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Disorders Presenting as Anaemia among Paediatric Population at a Tertiary Care Centre, Kerala, India: A Cross-sectional Study 在印度喀拉拉邦三级保健中心的儿科人群中表现为贫血的疾病:一项横断面研究
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/59725.2682
Unnikrishnan Govindakurup, Shiji K. Jacob, Febby K Philip
Introduction: Anaemia is a condition marked by low Haemoglobin (Hb) concentration and is an important risk factor for the poor health and development of children and adolescents. Anaemia is not a diagnosis, but merely an objective sign of disease. The correct treatment requires an understanding of the pathogenesis of the condition. Aim: To identify disorders presenting as anaemia in paediatric population. Also to analyse the data by grading of anaemia and to calculate the proportion of anaemia in various paediatric age groups. Materials and Methods: This cross-sectional study was conducted at Government Medical College, Ernakulum, Kerala, India, from September 2017 to February 2018, on 211 paediatric patients of age groups from newborn upto 18 years. After a detailed clinical history and examination, Complete Blood Count (CBC), peripheral smear preparation, reticulocyte count, renal function tests, liver function tests, and if necessary, radiological and bone marrow examination were done. The mean haemoglobin in the categories were compared with Comprehensive National Nutritional Survey Data. The data obtained were entered in Microsoft excel 365 and further analysed. Categorical variables were analyzed by Fisher’s- exact test and continuous variables by Analysis of Variance (ANOVA) and Kruskal-Wallis test and the significance level was set at p-value ≤ 0.05. Results: Of the 211 patients, 120 (56.87%) were males and 91 (43.13%) were females. The average haemoglobin level varies across age groups and sex. In the case of newborns, average Hb was 9.31 g/dL in males and 10.4 g/dL in females. A total of 211 patients presented with 339 disease conditions, with respiratory disorders in 98, followed by 83 nutritional diseases, 49 infections and 35 systemic diseases. Total of 132 patients in age group of 6 months to 4 years, presented with maximum disorders (206). A total of 186 (54.8%) cases presented with Microcytic Hypochromic Anaemia (MHA), 149 (43.95%) with Normocytic Normochromic Anaemia (NNA) and only 4 (1.18%) with Haemolytic Anaemia (HA). No cases of macrocytic anaemia were noted. Conclusion: Total of 76.8% cases of MHA (42.1% of total anaemia cases) are associated with Nutritional, Respiratory and Infectious conditions which can be managed by public health measures. The haemoglobin levels in neonates and less than 6 months age group were significantly less than population mean which needs to be addressed. In similar manner, girls in school going age group had significantly lower Hb than boys.
简介:贫血是一种以血红蛋白(Hb)浓度低为特征的疾病,是儿童和青少年健康和发育不良的重要危险因素。贫血不是一种诊断,而仅仅是疾病的客观迹象。正确的治疗需要了解病情的发病机制。目的:确定以贫血为表现的儿童疾病。还通过贫血分级分析数据,并计算不同儿科年龄组中贫血的比例。材料和方法:本横断面研究于2017年9月至2018年2月在印度喀拉拉邦埃纳库伦政府医学院进行,研究对象为211名新生儿至18岁年龄段的儿科患者。经过详细的临床病史和检查,全血细胞计数(CBC),外周涂片准备,网织红细胞计数,肾功能检查,肝功能检查,必要时进行放射和骨髓检查。这些类别的平均血红蛋白与全国综合营养调查数据进行比较。将得到的数据输入到Microsoft excel 365中进行进一步分析。分类变量采用Fisher’s- exact检验,连续变量采用方差分析(ANOVA)和Kruskal-Wallis检验,p值≤0.05。结果:211例患者中,男性120例(56.87%),女性91例(43.13%)。平均血红蛋白水平因年龄组和性别而异。在新生儿中,男性平均Hb为9.31 g/dL,女性为10.4 g/dL。共有211名患者出现339种疾病,其中呼吸系统疾病98例,营养疾病83例,感染49例,全身性疾病35例。共132例患者,年龄6个月至4岁,表现出最大障碍(206例)。186例(54.8%)为小细胞性低色贫血(MHA), 149例(43.95%)为正色性贫血(NNA),溶血性贫血(HA)仅4例(1.18%)。未发现大细胞性贫血病例。结论:共有76.8%的MHA病例(占总贫血病例的42.1%)与营养、呼吸和传染病相关,可通过公共卫生措施加以控制。新生儿和6个月以下年龄组的血红蛋白水平明显低于人口平均水平,这需要解决。同样,上学年龄组女孩的Hb明显低于男孩。
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引用次数: 0
Role of Oxidative Stress on Malarial Anaemia: Significance of Oxidative Stress Index in Patients with Malarial Infection 氧化应激在疟疾贫血中的作用:疟疾感染患者氧化应激指数的意义
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/48961.2557
Syed Ghouse Ali Hatim, D. Phaneendra, V. S. Kumar, Sasikala Thallapapaneni, Y. B. Suchetha
Introduction: An alteration of oxidant and antioxidant levels is thought to be involved in the pathogenesis of malaria. Limited data is found on association between oxidant and antioxidant status and significance of oxidative stress index in patients with malarial infection and anaemia in south Indian population. Aim: To measure the levels of oxidants and antioxidants and oxidative stress index in patients with malaria and their association with anaemia. Materials and Methods: The present case-control study was conducted in Department of Biochemistry, Osmania General Hospital, Hyderabad, India. A total of 50 subjects of malaria aged 20-45 years were included as cases based on inclusion criteria and exclusion criteria. Control group comprised of 50 healthy age and gender matched subjects. Haemoglobin (Hb), serum Malondialdehyde (MDA), Superoxide Dismutase (SOD), Total Antioxidant Capacity (TAC) was estimated in both the groups by standard methods using Ultraviolet Spectrophotometer. Independent sample t-test was used to test for the difference in all biochemical parameters among study and control groups. The study of orrelation among the parameters was done by Pearson’s correlation. Results: Both the groups were age and gender matched (p=0.39). MDA was significantly elevated in cases as compared to controls (p<0.0001). SOD, Ferric Reducing Ability of Plasma (FRAP), Hb were significantly lower in cases as compared to controls with p-value <0.0001. In the present study, it was found that there was a significant negative correlation between Hb and oxidative stress index (MDA/FRAP=-0.480) with p-value=0.0001 in patients with malaria. Conclusion: The present study concluded that oxidative stress might be a cause of malarial anaemia. Alterations in oxidant and antioxidant levels might have a role in pathogenesis of malaria. As compared to individual markers, oxidative stress index was found to be significantly associated with malarial anaemia denoting its role as a better marker in these patients. Antimalarial therapy targeting the above factors might decrease the pathogenesis, morbidity and mortality in patients with malaria.
简介:氧化剂和抗氧化剂水平的改变被认为与疟疾的发病机制有关。在印度南部疟疾感染和贫血患者中,氧化应激指数与氧化剂和抗氧化状态之间的关联数据有限。目的:测定疟疾患者抗氧化剂、抗氧化剂水平和氧化应激指数及其与贫血的关系。材料与方法:本病例对照研究在印度海得拉巴奥斯马尼亚总医院生物化学科进行。根据纳入标准和排除标准,共有50名年龄在20-45岁的疟疾患者被纳入病例。对照组由50名年龄和性别匹配的健康受试者组成。用紫外分光光度计标准方法测定两组患者血红蛋白(Hb)、血清丙二醛(MDA)、超氧化物歧化酶(SOD)、总抗氧化能力(TAC)。采用独立样本t检验检验各生化指标在研究组与对照组之间的差异。采用Pearson相关法研究各参数间的相关性。结果:两组患者年龄、性别匹配(p=0.39)。与对照组相比,病例中MDA显著升高(p<0.0001)。与对照组相比,SOD、血浆铁还原能力(FRAP)、Hb显著降低(p值<0.0001)。本研究发现,疟疾患者Hb与氧化应激指数(MDA/FRAP=-0.480)呈显著负相关,p值=0.0001。结论:氧化应激可能是引起疟疾贫血的原因之一。氧化剂和抗氧化剂水平的改变可能在疟疾的发病机制中起作用。与个体标记物相比,氧化应激指数被发现与疟疾贫血显著相关,表明其在这些患者中是更好的标记物。针对上述因素进行抗疟治疗可能会降低疟疾患者的发病、发病率和死亡率。
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引用次数: 1
Study of Blood Donor Deferral in a Tertiary Care Hospital, Northern India 印度北部一家三级保健医院推迟献血者的研究
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/50423.2569
H. Bhardwaj, D. Swarup, R. Bansal
Introduction: Blood donation programme is vital to any transfusion service. Deferral is a painful and sad experience both for the donor and the centre. Thus, every blood centre has to pivot between admissible quality and desired quantity. Aim: To find out incidence and pattern of donor deferral in a tertiary care hospital, Meerut, Uttar Pradesh, India. Materials and Methods: A retrospective cross-sectional study was conducted over a period of four years from January 2016 to December 2019 in a blood bank, Department of Pathology in a tertiary care hospital of Meerut, Uttar Pradesh, India. Details of donors who were deferred either temporarily or permanently during the study period were collected from the deferral files. Data analysis was done by calculating the percentage for every cause of donor deferral. Results: Out of the 29,663 donors who registered for blood donation during the study period, 2,626 donors were deferred due to several reasons. Temporary reasons (2592) were like anaemia, medications, alcohol, allergy, low-weight, fever, tattooing and permanent causes (34) were like hypertension, cardiac disorders, diabetes, asthma and thyroid disorders. Anaemia was the most common cause for deferral and total deferral rate came out to be 8.85%. Conclusion: Studying and analysing the profile of blood donors helps to identify categories of population which could be targeted to increase pool of voluntary blood donors. Education, motivation and treatment of these deferred donors due to anaemia or other temporary causes is an important aspect in blood banking, so that these donors may be recruited again.
献血规划对任何输血服务都是至关重要的。对捐赠者和中心来说,推迟是一种痛苦和悲伤的经历。因此,每个血液中心都必须在可接受的质量和所需的数量之间进行调整。目的:了解印度北方邦密鲁特某三级医院供体延迟的发生率和模式。材料和方法:从2016年1月至2019年12月,在印度北方邦密鲁特一家三级保健医院病理学部的血库进行了一项回顾性横断面研究,为期四年。在研究期间暂时或永久推迟的捐助者的详细资料从推迟档案中收集。数据分析是通过计算供体延迟的每个原因的百分比来完成的。结果:在研究期间登记献血的29663名献血者中,2626名献血者由于多种原因而推迟献血。暂时性原因(2592人)包括贫血、药物、酒精、过敏、体重过轻、发烧、纹身等,永久性原因(34人)包括高血压、心脏病、糖尿病、哮喘和甲状腺疾病等。贫血是最常见的延期原因,总延期率为8.85%。结论:研究和分析献血者的情况有助于确定有针对性的人群类别,增加自愿献血者的数量。对这些因贫血或其他暂时原因而推迟献血者进行教育、激励和治疗是血库工作的一个重要方面,以便再次招募这些献血者。
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引用次数: 0
Severe Cystoisospora belli Diarrhoea in Post Renal Transplant Patient 肾移植术后患者的严重腹膜囊异孢子虫腹泻
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/53583.2655
S. Tewari, S. Garg, S. Garg
Cystoisospora belli (C. belli) is an opportunistic protozoal parasite. It is prevalent in tropical and subtropical areas of the world. It is frequently encountered in immunocompromised patients with Acquired Immunodeficiency Syndrome (AIDS) and other immunodeficiency illnesses. Infection usually occurs due to faecal contamination of food and water. Chronic severe watery diarrhoea occurs in C. belli infected patients. C. belli is diagnosed by demonstration of characteristic oocyst in the stool sample. The common methods used for stool examination are wet saline mount, iodine mount, and modified acid fast staining. Although C. belli is distributed worldwide and more prevalent in developing countries but not much reported from India. Most of the cases reported from India are in Human Immunodeficiency Virus (HIV)-positive patients and not many cases reported in renal transplant cases. Here, a case of 27-year old male post renal transplant patient having severe diarrhoea has been presented. Patient complaining of watery diarrhoea off and on for last one month for which he had taken some medicine from his local level but not got relieved. The patient was negative for HIV and was on immunosuppressive drugs. Stool sample of the patient examined by direct wet mount, iodine mount and acid fast staining. On microscopy characteristic oocysts of C. belli were detected. The patient was given combination treatment to which he responded well.
贝利囊异孢子虫(C. belli)是一种机会性原生动物寄生虫。它在世界热带和亚热带地区流行。它经常出现在免疫功能低下的患者获得性免疫缺陷综合征(艾滋病)和其他免疫缺陷疾病。感染通常是由于粪便污染了食物和水。慢性严重水样腹泻发生在贝利梭菌感染的病人身上。通过在粪便样本中显示特征性卵囊来诊断大肠杆菌。常用的大便检查方法有湿盐涂片、碘涂片和改良抗酸染色。虽然贝利梭菌分布在世界各地,在发展中国家更为普遍,但在印度的报道不多。印度报告的大多数病例是人类免疫缺陷病毒(HIV)阳性患者,肾移植病例报告的病例不多。这里,一个27岁的男性肾移植后患者有严重的腹泻。病人抱怨过去一个月断断续续的水样腹泻,他已经从当地药房吃了一些药,但没有缓解。该患者HIV呈阴性,正在服用免疫抑制药物。采用直接湿法、碘法和抗酸染色对患者粪便标本进行检查。显微镜下观察到贝利梭菌卵囊的特征。病人接受了综合治疗,效果很好。
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引用次数: 0
Tumour Associated Tissue Eosinophilia in Oral Squamous Cell Carcinoma by Special Histochemical Analysis of Tissue Eosinophilia using Congo Red Staining 用刚果红染色对口腔鳞状细胞癌组织嗜酸性粒细胞的特殊组织化学分析
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/53615.2617
R. Sujatha, Rufaida Shafiuddin, M. V. Kulkarni, Y. Manjunatha
Introduction: Tumour Associated Tissue Eosinophilia (TATE) is an important phenomenon occurring in the tumour microenvironment and has a pivotal role. TATE is defined as “eosinophilic stromal infiltration of a tumour not associated with tumour necrosis or ulceration”. The exact role of TATE in malignancies is yet unclear but studies have shown that TATE usually has a favourable outcome in head and neck Squamous Cell Carcinoma (SCC). Therefore, more studies are needed to substantiate this data. Aim: To compare TATE between normal epithelium and Oral Squamous Cell Carcinoma (OSCC) and compare TATE between the histological grades of OSCC. Materials and Methods: A retrospective study was conducted at Dr. BR Ambedkar Medical College, Bangalore, Karnataka, India, from June 2019-January 2021 which included 50 cases, 10 from normal mucosa and 40 histopathologically diagnosed cases of OSCC. 1% congo red solution was used to stain 4 μm thick sections. The sections were examined at a high magnification (40X) and 10 microscopic fields were examined in succession for eosinophils. The average number of eosinophils observed were compared using univariate analysis, which included the Analysis of Variance (ANOVA) test and the Chi- square test and a p-value of 0.001 was considered statistically significant. Results: The mean value of tissue eosinophils increased in OSCC compared to normal mucosa, according to present study findings. When comparing different grades of carcinoma, statistical analysis revealed that well differentiated squamous cell carcinoma had a greater TATE than other grades, which was statistically significant (p-value <0.001). Conclusion: The higher eosinophil count in well differentiated OSCC compared to the other grades could be associated with a better clinical outcome for the patient. In OSCC, TATE can be utilised as a predictor of a good prognosis.
肿瘤相关组织嗜酸性粒细胞(tumor Associated Tissue Eosinophilia, TATE)是肿瘤微环境中发生的一种重要现象,具有举足轻重的作用。TATE定义为“肿瘤嗜酸性间质浸润,与肿瘤坏死或溃疡无关”。TATE在恶性肿瘤中的确切作用尚不清楚,但研究表明,TATE在头颈部鳞状细胞癌(SCC)中通常有良好的预后。因此,需要更多的研究来证实这一数据。目的:比较正常上皮与口腔鳞状细胞癌(OSCC)的TATE,并比较OSCC组织学分级之间的TATE。材料和方法:2019年6月至2021年1月,在印度卡纳塔克邦班加罗尔的Dr. BR Ambedkar医学院进行了一项回顾性研究,其中包括50例OSCC, 10例来自正常粘膜,40例组织病理学诊断的OSCC。1%刚果红溶液对4 μm厚的切片进行染色。在高倍显微镜下(40倍)检查切片,并连续检查10个显微镜视野中的嗜酸性粒细胞。观察到的嗜酸性粒细胞的平均数量采用单因素分析进行比较,其中包括方差分析(ANOVA)检验和卡方检验,p值为0.001被认为具有统计学意义。结果:根据目前的研究结果,与正常粘膜相比,组织嗜酸性粒细胞的平均值在OSCC中增加。在比较不同级别的癌时,统计分析显示,高分化鳞状细胞癌的TATE高于其他级别,差异有统计学意义(p值<0.001)。结论:与其他级别相比,高分化OSCC中较高的嗜酸性粒细胞计数可能与患者更好的临床结果相关。在OSCC中,TATE可以作为预后良好的预测指标。
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引用次数: 0
Immunohistochemical Study of Ki-67 Labelling Index in Neoplasms of Central Nervous System 中枢神经系统肿瘤Ki-67标记指数的免疫组化研究
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/52989.2599
Anuradha G. Patil, N. Bhargava, Megha M Wadone, A. Anita
Introduction: The central nervous system tumours show a varied histopathological spectrum. The cell proliferation index may provide an objective method for assessing tumour biology. The Ki-67 is considered to be the most reliable proliferative marker predicting the tumour behaviour of various systemic and intracranial neoplasms. As it reflects tumour proliferating potential, it helps in determining the grade and hence the likelihood of recurrence. This study was carried out considering that very few studies of Ki-67 Labelling Index (LI) is seen in Central Nervous System (CNS) neoplasms collectively. Aim: To study the Ki-67 LI in CNS neoplasms and the association of Ki-67 LI with different parameters like age, sex, World Health Organisation (WHO) grading and histological types. Materials and Methods: The present descriptive analytical study was conducted at Department of Pathology, Mahadevappa Rampure Medical College, Karnataka, India, attached to a tertiary care hospital, Kalaburagi, for a period of five years between 1st Aug 2013 to 31st July 2018 after approval from the Institutional Ethics Committee. The formalin-fixed and paraffin-embedded tissue sections were stained with haematoxylin and eosin. Immunohistochemistry (IHC) was carried out with Ki-67 antibody using standard protocol. The data was analysed using IBM SPSS software version 19.0. The descriptive statistics frequency and percentages were calculated. The morphological grading of CNS tumours was done and the distribution of Ki-67 LI values were analysed. Results: A total of 102 histopathologically diagnosed primary CNS tumours were included in the study. High incidence of CNS neoplasms was seen in 3rd to 4th decade with slight male preponderance. This study included 40 meningioma cases. Mean percentages of Ki-67 LI for grade I and grade II meningiomas were 3.3% and 4%, respectively. The Ki-67 mean value for Astrocytomas grade I was 5.6% and grade II was 8.7%. Grade IV Glioblastoma and Gliosarcoma showed mean value of 18% and 18.8%, respectively. It was observed that LI increased with increase in grade of the tumour. Schwannoma and Dysembryoplastic Neuroepethelial Tumour (DNET) showed Ki-67 LI of 2.9% and 2.6%, respectively. Mean value of Ki-67 LI of other primary CNS neoplasms were as follows: Medulloblastoma 53%, Atypical Teratoid/Rhabdoid Tumour (ATRT) 32%, Haemangiopericytoma 8%, Neurocytoma 4%, Malignant Peripheral Nerve Sheath Tumour (MPNST) 3%, Ganglioglioma 4% and Haemangioblastoma 4%. Conclusion: The Ki-67 LI is the simplest and the most reliable method for evaluating the cell proliferation. It has a great value in designating the exact grade of the tumour when used in combination with histopathological features. It can also be used for planning of adjuvant therapy in primary CNS neoplasms.
导言:中枢神经系统肿瘤表现出不同的组织病理谱。细胞增殖指数可为评价肿瘤生物学提供一种客观的方法。Ki-67被认为是预测各种全身和颅内肿瘤行为的最可靠的增殖标志物。由于它反映了肿瘤的增殖潜力,因此有助于确定肿瘤的级别和复发的可能性。本研究是考虑到Ki-67标记指数(LI)在中枢神经系统(CNS)肿瘤中的研究很少。目的:探讨中枢神经系统肿瘤的Ki-67 LI水平,以及Ki-67 LI与年龄、性别、世界卫生组织(WHO)分级及组织学类型的关系。材料和方法:经机构伦理委员会批准,本描述性分析研究于2013年8月1日至2018年7月31日在印度卡纳塔克邦Mahadevappa Rampure医学院病理学系进行,该医学院隶属于Kalaburagi三级保健医院,为期五年。福尔马林固定切片和石蜡包埋切片分别用苏木精和伊红染色。用Ki-67抗体按标准方案进行免疫组化(IHC)。采用IBM SPSS 19.0软件对数据进行分析。计算描述性统计频率和百分比。对中枢神经系统肿瘤进行形态学分级,分析Ki-67 LI值的分布。结果:本研究共纳入102例经组织病理学诊断的原发性中枢神经系统肿瘤。中枢神经系统肿瘤的高发见于第3至第4年,男性略占优势。本研究包括40例脑膜瘤病例。I级和II级脑膜瘤Ki-67 LI的平均百分比分别为3.3%和4%。星形细胞瘤I级Ki-67平均值为5.6%,II级为8.7%。IV级胶质母细胞瘤和胶质肉瘤的平均值分别为18%和18.8%。我们观察到LI随肿瘤分级的增加而增加。神经鞘瘤和胚胎发育异常神经上皮瘤Ki-67 LI分别为2.9%和2.6%。其他原发性中枢神经系统肿瘤Ki-67 LI平均值为:髓母细胞瘤53%,非典型畸胎瘤/横纹肌样瘤(ATRT) 32%,血管外皮细胞瘤8%,神经细胞瘤4%,恶性周围神经鞘瘤(MPNST) 3%,神经节胶质瘤4%,血管母细胞瘤4%。结论:Ki-67 LI是评价细胞增殖最简单、最可靠的方法。当与组织病理学特征结合使用时,它在指定肿瘤的确切分级方面具有很大的价值。它也可用于原发性中枢神经系统肿瘤的辅助治疗计划。
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引用次数: 0
Descriptive Study of the Spectrum of Disorders Presenting as Normocytic Normochromic Anaemia from a Tertiary Care Setting at Ernakulam, Kerala, India 在印度喀拉拉邦埃纳库拉姆的三级保健机构中,描述了以正红细胞、正色贫血为表现的疾病谱
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/53145.2601
Unnikrishnan Govind, Febby K Philip
Introduction: Anaemia is a common problem discovered on routine laboratory tests. Based on red cell morphology, anaemia can be classified as microcytic hypochromic, macrocytic and Normocytic Normochromic Anaemia (NNA). Anaemia is not a diagnosis in itself, but merely an objective sign of underlying disease. The correct treatment requires an understanding of the pathogenesis of the condition. Varied number of clinical disorders manifests as NNA and pose a great challenge to the clinician. Aim: To identify the spectrum of disorders presenting as NNA and to grade anaemia across age and sex of individual using World Health Organisation (WHO) criteria. Materials and Methods: This prospective descriptive study was conducted in a tertiary care teaching hospital, Ernakulam, Kerala, India during one year period of February 2017-January 2018. Total of 514 patients meeting the inclusion criteria were recruited for the study. After taking detailed history and clinical examination, investigations were done including Complete Blood Count (CBC), peripheral smear preparation, reticulocyte count, Renal Function Tests (RFT), Liver Function Tests (LFT) and if necessary, bone marrow study and radiological studies were done. The data obtained was statistically analysed using Microsoft Excel 365. Descriptive statistics viz., number of cases, percentage, concomitant involvement with other disorders, differential involvement with various age groups, male:female ratio, and grade of anaemia were utilised to describe the spectrum of disorders presenting as NNA. Results: Of the 514 patients, 433 were adults and 81 were in paediatric age group. The average age in adult males were 58 years and in females 57 years with Haemoglobin (Hb) being 9.04 g/dL and 8.99 g/dL, respectively. Paediatric population had an average Hb of 10.18 g/dL. A total of 106 conditions were seen among the 514 patients. The disease conditions were further categorised into 10 subtypes. Type 2 Diabetes Mellitus (T2DM) constituted single most common associated disorder (112 cases) seen along NNA followed by Coronary Artery Disease (CAD) (74 cases). Idiopathic cases constituted 79 cases. Conclusion: The NNA constituted 25% of the cases presented to the laboratory during the study period. T2DM was associated with NNA along with CAD. An understanding of the categories of anaemia along with a diagnostic protocol will go a long way in better management of the patient.
简介:贫血是在常规实验室检查中发现的常见问题。根据红细胞形态,贫血可分为小细胞性低色性贫血、大细胞性贫血和正色性贫血(NNA)。贫血本身并不是一种诊断,而仅仅是潜在疾病的客观迹象。正确的治疗需要了解病情的发病机制。不同种类的临床疾病表现为NNA,对临床医生提出了巨大的挑战。目的:确定表现为NNA的疾病谱系,并使用世界卫生组织(WHO)标准对个体的年龄和性别进行贫血分级。材料和方法:本前瞻性描述性研究于2017年2月至2018年1月在印度喀拉拉邦埃纳库拉姆的一家三级护理教学医院进行。共有514名符合纳入标准的患者被纳入研究。在详细的病史和临床检查后,进行了调查,包括全血细胞计数(CBC)、外周涂片准备、网织红细胞计数、肾功能检查(RFT)、肝功能检查(LFT),必要时还进行了骨髓检查和放射学检查。所得数据采用Microsoft Excel 365进行统计分析。描述性统计数据,即病例数、百分比、与其他疾病的合并、不同年龄组的不同累及、男女比例和贫血等级,被用于描述以NNA表现的疾病谱。结果:514例患者中,成人433例,儿童81例。成年男性平均年龄58岁,女性平均年龄57岁,血红蛋白(Hb)分别为9.04 g/dL和8.99 g/dL。儿科人群平均Hb为10.18 g/dL。514名患者共出现106种情况。将疾病状况进一步分为10个亚型。2型糖尿病(T2DM)是沿NNA最常见的相关疾病(112例),其次是冠状动脉疾病(CAD)(74例)。特发性病例79例。结论:NNA占研究期间提交实验室的病例的25%。T2DM与NNA及CAD相关。了解贫血的种类以及诊断方案将对更好地管理患者大有帮助。
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引用次数: 0
Clinical Epidemiology of Multidrug Resistant Tuberculosis in a Nodal Drug Resistant- TB Centre in Southern Odisha: A Cross-sectional Study 南奥里萨邦结核结核结核结核结核结核结核结核结核结核结核临床流行病学:横断面研究
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/53247.2591
Nisith Kr Das, Abinash Panda
Introduction: Multidrug-Resistant Tuberculosis (MDR-TB) is a significant public health problem. The number of MDR-TB cases is very high in India and the management is inadequate due to resource constraints. The assessment of MDR-TB burden has to be reliable for programmatic management of MDR-TB under the Revised National Tuberculosis Control Program (RNTCP) of India. Aim: To find the clinico-demographic profile and pattern of MDR-TB among the tuberculosis patients reporting to a nodal tuberculosis centre in Southern Odisha, India. Materials and Methods: The patient record based cross-sectional study was carried out on a convenience sample of 125 sputum positive MDR-TB cases admitted to the Directly Observed Treatment Short-course (DOTS) plus centre of the Nodal Tuberculosis Centre at Berhampur, Odisha, India, during the period from April 2017 to March 2018. A predesigned case record form was used to collect data on the socio-demographic profile, addictions, co-morbidity, Human Immunodeficiency Virus (HIV) status, Bacille Calmette-Guerin (BCG) immunisation status, pattern of drug resistance, history of anti-TB treatment, presenting symptoms at admission, adverse drug reactions observed during the treatment for MDR-TB. The data was analysed using GraphPad Prism trial version 7.0. Descriptive statistics were used to present the final data. Results: Highest number of study participants (95, 76%) were within 18-45 years age group and 90 (72%) of the patients were males. Rural habitation (90, 72%), engagement in labour works (65, 52%), low socio-economic status (75, 60%) were the common socio-economic characteristics. Resistance to rifampicin was the commonest variety 101 (80.8%) and 80 (64%) were newly diagnosed cases of tuberculosis. The commonest presenting symptom was cough in 97 (77.6%) patients and gastrointestinal upset was the commonest adverse drug reaction encountered during therapy. Conclusion: The MDR-TB affects the population in their most productive age. Rifampicin resistant TB was the predominant variety observed in the study population. The MDR-TB can be successfully treated with maximally effective and complete drug regimes.
耐多药结核病(MDR-TB)是一个重大的公共卫生问题。印度的耐多药结核病病例数量非常高,由于资源限制,管理工作不足。根据印度修订的国家结核病控制规划(RNTCP),耐多药结核病负担评估必须是可靠的,以便对耐多药结核病进行规划管理。目的:了解印度南奥里萨邦结核中心结核患者耐多药结核病的临床人口统计学特征和模式。材料和方法:在2017年4月至2018年3月期间,对印度奥里萨邦Berhampur淋巴结结核中心直接观察短程治疗(DOTS)加中心收治的125例痰阳性耐多药结核病患者进行了基于患者记录的横断面研究。使用预先设计的病例记录表收集有关社会人口统计学概况、成瘾、合并症、人类免疫缺陷病毒(HIV)状况、卡介苗(BCG)免疫状况、耐药模式、抗结核治疗史、入院时出现症状、耐多药结核病治疗期间观察到的药物不良反应等数据。使用GraphPad Prism 7.0试用版分析数据。最终数据采用描述性统计。结果:18-45岁年龄组的患者最多(95例,76%),其中90例(72%)为男性。农村居住(90,72%)、从事劳动(65,52%)、社会经济地位低(75,60%)是共同的社会经济特征。以利福平耐药最为常见,其中101例(80.8%)和80例(64%)为新诊断结核病例。97例(77.6%)患者最常见的临床表现为咳嗽,胃肠道不适是治疗过程中最常见的药物不良反应。结论:耐多药结核病主要发生在最具生产能力的年龄段。利福平耐药结核病是研究人群中观察到的主要品种。通过最有效和最完整的药物制度,可以成功治疗耐多药结核病。
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引用次数: 0
Langerhans Cell Histiocytosis without Eosinophilia and Lytic Lesions of Bone: A Rare Disease with Unusual Presentation 朗格汉斯细胞组织细胞增多症无嗜酸性粒细胞增多和骨溶解性病变:一种罕见的疾病与不寻常的表现
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/55124.2637
S. Chauhan, Sunita Sharma, Smita Singh, S. Mukherjee
LCH is a disease of abnormal clonal proliferation of langerhans cell of the bone marrow derived monocyte-macrophage lineage. Cells with characteristic coffee bean / grooved / indented nuclei with a background of histiocytes, lymphocytes, eosinophils and other inflammatory cells are seen. Clinical presentation varies from unifocal unisystem to multifocal unisystem to multifocal multisystem. We present a rare case of multisystem LCH involving high risk organs in a two and a half year old child. presented with the chief complaints of fever and red raised maculopapular lesions on trunk, palm, forehead and scalp for one and a half yrs with hepatosplenomegaly. There were no lytic lesions of the bones. Hematological parameters showed anaemia with thrombocytopenia while Bone Marrow Aspirate showed increase in histiocytic cell with some cells showing characteristic coffee bean, cleaved irregularly contoured nuclei. However, eosinophilia was not seen. Sections from the skin lesions showed cells with similar morphology without usually accompanied eosinophilia. The cells were CD1a and S100 positive. So a FINAL DIAGNOSIS of langerhans cell histiocytosis was made. The emphasis here lies on thorough analysis of the clinical presentations, imaging studies and scrupulous histomorphological and immunohistochemical examination, so that early diagnosis and timely intervention is ensured in such cases where the characteristic features like lytic lesions of bone and eosinophilia is not found.
LCH是一种来源于骨髓的单核-巨噬细胞谱系的朗格汉斯细胞异常克隆增生的疾病。细胞具有特征性的咖啡豆/沟槽/凹痕核,背景有组织细胞、淋巴细胞、嗜酸性粒细胞和其他炎症细胞。临床表现从单焦点单系统到多焦点单系统到多焦点多系统不等。我们报告一例罕见的涉及高危器官的多系统LCH病例,患者为两岁半的儿童。主诉为发热,躯干、手掌、前额和头皮上红色凸起的黄斑丘疹病变一年半,伴肝脾肿大。骨头没有溶解性损伤。血液学指标显示贫血伴血小板减少,骨髓抽吸显示组织细胞增多,部分细胞呈特有的咖啡豆状,细胞核呈不规则形状。但未见嗜酸性粒细胞增多。皮肤病变切片显示细胞形态相似,通常不伴有嗜酸性粒细胞增多。细胞CD1a和S100阳性。最终诊断为朗格汉斯细胞组织细胞增多症。重点在于充分分析临床表现、影像学检查,仔细进行组织形态学和免疫组化检查,在未发现骨溶解性病变、嗜酸性粒细胞增多等特征性表现的情况下,确保早期诊断和及时干预。
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引用次数: 0
Clinicopathological Spectrum of Salivary Gland Lesions - A Retrospective Study from Tertiary Care Research Institute, Andhra Pradesh 唾液腺病变的临床病理谱-来自安得拉邦三级保健研究所的回顾性研究
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/55950.2651
Sanuvada Vijay Rama Raja Sekhar, Regidi Swathi Ratnam, B. Gouthami, B. R. Chandra
Introduction: The salivary glands are subjected to various pathological conditions ranging from simple inflammation to most complex malignant lesions. Majority of these lesions can be diagnosed by simple histopathological examination. But, as these salivary gland lesions are not common, the incidence of these varies in different geographic locations. Aim: To study the spectrum of different salivary gland lesions and demographic data in a tertiary care hospital serving North East coastal area of Andhra Pradesh. Materials and Methods: This was a retrospective study conducted in Great Eastern Medical School and Hospital,Srikakulam, Andhra Pradesh, India. Total of 85 salivary gland lesions were analyzed for a period of 4 years (December 2015 to November 2019). From the records of Histopathology, Department of Pathology, data was retrieved. Typing of the salivary gland tumours were done using sections stained with Hematoxylin and Eosin (H&E). All the cases were analysed and divided according to the demographics and histological type. Descriptive statistics were used and data was tabulated in frequency and percentages. Results: A total of 85 salivary gland lesions were studied, of which 14 (16%) were non-neoplastic and 71 (84%) were neoplastic in nature. Among the neoplastic lesions, 56 (66%) were benign and 15 (18%) were malignant. There was slight male preponderance with a ratio of M:F=1.3:1. Majority of the tumours occurred in parotid gland (73), followed by submandibular gland (7) and minor salivary glands (5). All the tumours were classified and graded according to World Health Organization (WHO), while Brandwein Grading System was followed for mucoepidermoid carcinoma. Pleomorphic adenoma was the most frequent benign tumour and mucoepidermoid carcinoma was the most common malignant tumour. Conclusion: Though benign salivary gland tumours are more frequently encountered in the present study, malignant salivary gland tumours are not uncommon.
唾液腺遭受各种病理条件,从简单的炎症到最复杂的恶性病变。大多数病变可通过简单的组织病理学检查诊断。但是,由于这些唾液腺病变并不常见,这些发病率在不同的地理位置有所不同。目的:研究安得拉邦东北沿海地区某三级医院不同唾液腺病变的频谱和人口统计数据。材料和方法:本研究是在印度安得拉邦Srikakulam的大东方医学院和医院进行的回顾性研究。分析了4年(2015年12月至2019年11月)共85例唾液腺病变。从病理科组织病理学记录中检索数据。用苏木精和伊红(H&E)染色切片对涎腺肿瘤进行分型。根据人口统计学和组织学类型对所有病例进行分析和分类。采用描述性统计,数据以频率和百分比制成表格。结果:共85例唾液腺病变,其中非肿瘤性病变14例(16%),肿瘤性病变71例(84%)。其中良性56例(66%),恶性15例(18%)。男性有轻微优势,比例为M:F=1.3:1。大多数肿瘤发生在腮腺(73例),其次是颌下腺(7例)和少量唾液腺(5例)。所有肿瘤均按照世界卫生组织(WHO)分类和分级,粘液表皮样癌采用Brandwein分级系统。多形性腺瘤是最常见的良性肿瘤,粘液表皮样癌是最常见的恶性肿瘤。结论:虽然良性涎腺肿瘤在本研究中更为常见,但恶性涎腺肿瘤也不罕见。
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引用次数: 0
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National Journal of Laboratory Medicine
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