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Postgraduate Courses and Training in Paediatrics in Bangladesh Shishu Hospital & Institute Vol. 37(2) 孟加拉国Shishu医院和研究所的儿科研究生课程和培训第37卷(2)
Pub Date : 2022-12-11 DOI: 10.3329/dshj.v37i2.63226
The Editor
Abstract not available DS (Child) H J 2021; 37(2): 146
摘要不可用DS (Child) [J] 2021;37 (2): 146
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引用次数: 0
Complications of Paediatric Ventriculoperitoneal (VP) Shunt: Experience in A Tertiary Care Hospital 小儿脑室-腹膜(VP)分流术的并发症:一家三级医院的经验
Pub Date : 2022-12-11 DOI: 10.3329/dshj.v37i2.63221
Swapan Paul, R. Islam, P. K. Ghosh, P. K. Biswas, D. Hossain, Md. Aminur Rashid
Background: Ventricloperitoneal (VP) shunt is the most commonly used shunt procedure in children because of the capacity of the peritoneum to resorb fluid like Cerebrospinal fluid (CSF). Primary and subsequent peritoneal catheter placement is relatively easy procedure to be done. VP shunt procedures are associated with varieties of complications. Methods: A prospective study was done from July 2017 to June 2021 in Faculty of Paediatric Surgery, Bangladesh Shishu Hospital & Institute. A total number of cases underwent VP shunt surgery were 192. We had analyzed 82(42.71%) patients of VP shunt surgery who had various shunt related complications and analyzed the predisposing risk factors and spectrum of complications. Results: The mean age was 16±14 months and median age was11.75 months. Out of 82 patients 56 (68.29%) were male and 26(31.71%) were female. Seventy (85.37%) patients had single complication and 12(14.63%) had more than 1 complications. Twenty four (29.27%) patients had infective complication and 58(70.73%) had mechanical complication. Infective complications (24, 29.27%) include shunt tract abscess (41.66%), CSF leak (16.67%) exposure of shunt tube through anus (16.67%), wound infection (16.67%). Mechanical complications were present in 58(70.73%) cases and 40(48.78%) had ventricular end malformation, 24(29.27%) peritoneal end and 18(21.95%) had both end malformation. Conclusion: With this prospective study of complications of VP shunt, age at initial shunt surgery, insertion and important patient-related predictors of shunt failure. The different predominant etiological factors the interval between the age of initial shunt placement and onset of complications were the most responsible for early and late shunt failure were infective and mechanical complications respectively. DS (Child) H J 2021; 37(2): 129-134
背景:脑室-腹膜(VP)分流术是儿童最常用的分流术,因为腹膜具有吸收脑脊液(CSF)等液体的能力。最初和随后的腹膜导管放置相对容易完成。副静脉分流术与各种并发症有关。方法:一项前瞻性研究于2017年7月至2021年6月在孟加拉国Shishu医院和研究所儿科外科学院进行。接受VP分流术的病例共192例。我们分析了82例(42.71%)有各种分流相关并发症的VP分流手术患者,分析了并发症的易感危险因素和谱。结果:患者平均年龄16±14个月,中位年龄11.75个月。其中男性56例(68.29%),女性26例(31.71%)。单一并发症70例(85.37%),1种以上并发症12例(14.63%)。感染性并发症24例(29.27%),机械性并发症58例(70.73%)。感染并发症包括分流道脓肿(41.66%)、脑脊液漏(16.67%)、分流管经肛门暴露(16.67%)、伤口感染(16.67%)。机械并发症58例(70.73%),脑室端畸形40例(48.78%),腹膜端畸形24例(29.27%),双端畸形18例(21.95%)。结论:本前瞻性研究对VP分流术的并发症、初次分流术的年龄、插入年龄以及分流术失败的重要患者相关预测因素进行了研究。不同的主要病因(分流器初始放置年龄与并发症发生的时间间隔)对早期和晚期分流器失效的影响最大,分别为感染性和机械性并发症。DS(儿童)H J 2021;37 (2): 129 - 134
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引用次数: 0
Abstracts From Current Literature Vol. 37(2) 《当代文献》第37卷第2期摘要
Pub Date : 2022-12-11 DOI: 10.3329/dshj.v37i2.63224
The Editor
Abstract not available DS (Child) H J 2021; 37(2): 143-144
摘要不可用DS (Child) [J] 2021;37 (2): 143 - 144
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引用次数: 0
Experience of Paediatric Acute Lymphoblastic Leukemia Service in A Newly Established Haemato-Oncology Center in Bangladesh: Opportunities and Challenges 孟加拉国新成立的血液肿瘤中心儿科急性淋巴细胞白血病服务的经验:机遇与挑战
Pub Date : 2022-12-11 DOI: 10.3329/dshj.v37i2.63219
S. F. Sonia, A. Mishra, M. Gogoi, Azmeri Sultana, S. Afroze
Background: Acute lymphoblastic leukemia (ALL) is the most common childhood malignancy and its modern management is complex. We are reporting early experience of establishing a paediatric ALL service in a multidisciplinary paediatric hospital in Bangladesh. Methods: This is a retrospective review of children below 18 years of age with confirmed diagnosis of ALL from July 2020 to June 2021 in Dr. M R Khan Shishu Hospital and ICH, Dhaka, Bangladesh, who received treatment adapted from the standard arm of ICICLE (Indian Childhood Collaborative Leukemia Group) protocol. Data were collected which included demographic, clinical, laboratory features of all patients at the time of presentation and also morbidities and outcome during all phases of chemotherapy. Analysis was done using descriptive statistics. Results: Of 51 patients, 16 were newly diagnosed patients, 32 received continuation care and 3 had relapsed disease. Treatment was initiated in 12 (75%) of 16 patients with newly-diagnosed ALL. Median age was three years, 50% were girls, one had TALL and 5 (42%) had high presentation leucocyte count (³50,000/mm3). Complete cytogenetic testing was available for one patient alone, no patient had Ph+ ALL. Eleven (92%) showed good prednisolone response. All nine patients who completed the induction phase achieved morphological remission, with high minimal residual disease (³0·01%) in two (22%). At last follow-up (30-06-2021), two patients were midway through induction, two died from sepsis (one each in Induction and Consolidation, both high risk ALL) and eight (67%) are alive in remission, on treatment 2-12 months from diagnosis. Continuation care included intrathecal treatments (n=119) and vincristine-corticosteroid pulses (n=53); 94% patient remained in complete remission, while two (6%) relapsed during the course of treatment. Conclusion: Risk-stratified ALL treatment is feasible in a newly established resource limited setting but limited by availability of high-quality diagnostics, specifically cytogenetics. Our study revealed that, during intensive phase approximately two-third children and during maintenance phase majority of children remained in complete remission. DS (Child) H J 2021; 37(2): 116-122
背景:急性淋巴细胞白血病(ALL)是最常见的儿童恶性肿瘤,其现代治疗是复杂的。我们报告在孟加拉国一家多学科儿科医院建立儿科ALL服务的早期经验。方法:回顾性研究了2020年7月至2021年6月在孟加拉国达卡Khan Shishu医院和ICH接受ICICLE(印度儿童白血病合作组)标准组治疗的18岁以下确诊为ALL的儿童。收集的数据包括所有患者在出现时的人口学、临床、实验室特征以及化疗所有阶段的发病率和结果。采用描述性统计进行分析。结果:51例患者中,新诊断16例,继续治疗32例,复发3例。16例新诊断的ALL患者中有12例(75%)开始治疗。中位年龄为3岁,50%为女孩,1例为TALL, 5例(42%)表现为白细胞计数高(³50,000/mm3)。1例患者单独进行了完整的细胞遗传学检测,没有患者出现Ph+ ALL。11例(92%)强的松龙反应良好。所有完成诱导期的9例患者均实现了形态学缓解,2例(22%)的最小残留疾病(³·01%)较高。在最后一次随访中(2021年6月30日),2例患者在诱导过程中中途死亡,2例死于败血症(诱导和巩固各1例,均为高风险ALL), 8例(67%)在诊断后2-12个月治疗后缓解期存活。继续治疗包括鞘内治疗(n=119)和长春新碱-皮质类固醇脉冲治疗(n=53);94%的患者保持完全缓解,而2例(6%)在治疗过程中复发。结论:在新建立的资源有限的环境中,风险分层治疗ALL是可行的,但受高质量诊断的可用性,特别是细胞遗传学的限制。我们的研究显示,在强化阶段,大约三分之二的儿童和在维持阶段,大多数儿童仍然完全缓解。DS(儿童)H J 2021;37 (2): 116 - 122
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引用次数: 0
Students Qualified from Bangladesh Shishu Hospital & Institute (Former BICH) Vol. 37(1) 孟加拉国石树医院和研究所(原BICH)合格学生第37卷(1)
Pub Date : 2022-04-12 DOI: 10.3329/dshj.v37i1.59125
The Editor
Abstract not available DS (Child) H J 2021; 37(1): 82
摘要不可用DS (Child) [J] 2021;37 (1): 82
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引用次数: 0
Institute News Vol. 37(1) 研究所新闻第37卷(1)
Pub Date : 2022-04-12 DOI: 10.3329/dshj.v37i1.59123
The Editor
Abstract not available DS (Child) H J 2021; 37(1): 80
摘要不可用DS (Child) [J] 2021;37 (1): 80
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引用次数: 0
Clinico-pathological Profile of Childhood Nonhodgkin Lymphoma (NHL) in A Tertiary Care Hospital in Bangladesh 孟加拉国一家三级医院儿童非霍奇金淋巴瘤(NHL)的临床病理分析
Pub Date : 2022-04-12 DOI: 10.3329/dshj.v37i1.59089
K. Nahar, A. Hasan, A. Islam, C. Jamal
Background: Non-Hodgkin Lymphoma (NHL) is the third most common childhood malignancy. With histopathology based intensive chemotherapy and CNS-directed therapy, survival can reach more than 80%. Objective: The study was conducted to observe the clinico-pathological findings of NHL in Bangladeshi children. Methods: A prospective observational study was conducted in the Paediatric Haematology and Oncology Department of BSMMU from June 2012 to December 2012. Newly diagnosed NHL patients were included in the study. Patient’s initial clinical presentations, time interval from onset of symptoms to diagnosis were recorded. Diagnostic and staging workups were done by CBC, biochemistry, radio-imaging, histopathology (FNAC/excision biopsy), serous fluids/CSF cytology (cytospin), and bone marrow aspiration. Result: Among the 34 patients, BL had preponderance (n=23, 68%) then LL. Median age was 7.6 years. Male: female ratio was 2.1:1. Delayed diagnosis was found in 59% patient. Primary sites were abdomen (65%), thorax (32%), and head-neck (3%). At initial presentation, 83% patients of Burkitt NHL and 100% Lymphoblastic NHL patients came with advanced disease. Bone marrow involvement was found in 23.6% patients and 12% had CNS involvement at their presentation. Irrespective to histology, most common stage was stage-III, which was 53% and then stage-IV was 35%. Median LDH was 1719 U/L. Patient with abdominal variety of NHL came with abdominal complaint like pain (66%), distension (65%), ascites (48%), mass like hepatomegaly (39%), splenomegaly (26%), intussusceptions (8%), testicular involvement (4%). B symptoms were commonly found in 74% patient. Pallor (82%), anorexia, nausea & vomiting (48%), oedema (25%), peripheral lymphadenopathy (49%) were also noticed. In case of thoracic variety of NHL, most common presentation was respiratory distress (90%), superior mediastinal syndrome (SMS) (45%), with high incidence of B symptoms (90%), peripheral lymphadenopathy (72%) with other respiratory finding like chest bulging, mediastinal mass, pleural effusion was also found. Conclusions: About 59% childhood NHL patients tend to present with delayed diagnosis and 88% with advanced disease. Burkitt NHL is the commonest childhood lymphoma, mostly presented with abdominal complaint. Thoracic variety is mostly Lymphoblastic lymphoma. Histopathological findings following excisional biopsy is the most significant and confirmatory for diagnosis. Serum LDH were found significantly high level in both varieties. DS (Child) H J 2021; 37(1): 21-27
背景:非霍奇金淋巴瘤(NHL)是第三大最常见的儿童恶性肿瘤。通过组织病理学强化化疗和中枢神经系统指导治疗,生存率可达80%以上。目的:观察孟加拉儿童非霍奇金淋巴瘤的临床病理表现。方法:2012年6月至2012年12月在北京医科大学儿科血液科和肿瘤科进行前瞻性观察研究。新诊断的NHL患者被纳入研究。记录患者的初始临床表现,从症状出现到诊断的时间间隔。诊断和分期工作通过CBC、生化、放射成像、组织病理学(FNAC/切除活检)、浆液/CSF细胞学(细胞自旋)和骨髓穿刺完成。结果:34例患者中,BL(23例,68%)高于LL。中位年龄为7.6岁。男女比例为2.1:1。59%的患者发现延迟诊断。原发部位为腹部(65%)、胸部(32%)和头颈部(3%)。在初次就诊时,83%的伯基特型非霍奇金淋巴瘤患者和100%的淋巴母细胞型非霍奇金淋巴瘤患者病情进展。23.6%的患者骨髓受累,12%的患者出现中枢神经系统受累。与组织学无关,最常见的分期为iii期,占53%,其次是iv期,占35%。中位LDH为1719 U/L。腹部各种类型的NHL患者有腹部症状,如疼痛(66%)、腹胀(65%)、腹水(48%)、肿块样肝肿大(39%)、脾肿大(26%)、肠套迭(8%)、睾丸受累(4%)。B型症状常见于74%的患者。面色苍白(82%),厌食,恶心和呕吐(48%),水肿(25%),周围淋巴结病变(49%)也被注意到。对于胸椎型NHL,最常见的表现为呼吸窘迫(90%),上纵隔综合征(SMS) (45%), B型症状高发(90%),周围淋巴结病变(72%)伴有其他呼吸表现,如胸鼓、纵隔肿块、胸腔积液。结论:约59%的儿童NHL患者倾向于延迟诊断,88%的患者倾向于疾病晚期。伯基特NHL是最常见的儿童淋巴瘤,主要表现为腹部症状。胸型多为淋巴母细胞淋巴瘤。切除活检后的组织病理学结果是诊断最重要和最具确证性的。两品种血清乳酸脱氢酶水平均显著升高。DS(儿童)H J 2021;(1): 37 -
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引用次数: 0
Abstracts From Current Literature Vol. 37(1) 《当代文献》第37卷第1期摘要
Pub Date : 2022-04-12 DOI: 10.3329/dshj.v37i1.59122
The Editor
Abstract not available DS (Child) H J 2021; 37(1): 78-79
摘要不可用DS (Child) [J] 2021;37 (1): 78 - 79
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引用次数: 0
Postgraduate Courses and Training in Paediatrics in BSH&I Vol. 37(1) 儿科研究生课程及训练(BSH&I)第37卷(1)
Pub Date : 2022-04-12 DOI: 10.3329/dshj.v37i1.59124
The Editor
Abstract not available DS (Child) H J 2021; 37(1): 81
摘要不可用DS (Child) [J] 2021;37 (1): 81
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引用次数: 0
Alagille Syndrome: A Case Report 阿拉吉尔综合征1例报告
Pub Date : 2022-04-12 DOI: 10.3329/dshj.v37i1.59120
Madhabi Baidya, Syed Shafi Ahmed, Salauddin Mahmud
Abstract not available DS (Child) H J 2021; 37(1): 71-73
摘要不可用DS (Child) [J] 2021;37 (1): 71 - 73
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引用次数: 0
期刊
Dhaka Shishu (Children) Hospital Journal
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