discharge educational programs for discharging cancer patients. Method: The subjects of this study were 132 mothers whose children were diagnosed with cancer and being treated at 3 university hospitals in Busan. The data were collected from December 1 to February 28, 2005, and were analyzed Using SPSS WIN 10.0. Result: The degree of education at the time of discharge from hospital was statistically significantly lower than that of educational demand after the discharge. Such demand significantly varied in accordance with the length of period passed after the discharge. Mother’s educational demand was significantly different in accordance with generation characteristics of her child with cancer, especially the first period of hospitalization and change in weight Conclusions: mothers of children with cancer were higher in educational demand after the child’s discharge from hospital than in education provided at the time of the discharge. Such demand was different in accordance with the length of period passed after the child's discharge from hospital.

• Asian Pacific Journal of Cancer Prevention
• /
• 제15권8호
• /
• pp.3541-3546
• /
• 2014

TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL). This translocation is associated with a good prognosis and rarely shows chemotherapeutic resistance to 3-drug based remission induction phase of treatment as well as overall treatment. Thus, the higher the frequency of this fusion oncogene, the easier to manage childhood ALL in a given region with less intensive chemotherapy. Although global frequency of TEL-AML1 has been reported to be 20-30%, a very low frequency has been found in some geographical regions, including one study from Lahore, Punjab, Pakistan and others from India. The objective of present study was to investigate if this low frequency of TEL-AML1 in pediatric ALL is only in Lahore region or similar situation exists at other representative oncology centers of Pakistan. A total of 167 pediatric ALL patients were recruited from major pediatric oncology centers situated in Lahore, Faisalabad, Peshawar and Islamabad. Patients were tested for TEL-AML1 using nested reverse transcription polymerase chain reaction (RT-PCR). Only 17 out of 167 (10.2%) patients were found to be TEL-AML1 positive. TEL-AML1+ALL patients had favorable prognosis, most of them (82.4%, 14/17) showing early remission and good overall survival. Thus, our findings indicate an overall low frequency of TEL-AML1 in Pakistan pediatric ALL patients, in accordance with lower representation of this prognostically important genetic abnormality in other less developed countries, specifically in south Asia, thus associating it with poor living standards in these ethnic groups. It also indicates ethnic and geographical differences in the distribution of this prognostically important genetic abnormality among childhood ALL patients, which may have a significant bearing on ALL management strategies in different parts of the world.

• Asian Pacific Journal of Cancer Prevention
• /
• 제17권4호
• /
• pp.1717-1723
• /
• 2016

Background: This study assessed parental experiences with chemotherapy-induced alopecia among children with cancer treated at an Indonesian academic hospital. Materials and Methods: Fifty parents of childhood cancer patients were interviewed using semi-structured questionnaires. Results: The moment that hair fell out was the moment that parents (84%) had to admit their child had cancer. Alopecia was a traumatizing painful experience (46%). Active strategies to hide alopecia, mainly hats, were used by 66% of children, while 34% never covered their bald head. If money had not been an issue, 40% would use another strategy. Alopecia made children limit outdoor daily activities (78%) and engagement with others (60%). Significantly more children from high-educated (95%) than low-educated (60%) parents received sympathy from other people (P=0.012). Significantly more Christian (29%) than Muslim (0%) families confirmed that alopecia lowered the quality of life (P=0.046). Most parents (82%) had no prior plans about alopecia management, yet for significantly more girls (26%) than boys (0%) such plans existed (P=0.044). Parents received most information about alopecia from other parents (66%). Parents (92%) needed more alopecia education from doctors. Of all school-attending children, 53% were bullied and 47% did not want to attend school due to alopecia. Significantly more high-educated than low-educated families received pity from teachers and pupils (94% vs. 0%, P=0.004), and acceptance by pupils (81% vs. 0%, P=0.021). Conclusions: Alopecia is a severe, far-stretching side-effect of chemotherapy with physical, psychological and social consequences for children and parents. Parents should be better informed about occurrence and impact of alopecia. Extra attention is required to facilitate children's return to school. Healthcare providers should facilitate optimal supportive care through open dialogue and provision of educational m aterials for parents, children and their community.

• Clinical and Experimental Pediatrics
• /
• 제48권6호
• /
• pp.619-623
• /
• 2005

목 적 : 면역 저하된 소아 암 환자에서 균혈증은 조기에 적절한 치료를 하지 못하면 이환율과 사망률이 높아 질 수 있는 질환으로서 호발 원인균의 발생 빈도 및 항생제에 대한 감수성은 지역적 시기적으로 변화하는 경향이 있으므로 이를 조사하여 경험적 항생제 선택에 도움을 주고자 하였다. 방 법 : 1995년 9월부터 2003년 8월까지 영남대학교 의과대학부속병원 소아과에 입원한 소아 암 환자를 대상으로 병력지와 혈액배양검사 결과를 조사하여 균혈증이 확진된 39명, 58례를 대상으로 원인 균의 종류 및 항생제 감수성을 조사 분석하였다. 결 과 : 소아 암 환자에서 균혈증의 발생빈도는 균혈증이 의심되어 혈액배양을 시행한 1,022례 중 58례로 5.7%였다. 균혈증을 일으킨 가장 흔한 원인 균은 그람양성균으로 총 37례(63.8%) 였고 그람음성균은 총 21례(36.2%)였다. 그람양성균의 경우 Staphylococcus epidermidis (22례, 37.9%), Staphylococcus aureus (10례, 17.3%), Streptococcus (5례, 8.6%) 순이었고, 그람음성균의 경우 Escherichia coli (7례, 12%), Enterobacter (4례, 6.9%), Klebsiella (4례, 6.9%), Serratia (2례, 3.5%), Acinetobacter (2례, 3.5%), Proteus (1례, 1.7%), Morganella morganii (1례, 1.7%) 순으로 나타났다. 항생제 감수성 검사에서는 그람양성균 37례 중 6례(16%)에서만 penicillin 감수성을 나타내었고, 15례(40%)에서 oxacillin 감수성을 나타내었다. Staphylococcus aureus는 1례를 제외한 모든 예에서 vancomycin에, Staphylococcus epidermidis는 1례를 제외한 모든 예에서 teicoplanin에 감수성을 나타내었다. 그람음성균의 경우, 21례 중 2례(10%)만이 cefotaxime에, 4례(19%)에서만 ceftazidime에 감수성을 나타내었다. Aminoglycoside에는 21례 중 6례(29%) 에서만 감수성을 나타내었으며, 21례 모두에서 imipenem에 감수성을, 2000년 이후부터 감수성 검사를 시행한 meropenem에도 모든 예에서 감수성을 나타내었다. 결 론: 균혈증이 의심되는 소아 암 환자에서 그람양성균에 의한 균혈증이 증가하는 점과 그람양성균과 그람음성균 모두 항생제 다제내성 빈도가 증가하고 있음을 유념하여 적절한 항생제를 선택해야 할 것이다.

• Clinical and Experimental Pediatrics
• /
• 제53권4호
• /
• pp.465-470
• /
• 2010

The number of long-term survivors is increasing in the western countries due to remarkable improvements in the treatment of childhood cancer. The long-term complications of childhood cancer survivors in these countries were brought to light by the childhood cancer survivor studies. In Korea, the 5-year survival rate of childhood cancer patients is approaching 70%; therefore, it is extremely important to undertake similar long-term follow-up studies and comprehensive long-term care for our population. On the basis of the experiences of childhood cancer survivorship care of the western countries and the current Korean status of childhood cancer survivors, long-term follow-up study and long-term care systems need to be established in Korea in the near future. This system might contribute to the improvement of the quality of life of childhood cancer survivors through effective intervention strategies.

• Asian Pacific Journal of Cancer Prevention
• /
• 제16권3호
• /
• pp.1029-1031
• /
• 2015

Objective: Glypican-3 (GPC3) is reported to be an oncofetal protein that is a useful diagnostic immunomarker for hepatoblastoma. However, the results are not inclusive. This study systemically investigated the association between expression of GPC3 and pediatric hepatoblastoma. Methods: Clinical studies evaluating the association were identified using a predefined search strategy. GPC3 immunohistochemistry was applied in the pathological diagnosis of hepatoblastoma using the monoclonal antibodies with formalin-fixed and paraffin-embedded specimens. Positive predictive rates for the association between expression of GPC3 and pediatric hepatoblastoma were calculated. Results: Specimens from four clinical studies which including 134 patients with pediatric hepatoblastoma tested by GPC3 immunohistochemistry were considered eligible for inclusion. Systemic analysis showed that, in all patients, pooled positive predictive rate of the association between expression of GPC3 and pediatric hepatoblastoma was 95.5% (128/134). Conclusion: This systemic analysis suggests that the expression of glypican-3 is highly associated with the diagnosis of pediatric hepatoblastoma.